Prof. A.A.M. Wilde PhD publications

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Publications Prof. PhD A.A.M. Wilde

Position
Full Professor
Main activities
Patient care, Research, Other
Specialisation
Clinical aspects of heart failure and arrhythmias
Focus of research
  • Arrhythmias
  • Cardiomyopathy
  • Electrophysiology
  • Genetics
  • Sudden death

2021

  • Stiles Martin K, Wilde Arthur A M, Abrams Dominic J, Ackerman Michael J, Albert Christine M, Behr Elijah R, Chugh Sumeet S, Cornel Martina C, Gardner Karen, Ingles Jodie, James Cynthia A, Jimmy Juang Jyh-Ming, Kääb Stefan, Kaufman Elizabeth S, Krahn Andrew D, Lubitz Steven A, MacLeod Heather, Morillo Carlos A, Nademanee Koonlawee, Probst Vincent, Saarel Elizabeth V, Sacilotto Luciana, Semsarian Christopher, Sheppard Mary N, Shimizu Wataru, Skinner Jonathan R, Tfelt-Hansen Jacob, Wang Dao Wu 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families Heart rhythm 2021;18 (1):e1-e50 [PubMed]
  • Jansen M., Christiaans I., van der Crabben S. N., Michels M., Huurman R., Hoedemaekers Y. M., Dooijes D., Jongbloed J. D. H., Boven L. G., Lekanne Deprez R. H., Wilde A. A. M., Jans J. J. M., van der Velden J., de Boer R. A., van Tintelen J. P., Asselbergs F. W., Baas A. F. BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status Netherlands heart journal 2021 [PubMed]
  • Bleijendaal Hidde, Ramos Lucas A, Lopes Ricardo R, Verstraelen Tom E, Baalman Sarah W E, Oudkerk Pool Marinka D, Tjong Fleur V Y, Melgarejo-Meseguer Francisco M, Gimeno-Blanes F Javier, Gimeno-Blanes Juan R, Amin Ahmad S, Winter Michiel M, Marquering Henk A, Kok Wouter E M, Zwinderman Aeilko H, Wilde Arthur A M, Pinto Yigal M Computer versus cardiologist: Is a machine learning algorithm able to outperform an expert in diagnosing a phospholamban p.Arg14del mutation on the electrocardiogram? Heart rhythm 2021;18 (1):79-87 [PubMed]
  • Sarcon Anna, Hsia Henry, Postema Pieter G., Wilde Arthur A. M., Patocskai Bence, di Diego José M., Antzelevitch Charles, Scheinman Melvin Fractionated Epicardial Electrograms: Implication for Mechanism of the Brugada Pattern JACC. Clinical electrophysiology 2021;7 (2):258-270
  • van der Ree Martijn H., Vendrik Jeroen, Kors Jan A., Amin Ahmad S., Wilde Arthur A. M., Tan Hanno L., Postema Pieter G. Left axis deviation in brugada syndrome: Vectorcardiographic evaluation during ajmaline provocation testing reveals additional depolarization abnormalities International journal of molecular sciences 2021;22 (2):1-9 [PubMed]
  • Cadrin-Tourigny Julia, Bosman Laurens P., Wang Weijia, Tadros Rafik, Bhonsale Aditya, Bourfiss Mimount, Lie Øyvind H., Saguner Ardan M., Svensson Anneli, Andorin Antoine, Tichnell Crystal, Murray Brittney, Zeppenfeld Katja, van den Berg Maarten P., Asselbergs Folkert W., Wilde Arthur A. M., Krahn Andrew D., Talajic Mario, Rivard Lena, Chelko Stephen, Zimmerman Stefan L., Kamel Ihab R., Crosson Jane E., Judge Daniel P., Yap Sing-Chien, van der Heijden Jeroen F., Tandri Harikrishna, Jongbloed Jan D. H., van Tintelen J. Peter, Platonov Pyotr G., Duru Firat, Haugaa Kristina H., Khairy Paul, Hauer Richard N. W., Calkins Hugh, te Riele Anneline S. J. M., James Cynthia A. Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration Circulation. Arrhythmia and electrophysiology 2021;14 (1):e008509 [PubMed]

2020

  • Pflaumer Andreas, Wilde Arthur A. M., Charafeddine Fatme, Davis Andrew M. 50 Years of Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) – Time to Explore the Dark Side of the Moon Heart, lung & circulation 2020;29 (4):520-528 [PubMed]
  • Vink Arja Suzanne, Clur Sally-Ann B. , Postema Pieter G. , Blom Nico A. , Wilde Arthur A. M. Age, Sex and Racial Differences in Cardiac Repolarization and Arrhythmogenesisin: Nabil El-Sherif, editors. Cardiac Repolarization, Basic Science and Clinical Management. Springer; 2020. p. 119-130, ISBN 9783030226718
  • Wilde Arthur A. M., Lodder Elisabeth M. A highly specific biomarker for Brugada syndrome. Also too good to be true? European heart journal 2020;41 (28):2891-2893 [PubMed]
  • Adler Arnon, Novelli Valeria, Amin Ahmad S., Abiusi Emanuela, Care Melanie, Nannenberg Eline A., Feilotter Harriet, Amenta Simona, Mazza Daniela, Bikker Hennie, Sturm Amy C., Garcia John, Ackerman Michael J., Hershberger Raymond E., Perez Marco V., Zareba Wojciech, Ware James S., Wilde Arthur A. M., Gollob Michael H. An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome Circulation 2020;141 (6):418-428 [PubMed]
  • Ng Kevin, Titus Erron W., Lieve Krystien V., Roston Thomas M., Mazzanti Andrea, Deiter Frederick H., Denjoy Isabelle, Ingles Jodie, Till Jan, Robyns Tomas, Connors Sean P., Steinberg Christian, Abrams Dominic J., Pang Benjamin, Scheinman Melvin M., Bos J. Martijn, Duffett Stephen A., van der Werf Christian, Maltret Alice, Green Martin S., Rutberg Julie, Balaji Seshadri, Cadrin-Tourigny Julia, Orland Kate M., Knight Linda M., Brateng Caitlin, Wu Jeremy, Tang Anthony S., Skanes Allan C., Manlucu Jaimie, Healey Jeff S., January Craig T., Krahn Andrew D., Collins Kathryn K., Maginot Kathleen R., Fischbach Peter, Etheridge Susan P., Eckhardt Lee L., Hamilton Robert M., Ackerman Michael J., Noguer Ferran Rosés I., Semsarian Christopher, Jura Natalia, Leenhardt Antoine, Gollob Michael H., Priori Silvia G., Sanatani Shubhayan, Wilde Arthur A. M., Deo Rahul C., Roberts Jason D. An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia Circulation 2020;142 (10):932-947 [PubMed]
  • Roberts Jason D., Asaki S. Yukiko, Mazzanti Andrea, Bos J. Martijn, Tuleta Izabela, Muir Alison R., Crotti Lia, Krahn Andrew D., Kutyifa Valentina, Shoemaker M. Benjamin, Johnsrude Christopher L., Aiba Takeshi, Marcondes Luciana, Baban Anwar, Udupa Sharmila, Dechert Brynn, Fischbach Peter, Knight Linda M., Vittinghoff Eric, Kukavica Deni, Stallmeyer Birgit, Giudicessi John R., Spazzolini Carla, Shimamoto Keiko, Tadros Rafik, Cadrin-Tourigny Julia, Duff Henry J., Simpson Christopher S., Roston Thomas M., Wijeyeratne Yanushi D., el Hajjaji Imane, Yousif Maisoon D., Gula Lorne J., Leong-Sit Peter, Chavali Nikhil, Landstrom Andrew P., Marcus Gregory M., Dittmann Sven, Wilde Arthur A. M., Behr Elijah R., Tfelt-Hansen Jacob, Scheinman Melvin M., Perez Marco V., Kaski Juan Pablo, Gow Robert M., Drago Fabrizio, Aziz Peter F., Abrams Dominic J., Gollob Michael H., Skinner Jonathan R., Shimizu Wataru, Kaufman Elizabeth S., Roden Dan M., Zareba Wojciech, Schwartz Peter J., Schulze-Bahr Eric, Etheridge Susan P., Priori Silvia G., Ackerman Michael J. An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition Circulation 2020;141 (6):429-439 [PubMed]
  • Proost Virginnio M., Wilde Arthur A. M. Arrhythmogenic cardiomyopathyin: Martin Green, Andrew Krahn, Wael Alqarawi, editors. Electrocardiography of inherited arrhythmias and cardiomyopathies. Cham, Switzerland: Springer; 2020. p. 85-115, ISBN 9783030521721
  • Wilde Arthur A. M., Lodder Elisabeth M. Biomarkers in inherited arrhythmias: necessity for validation and collaboration European heart journal 2020;41 (47):4523-4524 [PubMed]
  • van der Ree Martijn H., Blanck Oliver, Limpens Jacqueline, Lee Charlie H., Balgobind Brian V., Dieleman Edith M. T., Wilde Arthur A. M., Zei Paul C., de Groot Joris R., Slotman Ben J., Cuculich Phillip S., Robinson Clifford G., Postema Pieter G. Cardiac radioablation—A systematic review Heart rhythm 2020;17 (8):1381-1392 [PubMed]
  • Wilde A. A. M., Nannenberg E., van der Werf C. Cardiogenetics, 25 years a growing subspecialism Netherlands heart journal 2020;28:39-43 [PubMed]
  • Roston Thomas M., van der Werf Christian, Cheung Christopher C., Grewal Jasmine, Davies Brianna, Wilde Arthur A. M., Krahn Andrew D. Caring for the pregnant woman with an inherited arrhythmia syndrome Heart rhythm 2020;17 (2):341–348 [PubMed]
  • Haanschoten D. M., Elvan A., Postema P. G., Smit J. J. J., Adiyaman A., ter Bekke R. M. A., Asaad N., Aanhaanen W. T. J., Misier A. R. Ramdat, Delnoy P. P. H. M., Crijns H. J. G. M., Wilde A. A. M. Catheter ablation in highly symptomatic Brugada patients: a Dutch case series Clinical research in cardiology 2020;109 (5):560-569 [PubMed]
  • Dijk Frederike Clinical implications of innovative pacemaker and defibrillator options 2020. 222p. ISBN 9789402818390. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Boersma Lucas, Wilde Arthur A. M.)
  • Makarawate Pattarapong, Glinge Charlotte, Khongphatthanayothin Apichai, Walsh Roddy, Mauleekoonphairoj John, Amnueypol Montawatt, Prechawat Somchai, Wongcharoen Wanwarang, Krittayaphong Rungroj, Anannab Alisara, Lichtner Peter, Meitinger Thomas, Tjong Fleur V Y, Lieve Krystien V V, Amin Ahmad S, Sahasatas Dujdao, Ngarmukos Tachapong, Wichadakul Duangdao, Payungporn Sanchai, Sutjaporn Boosamas, Wandee Pharawee, Poovorawan Yong, Tfelt-Hansen Jacob, Tanck Michael W T, Tadros Rafik, Wilde Arthur A M, Bezzina Connie R, Veerakul Gumpanart, Nademanee Koonlawee Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand Heart rhythm 2020;17 (12):2145-2153 [PubMed]
  • Postema Pieter G., Schwartz Peter J., Arbelo Elena, Bannenberg Wilbert J., Behr Elijah R., Belhassen Bernard, Brugada Josep, Brugada Pedro, John Camm A., Casado-Arroyo Ruben, 't Hoen Ellen, Hollak Carla E. M., Kääb Stefan, Lambiase Pier D., Leenhardt Antoine, Priori Silvia G., Probst Vincent, Stunnenberg Bas C., Tfelt-Hansen Jacob, van Engelen Baziel G. M., Veltmann Christian, Viskin Sami, Wilde Arthur A. M. Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine European heart journal 2020;41 (5):614-617 [PubMed]
  • Conte Giulio, Scherr Daniel, Lenarczyk Radoslaw, Gandjbachkh Estelle, Boulé Stéphane, Spartalis Michael D., Behr Elijah R., Wilde Arthur, Potpara Tatjana Diagnosis, family screening, and treatment of inherited arrhythmogenic diseases in Europe: results of the European Heart Rhythm Association Survey EP Europace 2020;22 (12):1904-1910 [PubMed]
  • Lahrouchi Najim Dissecting genetic risk in common and rare inherited disorders 2020. 394p. ISBN 9789464160925. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Bezzina Connie, Wilde Arthur A. M.)
  • Taha Karim, te Rijdt Wouter P., Verstraelen Tom E., Cramer Maarten J., de Boer Rudolf A., de Bruin-Bon Rianne H. A. C. M., Bouma Berto J., Asselbergs Folkert W., Wilde Arthur A. M., van den Berg Maarten P., Teske Arco J. Early Mechanical Alterations in Phospholamban Mutation Carriers: Identifying Subclinical Disease Before Onset of Symptoms JACC. Cardiovascular imaging 2020 [PubMed]
  • Offerhaus Joost A., Bezzina Connie R., Wilde Arthur A. M. Epidemiology of inherited arrhythmias Nature reviews. Cardiology 2020;17 (4):205-215 [PubMed]
  • Nielsen Jens Cosedis, Lin Yenn-Jiang, de Oliveira Figueiredo Marcio Jansen, Sepehri Shamloo Alireza, Alfie Alberto, Boveda Serge, Dagres Nikolaos, di Toro Dario, Eckhardt Lee L., Ellenbogen Kenneth, Hardy Carina, Ikeda Takanori, Jaswal Aparna, Kaufman Elizabeth, Krahn Andrew, Kusano Kengo, Kutyifa Valentina, Lim Han S., Lip Gregory Y. H., Nava-Townsend Santiago, Pak Hui-Nam, Rodríguez Diez Gerardo, Sauer William, Saxena Anil, Svendsen Jesper Hastrup, Vanegas Diego, Vaseghi Marmar, Wilde Arthur, Bunch T. Jared, Buxton Alfred E., Calvimontes Gonzalo, Chao Tze-Fan, Eckardt Lars, Estner Heidi, Gillis Anne M., Isa Rodrigo, Kautzner Josef, Maury Philippe, Moss Joshua D., Nam Gi-Byung, Olshansky Brian, Pava Molano Luis Fernando, Pimentel Mauricio, Prabhu Mukund, Tzou Wendy S., Sommer Philipp, Swampillai Janice, Vidal Alejandro, Deneke Thomas, Hindricks Gerhard European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population EP Europace 2020;22 (8):1147-1148 [PubMed]
  • Nielsen Jens Cosedis, Lin Yenn-Jiang, de Oliveira Figueiredo Marcio Jansen, Sepehri Shamloo Alireza, Alfie Alberto, Boveda Serge, Dagres Nikolaos, di Toro Dario, Eckhardt Lee L., Ellenbogen Kenneth, Hardy Carina, Ikeda Takanori, Jaswal Aparna, Kaufman Elizabeth, Krahn Andrew, Kusano Kengo, Kutyifa Valentina, S. Lim Han, Lip Gregory Y. H., Nava-Townsend Santiago, Pak Hui-Nam, Rodríguez Diez Gerardo, Sauer William, Saxena Anil, Svendsen Jesper Hastrup, Vanegas Diego, Vaseghi Marmar, Wilde Arthur, Bunch T. Jared European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population Journal of arrhythmia 2020;36 (4):553-607 [PubMed]
  • Nielsen Jens Cosedis, Lin Yenn-Jiang, de Oliveira Figueiredo Marcio Jansen, Sepehri Shamloo Alireza, Alfie Alberto, Boveda Serge, Dagres Nikolaos, di Toro Dario, Eckhardt Lee L., Ellenbogen Kenneth, Hardy Carina, Ikeda Takanori, Jaswal Aparna, Kaufman Elizabeth, Krahn Andrew, Kusano Kengo, Kutyifa Valentina, Lim Han S., Lip Gregory Y. H., Nava-Townsend Santiago, Pak Hui-Nam, Diez Gerardo Rodríguez, Sauer William, Saxena Anil, Svendsen Jesper Hastrup, Vanegas Diego, Vaseghi Marmar, Wilde Arthur, Bunch T. Jared, Buxton Alfred E., Calvimontes Gonzalo, Chao Tze-Fan, Eckardt Lars, Estner Heidi, Gillis Anne M., Isa Rodrigo, Kautzner Josef, Maury Philippe, Moss Joshua D., Nam Gi-Byung, Olshansky Brian, Pava Molano Luis Fernando, Pimentel Mauricio, Prabhu Mukund, Tzou Wendy S., Sommer Philipp, Swampillai Janice, Vidal Alejandro, Deneke Thomas, Hindricks Gerhard European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population Heart rhythm 2020;17 (9):e269-e316 [PubMed]
  • Li Zongzhe, Chen Peng, Li Chenze, Tan Lun, Xu Jinchao, Wang Hong, Sun Yang, Wang Yan, Zhao Chunxia, Link Mark S., Wilde Arthur A. M., Wang Dao Wu, Wang Dao Wen Genetic arrhythmias complicating patients with dilated cardiomyopathy Heart rhythm 2020;17 (2):305-312 [PubMed]
  • Giudicessi John R., Roden Dan M., Wilde Arthur A. M., Ackerman Michael J. Genetic Susceptibility for COVID-19-Associated Sudden Cardiac Death in African Americans Heart rhythm 2020;17 (9):1487-1492 [PubMed]
  • Lieve Krystien V. V., Dusi Veronica, van der Werf Christian, Bos J. Martijn, Lane Conor M., Stokke Mathis Korseberg, Roston Thomas M., Djupsjöbacka Aurora, Wada Yuko, Denjoy Isabelle, Bundgaard Henning, Noguer Ferran Roses I., Semsarian Christopher, Robyns Tomas, Hofman Nynke, Tanck Michael W., van den Berg Maarten P., Kammeraad Janneke A. E., Krahn Andrew D., Clur Sally-Ann B., Sacher Frederic, Till Jan, Skinner Jonathan R., Tfelt-Hansen Jacob, Probst Vincent, Leenhardt Antoine, Horie Minoru, Swan Heikki, Roberts Jason D., Sanatani Shubhayan, Haugaa Kristina H., Schwartz Peter J., Ackerman Michael J., Wilde Arthur A. M. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Circulation. Arrhythmia and electrophysiology 2020;13 (3):e007471 [PubMed]
  • Wilde Arthur A M Importance of Validating Guideline Recommendations Circulation journal 2020;84 (12):2136-2137 [PubMed]
  • Hermans Ben J. M., Bennis Frank C., Vink Arja S., Koopsen Tijmen, Lyon Aurore, Wilde Arthur A. M., Nuyens Dieter, Robyns Tomas, Pison Laurent, Postema Pieter G., Delhaas Tammo Improving long QT syndrome diagnosis by a polynomial-based T-wave morphology characterization Heart rhythm 2020;17 (5):752-758 [PubMed]
  • van der Stuijt Willeke, Quast Anne-Floor B. E., Baalman Sarah W. E., Olde Nordkamp Louise R. A., Wilde Arthur A. M., Knops Reinoud E. Improving the care for female subcutaneous ICD patients: A qualitative study of gender-specific issues International journal of cardiology 2020;317:91-95 [PubMed]
  • Peltenburg Puck J., Blom Nico A., Vink Arja S., Kammeraad Janneke A. E., Breur Hans J. M. P. J., Rammeloo Lukas A. J., Wilde Arthur A. M., Clur Sally-Ann B. In Children and Adolescents from Brugada Syndrome-Families, only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced by Fever Circulation 2020;142 (1):89-91 [PubMed]
  • Schwartz Peter J., Ackerman Michael J., Antzelevitch Charles, Bezzina Connie R., Borggrefe Martin, Cuneo Bettina F., Wilde Arthur A. M. Inherited cardiac arrhythmias Nature reviews. Disease primers 2020;6 (1) [PubMed]
  • Wilde Arthur A. M. Listen to your patient and act on the triggersin: Cardiac Electrophysiology. Springer International Publishing; 2020. p. 191-193, ISBN 9783030285319
  • Cuneo Bettina F., Kaizer Alexander M., Clur Sally Ann, Swan Heikki, Herberg Ulrike, Winbo Annika, Rydberg Annika, Haugaa Kristina, Etheridge Susan, Ackerman Michael J., Dagradi Federica, Killen Stacy A. S., Wacker-Gussmann Annette, Benson D. Woodrow, Wilde A. A. M., Pan Zhaoxing, Lam Aimee, Spazzolini Carla, Horigome Hitoshi, Schwartz Peter J. Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study American journal of obstetrics and gynecology 2020;222 (3):263.e1-263.e11 [PubMed]
  • Offerhaus Joost A., Wilde Arthur A. M., Remme Carol Ann Prophylactic (hydroxy)chloroquine in COVID-19: Potential relevance for cardiac arrhythmia risk Heart rhythm 2020;17 (9):1480-1486 [PubMed]
  • Wu Cheng-I., Postema Pieter G., Arbelo Elena, Behr Elijah R., Bezzina Connie R., Napolitano Carlo, Robyns Tomas, Probst Vincent, Schulze-Bahr Eric, Remme Carol Ann, Wilde Arthur A. M. SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes Heart rhythm 2020;17 (9):1456-1462 [PubMed]
  • Wijeyeratne Yanushi D., Tanck Michael W., Mizusawa Yuka, Batchvarov Velislav, Barc Julien, Crotti Lia, Bos J. Martijn, Tester David J., Muir Alison, Veltmann Christian, Ohno Seiko, Page Stephen P., Galvin Joseph, Tadros Rafik, Muggenthaler Martina, Raju Hariharan, Denjoy Isabelle, Schott Jean-Jacques, Gourraud Jean-Baptiste, Skoric-Milosavljevic Doris, Nannenberg Eline A., Redon Richard, Papadakis Michael, Kyndt Florence, Dagradi Federica, Castelletti Silvia, Torchio Margherita, Meitinger Thomas, Lichtner Peter, Ishikawa Taisuke, Wilde Arthur A. M., Takahashi Kazuhiro, Sharma Sanjay, Roden Dan M., Borggrefe Martin M., McKeown Pascal P., Shimizu Wataru, Horie Minoru, Makita Naomasa, Aiba Takeshi, Ackerman Michael J., Schwartz Peter J., Probst Vincent, Bezzina Connie R., Behr Elijah R. Scn5a mutation type and a genetic risk score associate variably with brugada syndrome phenotype in scn5a families Circulation. Genomic and precision medicine 2020:599-608 [PubMed]
  • Boukens Bastiaan J., Benjacholamas Vichai, van Amersfoort Shirley, Meijborg Veronique M., Schumacher Cees, Jensen Bjarke, Haissaguerre Michel, Wilde Arthur, Prechawat Somchai, Huntrakul Anurut, Nademanee Koonlawee, Coronel Ruben Structurally Abnormal Myocardium Underlies Ventricular Fibrillation Storms in a Patient Diagnosed With the Early Repolarization Pattern JACC. Clinical electrophysiology 2020;6 (11):1395-1404 [PubMed]
  • Knops Reinoud E., Olde Nordkamp Louise R. A., Delnoy Peter-Paul H. M., Boersma Lucas V. A., Kuschyk J. rgen, el-Chami Mikhael F., Bonnemeier Hendrik, Behr Elijah R., Brouwer Tom F., Kääb Stefan, Mittal Suneet, Quast Anne-Floor B. E., Smeding Lonneke, van der Stuijt Willeke, de Weger Anouk, de Wilde Koen C., Bijsterveld Nick R., Richter Sergio, Brouwer Marc A., de Groot Joris R., Kooiman Kirsten M., Lambiase Pier D., Neuzil Petr, Vernooy Kevin, Alings Marco, Betts Tim R., Bracke Frank A. L. E., Burke Martin C., de Jong Jonas S. S. G., Wright David J., Tijssen Jan G. P., Wilde Arthur A. M., Study group members AMC , Driessen Antonius H. G. Subcutaneous or Transvenous Defibrillator Therapy New England journal of medicine 2020;383 (6):526-536 [PubMed]
  • van Hattum J. C., Verwijs S. M., Rienks R., Bijsterveld N. R., de Vries S. T., Pinto Y. M., Wilde A. A. M., Jørstad H. T. The Netherlands Sports Cardiology Map: a step towards sports cardiology network medicine for patient and athlete care Netherlands heart journal 2020 [PubMed]
  • Wilde A. A. M., Offerhaus J. A. The ‘president’s drug’ Netherlands heart journal 2020;28 (7-8):363-365 [PubMed]
  • Hulleman Michiel The rhythm of the arrest: Epidemiological and electrocardiographic analyses in out-of-hospital cardiac arrest 2020. 245p. ISBN 9789402821017. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde Arthur A. M.; Co-supervisors: Koster Ruud W., Blom Marieke T.)
  • Lahrouchi Najim, Raju Hariharan, Lodder Elisabeth M., Papatheodorou Stathis, Miles Chris, Ware James S., Papadakis Michael, Tadros Rafik, Cole Della, Skinner Jonathan R., Crawford Jackie, Love Donald R., Pua Chee J., Soh Bee Y., Bhalshankar Jaydutt D., Govind Risha, Tfelt-Hansen Jacob, Winkel Bo G., van der Werf Christian, Wijeyeratne Yanushi D., Mellor Greg, Till Janice, Cohen Marta, Tome-Esteban Maria, Sharma Sanjay, Wilde Arthur A. M., Cook Stuart A., Sheppard Mary N., Bezzina Connie R., Behr Elijah R. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy European journal of human genetics 2020;28 (1):17-22 [PubMed]
  • Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G., Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L., Mazzanti Andrea, Beckmann Britt M., Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D., Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A., Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M. Ben, Weeke Peter E., Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J., Bos J. Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G., Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A., Veldink Jan H., van den Berg Leonard H., Al-Chalabi Ammar, Shaw Christopher E., Shaw Pamela J., Morrison Karen E., Andersen Peter M., Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C., Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J. Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D., Antzelevitch Charles, Roden Dan M., Saenen Johan, Borggrefe Martin, Odening Katja E., Ellinor Patrick T., Tfelt-Hansen Jacob, Skinner Jonathan R., van den Berg Maarten P., Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R., Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G., Guicheney Pascale, Tan Hanno L., Newton-Cheh Christopher, Ackerman Michael J., Schwartz Peter J., Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A., Tanck Michael W. T., Bezzina Connie R. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome Circulation 2020;142 (4):324-338 [PubMed]

2019

  • Towbin Jeffrey A., McKenna William J., Abrams Dominic J., Ackerman Michael J., Calkins Hugh, Darrieux Francisco C. C., Daubert James P., de Chillou Christian, DePasquale Eugene C., Desai Milind Y., Estes N. A. Mark, Hua Wei, Indik Julia H., Ingles Jodie, James Cynthia A., John Roy M., Judge Daniel P., Keegan Roberto, Krahn Andrew D., Link Mark S., Marcus Frank I., McLeod Christopher J., Mestroni Luisa, Priori Silvia G., Saffitz Jeffrey E., Sanatani Shubhayan, Shimizu Wataru, van Tintelen J. Peter, Wilde Arthur A. M., Zareba Wojciech 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy Heart rhythm 2019;16 (11):e301-e372 [PubMed]
  • Towbin Jeffrey A., McKenna William J., Abrams Dominic J., Ackerman Michael J., Calkins Hugh, Darrieux Francisco C. C., Daubert James P., de Chillou Christian, DePasquale Eugene C., Desai Milind Y., Estes N. A. Mark, Hua Wei, Indik Julia H., Ingles Jodie, James Cynthia A., John Roy M., Judge Daniel P., Keegan Roberto, Krahn Andrew D., Link Mark S., Marcus Frank I., McLeod Christopher J., Mestroni Luisa, Priori Silvia G., Saffitz Jeffrey E., Sanatani Shubhayan, Shimizu Wataru, van Tintelen J. Peter, Wilde Arthur A. M., Zareba Wojciech 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary Heart rhythm 2019;16 (11):e373-e407 [PubMed]
  • Cadrin-Tourigny Julia, Bosman Laurens P., Nozza Anna, Wang Weijia, Tadros Rafik, Bhonsale Aditya, Bourfiss Mimount, Fortier Annik, Lie Øyvind H., Saguner Ardan M., Svensson Anneli, Andorin Antoine, Tichnell Crystal, Murray Brittney, Zeppenfeld Katja, van den Berg Maarten P., Asselbergs Folkert W., Wilde Arthur A. M., Krahn Andrew D., Talajic Mario, Rivard Lena, Chelko Stephen, Zimmerman Stefan L., Kamel Ihab R., Crosson Jane E., Judge Daniel P., Yap Sing-Chien, van der Heijden Jeroen F., Tandri Harikrishna, Jongbloed Jan D. H., Guertin Marie-Claude, van Tintelen J. Peter, Platonov Pyotr G., Duru Firat, Haugaa Kristina H., Khairy Paul, Hauer Richard N. W., Calkins Hugh, te Riele Anneline S. J. M., James Cynthia A. A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy European heart journal 2019;40 (23):1850-1858 [PubMed]
  • Roberts Jason D., Murphy Nathaniel P., Hamilton Robert M., Lubbers Ellen R., James Cynthia A., Kline Crystal F., Gollob Michael H., Krahn Andrew D., Sturm Amy C., Musa Hassan, el-Refaey Mona, Koenig Sara, Aneq Meriam Åström, Hoorntje Edgar T., Graw Sharon L., Davies Robert W., Rafiq Muhammad Arshad, Koopmann Tamara T., Aafaqi Shabana, Fatah Meena, Chiasson David A., Taylor Matthew Rg, Simmons Samantha L., Han Mei, van Opbergen Chantal Jm, Wold Loren E., Sinagra Gianfranco, Mittal Kirti, Tichnell Crystal, Murray Brittney, Codima Alberto, Nazer Babak, Nguyen Duy T., Marcus Frank I., Sobriera Nara, Lodder Elisabeth M., van den Berg Maarten P., Spears Danna A., Robinson John F., Ursell Philip C., Green Anna K., Skanes Allan C., Tang Anthony S., Gardner Martin J., Hegele Robert A., van Veen Toon Ab, Wilde Arthur A. M., Healey Jeff S., Janssen Paul M. L., Mestroni Luisa, van Tintelen J. Peter, Calkins Hugh, Judge Daniel P., Hund Thomas J., Scheinman Melvin M., Mohler Peter J. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy Journal of clinical investigation 2019;130:3171-3184 [PubMed]
  • Quast Anne-Floor B. E., Baalman Sarah W. E., Brouwer Tom F., Smeding Lonneke, Wilde Arthur A. M., Burke Martin C., Knops Reinoud E. A novel tool to evaluate the implant position and predict defibrillation success of the subcutaneous implantable cardioverter-defibrillator: The PRAETORIAN score Heart rhythm 2019;16 (3):403-410 [PubMed]
  • Giudicessi John R., Lieve Krystien V. V., Rohatgi Ram K., Koca Faruk, Tester David J., van der Werf Christian, Martijn Bos J., Wilde Arthur A. M., Ackerman Michael J. Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance Circulation. Genomic and precision medicine 2019;12 (5):e002510 [PubMed]
  • Patel Riyaz S., Schmidt Amand F., Tragante Vinicius, McCubrey Raymond O., Holmes Michael V., Howe Laurence J., Direk Kenan, Åkerblom Axel, Leander Karin, Virani Salim S., Kaminski Karol A., Muehlschlegel Jochen D., Dubé Marie Pierre, Allayee Hooman, Almgren Peter, Alver Maris, Baranova Ekaterina V., Behlouli Hassan, Boeckx Bram, Braund Peter S., Breitling Lutz P., Delgado Graciela, Duarte Nubia E., Dufresne Line, Eriksson Niclas, Foco Luisa, Gijsberts Crystel M., Gong Yan, Hartiala Jaana, Heydarpour Mahyar, Hubacek Jaroslav A., Kleber Marcus, Kofink Daniel, Kuukasjärvi Pekka, Lee Vei Vei, Leiherer Andreas, Lenzini Petra A., Levin Daniel, Lyytikäinen Leo Pekka, Martinelli Nicola, Mons Ute, Nelson Christopher P., Nikus Kjell, Pilbrow Anna P., Ploski Rafal, Tanck Michael W.T., Wilde Arthur A.M., Bezzina Connie R., Hovingh G. Kees, Maitland-Van der Zee Anke H. Association of chromosome 9p21 with subsequent coronary heart disease events: A GENIUS-CHD study of individual participant data Circulation. Genomic and precision medicine 2019;12 (4):161-172 [PubMed]
  • Crotti Lia, Spazzolini Carla, Tester David J., Ghidoni Alice, Baruteau Alban-Elouen, Beckmann Britt-Maria, Behr Elijah R., Bennett Jeffrey S., Bezzina Connie R., Bhuiyan Zahurul A., Celiker Alpay, Cerrone Marina, Dagradi Federica, de Ferrari Gaetano M., Etheridge Susan P., Fatah Meena, Garcia-Pavia Pablo, Al-Ghamdi Saleh, Hamilton Robert M., Al-Hassnan Zuhair N., Horie Minoru, Jimenez-Jaimez Juan, Kanter Ronald J., Kaski Juan P., Kotta Maria-Christina, Lahrouchi Najim, Makita Naomasa, Norrish Gabrielle, Odland Hans H., Ohno Seiko, Papagiannis John, Parati Gianfranco, Sekarski Nicole, Tveten Kristian, Vatta Matteo, Webster Gregory, Wilde Arthur A. M., Wojciak Julianne, George Alfred L., Ackerman Michael J., Schwartz Peter J. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry European heart journal 2019;40 (35):2964-2975 [PubMed]
  • Laracuente Ronald, Waase Marc Paul, Kalia Isha, Wilde Arthur A. M., Chung Wendy K. Cases in precision medicine: Genetic assessment after a sudden cardiac death in the family Annals of internal medicine 2019;170 (10):710-716 [PubMed]
  • Skinner Jonathan R., Winbo Annika, Abrams Dominic, Vohra Jitendra, Wilde Arthur A. Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects Heart, lung & circulation 2019;28 (1):22-30 [PubMed]
  • Panhuyzen-Goedkoop Nicole, Wilde Arthur Channelopathy in athletesin: A Pelliccia, H Heidbuchel, D Corrado, M Borjesson, S Sharma, editors. The ESC textbook of Sports Cardiology. Oxford: Oxford Unitersity Press Inc; 2019. p. 253-264, ISBN 9780198779742
  • Michowitz Yoav, Milman Anat, Andorin Antoine, Sarquella-Brugada Georgia, Gonzalez Corcia M. Cecilia, Gourraud Jean-Baptiste, Conte Giulio, Sacher Frederic, Juang Jimmy J. M., Kim Sung-Hwan, Leshem Eran, Mabo Philippe, Postema Pieter G., Hochstadt Aviram, Wijeyeratne Yanushi D., Denjoy Isabelle, Giustetto Carla, Mizusawa Yuka, Huang Zhengrong, Jespersen Camilla H., Maeda Shingo, Takahashi Yoshihide, Kamakura Tsukasa, Aiba Takeshi, Arbelo Elena, Mazzanti Andrea, Allocca Giuseppe, Brugada Ramon, Casado-Arroyo Ruben, Champagne Jean, Priori Silvia G., Veltmann Christian, Delise Pietro, Corrado Domenico, Brugada Josep, Kusano Kengo F., Hirao Kenzo, Calo Leonardo, Takagi Masahiko, Tfelt-Hansen Jacob, Yan Gan-Xin, Gaita Fiorenzo, Leenhardt Antoine, Behr Elijah R., Wilde Arthur A. M., Nam Gi-Byoung, Brugada Pedro, Probst Vincent, Belhassen Bernard Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome Journal of the American College of Cardiology 2019;73 (14):1756-1765 [PubMed]
  • Wilde Arthur A.M. Creating certainty out of uncertainty European heart journal 2019;40 (10):839-841 [PubMed]
  • Milman Anat, Andorin Antoine, Postema Pieter G., Gourraud Jean-Baptiste, Sacher Frederic, Mabo Philippe, Kim Sung-Hwan, Maeda Shingo, Takahashi Yoshihide, Kamakura Tsukasa, Aiba Takeshi, Conte Giulio, Juang Jimmy J. M., Leshem Eran, Michowitz Yoav, Fogelman Rami, Hochstadt Aviram, Mizusawa Yuka, Giustetto Carla, Arbelo Elena, Huang Zhengrong, Corrado Domenico, Delise Pietro, Allocca Giuseppe, Takagi Masahiko, Wijeyeratne Yanushi D., Mazzanti Andrea, Brugada Ramon, Casado-Arroyo Ruben, Champagne Jean, Calo Leonardo, Sarquella-Brugada Georgia, Jespersen Camilla H., Tfelt-Hansen Jacob, Veltmann Christian, Priori Silvia G., Behr Elijah R., Yan Gan-Xin, Brugada Josep, Gaita Fiorenzo, Wilde Arthur A. M., Brugada Pedro, Kusano Kengo F., Hirao Kenzo, Nam Gi-Byoung, Probst Vincent, Belhassen Bernard Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome Heart rhythm 2019;16 (10):1468-1474 [PubMed]
  • Fellmann Florence, van el Carla G., Charron Philippe, Michaud Katarzyna, Howard Heidi C., Boers Sarah N., Clarke Angus J., Duguet Anne-Marie, Forzano Francesca, Kauferstein Silke, Kayserili H. lya, Lucassen Anneke, Mendes Álvaro, Patch Christine, Radojkovic Dragica, Rial-Sebbag Emmanuelle, Sheppard Mary N., Tassé Anne-Marie, Temel Sehime G., Sajantila Antti, Basso Cristina, Wilde Arthur A. M., Cornel Martina C. European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death European journal of human genetics 2019;27 (12):1763-1773 [PubMed]
  • Jansweijer Joeri A., van Spaendonck-Zwarts Karin Y., Tanck Michael W. T., Peter van Tintelen J., Christiaans Imke, van der Smagt Jasper, Vermeer Alexa, Bos J. Martijn, Moss Arthur J., Swan Heikki, Priori Sylvia, Rydberg Annika, Tfelt-Hansen Jacob, Ackerman Michael, Olivotto Iacopo, Charron Philippe, Gimeno Juan R., van den Berg Maarten, Wilde Arthur, Pinto Yigal M. Heritability in genetic heart disease: The role of genetic background Open heart 2019;6 (1) [PubMed]
  • Beurskens Niek E. G., Tjong Fleur V. Y., de Bruin-Bon Rianne H. A., Dasselaar Kosse J., Kuijt Wichert J., Wilde Arthur A. M., Knops Reinoud E. Impact of Leadless Pacemaker Therapy on Cardiac and Atrioventricular Valve Function Through 12 Months of Follow-Up Circulation. Arrhythmia and electrophysiology 2019;12 (5):e007124 [PubMed]
  • van der Werf Christian, Lieve Krystien V, Bos J Martijn, Lane Conor M, Denjoy Isabelle, Roses-Noguer Ferran, Aiba Takeshi, Wada Yuko, Ingles Jodie, Leren Ida S, Rudic Boris, Schwartz Peter J, Maltret Alice, Sacher Frederic, Skinner Jonathan R, Krahn Andrew D, Roston Thomas M, Tfelt-Hansen Jacob, Swan Heikki, Robyns Tomas, Ohno Seiko, Roberts Jason D, van den Berg Maarten P, Kammeraad Janneke A, Probst Vincent, Kannankeril Prince J, Blom Nico A, Behr Elijah R, Borggrefe Martin, Haugaa Kristina H, Semsarian Christopher, Horie Minoru, Shimizu Wataru, Till Janice A, Leenhardt Antoine, Ackerman Michael J, Wilde Arthur A Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest European heart journal 2019;40 (35):2953-2961 [PubMed]
  • Blom Lennart J., Visser Marloes, Christiaans Imke, Scholten Marcoen F., Bootsma Marianne, van den Berg Maarten P., Yap Sing-Chien, van der Heijden Jeroen F., Doevendans Pieter A., Loh Peter, Postema Pieter G., Barge-Schaapsveld Daniela Q., Hofman Nynke, Volders Paul G. A., Wilde Arthur A., Hassink Rutger J. Incidence and predictors of implantable cardioverter-defibrillator therapy and its complications in idiopathic ventricular fibrillation patients EP Europace 2019;21 (10):1519-1526 [PubMed]
  • Vermeer Alexa M. C. Inherited cardiomyopathies and phenocopies 2019. 180p. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M. , Bezzina C.; Co-supervisor: Christiaans I.)
  • Beurskens Niek E. G., Tjong Fleur V. Y., Dasselaar Kosse J., Kuijt Wichert J., Wilde Arthur A. M., Knops Reinoud E. Leadless pacemaker implantation after explantation of infected conventional pacemaker systems: A viable solution? Heart rhythm 2019;16 (1):66-71 [PubMed]
  • Lieve Krystien V.V., Verhagen Judith M.A., Wei Jinhong, Bos J. Martijn, van der Werf Christian, Rosés i Noguer Ferran, Mancini Grazia M.S., Guo Wenting, Wang Ruiwu, van den Heuvel Freek, Frohn-Mulder Ingrid M.E., Shimizu Wataru, Nogami Akihiko, Horigome Hitoshi, Roberts Jason D., Leenhardt Antoine, Crijns Harry J.G., Blank Andreas C., Aiba Takeshi, Wiesfeld Ans C.P., Blom Nico A., Sumitomo Naokata, Till Jan, Ackerman Michael J., Chen S. R.Wayne, van de Laar Ingrid M.B.H., Wilde Arthur A.M. Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia Heart rhythm 2019;16 (2):220-228 [PubMed]
  • Quast Anne-Floor B. E., Baalman Sarah W. E., van der Stuijt Willeke, Wilde Arthur A. M., Knops Reinoud E. Minimal defibrillation thresholds and the correlation with implant position in subcutaneous implantable-defibrillator patients Journal of cardiovascular electrophysiology 2019;30 (11):2441-2447 [PubMed]
  • Jansen Mark, Baas Annette F., van Spaendonck-Zwarts Karin Y., Ummels Amber S., van den Wijngaard Arthur, Jongbloed Jan D. H., van Slegtenhorst Marjon A., Lekanne Deprez Ronald H., Wessels Marja W., Michels Michelle, Houweling Arjan C., Hoorntje Edgar T., Helderman-van den Enden Paula J. T. M., Barge-Schaapveld Daniela Q. C. M., Peter van Tintelen J., van den Berg Maarten P., Wilde Arthur A. M., Ploos van Amstel Hans K., Hennekam Eric A. M., Asselbergs Folkert W., Sijbrands Eric J. G., Dooijes Dennis Mortality Risk Associated With Truncating Founder Mutations in Titin Circulation. Genomic and precision medicine 2019;12 (5):e002436 [PubMed]
  • te Rijdt Wouter P., ten Sande Judith N., Gorter Thomas M., van der Zwaag Paul A., van Rijsingen Ingrid A., Boekholdt S. Matthijs, van Tintelen J. Peter, van Haelst Paul L., Planken R. Nils, de Boer Rudolf A., Suurmeijer Albert J. H., van Veldhuisen Dirk J., Wilde Arthur A. M., Willems Tineke P., van Dessel Pascal F. H. M., van den Berg Maarten P. Myocardial fibrosis as an early feature in phospholamban p.Arg14del mutation carriers: phenotypic insights from cardiovascular magnetic resonance imaging European heart journal cardiovascular Imaging 2019;20 (1):92-100 [PubMed]
  • Raju Hariharan, Ware James S., Skinner Jonathan R., Hedley Paula L., Arno Gavin, Love Donald R., van der Werf Christian, Tfelt-Hansen Jacob, Winkel Bo Gregers, Cohen Marta C., Li Xinzhong, John Shibu, Sharma Sanjay, Jeffery Steve, Wilde Arthur A. M., Christiansen Michael, Sheppard Mary N., Behr Elijah R. Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy BMC cardiovascular disorders 2019;19 (1) [PubMed]
  • Tadros Rafik, Tan Hanno L., el Mathari Sulayman, Kors Jan A., Postema Pieter G., Lahrouchi Najim, Beekman Leander, Radivojkov-Blagojevic Milena, Amin Ahmad S., Meitinger Thomas, Tanck Michael W., Wilde Arthur A., Bezzina Connie R. Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores European heart journal 2019;40 (37):3097-3107 [PubMed]
  • Cheung Christopher C., Lieve Krystien V., Roston Thomas M., van der Ree Martijn H., Deyell Marc W., Andrade Jason G., Laksman Zachary W., Nannenberg Eline A., Tadros Rafik, Pang Benjamin, Rutberg Julie, Green Martin S., Conacher Susan, Seifer Colette M., Roberts Jason D., Steinberg Christian, Sanatani Shubhayan, Wilde Arthur A., Krahn Andrew D. Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia JACC. Clinical electrophysiology 2019;5 (3):387-394 [PubMed]
  • Quast Anne-Floor B. E., Baalman Sarah W. E., Betts Tim R., Boersma Lucas V. A., Bonnemeier Hendrik, Boveda Serge, Brouwer Tom F., Burke Martin C., Delnoy Peter Paul H. M., el-Chami Mikhael, Kuschyk Juergen, Lambiase Pier, Marquie Christelle, Miller Marc A., Smeding Lonneke, Wilde Arthur A. M., Knops Reinoud E. Rationale and design of the PRAETORIAN-DFT trial: A prospective randomized CompArative trial of SubcutanEous ImplanTable CardiOverter-DefibrillatoR ImplANtation with and without DeFibrillation testing American heart journal 2019;214:167-174 [PubMed]
  • Wilde Arthur A. M., Gollob Michael H. Response by Wilde and Gollob to Letter Regarding Article, "Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome" Circulation 2019;139 (14):1760-1761 [PubMed]
  • Wilde Arthur A.M., Garan Hasan, Boyden Penelope A. Role of the Purkinje system in heritable arrhythmias Heart rhythm 2019;16 (7):1121-1126 [PubMed]
  • Walsh Roddy, Wilde Arthur A. M. SCN5A variants in Brugada syndrome: True, true false, or false true Journal of cardiovascular electrophysiology 2019;30 (1):128-131 [PubMed]
  • Quast Anne Floor B. E. Subcutaneous implantable cardioverter-defibrillator therapy and other alternatives for transvenous leads 2019. 185p. ISBN 9789402816112. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Knops R. E.)
  • Patel Riyaz S., Tragante Vinicius, Schmidt Amand F., McCubrey Raymond O., Holmes Michael V., Howe Laurence J., Direk Kenan, Åkerblom Axel, Leander Karin, Virani Salim S., Kaminski Karol A., Muehlschlegel Jochen D., Allayee Hooman, Almgren Peter, Alver Maris, Baranova Ekaterina V., Behloui Hassan, Boeckx Bram, Braund Peter S., Breitling Lutz P., Delgado Graciela, Duarte Nubia E., Dubé Marie-Pierre, Dufresne Line, Eriksson Niclas, Foco Luisa, Scholz Markus, Gijsberts Crystel M., Glinge Charlotte, Gong Yan, Hartiala Jaana, Heydarpour Mahyar, Hubacek Jaroslav A., Kleber Marcus, Kofink Daniel, Kotti Salma, Kuukasjärvi Pekka, Lee Vei-Vei, Leiherer Andreas, Lenzini Petra A., Levin Daniel, Lyytikäinen Leo-Pekka, Martinelli Nicola, Mons Ute, Nelson Christopher P., Nikus Kjell, Pilbrow Anna P., Ploski Rafal, Sun Yan V., Tanck Michael W. T., Tang W. H. Wilson, Trompet Stella, van der Laan Sander W., van Setten Jessica, Vilmundarson Ragnar O., Viviani Anselmi Chiara, Vlachopoulou Efthymia, Al Ali Lawien, Boerwinkle Eric, Briguori Carlo, Carlquist John F., Carruthers Kathryn F., Casu Gavino, Deanfield John, Deloukas Panos, Dudbridge Frank, Engstrøm Thomas, Fitzpatrick Natalie, Fox Kim, Gigante Bruna, James Stefan, Lokki Marja-Liisa, Lotufo Paulo A., Marziliano Nicola, Mordi Ify R., Muhlestein Joseph B., Newton-Cheh Christopher, Pitha Jan, Saely Christoph H., Samman-Tahhan Ayman, Sandesara Pratik B., Teren Andrej, Timmis Adam, van de Werf Frans, Wauters Els, Wilde Arthur A. M., Ford Ian, Stott David J., Algra Ale, Andreassi Maria G., Ardissino Diego, Arsenault Benoit J., Ballantyne Christie M., Bergmeijer Thomas O., Bezzina Connie R., Body Simon C., Boersma Eric H., Bogaty Peter, Bots Michiel L., Brenner Hermann, Brugts Jasper J., Burkhardt Ralph, Carpeggiani Clara, Condorelli Gianluigi, Cooper-DeHoff Rhonda M., Cresci Sharon, Danchin Nicolas, de Faire Ulf, Doughty Robert N., Drexel Heinz, Engert James C., Fox Keith A. A., Girelli Domenico, Grobbee Diederick E., Hagström Emil, Hazen Stanley L., Held Claes, Hemingway Harry, Hoefer Imo E., Hovingh G. Kees, Jabbari Reza, Johnson Julie A., Jukema J. Wouter, Kaczor Marcin P., Kähönen Mika, Kettner Jiri, Kiliszek Marek, Klungel Olaf H., Lagerqvist Bo, Lambrechts Diether, Laurikka Jari O., Lehtimäki Terho, Lindholm Daniel, Mahmoodi B. K., Maitland-van der Zee Anke H., McPherson Ruth, Melander Olle, Metspalu Andres, Niemcunowicz-Janica Anna, Olivieri Oliviero, Opolski Grzegorz, Palmer Colin N., Pasterkamp Gerard, Pepine Carl J., Pereira Alexandre C., Pilote Louise, Quyyumi Arshed A., Richards A. Mark, Sanak Marek, Siegbahn Agneta, Simon Tabassome, Sinisalo Juha, Smith J. Gustav, Spertus John A., Stender Steen, Stewart Alexandre F. R., Szczeklik Wojciech, Szpakowicz Anna, Tardif Jean-Claude, ten Berg Jurriën M., Tfelt-Hansen Jacob, Thanassoulis George, Thiery Joachim, Torp-Pedersen Christian, van der Graaf Yolanda, Visseren Frank L. J., Waltenberger Johannes, Weeke Peter E., van der Harst Pim, Lang Chim C., Sattar Naveed, Cameron Vicky A., Anderson Jeffrey L., Brophy James M., Pare Guillaume, Horne Benjamin D., März Winfried, Wallentin Lars, Samani Nilesh J., Hingorani Aroon D., Asselbergs Folkert W. Subsequent Event Risk in Individuals With Established Coronary Heart Disease Circulation. Genomic and precision medicine 2019;12 (4):e002470 [PubMed]
  • Podliesna Svitlana, Delanne Julian, Miller Lindsey, Tester David J., Uzunyan Merujan, Yano Shoji, Klerk Mischa, Cannon Bryan C., Khongphatthanayothin Apichai, Laurent Gabriel, Bertaux Geraldine, Falcon-Eicher Sylvie, Wu Shengnan, Yen Hai-Yun, Gao Hanlin, Wilde Arthur A. M., Faivre Laurence, Ackerman Michael J., Lodder Elisabeth M., Bezzina Connie R. Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys) Heart rhythm 2019;16 (1):98-105 [PubMed]
  • Bosman L. P., Verstraelen T. E., van Lint F. H. M., Cox M. G. P. J., Groeneweg J. A., Mast T. P., van der Zwaag P. A., Volders P. G. A., Evertz R., Wong L., de Groot N. M. S., Zeppenfeld K., van der Heijden J. F., van den Berg M. P., Wilde A. A. M., Asselbergs F. W., Hauer R. N. W., te Riele A. S. J. M., van Tintelen J. P., Baas A. F., Barge-Schaapveld D. Q. C. M., Boekholdt S. M., Cramer M. J. M., Dooijes D., Jongbloed J. D. H., Loh P., Planken R. N., Prakken N. H. J., van der Smagt J. J., van der Wal A. C., Teske A. J., van Veen T. A. B., Velthuis B. K., Vink A., Yap S. C. The Netherlands Arrhythmogenic Cardiomyopathy Registry: design and status update Netherlands heart journal 2019;27 (10):480-486 [PubMed]
  • Milman Anat, Hochstadt Aviram, Andorin Antoine, Gourraud Jean-Baptiste, Sacher Frederic, Mabo Philippe, Kim Sung-Hwan, Conte Giulio, Arbelo Elena, Kamakura Tsukasa, Aiba Takeshi, Napolitano Carlo, Giustetto Carla, Denjoy Isabelle, Juang Jimmy J. M., Maeda Shingo, Takahashi Yoshihide, Leshem Eran, Michowitz Yoav, Rahkovich Michael, Jespersen Camilla H., Wijeyeratne Yanushi D., Champagne Jean, Calo Leonardo, Huang Zhengrong, Mizusawa Yuka, Postema Pieter G., Brugada Ramon, Wilde Arthur A. M., Yan Gan-Xin, Behr Elijah R., Tfelt-Hansen Jacob, Hirao Kenzo, Veltmann Christian, Leenhardt Antoine, Corrado Domenico, Gaita Fiorenzo, Priori Silvia G., Kusano Kengo F., Takagi Masahiko, Delise Pietro, Brugada Josep, Brugada Pedro, Nam Gi-Byoung, Probst Vincent, Belhassen Bernard Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS) EP Europace 2019;21 (5):796-802 [PubMed]
  • Mellor Greg J., Panwar Pankaj, Lee Andrea K., Steinberg Christian, Hathaway Julie A., Bartels Kirsten, Christian Susan, Balaji Seshadri, Roberts Jason D., Simpson Chris S., Boczek Nicole J., Tester David J., Radbill Andrew E., Mok Ngai-Shing, Hamilton Robert M., Kaufman Elizabeth S., Eugenio Paul L., Weiss Raul, January Craig, McDaniel George M., Leather Richard A., Erickson Christopher, Falik Shelley, Behr Elijah R., Wilde Arthur A. M., Sanatani Shubhayan, Ackerman Michael J., van Petegem Filip, Krahn Andrew D., Laksman Zachary Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site EP Europace 2019;21 (11):1725-1732 [PubMed]
  • Wilde Arthur A.M., Viskin Sami Using registries to predict outcome: The implantable cardioverter-defibrillator in long QT syndrome Europace : European pacing, arrhythmias, and cardiac electrophysiology 2019;21 (2):188-189 [PubMed]
  • van der Werf Christian, Wilde Arthur A. M. Why did this patient experience a sudden cardiac arrest? Follow your curiosity! Heart rhythm 2019;16 (8):1240-1241 [PubMed]

2018

  • Rivaud Mathilde R., Jansen John A., Postema Pieter G., Nannenberg Eline A., Mizusawa Yuka, van der Nagel Roel, Wolswinkel Rianne, van der Made Ingeborg, Marchal Gerard A., Rajamani Sridharan, Belardinelli Luiz, van Tintelen J. Peter, Tanck Michael W. T., van DerWal Allard C., de Bakker Jacques M. T., van Rijen Harold V., Creemers Esther E., Wilde Arthur A. M., van den Berg Maarten P., van Veen Toon A. B., Bezzina Connie R., Remme Carol Ann A common co-morbiditymodulates disease expression and treatment efficacy in inherited cardiac sodiumchannelopathy European heart journal 2018;39 (31):2898-2907 [PubMed]
  • Ashar Foram N., Mitchell Rebecca N., Albert Christine M., Newton-Cheh Christopher, Brody Jennifer A., Müller-Nurasyid Martina, Moes Anna, Meitinger Thomas, Mak Angel, Huikuri Heikki, Junttila M. Juhani, Goyette Philippe, Pulit Sara L., Pazoki Raha, Tanck Michael W., Blom Marieke T., Zhao XiaoQing, Havulinna Aki S., Jabbari Reza, Glinge Charlotte, Tragante Vinicius, Escher Stefan A., Chakravarti Aravinda, Ehret Georg, Coresh Josef, Li Man, Prineas Ronald J., Franco Oscar H., Kwok Pui-Yan, Lumley Thomas, Dumas Florence, McKnight Barbara, Rotter Jerome I., Lemaitre Rozenn N., Heckbert Susan R., O'Donnell Christopher J., Hwang Shih-Jen, Tardif Jean-Claude, VanDenburgh Martin, Uitterlinden André G., Hofman Albert, Stricker Bruno H. C., de Bakker Paul I. W., Franks Paul W., Jansson Jan-Hakan, Asselbergs Folkert W., Halushka Marc K., Maleszewski Joseph J., Tfelt-Hansen Jacob, Engstrøm Thomas, Salomaa Veikko, Virmani Renu, Kolodgie Frank, Wilde Arthur A. M., Tan Hanno L., Bezzina Connie R., Eijgelsheim Mark, Rioux John D., Jouven Xavier, Kääb Stefan, Psaty Bruce M., Siscovick David S., Arking Dan E., Sotoodehnia Nona A comprehensive evaluation of the genetic architecture of sudden cardiac arrest European heart journal 2018;39 (44):3961-3969 [PubMed]
  • Bundgaard Henning, Jøns Christian, Lodder Elisabeth M., Izarzugaza Jose M. G., Romero Herrera Jose A., Pehrson Steen, Tfelt-Hansen Jacob, Ahlberg Gustav, Olesen Morten S., Holst Anders G., Wellens Hein, de Villiers Carin, Hastings Robert, Stuart Graham, Brunak S. ren, Wilde Arthur A. M., Watkins Hugh, Christensen Alex H. A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression New England journal of medicine 2018;379 (18):1780-1781 [PubMed]
  • Vink Arja Suzanne, Kuipers Irene M., de Bruin-Bon Rianne H. A. C. M., Wilde Arthur A. M., Blom Nico A., Clur Sally-Ann B. A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children Pediatric cardiology 2018;39 (7):1413-1422 [PubMed]
  • Smit Nicoline W. Arrhythmogenic consequences of stem cell therapy for cardiac regeneration 2018. ISBN 9789402809237. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Coronel R.; Co-supervisor: Meijborg V. M. F.)
  • Panhuyzen-Goedkoop N. M., Wilde A. A. M. Athletes with channelopathy may be eligible to play Netherlands heart journal 2018;26 (3):146-153 [PubMed]
  • Giudicessi John R., Roden Dan M., Wilde Arthur A. M., Ackerman Michael J. Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing Circulation 2018;137 (6):619-630 [PubMed]
  • Quast Anne-Floor B. E., Brouwer Tom F., Tjong Fleur V. Y., Wilde Arthur A. M., Knops Reinoud E. Clinical parameters to optimize patient selection for subcutaneous and transvenous implantable defibrillator therapy Pacing and clinical electrophysiology 2018;41 (8):990-995 [PubMed]
  • Wilde Arthur A. M., Amin Ahmad S. Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy JACC. Clinical electrophysiology 2018;4 (5):569-579 [PubMed]
  • Quast A. B. E., Brouwer T. F., Kooiman K. M., van Dessel P. F. H. M., Blom N. A., Wilde A. A. M., Knops R. E. Comparison of complications and shocks in paediatric and young transvenous and subcutaneous implantable cardioverter-defibrillator patients Netherlands heart journal 2018;26 (12):612-619 [PubMed]
  • Boriani Giuseppe, Proietti Marco, Laroche C. cile, Fauchier Laurent, Marin Francisco, Nabauer Michael, Potpara Tatjana, Dan Gheorghe-Andrei, Kalarus Zbigniew, Diemberger Igor, Tavazzi Luigi, Maggioni Aldo P., Lip Gregory Y. H., Boriani G., Lip G. Y. H., Tavazzi L., Maggioni A. P., Dan G. A., Potpara T., Nabauer M., Marin F., Kalarus Z., Fauchier L., Goda A., Mairesse G., Shalganov T., Antoniades L., Taborsky M., Riahi S., Muda P., García Bolao I., Piot O., Nabauer M., Etsadashvili K., Simantirakis E., Haim M., Azhari A., Najafian J., Santini M., Mirrakhimov E., Kulzida K. A., Erglis A., Poposka L., Burg M., Crijns H., Erküner Ö, Atar D., Lenarczyk R., Martins Oliveira M., Shah D., de Groot Joris R., Neefs J., van den Berg N., Piersma F., Wilde A., et al Contemporary stroke prevention strategies in 11 096 European patients with atrial fibrillation: A report from the EURObservational Research Programme on Atrial Fibrillation (EORP-AF) Long-Term General Registry Europace : European pacing, arrhythmias, and cardiac electrophysiology 2018;20 (5):747-757 [PubMed]
  • van Dongen Ivo M. Contraction, collaterals and conduction in patients with a chronic total coronary occlusion 2018. ISBN 9789402810219. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Henriques J. P. S., Wilde A. A. M.; Co-supervisors: Delewi R., Claessen B. E. P. M.)
  • Vink Arja Suzanne, Neumann Benjamin, Lieve Krystien V V, Sinner Moritz F, Hofman Nynke, El Kadi Soufiane, Schoenmaker Melissa H A, Slaghekke Hanneke M J, de Jong Jonas S S G, Clur Sally-Ann B, Blom Nico A, Kääb Stefan, Wilde Arthur A M, Postema Pieter G Determination and Interpretation of the QT Interval Circulation 2018;138 (21):2345-2358 [PubMed]
  • Quast Anne-Floor B. E., Tjong Fleur V. Y., Koop Brendan E., Wilde Arthur A. M., Knops Reinoud E., Burke Martin C. Device orientation of a leadless pacemaker and subcutaneous implantable cardioverter-defibrillator in canine and human subjects and the effect on intrabody communication Europace : European pacing, arrhythmias, and cardiac electrophysiology 2018;20 (11):1866-1871 [PubMed]
  • Vink Arja Suzanne, Clur Sally-Ann B., Wilde Arthur A. M., Blom Nico A. Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndrome Trends in cardiovascular medicine 2018;28 (1):64-75 [PubMed]
  • Nannenberg Eline A., van Rijsingen Ingrid A. W., van der Zwaag Paul A., van den Berg Maarten P., van Tintelen J. Peter, Tanck Michael W. T., Ackerman Michael J., Wilde Arthur A. M., Christiaans Imke Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases Circulation. Genomic and precision medicine 2018;11 (10):e001797 [PubMed]
  • van Dongen Ivo M., Yilmaz Dilek, Elias Joëlle, Claessen Bimmer E. P. M., Delewi Ronak, Knops Reinoud E., Wilde Arthur A. M., van Erven Lieselot, Schalij Martin J., Henriques José P. S. Evaluation of the impact of a chronic total coronary occlusion on ventricular arrhythmias and long-term mortality in patients with ischemic cardiomyopathy and an implantable cardioverter- defibrillator (the eCTOpy-in-ICD study) Journal of the American Heart Association 2018;7 (10) [PubMed]
  • Michowitz Yoav, Milman Anat, Sarquella-Brugada Georgia, Andorin Antoine, Champagne Jean, Postema Pieter G., Casado-Arroyo Ruben, Leshem Eran, Juang Jimmy J. M., Giustetto Carla, Tfelt-Hansen Jacob, Wijeyeratne Yanushi D., Veltmann Christian, Corrado Domenico, Kim Sung-Hwan, Delise Pietro, Maeda Shingo, Gourraud Jean-Baptiste, Sacher Frederic, Mabo Philippe, Takahashi Yoshihide, Kamakura Tsukasa, Aiba Takeshi, Conte Giulio, Hochstadt Aviram, Mizusawa Yuka, Rahkovich Michael, Arbelo Elena, Huang Zhengrong, Denjoy Isabelle, Napolitano Carlo, Brugada Ramon, Calo Leonardo, Priori Silvia G., Takagi Masahiko, Behr Elijah R., Gaita Fiorenzo, Yan Gan-Xin, Brugada Josep, Leenhardt Antoine, Wilde Arthur A. M., Brugada Pedro, Kusano Kengo F., Hirao Kenzo, Nam Gi-Byoung, Probst Vincent, Belhassen Bernard Fever-related arrhythmic events in the multicenter Survey on Arrhythmic Events in Brugada Syndrome Heart rhythm 2018;15 (9):1394-1401 [PubMed]
  • Milman Anat, Gourraud Jean-Baptiste, Andorin Antoine, Postema Pieter G., Sacher Frederic, Mabo Philippe, Conte Giulio, Giustetto Carla, Sarquella-Brugada Georgia, Hochstadt Aviram, Kim Sung-Hwan, Juang Jimmy J. M., Maeda Shingo, Takahashi Yoshihide, Kamakura Tsukasa, Aiba Takeshi, Leshem Eran, Michowitz Yoav, Rahkovich Michael, Mizusawa Yuka, Arbelo Elena, Huang Zhengrong, Denjoy Isabelle, Wijeyeratne Yanushi D., Napolitano Carlo, Brugada Ramon, Casado-Arroyo Ruben, Champagne Jean, Calo Leonardo, Tfelt-Hansen Jacob, Priori Silvia G., Takagi Masahiko, Veltmann Christian, Delise Pietro, Corrado Domenico, Behr Elijah R., Gaita Fiorenzo, Yan Gan-Xin, Brugada Josep, Leenhardt Antoine, Wilde Arthur A. M., Brugada Pedro, Kusano Kengo F., Hirao Kenzo, Nam Gi-Byoung, Probst Vincent, Belhassen Bernard Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients Heart rhythm 2018;15 (10):1457-1465 [PubMed]
  • Saprungruang Ankavipar, Khongphatthanayothin Apichai, Mauleekoonphairoj John, Wandee Pharawee, Kanjanauthai Supaluck, Bhuiyan Zahurul A., Wilde Arthur A. M., Poovorawan Yong Genotype and clinical characteristics of congenital long QT syndrome in Thailand Indian pacing and electrophysiology journal 2018;18 (5):165-171 [PubMed]
  • Tjong Fleur V. Y., Beurskens Niek E. G., de Groot Joris R., Waweru Catherine, Liu Shufeng, Ritter Philippe, Reynolds Dwight, Wilde Arthur A. M., Knops Reinoud E. Health-related quality of life impact of a transcatheter pacing system Journal of cardiovascular electrophysiology 2018;29 (12):1697-1704 [PubMed]
  • Murray Brittney, Hoorntje Edgar T., te Riele Anneline S. J. M., Tichnell Crystal, van der Heijden Jeroen F., Tandri Harikrishna, van den Berg Maarten P., Jongbloed Jan D. H., Wilde Arthur A. M., Hauer Richard N. W., Calkins Hugh, Judge Daniel P., James Cynthia A., van Tintelen J. Peter, Dooijes Dennis Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC) Journal of cardiovascular electrophysiology 2018;29 (7):1004-1009 [PubMed]
  • Amin Ahmad S., Wilde Arthur A. M. Inheritable Potassium Channel Diseasesin: Douglas P. Zipes, José Jalife, William Gregory Stevenson, editors. Cardiac Electrophysiology; From Cell to Bedside. Philadelphia: Elsevier; 2018. p. 494, ISBN 9780323447331
  • Postema Pieter G., Lieve Krystien V. V., Wilde Arthur A. M. Inherited arrhythmias: Brugada syndrome and early repolarisation syndromein: Dhavendra Kumar, Perry Elliott, editors. Cardiovascular Genetics and Genomics: Principles and Clinical Practice. Cham, Switzerland: Springer International Publishing; 2018. p. 437-480, ISBN 9783319661124
  • O'Mahony Constantinos, Jichi Fatima, Ommen Steve R., Christiaans Imke, Arbustini Eloisa, Garcia-Pavia Pablo, Cecchi Franco, Olivotto Iacopo, Kitaoka Hiroaki, Gotsman Israel, Carr-White Gerald, Mogensen Jens, Antoniades Loizos, Mohiddin Saidi A., Maurer Mathew S., Tang Hak Chiaw, Geske Jeffrey B., Siontis Konstantinos C., Mahmoud Karim D., Vermeer Alexa, Wilde Arthur, Favalli Valentina, Guttmann Oliver P., Gallego-Delgado Maria, Dominguez Fernando, Tanini Ilaria, Kubo Toru, Keren Andre, Bueser Teofila, Waters Sarah, Issa Issa F., Malcolmson James, Burns Tom, Sekhri Neha, Hoeger Christopher W., Omar Rumana Z., Elliott Perry M. International external validation study of the 2014 European society of cardiology guidelines on sudden cardiac death prevention in hypertrophic cardiomyopathy (EVIDENCE-HCM) Circulation 2018;137 (10):1015-1023 [PubMed]
  • Gray Belinda, Hasdemir Can, Ingles Jodie, Aiba Takeshi, Makita Naomasa, Probst Vincent, Wilde Arthur A. M., Newbury-Ecob Ruth, Sheppard Mary N., Semsarian Christopher, Sy Raymond W., Behr Elijah R. Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants Heart rhythm 2018;15 (7):1051-1057 [PubMed]
  • Clur Sally-Ann B., Vink Arja S., Etheridge Susan P., Robles de Medina Pascale G., Rydberg Annika, Ackerman Michael J., Wilde Arthur A., Blom Nico A., Benson D. Woodrow, Herberg Ulrike, Donofrio Mary T., Cuneo Bettina F. Left Ventricular Isovolumetric Relaxation Time Is Prolonged in Fetal Long-QT Syndrome Circulation. Arrhythmia and electrophysiology 2018;11 (4) [PubMed]
  • Blom L. J., Volders P. G. A., Wilde A. A., Hassink R. J. Life-long tailoring of diagnosis and management of patients with idiopathic ventricular fibrillation—future perspectives in research Netherlands heart journal 2018;26 (7-8):367-374 [PubMed]
  • Tjong Fleur V. Y., Knops Reinoud E., Neuzil Petr, Petru Jan, Sediva Lucie, Wilde Arthur A. M., Sperzel Johannes, Reddy Vivek Y. Midterm Safety and Performance of a Leadless Cardiac Pacemaker: 3-Year Follow-up to the LEADLESS Trial (Nanostim Safety and Performance Trial for a Leadless Cardiac Pacemaker System) Circulation 2018;137 (6):633-635 [PubMed]
  • Hoorntje Edgar T., Posafalvi Anna, Syrris Petros, van der Velde K. Joeri, Bolling Marieke C., Protonotarios Alexandros, Boven Ludolf G., Amat-Codina Nuria, Groeneweg Judith A., Wilde Arthur A., Sobreira Nara, Calkins Hugh, Hauer Richard N. W., Jonkman Marcel F., McKenna William J., Elliott Perry M., Sinke Richard J., van den Berg Maarten P., Chelko Stephen P., James Cynthia A., van Tintelen J. Peter, Judge Daniel P., Jongbloed Jan D. H. No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy PLoS ONE 2018;13 (8) [PubMed]
  • Tjong Fleur V. Y. Novel therapies in cardiac rhythm management: The start of the leadless era 2018. ISBN 9789082901504. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Reddy V. Y.; Co-supervisors: Knops R. E., de Groot J. R.)
  • Stunnenberg B. C., Raaphorst J., Deenen J. C. W., Links T. P., Wilde A. A., Verbove D. J., Kamsteeg E. J., van den Wijngaard A., Faber C. G., van der Wilt G. J., van Engelen B. G. M., Drost G., Ginjaar H. B. Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands Neuromuscular disorders 2018;28 (5):402-407 [PubMed]
  • Milman Anat, Andorin Antoine, Gourraud Jean-Baptiste, Postema Pieter G., Sacher Frederic, Mabo Philippe, Kim Sung-Hwan, Juang Jimmy J. M., Maeda Shingo, Takahashi Yoshihide, Kamakura Tsukasa, Aiba Takeshi, Conte Giulio, Sarquella-Brugada Georgia, Leshem Eran, Rahkovich Michael, Hochstadt Aviram, Mizusawa Yuka, Arbelo Elena, Huang Zhengrong, Denjoy Isabelle, Giustetto Carla, Wijeyeratne Yanushi D., Napolitano Carlo, Michowitz Yoav, Brugada Ramon, Casado-Arroyo Ruben, Champagne Jean, Calo Leonardo, Tfelt-Hansen Jacob, Priori Silvia G., Takagi Masahiko, Veltmann Christian, Delise Pietro, Corrado Domenico, Behr Elijah R., Gaita Fiorenzo, Yan Gan-Xin, Brugada Josep, Leenhardt Antoine, Wilde Arthur A. M., Brugada Pedro, Kusano Kengo F., Hirao Kenzo, Nam Gi-Byoung, Probst Vincent, Belhassen Bernard Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS) Heart rhythm 2018;15 (5):716-724 [PubMed]
  • Hosseini S. Mohsen, Kim Raymond, Udupa Sharmila, Costain Gregory, Jobling Rebekah, Liston Eriskay, Jamal Seema M., Szybowska Marta, Morel Chantal F., Bowdin Sarah, Garcia John, Care Melanie, Sturm Amy C., Novelli Valeria, Ackerman Michael J., Ware James S., Hershberger Ray E., Wilde Arthur A. M., Gollob Michael H. Reappraisal of Reported Genes for Sudden Arrhythmic Death Circulation 2018;138 (12):1195-1205 [PubMed]
  • Amin Ahmad S., Wilde Arthur A. M., Tan Hanno L. Response to letter from Drs. Li et al. regarding our paper in Int. J. Cardiol. 2018. Doi: 10.1016/j.ijcard.2017.09.010: SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers International journal of cardiology 2018;271:124 [PubMed]
  • Baruteau Alban-Elouen, Kyndt Florence, Behr Elijah R., Vink Arja S., Lachaud Matthias, Joong Anna, Schott Jean-Jacques, Horie Minoru, Denjoy Isabelle, Crotti Lia, Shimizu Wataru, Bos Johan M., Stephenson Elizabeth A., Wong Leonie, Abrams Dominic J., Davis Andrew M., Winbo Annika, Dubin Anne M., Sanatani Shubhayan, Liberman Leonardo, Kaski Juan Pablo, Rudic Boris, Kwok Sit Yee, Rieubland Claudine, Tfelt-Hansen Jacob, van Hare George F., Guyomarc'h-Delasalle B. atrice, Blom Nico A., Wijeyeratne Yanushi D., Gourraud Jean-Baptiste, Marec Hervé Le, Ozawa Junichi, Fressart V. ronique, Lupoglazoff Jean-Marc, Dagradi Federica, Spazzolini Carla, Aiba Takeshi, Tester David J., Zahavich Laura A., Beauséjour-Ladouceur Virginie, Jadhav Mangesh, Skinner Jonathan R., Franciosi Sonia, Krahn Andrew D., Abdelsayed Mena, Ruben Peter C., Yung Tak-Cheung, Ackerman Michael J., Wilde Arthur A., Schwartz Peter J., Probst Vincent SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups European heart journal 2018;39 (31):2879-2887 [PubMed]
  • Amin Ahmad S., Reckman Yolan J., Arbelo Elena, Spanjaart Anne M., Postema Pieter G., Tadros Rafik, Tanck Michael W., van den Berg Maarten P., Wilde Arthur A. M., Tan Hanno L. SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers International journal of cardiology 2018;266:128-132 [PubMed]
  • Brouwer Tom F. Subcutaneous defibrillation: The new kid on the block 2018. ISBN 9789463750509. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Knops R. E.)
  • Hermans Ben J. M., Stoks Job, Bennis Frank C., Vink Arja S., Garde Ainara, Wilde Arthur A. M., Pison Laurent, Postema Pieter G., Delhaas Tammo Support vector machine-based assessment of the T-wave morphology improves long QT syndrome diagnosis Europace : European pacing, arrhythmias, and cardiac electrophysiology 2018;20 (3):iii113-iii119 [PubMed]
  • Filippini L. H. P. M., Postema P. G., Zoubin K., Hermans B. J. M., Blom N. A., Delhaas T., Wilde A. A. M. The brisk-standing-test for long QT syndrome in prepubertal school children: defining normal Europace : European pacing, arrhythmias, and cardiac electrophysiology 2018;20 (F11):f108–f112 [PubMed]
  • Zijlstra Jolande A. The contribution of lay rescuers in out-of-hospital cardiac arrest 2018. ISBN 9789492917010. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Koster R. W.)
  • van Dongen Ivo M., Kolk Maarten Z. H., Elias Joëlle, Meijborg Veronique M. F., Coronel Ruben, de Bakker Jacques M. T., Claessen Bimmer E. P. M., Delewi Ronak, Ouweneel Dagmar M., Scheunhage Esther M., van der Schaaf René J., Suttorp Maarten-Jan, Bax Matthijs, Marques Koen M., Postema Pieter G., Wilde Arthur A. M., Henriques José P. S. The effect of revascularization of a chronic total coronary occlusion on electrocardiographic variables. A sub-study of the EXPLORE trial Journal of electrocardiology 2018;51 (5):906-912 [PubMed]
  • Giudicessi John R., Wilde Arthur A. M., Ackerman Michael J. The genetic architecture of long QT syndrome: A critical reappraisal Trends in cardiovascular medicine 2018;28 (7):453-464 [PubMed]
  • Amin Ahmad S., Wilde Arthur A. M. The phenotype is equally important in promoting variants from benign to pathogenic as well as in demoting variants from pathogenic to benign Heart rhythm 2018;15 (4):562-563 [PubMed]
  • Wilde Arthur A. M., Remme Carol Ann Therapeutic approaches for Long QT syndrome type 3: an update Europace : European pacing, arrhythmias, and cardiac electrophysiology 2018;20 (2):222-224 [PubMed]
  • Wilde Arthur A. M. The Shanghai Score System in Brugada Syndrome: Using it Beyond a Diagnostic Score ∗ JACC. Clinical electrophysiology 2018;4 (6):731-732 [PubMed]
  • Werf Christian van der, Wilde Arthur A. M. Ventricular Tachycardias in Catecholaminergic Cardiomyopathy (Catecholaminergic Polymorphic Ventricular Tachycardia)in: Douglas P. Zipes, José Jalife, William Gregory Stevenson, editors. Cardiac Electrophysiology; From Cell to Bedside. Philadelphia: Elsevier; 2018. p. 850-857, ISBN 9780323447331
  • Kapplinger Jamie D., Pundi Krishna N., Larson Nicholas B., Callis Thomas E., Tester David J., Bikker Hennie, Wilde Arthur A. M., Ackerman Michael J. Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation Circulation. Genomic and precision medicine 2018;11 (2):e001424 [PubMed]

2017

  • Tjong Fleur V.Y., Brouwer Tom F., Koop Brendan, Soltis Brian, Shuros Allan, Schmidt Brian, Swackhamer Bryan, Quast Anne Floor E.B., Wilde Arthur A.M., Burke Martin C., Knops Reinoud E. Acute and 3-Month Performance of a Communicating Leadless Antitachycardia Pacemaker and Subcutaneous Implantable Defibrillator JACC. Clinical electrophysiology 2017;3 (13):1487-1498 [PubMed]
  • Milman Anat, Andorin Antoine, Gourraud Jean-Baptiste, Sacher Frederic, Mabo Philippe, Kim Sung-Hwan, Maeda Shingo, Takahashi Yoshihide, Kamakura Tsukasa, Aiba Takeshi, Conte Giulio, Juang Jimmy J. M., Leshem Eran, Rahkovich Michael, Hochstadt Aviram, Mizusawa Yuka, Postema Pieter G., Arbelo Elena, Huang Zhengrong, Denjoy Isabelle, Giustetto Carla, Wijeyeratne Yanushi D., Napolitano Carlo, Michowitz Yoav, Brugada Ramon, Casado-Arroyo Ruben, Champagne Jean, Calo Leonardo, Sarquella-Brugada Georgia, Tfelt-Hansen Jacob, Priori Silvia G., Takagi Masahiko, Veltmann Christian, Delise Pietro, Corrado Domenico, Behr Elijah R., Gaita Fiorenzo, Yan Gan-Xin, Brugada Josep, Leenhardt Antoine, Wilde Arthur A. M., Brugada Pedro, Kusano Kengo F., Hirao Kenzo, Nam Gi-Byoung, Probst Vincent, Belhassen Bernard Age of First Arrhythmic Event in Brugada Syndrome Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients Circulation. Arrhythmia and electrophysiology 2017;10 (12) [PubMed]
  • Postema Pieter G., Wilde Arthur A.M. Aging in Brugada Syndrome: What About Risks? JACC. Clinical electrophysiology 2017;3 (1):68-70 [PubMed]
  • Knops Reinoud E. A new era for cardiac rhythm management devices: Solutions for transvenous lead complications 2017. 295p. ISBN 9789462335752. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: de Groot J. R.)
  • Portero Vincent, Casini Simona, Hoekstra Maaike, Verkerk Arie O., Mengarelli Isabella, Belardinelli Luiz, Rajamani Sridharan, Wilde Arthur A. M., Bezzina Connie R., Veldkamp Marieke W., Remme Carol Ann Anti-arrhythmic potential of the late sodium current inhibitor GS-458967 in murine Scn5a-1798insD+/- and human SCN5A-1795insD+/- iPSC-derived cardiomyocytes Cardiovascular research 2017;113 (7):829-838 [PubMed]
  • Brouwer Tom F., Smeding Lonneke, Berger Wouter R., Driessen Antoine H. G., de Groot Joris R., Wilde Arthur A. M., Knops Reinoud E. Assessment of the Extravascular Implantable Defibrillator: Feasibility of Substernal Ventricular Pacing Journal of cardiovascular electrophysiology 2017;28 (6):674-676 [PubMed]
  • Bdier Amnah Y., Al-Ghamdi Saleh, Verma Prashant K., Dagriri Khalid, Alshehri Bandar, Jiman Omamah A., Ahmed Sherif E., Wilde Arthur A. M., Bhuiyan Zahurul A., Al-Aama Jumana Y. Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia Molecular genetics and genomic medicine 2017;5 (5):592-601 [PubMed]
  • Schwartz Peter J., Ackerman Michael J., Wilde Arthur A. M. Channelopathies as Causes of Sudden Cardiac Death Cardiac electrophysiology clinics 2017;9 (4):537-549 [PubMed]
  • Wilde Arthur A. M., Amin Ahmad Channelopathies, genetic testing and risk stratification International journal of cardiology 2017;237:53-55 [PubMed]
  • van Barreveld M., Dijkgraaf M. G. W., Hulleman M., Boersma L. V. A., Delnoy P. P. H. M., Meine M., Tuinenburg A. E., Theuns D. A. M. J., van der Voort P. H., Kimman G. P., Buskens E., Tijssen J. P. G., Bruinsma N., Verstraelen T. E., Zwinderman A. H., van Dessel P. H. F. M., Wilde A. A. M. Dutch outcome in implantable cardioverter-defibrillator therapy (DO-IT): registry design and baseline characteristics of a prospective observational cohort study to predict appropriate indication for implantable cardioverter-defibrillator Netherlands heart journal 2017;25 (10):574-580 [PubMed]
  • Vink Arja S., Clur Sally-Ann B., Geskus Ronald B., Blank Andreas C., de Kezel Charlotte C. A., Yoshinaga Masao, Hofman Nynke, Wilde Arthur A. M., Blom Nico A. Effect of Age and Sex on the QTc Interval in Children and Adolescents With Type 1 and 2 Long-QT Syndrome Circulation. Arrhythmia and electrophysiology 2017;10 (4) [PubMed]
  • Vermeer Alexa M., Lodder Elisabeth M., Christiaans Imke, van Langen Irene M., Wilde Arthur A., Bezzina Connie R., Tadros Rafik Familial Disease Is Not Always Genetic: A Family With Atrioventricular Block and Mitral Regurgitation Canadian journal of cardiology 2017;33 (4):554.e9-554.e11 [PubMed]
  • Lieve Krystien V., Verkerk Arie O., Podliesna Svitlana, van der Werf Christian, Tanck Michael W., Hofman Nynke, van Bergen Paul F., Beekman Leander, Bezzina Connie R., Wilde Arthur A. M., Lodder Elisabeth M. Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation International journal of cardiology 2017;236:187-193 [PubMed]
  • Semsarian Christopher, Wilde Arthur A. M. Genetic Causes in Cardiac Arrest Survivors Fake News or the Real Deal? Circulation. Cardiovascular genetics 2017;10 (3):UNSP e001784 [PubMed]
  • Jenewein T., Beckmann B. M., Rose S., Osterhues H. H., Schmidt U., Wolpert C., Miny P., Marschall C., Alders M., Bezzina C. R., Wilde A. A. M., Kääb S., Kauferstein S. Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene Forensic science international 2017;275:187-194 [PubMed]
  • Gho Johannes M. I. H., Postema Pieter G., Conijn Maartje, Bruinsma Nienke, de Jong Jonas S. S. G., Bezzina Connie R., Wilde Arthur A. M., Asselbergs Folkert W. Heart failure following STEMI: a contemporary cohort study of incidence and prognostic factors Open heart 2017;4 (2) [PubMed]
  • Hu Yi Juan, Schmidt Amand F., Dudbridge Frank, Holmes Michael V., Brophy James M., Tragante Vinicius, Li Ziyi, Liao Peizhou, Quyyumi Arshed A., McCubrey Raymond O., Horne Benjamin D., Hingorani Aroon D., Asselbergs Folkert W., Patel Riyaz S., Long Qi, Åkerblom Axel, Algra Ale, Allayee Hooman, Almgren Peter, Anderson Jeffrey L., Andreassi Maria G., Anselmi Chiara V., Ardissino Diego, Arsenault Benoit J., Ballantyne Christie M., Baranova Ekaterina V., Behloui Hassan, Bergmeijer Thomas O., Bezzina Connie R., Bjornsson Eythor, Body Simon C., Boeckx Bram, Boersma Eric H., Boerwinkle Eric, Bogaty Peter, Braund Peter S., Breitling Lutz P., Brenner Hermann, Briguori Carlo, Brugts Jasper J., Burkhardt Ralph, Cameron Vicky A., Carlquist John F., Carpeggiani Clara, Carruthers Kathryn F., Casu Gavino, Hovingh Kees, Maitland-Van Der Zee Anke H., Tanck Michael W.T., Wilde Arthur A.M. Impact of Selection Bias on Estimation of Subsequent Event Risk Circulation. Cardiovascular genetics 2017;10 (5)
  • Brouwer Tom F., Miller Marc A., Quast Anne-Floor B. E., Palaniswamy Chandrasekar, Dukkipati Srinivas R., Reddy Vivek, Wilde Arthur A., Willner Jonathan M., Knops Reinoud E. Implantation of the Subcutaneous Implantable Cardioverter-Defibrillator: An Evaluation of 4 Implantation Techniques Circulation. Arrhythmia and electrophysiology 2017;10 (1):e004663 [PubMed]
  • Veerman Christiaan C. Inherited arrhythmia syndromes: From genotype to phenotype in hiPSC-derived cardiomyocytes 2017. 244p. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Bezzina C. R., Wilde A. A. M.; Co-supervisor: Verkerk A. O.)
  • Wilde Arthur A. M., Semsarian Christopher In search of the holy grail in the channelopathy field: Proving pathogenicity of long QT syndrome-associated variants? Heart rhythm 2017;14 (8):1180-1181 [PubMed]
  • Antzelevitch Charles, Yan Gan-Xin, Ackerman Michael J., Borggrefe Martin, Corrado Domenico, Guo Jihong, Gussak Ihor, Hasdemir Can, Horie Minoru, Huikuri Heikki, Ma Changsheng, Morita Hiroshi, Nam Gi-Byoung, Sacher Frederic, Shimizu Wataru, Viskin Sami, Wilde Arthur A. M. J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge Europace : European pacing, arrhythmias, and cardiac electrophysiology 2017;19 (4):665-694 [PubMed]
  • Blom Nicolaas A., Gorgels Anton P. M., Hauer Richard N. W., van Hemel Norbert M., Wilde Arthur A. M. Klinische elektrocardiografie: Een handleiding voor zelfstandige beoordeling van het ECG.Houten: Bohn Stafleu Van Loghum; 2017. 318p. ISBN 9789036803298
  • Hoorntje Edgar T., Bollen Ilse A., Barge-Schaapveld Daniela Q., van Tienen Florence H., te Meerman Gerard J., Jansweijer Joeri A., van Essen Anthonie J., Volders Paul G., Constantinescu Alina A., van den Akker Peter C., van Spaendonck-Zwarts Karin Y., Oldenburg Rogier A., Marcelis Carlo L., van der Smagt Jasper J., Hennekam Eric A., Vink Aryan, Bootsma Marianne, Aten Emmelien, Wilde Arthur A., van den Wijngaard Arthur, Broers Jos L., Jongbloed Jan D., van der Velden Jolanda, van den Berg Maarten P., van Tintelen J. Peter Lamin A/C-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation Circulation. Cardiovascular genetics 2017;10 (4) [PubMed]
  • Roberts Jason D., Krahn Andrew D., Ackerman Michael J., Rohatgi Ram K., Moss Arthur J., Nazer Babak, Tadros Rafik, Gerull Brenda, Sanatani Shubhayan, Wijeyeratne Yanushi D., Baruteau Alban-Elouen, Muir Alison R., Pang Benjamin, Cadrin-Tourigny Julia, Talajic Mario, Rivard Lena, Tester David J., Liu Taylor, Whitman Isaac R., Wojciak Julianne, Conacher Susan, Gula Lorne J., Leong-Sit Peter, Manlucu Jaimie, Green Martin S., Hamilton Robert, Healey Jeff S., Lopes Coeli M., Behr Elijah R., Wilde Arthur A., Gollob Michael H., Scheinman Melvin M. Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? Circulation. Arrhythmia and electrophysiology 2017;10 (8) [PubMed]
  • ten Sande Judith N. Modulators of ventricular arrhythmias in structurally normal and abnormal hearts 2017. 175p. ISBN 9789077595176. [UvA Dissertations Online] University of Amsterdam. (Supervisors: de Bakker J. M. T., Wilde A. A. M.; Co-supervisors: van Dessel P. F. H. M., Coronel R.)
  • te Riele Anneline S. J. M., Agullo-Pascual Esperanza, James Cynthia A., Leo-Macias Alejandra, Cerrone Marina, Zhang Mingliang, Lin Xianming, Lin Bin, Sobreira Nara L., Amat-Alarcon Nuria, Marsman Roos F., Murray Brittney, Tichnell Crystal, van der Heijden Jeroen F., Dooijes Dennis, van Veen Toon A. B., Tandri Harikrishna, Fowler Steven J., Hauer Richard N. W., Tomaselli Gordon, van den Berg Maarten P., Taylor Matthew R. G., Brun Francesca, Sinagra Gianfranco, Wilde Arthur A. M., Mestroni Luisa, Bezzina Connie R., Calkins Hugh, van Tintelen J. Peter, Bu Lei, Delmar Mario, Judge Daniel P. Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis Cardiovascular research 2017;113 (1):102-111 [PubMed]
  • Quast A. F. B. E., van Dijk V. F., Wilde A. A. M., Knops R. E., Boersma L. V. A. Outpatient treatment with the wearable cardioverter defibrillator: clinical experience in two Dutch centres Netherlands heart journal 2017;25 (5):312-317 [PubMed]
  • Vermeer Alexa M. C., Clur Sally-Ann B., Blom Nico A., Wilde Arthur A. M., Christiaans Imke Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive Journal of pediatrics 2017;188:91-95 [PubMed]
  • Nademanee Koonlawee, Wilde Arthur A.M. Repolarization Versus Depolarization Defects in Brugada Syndrome: A Tale of 2 Different Electrophysiologic Settings? JACC. Clinical electrophysiology 2017;3 (4):364-366 [PubMed]
  • Veerman Christiaan C., Wilders Ronald, Wilde Arthur A., Coronel Ruben, Remme Carol Ann, Verkerk Arie O., Bezzina Connie R. Response by Veerman et al to Letter Regarding Article, "The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity" Circulation research 2017;121 (5):E21 [PubMed]
  • Tadros Rafik, Wilde Arthur A. M. Revisiting the sensitivity of sodium channel blocker testing in Brugada syndrome using obligate transmittance International journal of cardiology 2017;245:183-184 [PubMed]
  • Veerman Christiaan C., Mengarelli Isabella, Lodder Elisabeth M., Kosmidis Georgios, Bellin Milena, Zhang Miao, Dittmann Sven, Guan Kaomei, Wilde Arthur A. M., Schulze-Bahr Eric, Greber Boris, Bezzina Connie R., Verkerk Arie O. Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation Journal of the American Heart Association 2017;6 (7) [PubMed]
  • Veerman Christiaan C., Podliesna Svitlana, Tadros Rafik, Lodder Elisabeth M., Mengarelli Isabella, de Jonge Berend, Beekman Leander, Barc Julien, Wilders Ronald, Wilde Arthur A., Boukens Bastiaan J., Coronel Ruben, Verkerk Arie, Remme Carol Ann, Bezzina Connie R. The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity Circulation research 2017;121 (5):537-548 [PubMed]
  • Hermans Ben J. M., Vink Arja S., Bennis Frank C., Filippini Luc H., Meijborg Veronique M. F., Wilde Arthur A. M., Pison Laurent, Postema Pieter G., Delhaas Tammo The development and validation of an easy to use automatic QT-interval algorithm PLoS ONE 2017;12 (9) [PubMed]
  • Amin Ahmad S., Wilde Arthur A.M. The future of sudden cardiac death research Progress in pediatric cardiology 2017;45:49-54
  • Kluin Jolanda, Wilde Arthur A. M., Pinto Yigal, van Herwerden Lex A. To Add or Not to Add Mitral Valve Surgery to Septal Myectomy in HOCM Patients Journal of the American College of Cardiology 2017;69 (17):2250 [PubMed]
  • Vermeer Alexa M. C., Janssen Anneloes, Boorsma Peter C., Mannens Marcel M. A. M., Wilde Arthur A. M., Christiaans Imke Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy Amyloid : the international journal of experimental and clinical investigation 2017;24 (2):87-91 [PubMed]
  • Jansweijer Joeri A., Nieuwhof Karin, Russo Francesco, Hoorntje Edgar T., Jongbloed Jan D. H., Lekanne Deprez Ronald H., Postma Alex V., Bronk Marieke, van Rijsingen Ingrid A. W., de Haij Simone, Biagini Elena, van Haelst Paul L., van Wijngaarden Jan, van den Berg Maarten P., Wilde Arthur A. M., Mannens Marcel M. A. M., de Boer Rudolf A., van Spaendonck-Zwarts Karin Y., van Tintelen J. Peter, Pinto Yigal M. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy European journal of heart failure 2017;19 (4):512-521 [PubMed]
  • Lahrouchi Najim, Raju Hariharan, Lodder Elisabeth M., Papatheodorou Efstathios, Ware James S., Papadakis Michael, Tadros Rafik, Cole Della, Skinner Jonathan R., Crawford Jackie, Love Donald R., Pua Chee J., Soh Bee Y., Bhalshankar Jaydutt D., Govind Risha, Tfelt-Hansen Jacob, Winkel Bo G., van der Werf Christian, Wijeyeratne Yanushi D., Mellor Greg, Till Jan, Cohen Marta C., Tome-Esteban Maria, Sharma Sanjay, Wilde Arthur A. M., Cook Stuart A., Bezzina Connie R., Sheppard Mary N., Behr Elijah R. Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome Journal of the American College of Cardiology 2017;69 (17):2134-2145 [PubMed]
  • Tadros Rafik, Nannenberg Eline A., Lieve Krystien V. , Skoric-Milosavljevic Doris, Lahrouchi Najim, Lekanne Dit Deprez Ronald H., Vendrik Jeroen, Reckman Yolan J. , Postema Pieter G., Amin Ahmad S., Bezzina Connie R. , Wilde Arthur A. M., Tan Hanno L. Yield and pitfalls of ajmaline testing in the evaluation of unexplained cardiac arrest and sudden unexplained death: Single centre experience of 482 families. Journal of the American College of Cardiology Clinical Electrophysiology 2017;3 (12):1400-1408 [PubMed]

2016

  • Itoh Hideki, Berthet Myriam, Fressart Véronique, Denjoy Isabelle, Maugenre Svetlana, Klug Didier, Mizusawa Yuka, Makiyama Takeru, Hofman Nynke, Stallmeyer Birgit, Zumhagen Sven, Shimizu Wataru, Wilde Arthur A. M., Schulze-Bahr Eric, Horie Minoru, Tezenas du Montcel Sophie, Guicheney Pascale Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction European journal of human genetics 2016;24 (8):1160-1166 [PubMed]
  • Krul Sébastien P. J. Autonomic and surgical substrate modulation of atrial fibrillation 2016. 217p. ISBN 9789461698551. [UvA Dissertations Online] University of Amsterdam. (Supervisors: de Bakker J. M. T., Wilde A. A. M.; Co-supervisors: de Groot J. R., de Mol B. A.)
  • Olde Nordkamp Louise R. A., Conte Giulio, Rosenmöller Boudewijn R. A. M., Warnaars Joppe L. F., Tan Hanno L., Caputo Maria L., Regoli Francois, Moccetti Tiziano, Auricchio Angelo, Knops Reinoud E., Wilde Arthur A. M. Brugada Syndrome and the Subcutaneous Implantable Cardioverter-Defibrillator Journal of the American College of Cardiology 2016;68 (6):665-666 [PubMed]
  • van der Bilt Ivo A. C. Cardiac abnormalities after aneurysmal subarachnoid hemorrhageEde: GVO drukkers & vormgevers B.V.; 2016. 136p. ISBN 9789090297057. [UvA Dissertations Online] Universiteit Utrecht. (Supervisors: Rinkel G., Wilde A. A. M.; Co-supervisor: Hasan D.)
  • Lieve Krystien V., van der Werf Christian, Wilde Arthur A. Catecholaminergic Polymorphic Ventricular Tachycardia Circulation journal 2016;80 (6):1285-1291 [PubMed]
  • Wilde Arthur A. M. Challenging the unifying pathophysiological concept of J-wave syndromes Heart rhythm 2016;13 (8):1729-1730 [PubMed]
  • Wilde Arthur A. M., Moss Arthur J., Kaufman Elizabeth S., Shimizu Wataru, Peterson Derick R., Benhorin Jesaia, Lopes Coeli, Towbin Jeffrey A., Spazzolini Carla, Crotti Lia, Zareba Wojciech, Goldenberg Ilan, Kanters Jørgen K., Robinson Jennifer L., Qi Ming, Hofman Nynke, Tester David J., Bezzina Connie R., Alders Marielle, Aiba Takeshi, Kamakura Shiro, Miyamoto Yoshihiro, Andrews Mark L., McNitt Scott, Polonsky Bronislava, Schwartz Peter J., Ackerman Michael J. Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study Circulation 2016;134 (12):872-882 [PubMed]
  • Tjong F. V. Y., Brouwer T. F., Smeding L., Kooiman K. M., de Groot J. R., Ligon D., Sanghera R., Schalij M. J., Wilde A. A. M., Knops R. E. Combined leadless pacemaker and subcutaneous implantable defibrillator therapy: feasibility, safety, and performance Europace : European pacing, arrhythmias, and cardiac electrophysiology 2016;18 (11):1740-1747 [PubMed]
  • Tjong Fleur V. Y., Brouwer Tom F., Kooiman Kirsten M., Smeding Lonneke, Koop Brendan, Soltis Brian, Shuros Allan, Wilde Arthur A. M., Burke Martin, Knops Reinoud E. Communicating Antitachycardia Pacing-Enabled Leadless Pacemaker and Subcutaneous Implantable Defibrillator Journal of the American College of Cardiology 2016;67 (15):1865-1866 [PubMed]
  • Lahrouchi N., Wilde A. A.M. Complexity of Molecular Genetics in the Inherited Cardiac Arrhythmiasin: Ion Channels in Health and Disease. Elsevier Inc.; 2016. p. 345-368, ISBN 9780128020029
  • Tan Hanno L., Wilde Arthur A. M. Contra-indicaties: Brugada-syndroomin: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2016/2017. Houten: Health Base; 2016. p. 960-961, ISBN 9789074027397
  • Wilde Arthur A. M. Contra-indicaties: Lang-QT-intervalsyndroom (LQTS)in: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2016/2017. Houten: Health Base; 2016. p. 818-824, ISBN 9789074027397
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Contra-indicaties: Tachy-aritmieënin: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2016/2017. Houten: Health Base; 2016. p. 766-768, ISBN 9789074027397
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Contra-indicaties: Wolff-Parkinson-White-syndroom (WPW)in: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2016/2017. Houten: Health Base; 2016. p. 962-963, ISBN 9789074027397
  • ten Sande Judith N., Postema Pieter G., Boekholdt S. Matthijs, Tan Hanno L., van der Heijden Jeroen F., de Groot Natasja M. S., Volders Paul G. A., Zeppenfeld Katja, Boersma Lucas V. A., Nannenberg Eline A., Christiaans Imke, Wilde Arthur A. M. Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus Heart rhythm 2016;13 (4):905-912 [PubMed]
  • Vermeer Alexa M. C., Lodder Elisabeth M., Thomas Dierk, Duijkers Floor A. M., Marcelis Carlo, van Gorselen Edwin O. F., Fortner Philipp, Buss Sebastian J., Mereles Derliz, Katus Hugo A., Wilde Arthur A. M., Bezzina Connie R., Boekholdt S. Matthijs, Schweizer Patrick A., Christiaans Imke Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 Mutations Journal of the American College of Cardiology 2016;67 (19):2313-2315 [PubMed]
  • Berger Wouter R., Krul Sébastien P. J., van der Pol Joy A., van Dessel Pascal F. H. M., Conrath Chantal E., Wilde Arthur A. M., de Groot Joris R. Documented atrial fibrillation recurrences after pulmonary vein isolation are associated with diminished quality of life Journal of cardiovascular medicine (Hagerstown, Md.) 2016;17 (3):201-208 [PubMed]
  • Elliott Perry, Charron Philippe, Blanes Juan Ramon Gimeno, Tavazzi Luigi, Tendera Michal, Konté Marème, Laroche Cécile, Maggioni Aldo P., Anastasakis Aris, Arbustini Eloisa, Asselbergs Folkert W., Axelsson Anna, Brito Dulce, Caforio Alida L.P., Carr-White Gerald, Czekaj Agata, Damy Thibaud, Devoto Emmanuela, Favalli Valentina, Findlay Iain, Garcia-Pavia Pablo, Hagège Albert, Heliö Tiina, Iliceto Sabino, Isnard Richard, Jansweijer Joeri A., Limongelli Giuseppe, Linhart Ales, Cuenca David López, Mansencal Nicolas, McKeown Pascal, Mogensen Jens, Mohiddin Saidi A., Monserrat Lorenzo, Olivotto Iacopo, Rapezzi Claudio, Rigopoulos A. G., Rosmini Stefania, Pfeiffer Barbara, Wicks Eleanor, Podzimkova J., Kuchynka P., Palecek T., Bundgaard H., Thune J. J., Kumme A., Due Vestergaard L., Wilde A.A.M., Pinto Y., Van Der Heijden J. F. European cardiomyopathy pilot registry: EURObservational research programme of the European society of cardiology European heart journal 2016;37 (2):164-173 [PubMed]
  • Gottschalk Byron H., Anselm Daniel D., Brugada Josep, Brugada Pedro, Wilde Arthur A., Chiale Pablo A., Pérez-Riera Andres R., Elizari Marcelo V., de Luna Antoni Bayés, Krahn Andrew D., Tan Hanno L., Postema Pieter G., Baranchuk Adrian Expert cardiologists cannot distinguish between Brugada phenocopy and Brugada syndrome electrocardiogram patterns Europace : European pacing, arrhythmias, and cardiac electrophysiology 2016;18 (7):1095-1100 [PubMed]
  • Padfield Gareth J., AlAhmari Leenah, Lieve Krystien V. V., AlAhmari Tasneem, Roston Thomas M., Wilde Arthur A., Krahn Andrew D., Sanatani Shubhayan Flecainide monotherapy is an option for selected patients with catecholaminergic polymorphic ventricular tachycardia intolerant of β-blockade Heart rhythm 2016;13 (2):609-613 [PubMed]
  • Mizusawa Yuka Genetic and environmental factors in cardiac sodium channel disease 2016. 280p. ISBN 9789461699008. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Bezzina C. R.; Co-supervisors: Tan H. L., Postema P. G.)
  • Amin Ahmad S., Wilde Arthur A. M. Genetic Control of Potassium Channels Cardiac electrophysiology clinics 2016;8 (2):285-306 [PubMed]
  • Amin Ahmad S., Wilde Arthur A. M. Genetic screening in acquired long QT syndrome? CAUTION: proceed carefully European heart journal 2016;37 (18):1465-1468 [PubMed]
  • Lodder Elisabeth M., de Nittis Pasquelena, Koopman Charlotte D., Wiszniewski Wojciech, Moura de Souza Carolina Fischinger, Lahrouchi Najim, Guex Nicolas, Napolioni Valerio, Tessadori Federico, Beekman Leander, Nannenberg Eline A., Boualla Lamiae, Blom Nico A., de Graaff Wim, Kamermans Maarten, Cocciadiferro Dario, Malerba Natascia, Mandriani Barbara, Akdemir Zeynep Hande Coban, Fish Richard J., Eldomery Mohammad K., Ratbi Ilham, Wilde Arthur A. M., de Boer Teun, Simonds William F., Neerman-Arbez Marguerite, Sutton V. Reid, Kok Fernando, Lupski James R., Reymond Alexandre, Bezzina Connie R., Bakkers Jeroen, Merla Giuseppe GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability American journal of human genetics 2016;99 (3):704-710 [PubMed]
  • Veerman Christiaan C., Mengarelli Isabella, Guan Kaomei, Stauske Michael, Barc Julien, Tan Hanno L., Wilde Arthur A. M., Verkerk Arie O., Bezzina Connie R. hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities Scientific reports 2016;6:30967 [PubMed]
  • Vermeer Alexa M. C., Wilde Arthur A. M., Christiaans Imke Human genetics of cardiomyopathiesin: Silke Rickert-Sperling, Robert G. Kelly, D. J. Driscoll, editors. Congenital heart diseases: the broken heart; clinical features, human genetics and molecular pathways. Wenen: Springer-Verlag; 2016. p. 675-686, ISBN 9783709118825
  • Visser Marloes, van der Heijden Jeroen F., Doevendans Pieter A., Loh Peter, Wilde Arthur A., Hassink Rutger J. Idiopathic Ventricular Fibrillation: The Struggle for Definition, Diagnosis, and Follow-Up Circulation. Arrhythmia and electrophysiology 2016;9 (5):e003817 [PubMed]
  • Andorin Antoine, Behr Elijah R., Denjoy Isabelle, Crotti Lia, Dagradi Federica, Jesel Laurence, Sacher Fréderic, Petit Bertrand, Mabo Philippe, Maltret Alice, Wong Leonie C. H., Degand Bruno, Bertaux Géraldine, Maury Philippe, Dulac Yves, Delasalle Béatrice, Gourraud Jean-Baptiste, Babuty Dominique, Blom Nico A., Schwartz Peter J., Wilde Arthur A., Probst Vincent Impact of clinical and genetic findings on the management of young patients with Brugada syndrome Heart rhythm 2016;13 (6):1274-1282 [PubMed]
  • Olde Nordkamp Louise R. A., Wilde Arthur A. M. Implantable cardiac defibrillation in inherited arryhthmia syndromesin: Kenneth A. Ellenbogen, Bruce L. Wilkoff, G. Neal Kay, Chu-Pak Lau, Angelo Auricchio, editors. Clinical cardiac pacing, defibrillation and resynchronization therapy (5th ed.). S.l.: Elsevier; 2016. p. 566-578, ISBN 9780323378048; 9780323394833
  • Olde Nordkamp Louise R. A., Postema Pieter G., Knops Reinoud E., van Dijk Nynke, Limpens Jacqueline, Wilde Arthur A. M., de Groot Joris R. Implantable cardioverter-defibrillator harm in young patients with inherited arrhythmia syndromes: A systematic review and meta-analysis of inappropriate shocks and complications Heart rhythm 2016;13 (2):443-454 [PubMed]
  • van der Werf Christian, Hendrix Anneke, Birnie Erwin, Bots Michiel L., Vink Aryan, Bardai Abdennasser, Blom Marieke T., Bosch Jan, Bruins Wendy, Das C. Kees, Koster Rudolph W., Naujocks Tatjana, Schaap Balthasar, Tan Hanno L., de Vos Ronald, de Vries Philip, Woonink Frits, Doevendans Pieter A., van Weert Henk C., Wilde Arthur A. M., Mosterd Arend, van Langen Irene M. Improving usual care after sudden death in the young with focus on inherited cardiac diseases (the CAREFUL study): a community-based intervention study Europace : European pacing, arrhythmias, and cardiac electrophysiology 2016;18 (4):592-601 [PubMed]
  • Wilde Arthur A. M. Interactiemechanismen: Verlenging QT-intervalin: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2016/2017. Houten: Health Base; 2016. p. 23-25, ISBN 9789074027397
  • Antzelevitch Charles, Yan Gan-Xin, Ackerman Michael J., Borggrefe Martin, Corrado Domenico, Guo Jihong, Gussak Ihor, Hasdemir Can, Horie Minoru, Huikuri Heikki, Ma Changsheng, Morita Hiroshi, Nam Gi-Byoung, Sacher Frederic, Shimizu Wataru, Viskin Sami, Wilde Arthur A. M. J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge Heart rhythm 2016;13 (10):E295-E324 [PubMed]
  • Antzelevitch Charles, Yan Gan-Xin, Ackerman Michael J., Borggrefe Martin, Corrado Domenico, Guo Jihong, Gussak Ihor, Hasdemir Can, Horie Minoru, Huikuri Heikki, Ma Changsheng, Morita Hiroshi, Nam Gi-Byoung, Sacher Frederic, Shimizu Wataru, Viskin Sami, Wilde Arthur A. M. J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge Journal of arrhythmia 2016;32 (5):315-339 [PubMed]
  • Amin Ahmad S., Pinto Yigal M., Ackerman Michael J., Wilde Arthur A. M. Letter by Amin et al Regarding Article, "Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3 ' Untranslated Region of KCNQ1?" Circulation. Cardiovascular genetics 2016;9 (6):580 [PubMed]
  • Brouwer Tom F., Yilmaz Dilek, Lindeboom Robert, Buiten Maurits S., Olde Nordkamp Louise R. A., Schalij Martin J., Wilde Arthur A., van Erven Lieselot, Knops Reinoud E. Long-Term Clinical Outcomes of Subcutaneous Versus Transvenous Implantable Defibrillator Therapy Journal of the American College of Cardiology 2016;68 (19):2047-2055 [PubMed]
  • Visser Marloes, van der Heijden Jeroen F., van der Smagt Jasper J., Doevendans Pieter A., Wilde Arthur A., Loh Peter, Hassink Rutger J. Long-Term Outcome of Patients Initially Diagnosed With Idiopathic Ventricular Fibrillation: A Descriptive Study Circulation. Arrhythmia and electrophysiology 2016;9 (10):e004258 [PubMed]
  • Kutty Shelby Modern echocardiography in pediatric right heart assessment 2016. 182p. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Sreeram N.)
  • van der Bilt Ivo A. C., Vendeville Jean-Paul, van de Hoef Tim P., Begieneman Mark P. V., Lagrand Wim K., Kros Johan M., Wilde Arthur A. M., Rinkel Gabriel J. E., Niessen Hans W. M. Myocarditis in patients with subarachnoid hemorrhage: A histopathologic study Journal of critical care 2016;32:196-200 [PubMed]
  • Batchvarov Velislav N., Bastiaenen Rachel, Postema Pieter G., Clark Elaine N., Macfarlane Peter W., Wilde Arthur A. M., Behr Elijah R. Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy Europace : European pacing, arrhythmias, and cardiac electrophysiology 2016;18 (9):1420-1426 [PubMed]
  • Hodes Anke R., Tichnell Crystal, te Riele Anneline S. J. M., Murray Brittney, Groeneweg Judith A., Sawant Abhishek C., Russell Stuart D., van Spaendonck-Zwarts Karin Y., van den Berg Maarten P., Wilde Arthur A., Tandri Harikrishna, Judge Daniel P., Hauer Richard N. W., Calkins Hugh, van Tintelen J. Peter, James Cynthia A. Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy Heart (British Cardiac Society) 2016;102 (4):303-312 [PubMed]
  • Wilde Arthur A.M., Postema Pieter G. Prevalence and clinical characteristics of brugada syndromein: J Wave Syndromes. Springer International Publishing; 2016. p. 121-138, ISBN 9783319315768
  • Mizusawa Yuka, Morita Hiroshi, Adler Arnon, Havakuk Ofer, Thollet Aurélie, Maury Philippe, Wang Dao W., Hong Kui, Gandjbakhch Estelle, Sacher Frédéric, Hu Dan, Amin Ahmad S., Lahrouchi Najim, Tan Hanno L., Antzelevitch Charles, Probst Vincent, Viskin Sami, Wilde Arthur A. M. Prognostic significance of fever-induced Brugada syndrome Heart rhythm 2016;13 (7):1515-1520 [PubMed]
  • Sroubek Jakub, Probst Vincent, Mazzanti Andrea, Delise Pietro, Hevia Jesus Castro, Ohkubo Kimie, Zorzi Alessandro, Champagne Jean, Kostopoulou Anna, Yin Xiaoyan, Napolitano Carlo, Milan David J., Wilde Arthur, Sacher Frederic, Borggrefe Martin, Ellinor Patrick T., Theodorakis George, Nault Isabelle, Corrado Domenico, Watanabe Ichiro, Antzelevitch Charles, Allocca Giuseppe, Priori Silvia G., Lubitz Steven A. Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis Circulation 2016;133 (7):622-630 [PubMed]
  • Kosmidis Georgios, Veerman Christiaan C., Casini Simona, Verkerk Arie O., van de Pas Simone, Bellin Milena, Wilde Arthur A. M., Mummery Christine L., Bezzina Connie R. Readthrough-Promoting Drugs Gentamicin and PTC124 Fail to Rescue Nav1.5 Function of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes Carrying Nonsense Mutations in the Sodium Channel Gene SCN5A Circulation. Arrhythmia and electrophysiology 2016;9 (11):e004227 [PubMed]
  • Cremers Charlotte H. P., van der Bilt Ivo A. C., van der Schaaf Irene C., Vergouwen Mervyn D. I., Dankbaar Jan Willem, Cramer Maarten J., Wilde Arthur A. M., Rinkel Gabriel J. E., Velthuis Birgitta K. Relationship Between Cardiac Dysfunction and Cerebral Perfusion in Patients with Aneurysmal Subarachnoid Hemorrhage Neurocritical care 2016;24 (2):202-206 [PubMed]
  • Nademanee Koonlawee, Raju Hariharan, de Noronha Sofia, Papadakis Michael, Robinson Laurence, Rothery Stephen, Makita Naomasa, Kowase Shinya, Boonmee Nakorn, Vitayakritsirikul Vorapot, Ratanarapee Samrerng, Sharma Sanjay, van der Wal Allard C., Christiansen Michael, Tan Hanno L., Wilde Arthur A., Nogami Akihiko, Sheppard Mary N., Veerakul Gumpanart, Behr Elijah R. REPLY: Search for Evidence-Based Medicine for Brugada Syndrome The Complex Network of the Brugada Syndrome Journal of the American College of Cardiology 2016;67 (13):1658-1659 [PubMed]
  • de Ferrari Gaetano M., Dusi Veronica, Spazzolini Carla, Bos J. Martijn, Abrams Dominic J., Berul Charles I., Crotti Lia, Eldar Michael, Kharlap Maria, Khoury Asaad, Krahn Andrew D., Leenhardt Antoine, Moir Christopher R., Odero Attilio, Nordkamp Louise Olde, Paul Thomas, I Noguer Ferran Rosés, Shkolnikova Maria, Till Jan, Wilde Arthur A. M., Ackerman Michael J., Schwartz Peter J. Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation" Circulation 2016;133 (4):e366-e367 [PubMed]
  • Wilde Arthur A. M., Postema Pieter G. Risk Stratification in Brugada Syndrome: The "Impossible" Made Possible? Journal of the American College of Cardiology 2016;67 (12):1441-1443 [PubMed]
  • Postema Pieter G., Wilde Arthur A. M. Risk stratification in Brugada syndrome: Where is the finish line? Heart rhythm 2016;13 (10):1955-1956 [PubMed]
  • Hofman Nynke, Wilde Arthur A. M. Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal Hearts Cardiac electrophysiology clinics 2016;8 (3):515-523 [PubMed]
  • Ruwald Martin H., Xu Parks Xiaorong, Moss Arthur J., Zareba Wojciech, Baman Jayson, McNitt Scott, Kanters Jorgen K., Shimizu Wataru, Wilde Arthur A., Jons Christian, Lopes Coeli M. Stop-codon and C-terminal nonsense mutations are associated with a lower risk of cardiac events in patients with long QT syndrome type 1 Heart rhythm 2016;13 (1):122-131 [PubMed]
  • Milano Annalisa, Blom Marieke T., Lodder Elisabeth M., van Hoeijen Daniel A., Barc Julien, Koopmann Tamara T., Bardai Abdennasser, Beekman Leander, Lichtner Peter, van den Berg Maarten P., Wilde Arthur A. M., Bezzina Connie R., Tan Hanno L. Sudden Cardiac Arrest and Rare Genetic Variants in the Community Circulation. Cardiovascular genetics 2016;9 (2):147-153 [PubMed]
  • Brouwer Tom F., Driessen Antoine H.G., Olde Nordkamp Louise R.A., Kooiman Kirsten M., De Groot Joris R., Wilde Arthur A.M., Knops Reinoud E. Surgical management of implantation-related complications of the subcutaneous implantable cardioverter-defibrillator JACC. Clinical electrophysiology 2016;2 (1):89-96
  • Devalla Harsha D., Gélinas Roselle, Aburawi Elhadi H., Beqqali Abdelaziz, Goyette Philippe, Freund Christian, Chaix Marie-A., Tadros Rafik, Jiang Hui, Le Béchec Antony, Monshouwer-Kloots Jantine J., Zwetsloot Tom, Kosmidis Georgios, Latour Frédéric, Alikashani Azadeh, Hoekstra Maaike, Schlaepfer Jurg, Mummery Christine L., Stevenson Brian, Kutalik Zoltan, de Vries Antoine Af, Rivard Léna, Wilde Arthur Am, Talajic Mario, Verkerk Arie O., Al-Gazali Lihadh, Rioux John D., Bhuiyan Zahurul A., Passier Robert TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT EMBO molecular medicine 2016;8 (12):1390-1408 [PubMed]
  • Lieve Krystien V. V., Wilde Arthur A., van der Werf Christian The Role of Flecainide in the Management of Catecholaminergic Polymorphic Ventricular Tachycardia Arrhythmia & electrophysiology review 2016;5 (1):45-49 [PubMed]
  • Yagihara Nobue, Watanabe Hiroshi, Barnett Phil, Duboscq-Bidot Laetitia, Thomas Atack C., Yang Ping, Ohno Seiko, Hasegawa Kanae, Kuwano Ryozo, Chatel Stéphanie, Redon Richard, Schott Jean-Jacques, Probst Vincent, Koopmann Tamara T., Bezzina Connie R., Wilde Arthur A. M., Nakano Yukiko, Aiba Takeshi, Miyamoto Yoshihiro, Kamakura Shiro, Darbar Dawood, Donahue Brian S., Shigemizu Daichi, Tanaka Toshihiro, Tsunoda Tatsuhiko, Suda Masayoshi, Sato Akinori, Minamino Tohru, Endo Naoto, Shimizu Wataru, Horie Minoru, Roden Dan M., Makita Naomasa Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes Journal of the American Heart Association 2016;5 (9):e003644 [PubMed]

2015

  • Kolder Iris C. R. M., Tanck Michael W. T., Postema Pieter G., Barc Julien, Sinner Moritz F., Zumhagen Sven, Husemann Anja, Stallmeyer Birgit, Koopmann Tamara T., Hofman Nynke, Pfeufer Arne, Lichtner Peter, Meitinger Thomas, Beckmann Britt M., Myerburg Robert J., Bishopric Nanette H., Roden Dan M., Kääb Stefan, Wilde Arthur A. M., Schott Jean-Jacques, Schulze-Bahr Eric, Bezzina Connie R. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2 Circulation. Cardiovascular genetics 2015;8 (3):447-456 [PubMed]
  • Kuiper Mathijs, Willems Albert, Wilde Arthur A. M. An unexpected ECG finding Netherlands heart journal 2015;23 (12):613-616 [PubMed]
  • Haas Jan, Frese Karen S., Peil Barbara, Kloos Wanda, Keller Andreas, Nietsch Rouven, Feng Zhu, Müller Sabine, Kayvanpour Elham, Vogel Britta, Sedaghat-Hamedani Farbod, Lim Wei-Keat, Zhao Xiaohong, Fradkin Dmitriy, Köhler Doreen, Fischer Simon, Franke Jennifer, Marquart Sabine, Barb Ioana, Li Daniel Tian, Amr Ali, Ehlermann Philipp, Mereles Derliz, Weis Tanja, Hassel Sarah, Kremer Andreas, King Vanessa, Wirsz Emil, Isnard Richard, Komajda Michel, Serio Alessandra, Grasso Maurizia, Syrris Petros, Wicks Eleanor, Plagnol Vincent, Lopes Luis, Gadgaard Tenna, Eiskjær Hans, Jørgensen Mads, Garcia-Giustiniani Diego, Ortiz-Genga Martin, Crespo-Leiro Maria G., Deprez Rondal H. Lekanne Dit, Christiaans Imke, van Rijsingen Ingrid A., Wilde Arthur A., Waldenstrom Anders, Bolognesi Martino, Bellazzi Riccardo, Mörner Stellan, Bermejo Justo Lorenzo, Monserrat Lorenzo, Villard Eric, Mogensen Jens, Pinto Yigal M., Charron Philippe, Elliott Perry, Arbustini Eloisa, Katus Hugo A., Meder Benjamin Atlas of the clinical genetics of human dilated cardiomyopathy European heart journal 2015;36 (18):1123-135a [PubMed]
  • Amin Ahmad Shoaib, Peters René H. J., Verstraaten Maaike, Wilde Arthur A. M., Buijs Eugène M. Baseline NT-ProBNP level predicts success of cardioversion of atrial fibrillation with flecainide Netherlands heart journal 2015;23 (3):182-189 [PubMed]
  • Wilde Arthur A. M., Postema Pieter G. Bringing home the bacon? The next step in cardiac sodium channelopathies Journal of clinical investigation 2015;125 (1):99-101 [PubMed]
  • van Brussel Peter M., Lieve Krystien V. V., de Winter Robbert J., Wilde Arthur A. M. Cardiorenal axis and arrhythmias: Will renal sympathetic denervation provide additive value to the therapeutic arsenal? Heart rhythm 2015;12 (5):1080-1087 [PubMed]
  • van der Werf Christian, Wilde Arthur A. M. Catecholaminergic polymorphic ventricular tachycardia: disease with different faces Circulation. Arrhythmia and electrophysiology 2015;8 (3):523-525 [PubMed]
  • Chockalingam Priya, Mizusawa Yuka, Wilde Arthur A. M. Channelopathies - emerging trends in the management of inherited arrhythmias Indian pacing and electrophysiology journal 2015;15 (1):43-54 [PubMed]
  • Scicluna Brendon P., Remme Carol Ann, Rivaud Mathilde, Wilde Arthur A. M., Bezzina Connie R., Verkerk Arie O. Chemokine ligand 9 modulates cardiac repolarization via Cxcr3 receptor binding International journal of cardiology 2015;201:49-52 [PubMed]
  • Knops Reinoud E., Tjong Fleur V. Y., Neuzil Petr, Sperzel Johannes, Miller Marc A., Petru Jan, Simon Jaroslav, Sediva Lucie, de Groot Joris R., Dukkipati Srinivas R., Koruth Jacob S., Wilde Arthur A. M., Kautzner Josef, Reddy Vivek Y. Chronic performance of a leadless cardiac pacemaker: 1-year follow-up of the LEADLESS trial Journal of the American College of Cardiology 2015;65 (15):1497-1504 [PubMed]
  • Bardai Abdenasser Clinical, electrocardiographic and genetic risk factors for sudden cardiac death 2015. 263p. ISBN 9789462951136. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Tan H. L.)
  • de Ferrari Gaetano M., Dusi Veronica, Spazzolini Carla, Bos J. Martijn, Abrams Dominic J., Berul Charles I., Crotti Lia, Davis Andrew M., Eldar Michael, Kharlap Maria, Khoury Asaad, Krahn Andrew D., Leenhardt Antoine, Moir Christopher R., Odero Attilio, Olde Nordkamp Louise, Paul Thomas, Rosés I Noguer Ferran, Shkolnikova Maria, Till Jan, Wilde Arthur A. M., Ackerman Michael J., Schwartz Peter J. Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia The Role of Left Cardiac Sympathetic Denervation Circulation 2015;131 (25):2185-2193 [PubMed]
  • Groeneweg Judith A., Bhonsale Aditya, James Cynthia A., te Riele Anneline S., Dooijes Dennis, Tichnell Crystal, Murray Brittney, Wiesfeld Ans C. P., Sawant Abhishek C., Kassamali Bina, Atsma Douwe E., Volders Paul G., de Groot Natasja M., de Boer Karin, Zimmerman Stefan L., Kamel Ihab R., van der Heijden Jeroen F., Russell Stuart D., Jan Cramer Maarten, Tedford Ryan J., Doevendans Pieter A., van Veen Toon A., Tandri Harikrishna, Wilde Arthur A., Judge Daniel P., van Tintelen J. Peter, Hauer Richard N., Calkins Hugh Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members Circulation. Cardiovascular genetics 2015;8 (3):437-446 [PubMed]
  • Tan Hanno L., Wilde Athur A. M. Contra-Indicaties - Brugada-syndroomin: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, M. Heringa, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2015/2016. Houten: Health Base; 2015. p. 964-965, ISBN 9789074027380
  • Wilde Arthur A. M. Contra-Indicaties - Lang-QT-intervalsyndroom (LQTS)in: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, M. Heringa, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2015/2016. Houten: Health Base; 2015. p. 822-828, ISBN 9789074027380
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Contra-Indicaties - Tachy-aritmieënin: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, M. Heringa, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2015/2016. Houten: Health Base; 2015. p. 775-777, ISBN 9789074027380
  • Wilde Arthur A. M. Contra-Indicaties - Wolff-Parkinson-White-syndroom (WPW)in: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, M. Heringa, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2015/2016. Houten: Health Base; 2015. p. 966-967, ISBN 9789074027380
  • Chorin Ehud, Havakuk Ofer, Adler Arnon, Steinvil Arie, Rozovski Uri, van der Werf Christian, Postema Pieter G., Topaz Guy, Wilde Arthur A. M., Viskin Sami, Rosso Raphael Diagnostic value of T-wave morphology changes during "QT stretching" in patients with long QT syndrome Heart rhythm 2015;12 (11):2263-2271 [PubMed]
  • Kapplinger Jamie D., Giudicessi John R., Ye Dan, Tester David J., Callis Thomas E., Valdivia Carmen R., Makielski Jonathan C., Wilde Arthur A., Ackerman Michael J. Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel Circulation. Cardiovascular genetics 2015;8 (4):582-595 [PubMed]
  • Kapplinger Jamie D., Tseng Andrew S., Salisbury Benjamin A., Tester David J., Callis Thomas E., Alders Marielle, Wilde Arthur A. M., Ackerman Michael J. Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel Journal of cardiovascular translational research 2015;8 (3):187-197 [PubMed]
  • Wilde Arthur A. M., Nademanee Koonlawee Epicardial Substrate Ablation in Brugada Syndrome: Time for a Randomized Trial! Circulation. Arrhythmia and electrophysiology 2015;8 (6):1306-1308 [PubMed]
  • Viskin Sami, Rosso Raphael, Friedensohn Limor, Havakuk Ofer, Wilde Arthur A. M. Everybody has Brugada syndrome until proven otherwise? Heart rhythm 2015;12 (7):1595-1598 [PubMed]
  • Nademanee Koonlawee, Raju Hariharan, de Noronha Sofia V., Papadakis Michael, Robinson Laurence, Rothery Stephen, Makita Naomasa, Kowase Shinya, Boonmee Nakorn, Vitayakritsirikul Vorapot, Ratanarapee Samrerng, Sharma Sanjay, van der Wal Allard C., Christiansen Michael, Tan Hanno L., Wilde Arthur A., Nogami Akihiko, Sheppard Mary N., Veerakul Gumpanart, Behr Elijah R. Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome Journal of the American College of Cardiology 2015;66 (18):1976-1986 [PubMed]
  • Wilde Arthur A. M., Viskin Sami From whole exome sequencing to patient-specific therapy: another example of how basic research pays off in patient care Journal of the American Heart Association 2015;4 (5):e002085 [PubMed]
  • Al-Aama J. Y., Al-Ghamdi S., Bdier A. Y., Alqarawi A., Jiman O. A., Al-Aama N., Al-Aata J., Wilde A. A. M., Bhuiyan Z. A. Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia Clinical genetics 2015;87 (1):74-79 [PubMed]
  • Bhonsale Aditya, Groeneweg Judith A., James Cynthia A., Dooijes Dennis, Tichnell Crystal, Jongbloed Jan D. H., Murray Brittney, te Riele Anneline S. J. M., van den Berg Maarten P., Bikker Hennie, Atsma Douwe E., de Groot Natasja M., Houweling Arjan C., van der Heijden Jeroen F., Russell Stuart D., Doevendans Pieter A., van Veen Toon A., Tandri Harikrishna, Wilde Arthur A., Judge Daniel P., van Tintelen J. Peter, Calkins Hugh, Hauer Richard N. Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers European heart journal 2015;36 (14):847-855 [PubMed]
  • Olde Nordkamp Louise R. A., Brouwer Tom F., Barr Craig, Theuns Dominic A. M. J., Boersma Lucas V. A., Johansen Jens B., Neuzil Petr, Wilde Arthur A. M., Carter Nathan, Husby Michael, Lambiase Pier D., Knops Reinoud E. Inappropriate shocks in the subcutaneous ICD: Incidence, predictors and management International journal of cardiology 2015;195:126-133 [PubMed]
  • Lieve Krystien V. V., Wilde Arthur A. M. Inherited ion channel diseases: a brief review Europace : European pacing, arrhythmias, and cardiac electrophysiology 2015;17 (Suppl. 2):ii1-ii6 [PubMed]
  • Wilde Arthur A. M. Interactiemechanismen - Verlenging QT-intervalin: S. D. Borgsteede, C. G. Colijn, V. M. Eimermann, M. Heringa, S. W. G. Neutkens, Kayan Tsoi, editors. Commentaren Medicatiebewaking 2015/2016. Houten: Health Base; 2015. p. 24-26, ISBN 9789074027380
  • Olde Nordkamp Louise Rosalia Antoinne Invasive therapy for inherited cardiac arrhythmias: towards a better benefit-risk equilibrium 2015. 272p. ISBN 9789461696113. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisors: van Dijk N., de Groot J. R.)
  • Lieve Krystien V. V., Wilde Arthur A. M., van der Werf Christian Plotse dood en wegrakingen door een erfelijke hartritmestoornis; mogelijke diagnose bij wegrakingen en plots overlijden van familieleden Nederlands tijdschrift voor geneeskunde 2015;159:A8205 [PubMed]
  • Tjong Fleur V. Y., Stam Olga C. G., van der Wal Allard C., Beenen Ludo F., Bouma Berto J., de Groot Joris R., Wilde Arthur A. M., Knops Reinoud E. Postmortem Histopathological Examination of a Leadless Pacemaker Shows Partial Encapsulation After 19 Months Circulation. Arrhythmia and electrophysiology 2015;8 (5):1293-1295 [PubMed]
  • Beesems Stefanie Gerarda Quality and outcome of cardiopulmonary resuscitation 2015. 185p. ISBN 9789462330047. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Koster R. W.)
  • Verkerk Agnes J., Vermeer Alexa M., Smets Ellen M., Dekker Lukas R., Wilde Arthur A., van Langen Irene M., Christiaans Imke, Nieuwkerk Pythia T. Quality of Life in Young Adult Patients with a Cardiogenetic Condition Receiving an ICD for Primary Prevention of Sudden Cardiac Death Pacing and clinical electrophysiology 2015;38 (7):870-877 [PubMed]
  • Behr Elijah R., Savio-Galimberti Eleonora, Barc Julien, Holst Anders G., Petropoulou Evmorfia, Prins Bram P., Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A., Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J., Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M., Bezzina Connie R., Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, Jamshidi Yalda Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study Cardiovascular research 2015;106 (3):520-529 [PubMed]
  • ten Sande Judith N., Coronel Ruben, Conrath Chantal E., Driessen Antoine H. G., de Groot Joris R., Tan Hanno L., Nademanee Koonlawee, Wilde Arthur A. M., de Bakker Jacques M. T., van Dessel Pascal F. H. M. ST-Segment Elevation and Fractionated Electrograms in Brugada Syndrome Patients Arise From the Same Structurally Abnormal Subepicardial RVOT Area but Have a Different Mechanism Circulation. Arrhythmia and electrophysiology 2015;8 (6):1382-1392 [PubMed]
  • Pazoki Raha Subtle killers and sudden death: Genetic variants modulating ventricular fibrillation in the setting of myocardial infarction 2015. 180p. ISBN 9789461696311. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Bezzina C. R., Wilde A. A. M.; Co-supervisor: Tanck M. W. T.)
  • Semsarian Christopher, Ingles Jodie, Wilde Arthur A. M. Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives European heart journal 2015;36 (21):1290-1296 [PubMed]
  • Olde Nordkamp Louise R. A., Vink Arja S., Wilde Arthur A. M., de Lange Freek J., de Jong Jonas S. S. G., Wieling Wouter, van Dijk Nynke, Tan Hanno L. Syncope in Brugada syndrome: prevalence, clinical significance, and clues from history taking to distinguish arrhythmic from nonarrhythmic causes Heart rhythm 2015;12 (2):367-375 [PubMed]
  • Veerman Christiaan C., Wilde Arthur A. M., Lodder Elisabeth M. The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology Gene 2015;573 (2):177-187 [PubMed]
  • Vermeer Alexa, Christiaans Imke, Wilde Arthur The Need to Continue Screening for Hypertrophic Cardiomyopathy After Adolescence American journal of cardiology 2015;115 (7):1002 [PubMed]
  • Meijborg Veronique Marlinde Frederica The T wave: Physiology and pathophysiology 2015. 168p. ISBN 9789461697103. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., de Bakker J. M. T.; Co-supervisors: Coronel R., Conrath C. E.)
  • van der Bilt Ivo A., Hasan Djo, van den Brink Renee B., Cramer Maarten J., van der Jagt Mathieu, van Kooten Fop, Regtien Joost G., van den Berg Maarten P., Groen Rob J., ten Cate Folkert J., Kamp Otto, Götte Marco J., Horn Janneke, Girbes Armand R., Vandertop W. Peter, Algra Ale, Rinkel Gabriel J., Wilde Arthur A. Time Course and Risk Factors for Myocardial Dysfunction After Aneurysmal Subarachnoid Hemorrhage Neurosurgery 2015;76 (6):700-705 [PubMed]
  • Krul Sébastien P.J., Berger Wouter R., Veldkamp Marieke W., Driessen Antoine H.G., Wilde Arthur A.M., Deneke Thomas, De Bakker Jacques M.T., Coronel Ruben, De Groot Joris R. Treatment of Atrial and Ventricular Arrhythmias Through Autonomic Modulation JACC. Clinical electrophysiology 2015;1 (6):496-508

2014

  • Wilde A. A. M. A common arrhythmia, not so common at an old age Netherlands heart journal 2014;22 (2):88 [PubMed]
  • de Jong Jonas S. S. G., Nieuwland Rienk, Meijers Joost C. M., Korporaal Suzanne J., Akkerman Jan Willem N., Wilde Arthur A. A. M., Dekker Lukas R. C. Altered platelet contents in survivors of early ischemic ventricular fibrillation: preliminary findings Platelets 2014;25 (1):71-74 [PubMed]
  • Marsman Roos F., Barc Julien, Beekman Leander, Alders Marielle, Dooijes Dennis, van den Wijngaard Arthur, Ratbi Ilham, Sefiani Abdelaziz, Bhuiyan Zahurul A., Wilde Arthur A. M., Bezzina Connie R. A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence Journal of the American College of Cardiology 2014;63 (3):259-266 [PubMed]
  • Buxton Alfred E., Wilde Arthur A. M., Chen Peng-Sheng A new ECG section in HeartRhythm by Josephson and Wellens Heart rhythm 2014;11 (12):2328 [PubMed]
  • Wilde Arthur A. M., Ackerman Michael J. Beta-Blockers in the Treatment of Congenital Long QT Syndrome Is One Beta-Blocker Superior to Another? Journal of the American College of Cardiology 2014;64 (13):1359-1361 [PubMed]
  • Stunnenberg Bas C., Deinum Jaap, Links Thera P., Wilde Arthur A., Franssen Hessel, Drost Gea Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause? Muscle & nerve 2014;50 (3):327-332 [PubMed]
  • van der Bilt Ivo, Hasan Djo, van den Brink Renee, Cramer Maarten-Jan, van der Jagt Mathieu, van Kooten Fop, Meertens John, van den Berg Maarten, Groen Rob, ten Cate Folkert, Kamp Otto, Götte Marco, Horn Janneke, Groeneveld Johan, Vandertop Peter, Algra Ale, Visser Frans, Wilde Arthur, Rinkel Gabriel Cardiac dysfunction after aneurysmal subarachnoid hemorrhage: relationship with outcome Neurology 2014;82 (4):351-358 [PubMed]
  • Schade van Westrum Steven M., Dekker Lukas R. C., de Voogt Willem G., Wilde Arthur A. M., Ginjaar Ieke B., de Visser Marianne, van der Kooi Anneke J. Cardiac involvement in Dutch patients with sarcoglycanopathy: a cross-sectional cohort and follow-up study Muscle & nerve 2014;50 (6):909-913 [PubMed]
  • Boczek Nicole J., Ye Dan, Johnson Eric K., Wang Wei, Crotti Lia, Tester David J., Dagradi Federica, Mizusawa Yuka, Torchio Margherita, Alders Marielle, Giudicessi John R., Wilde Arthur A. M., Schwartz Peter J., Nerbonne Jeanne M., Ackerman Michael J. Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome Circulation research 2014;115 (4):460-469 [PubMed]
  • Tan Hanno L., Wilde Arthur A. M. Contra-Indicaties - Brugada-syndroomin: Sander D. Borgsteede, C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. S. Lagas, M. Heringa, J. C. Klaucke, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2014/2015. Houten: Health Base; 2014. p. 914-915, ISBN 9789074027366
  • Wilde Arthur A. M. Contra-Indicaties - Lang-QT-intervalsyndroom (LQTS)in: Sander D. Borgsteede, C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. S. Lagas, M. Heringa, J. C. Klaucke, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2014/2015. Houten: Health Base; 2014. p. 776-782, ISBN 9789074027366
  • MacGillavry Melvin R., Wilde Arthur A. M. Contra-Indicaties - Tachy-aritmieënin: Sander D. Borgsteede, C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. S. Lagas, M. Heringa, J. C. Klaucke, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2014/2015. Houten: Health Base; 2014. p. 731-733, ISBN 9789074027366
  • Mac Gillavry Melvin R., Wilde Athur A. M. Contra-Indicaties - Wolff-Parkinson-White-syndroom (WPW)in: Sander D. Borgsteede, C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. S. Lagas, M. Heringa, J. C. Klaucke, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2014/2015. Houten: Health Base; 2014. p. 916-917, ISBN 9789074027366
  • Marsman Roos F. J., Bezzina Connie R., Freiberg Fabian, Verkerk Arie O., Adriaens Michiel E., Podliesna Svitlana, Chen Chen, Purfürst Bettina, Spallek Bastian, Koopmann Tamara T., Baczko Istvan, dos Remedios Cristobal G., George Alfred L., Bishopric Nanette H., Lodder Elisabeth M., de Bakker Jacques M. T., Fischer Robert, Coronel Ruben, Wilde Arthur A. M., Gotthardt Michael, Remme Carol Ann Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia Journal of the American College of Cardiology 2014;63 (6):549-559 [PubMed]
  • Al-Aama J. Y., Al-Ghamdi S., Bdier A. Y., Wilde A. A. M., Bhuiyan Zahurul A. De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome Clinical genetics 2014;86 (5):492-495 [PubMed]
  • Krul Sébastien P. J., Meijborg Veronique M. F., Berger Wouter R., Linnenbank André C., Driessen Antoine H. G., van Boven Wim-Jan, Wilde Arthur A. M., de Bakker Jacques M., Coronel Ruben, de Groot Joris R. Disparate response of high-frequency ganglionic plexus stimulation on sinus node function and atrial propagation in patients with atrial fibrillation Heart rhythm 2014;11 (10):1743-1751 [PubMed]
  • Wilde Arthur A. M., Lieve Krystien V. V. Double trouble, stick to the basics should be the rule! Heart rhythm 2014;11 (11):2105-2106 [PubMed]
  • Kraaier Karin, Scholten Marcoen F., Tijssen Jan G. P., Theuns Dominic A. M. J., Jordaens Luc J. L. M., Wilde Arthur A. M., van Dessel Pascal F. H. M. Early mortality in prophylactic implantable cardioverter-defibrillator recipients: development and validation of a clinical risk score Europace : European pacing, arrhythmias, and cardiac electrophysiology 2014;16 (1):40-46 [PubMed]
  • Krul Sebastien P. J., Pison Laurent, la Meir Mark, Driessen Antoine H. G., Wilde Arthur A. M., Maessen Jos G., de Mol Bas A. J. M., Crijns Harry J. G. M., de Groot Joris R. Epicardial and endocardial electrophysiological guided thoracoscopic surgery for atrial fibrillation: a multidisciplinary approach of atrial fibrillation ablation in challenging patients International journal of cardiology 2014;173 (2):229-235 [PubMed]
  • Priori Silvia G., Wilde Arthur A., Horie Minoru, Cho Yongkeun, Behr Elijah R., Berul Charles, Blom Nico, Brugada Josep, Chiang Chern En, Huikuri Heikki, Kannankeril Prince, Krahn Andrew, Leenhardt Antoine, Moss Arthur, Schwartz Peter J., Shimizu Wataru, Tomaselli Gordon, Tracy Cynthia Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes Journal of arrhythmia 2014;30 (1):29-47
  • Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J.E., Michels M., Postema P. G., Majoor-Krakauer D., Van Den Wijngaard A., Mannens M. M.A.M., Van Tintelen J. P., Van Langen I. M., Wilde A. A.M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlandsin: Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu von Loghum; 2014. p. 37-42, ISBN 9036807042; 9789036807043
  • Wilde Arthur A. M., van Tintelen J. Peter Founder mutations in inherited cardiac diseases in the NetherlandsHouten: Bohn Stafleu Van Loghum; 2014. ISBN 9789036807043
  • Groeneweg Judith A., Ummels Amber, Mulder Marcel, Bikker Hennie, van der Smagt Jasper J., van Mil Anneke M., Homfray Tessa, Post Jan G., Elvan Arif, van der Heijden Jeroen F., Houweling Arjan C., Jongbloed Jan D. H., Wilde Arthur A. M., van Tintelen J. Peter, Hauer Richard N., Dooijes Dennis Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy Heart rhythm 2014;11 (11):2010-2017 [PubMed]
  • Witjas-Paalberends E. Rosalie, Güçlü Ahmet, Germans Tjeerd, Knaapen Paul, Harms Hendrik J., Vermeer Alexa M. C., Christiaans Imke, Wilde Arthur A. M., dos Remedios Cris, Lammertsma Adriaan A., van Rossum Albert C., Stienen Ger J. M., van Slegtenhorst Marjon, Schinkel Arend F., Michels Michelle, Ho Carolyn Y., Poggesi Corrado, van der Velden Jolanda Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations Cardiovascular research 2014;103 (2):248-257 [PubMed]
  • Mizusawa Yuka, Horie Minoru, Wilde Arthur A. M. Genetic and clinical advances in congenital long QT syndrome Circulation journal 2014;78 (12):2827-2833 [PubMed]
  • Arking Dan E., Pulit Sara L., Crotti Lia, van der Harst Pim, Munroe Patricia B., Koopmann Tamara T., Sotoodehnia Nona, Rossin Elizabeth J., Morley Michael, Wang Xinchen, Johnson Andrew D., Lundby Alicia, Gudbjartsson Daníel F., Noseworthy Peter A., Eijgelsheim Mark, Bradford Yuki, Tarasov Kirill V., Dörr Marcus, Müller-Nurasyid Martina, Lahtinen Annukka M., Nolte Ilja M., Smith Albert Vernon, Bis Joshua C., Isaacs Aaron, Newhouse Stephen J., Evans Daniel S., Post Wendy S., Waggott Daryl, Lyytikäinen Leo-Pekka, Hicks Andrew A., Eisele Lewin, Ellinghaus David, Hayward Caroline, Navarro Pau, Ulivi Sheila, Tanaka Toshiko, Tester David J., Chatel Stéphanie, Gustafsson Stefan, Kumari Meena, Morris Richard W., Naluai Åsa T., Padmanabhan Sandosh, Kluttig Alexander, Strohmer Bernhard, Panayiotou Andrie G., Torres Maria, Knoflach Michael, Hubacek Jaroslav A., Slowikowski Kamil, Raychaudhuri Soumya, Kumar Runjun D., Harris Tamara B., Launer Lenore J., Shuldiner Alan R., Alonso Alvaro, Bader Joel S., Ehret Georg, Huang Hailiang, Kao W. H. Linda, Strait James B., Macfarlane Peter W., Brown Morris, Caulfield Mark J., Samani Nilesh J., Kronenberg Florian, Willeit Johann, Smith J. Gustav, Greiser Karin H., Meyer zu Schwabedissen Henriette, Werdan Karl, Carella Massimo, Zelante Leopoldo, Heckbert Susan R., Psaty Bruce M., Rotter Jerome I., Kolcic Ivana, Polašek Ozren, Wright Alan F., Griffin Maura, Daly Mark J., Arnar David O., Hólm Hilma, Thorsteinsdottir Unnur, Denny Joshua C., Roden Dan M., Zuvich Rebecca L., Emilsson Valur, Plump Andrew S., Larson Martin G., O'Donnell Christopher J., Yin Xiaoyan, Bobbo Marco, D'Adamo Adamo P., Iorio Annamaria, Sinagra Gianfranco, Carracedo Angel, Cummings Steven R., Nalls Michael A., Jula Antti, Kontula Kimmo K., Marjamaa Annukka, Oikarinen Lasse, Perola Markus, Porthan Kimmo, Erbel Raimund, Hoffmann Per, Jöckel Karl-Heinz, Kälsch Hagen, Nöthen Markus M., den Hoed Marcel, Loos Ruth J. F., Thelle Dag S., Gieger Christian, Meitinger Thomas, Perz Siegfried, Peters Annette, Prucha Hanna, Sinner Moritz F., Waldenberger Melanie, de Boer Rudolf A., Franke Lude, van der Vleuten Pieter A., Beckmann Britt Maria, Martens Eimo, Bardai Abdennasser, Hofman Nynke, Wilde Arthur A. M., Behr Elijah R., Dalageorgou Chrysoula, Giudicessi John R., Medeiros-Domingo Argelia, Barc Julien, Kyndt Florence, Probst Vincent, Ghidoni Alice, Insolia Roberto, Hamilton Robert M., Scherer Stephen W., Brandimarto Jeffrey, Margulies Kenneth, Moravec Christine E., del Greco M Fabiola, Fuchsberger Christian, O'Connell Jeffrey R., Lee Wai K., Watt Graham C. M., Campbell Harry, Wild Sarah H., El Mokhtari Nour E., Frey Norbert, Asselbergs Folkert W., Mateo Leach Irene, Navis Gerjan, van den Berg Maarten P., van Veldhuisen Dirk J., Kellis Manolis, Krijthe Bouwe P., Franco Oscar H., Hofman Albert, Kors Jan A., Uitterlinden André G., Witteman Jacqueline C. M., Kedenko Lyudmyla, Lamina Claudia, Oostra Ben A., Abecasis Gonçalo R., Lakatta Edward G., Mulas Antonella, Orrú Marco, Schlessinger David, Uda Manuela, Markus Marcello R. P., Völker Uwe, Snieder Harold, Spector Timothy D., Ärnlöv Johan, Lind Lars, Sundström Johan, Syvänen Ann-Christine, Kivimaki Mika, Kähönen Mika, Mononen Nina, Raitakari Olli T., Viikari Jorma S., Adamkova Vera, Kiechl Stefan, Brion Maria, Nicolaides Andrew N., Paulweber Bernhard, Haerting Johannes, Dominiczak Anna F., Nyberg Fredrik, Whincup Peter H., Hingorani Aroon D., Schott Jean-Jacques, Bezzina Connie R., Ingelsson Erik, Ferrucci Luigi, Gasparini Paolo, Wilson James F., Rudan Igor, Franke Andre, Mühleisen Thomas W., Pramstaller Peter P., Lehtimäki Terho J., Paterson Andrew D., Parsa Afshin, Liu Yongmei, van Duijn Cornelia M., Siscovick David S., Gudnason Vilmundur, Jamshidi Yalda, Salomaa Veikko, Felix Stephan B., Sanna Serena, Ritchie Marylyn D., Stricker Bruno H., Stefansson Kari, Boyer Laurie A., Cappola Thomas P., Olsen Jesper V., Lage Kasper, Schwartz Peter J., Kääb Stefan, Chakravarti Aravinda, Ackerman Michael J., Pfeufer Arne, de Bakker Paul I. W., Newton-Cheh Christopher Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization Nature genetics 2014;46 (8):826-836 [PubMed]
  • Marsman Roos F. J. Genetic risk factors for common and rare cardiac rhythm disorders 2014. 264p. ISBN 9789461086068. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Bezzina C. R., Wilde A. A. M.; Co-supervisors: Barnett P., Remme C. A.)
  • Milano Annalisa, Vermeer Alexa M. C., Lodder Elisabeth M., Barc Julien, Verkerk Arie O., Postma Alex V., van der Bilt Ivo A. C., Baars Marieke J. H., van Haelst Paul L., Caliskan Kadir, Hoedemaekers Yvonne M., Le Scouarnec Solena, Redon Richard, Pinto Yigal M., Christiaans Imke, Wilde Arthur A., Bezzina Connie R. HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy Journal of the American College of Cardiology 2014;64 (8):745-756 [PubMed]
  • Priori Silvia G., Wilde Arthur A., Horie Minoru, Cho Yongkeun, Behr Elijah R., Berul Charles, Blom Nico, Brugada Josep, Chiang Chern En, Huikuri Heikki, Kannankeril Prince, Krahn Andrew, Leenhardt Antoine, Moss Arthur, Schwartz Peter J., Shimizu Wataru, Tomaselli Gordon, Tracy Cynthia HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes Journal of arrhythmia 2014;30 (1):1-28
  • Kooiman Kirsten M., Knops Reinoud E., Olde Nordkamp Louise, Wilde Arthur A. M., de Groot Joris R. Inappropriate subcutaneous implantable cardioverter-defibrillator shocks due to T-wave oversensing can be prevented: implications for management Heart rhythm 2014;11 (3):426-434 [PubMed]
  • Chockalingam Priya, Wilde Arthur A. Inherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective Indian heart journal 2014;66 (Suppl. 1):S49-S57 [PubMed]
  • Wilde Arthur A. M. Interactiemechanismen - Verlenging QT-intervalin: Sander D. Borgsteede, C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. S. Lagas, M. Heringa, J. C. Klaucke, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2014/2015. Houten: Health Base; 2014. p. 23-25, ISBN 9789074027366
  • Olde Nordkamp L. R. A., Driessen A. H. G., Odero A., Blom N. A., Koolbergen D. R., Schwartz P. J., Wilde A. A. M. Left cardiac sympathetic denervation in the Netherlands for the treatment of inherited arrhythmia syndromes Netherlands heart journal 2014;22 (4):160-166 [PubMed]
  • van der Werf Christian, Stiekema Lotte, Tan Hanno L., Hofman Nynke, Alders Marielle, van der Wal Allard C., van Langen Irene M., Wilde Arthur A. M. Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up Heart rhythm 2014;11 (10):1728-1732 [PubMed]
  • Nannenberg Eline Alberdina Mortality in inherited cardiac diseases: Directing care in affected families 2014. 176p. ISBN 9789462593886. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Sijbrands E. J. G.; Co-supervisor: Christiaans I.)
  • van Rijsingen Ingrid A. W., van der Zwaag Paul A., Groeneweg Judith A., Nannenberg Eline A., Jongbloed Jan D. H., Zwinderman Aeilko H., Pinto Yigal M., Dit Deprez Ronald H. Lekanne, Post Jan G., Tan Hanno L., de Boer Rudolf A., Hauer Richard N. W., Christiaans Imke, van den Berg Maarten P., van Tintelen J. Peter, Wilde Arthur A. M. Outcome in phospholamban R14del carriers: results of a large multicentre cohort study Circulation. Cardiovascular genetics 2014;7 (4):455-465 [PubMed]
  • Reddy Vivek Y., Knops Reinoud E., Sperzel Johannes, Miller Marc A., Petru Jan, Simon Jaroslav, Sediva Lucie, de Groot Joris R., Tjong Fleur V. Y., Jacobson Peter, Ostrosff Alan, Dukkipati Srinivas R., Koruth Jacob S., Wilde Arthur A. M., Kautzner Josef, Neuzil Petr Permanent leadless cardiac pacing: results of the LEADLESS trial Circulation 2014;129 (14):1466-1471 [PubMed]
  • Kraaier K., Olimulder M. A. G. M., van Dessel P. F. H. M., Wilde A. A. M., Scholten M. F. Prognostic value of microvolt T-wave alternans in a real-world ICD population. Twente ICD Cohort Studie (TICS) Netherlands heart journal 2014;22 (10):440-445 [PubMed]
  • Wellens Hein J. J., Schwartz Peter J., Lindemans Fred W., Buxton Alfred E., Goldberger Jeffrey J., Hohnloser Stefan H., Huikuri Heikki V., Kääb Stefan, La Rovere Maria Teresa, Malik Marek, Myerburg Robert J., Simoons Maarten L., Swedberg Karl, Tijssen Jan, Voors Adriaan A., Wilde Arthur A. Risk stratification for sudden cardiac death: current status and challenges for the future European heart journal 2014;35 (25):1642-1651 [PubMed]
  • Kraaier Karin, Olimulder Marlon A. G. M., Galjee Michel A., van Dessel Pascal F. H. M., van der Palen Job, Wilde Arthur A. M., Scholten Marcoen F. Scar tissue and microvolt T-wave alternans international journal of cardiovascular imaging 2014;30 (4):773-779 [PubMed]
  • Elias J., Willems A. R., Wilde A. A. M. Should you be worried? Netherlands heart journal 2014;22 (3):129-130 [PubMed]
  • Blom Marieke Tabo Sudden cardiac arrest:: Studies on risk and outcome 2014. 234p. ISBN 9789088919602. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., de Boer A. [=Anthonius]; Co-supervisor: Tan H. L.)
  • Olde Nordkamp Louise R. A., Ruwald Martin H., Goldenberg Ilan, Wieling Wouter, McNitt Scott, Polonsky Bronislava, Wilde Arthur A. M., van Dijk Nynke, Moss Arthur J. Syncope in genotype-negative long QT syndrome family members American journal of cardiology 2014;114 (8):1223-1228 [PubMed]
  • Remme Carol Ann, Wilde Arthur A. M. Targeting sodium channels in cardiac arrhythmia Current opinion in pharmacology 2014;15:53-60 [PubMed]
  • Rizzo Stefania, Basso Cristina, Troost Dirk, Aronica Eleonora, Frigo Anna Chiara, Driessen Antoine H. G., Thiene Gaetano, Wilde Arthur A. M., van der Wal Allard C. T-Cell-Mediated Inflammatory Activity in the Stellate Ganglia of Patients With Ion-Channel Disease and Severe Ventricular Arrhythmias Circulation. Arrhythmia and electrophysiology 2014;7 (2):224-229 [PubMed]
  • Postema Pieter G., Wilde Arthur A. M. The measurement of the QT interval Current cardiology reviews 2014;10 (3):287-294 [PubMed]
  • Wilde A. A. M. Think twice before you tell Netherlands heart journal 2014;22 (4):190-+ [PubMed]
  • Kraaier Karin To implant or not to implant: Better risk stratification in ICD candidates 2014. 200p. ISBN 9789462284401. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisors: van Dessel P. F. H. M., Scholten M. F.)
  • ten Sande Judith N., Damman Peter, Tijssen Jan G. P., de Groot Joris R., Knops Reinoud E., Wilde Arthur A. M., van Dessel Pascal F. H. M. Value of Serial Heart Rate Variability Measurement for Prediction of Appropriate ICD Discharge in Patients with Heart Failure Journal of cardiovascular electrophysiology 2014;25 (1):60-65 [PubMed]
  • Olde Nordkamp Louise R. A., Warnaars Joppe L. F., Kooiman Kirsten M., de Groot Joris R., Rosenmöller Boudewijn R. A. M., Wilde Arthur A. M., Knops Reinoud E. Which patients are not suitable for a subcutaneous ICD: incidence and predictors of failed QRS-T-wave morphology screening Journal of cardiovascular electrophysiology 2014;25 (5):494-499 [PubMed]

2013

  • Faggioni Michela, Hwang Hyun Seok, van der Werf Christian, Nederend Ineke, Kannankeril Prince J., Wilde Arthur A. M., Knollmann Björn C. Accelerated sinus rhythm prevents catecholaminergic polymorphic ventricular tachycardia in mice and in patients Circulation research 2013;112 (4):689-697 [PubMed]
  • Postema Pieter G., Tan Hanno L., Wilde Arthur A. M. Ageing and Brugada syndrome: considerations and recommendations Journal of geriatric cardiology 2013;10 (1):75-81 [PubMed]
  • Wilde A. A. M. An atypical arrhythmia Netherlands heart journal 2013;21 (5):255-+
  • Wilde Arthur A. M. Andersen-Tawil syndrome, scarier for the doctor than for the patient? Who, when, and how to treat Europace : European pacing, arrhythmias, and cardiac electrophysiology 2013;15 (12):1690-1692 [PubMed]
  • van de Meerakker Judith B. A., Christiaans Imke, Barnett Phil, Lekanne Deprez Ronald H., Ilgun Aho, Mook Olaf R. F., Mannens Marcel M. A. M., Lam Jan, Wilde Arthur A. M., Moorman Antoon F. M., Postma Alex V. A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH 2013;1833 (4):833-839 [PubMed]
  • Groeneweg Judith A., van der Zwaag Paul A., Olde Nordkamp Louise R. A., Bikker Hennie, Jongbloed Jan D. H., Jongbloed Roselie, Wiesfeld Ans C. P., Cox Moniek G. P. J., van der Heijden Jeroen F., Atsma Douwe E., de Boer Karin, Doevendans Pieter A., Vink Aryan, van Veen Toon A. B., Dooijes Dennis, van den Berg Maarten P., Wilde Arthur A. M., van Tintelen J. Peter, Hauer Richard N. Arrhythmogenic right ventricular dysplasia/cardiomyopathy according to revised 2010 task force criteria with inclusion of non-desmosomal phospholamban mutation carriers American journal of cardiology 2013;112 (8):1197-1206 [PubMed]
  • Mac Gillavry Melvin R., Tan Hanno L., Wilde Arthur A. M. Brugada-syndroomin: C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. Hartman, M. Heringa, J. C. Klaucke, H. Mulder, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2013/2014. Houten: Health Base; 2013. p. 879-880, ISBN 9789074027359
  • van der Werf Christian, Wilde Arthur A. M. Catecholaminergic polymorphic ventricular tachycardia: from bench to bedside Heart (British Cardiac Society) 2013;99 (7):497-504 [PubMed]
  • Beckmann Britt-Maria, Wilde Arthur A. M., Kääb Stefan Clinical utility gene card for: long-QT syndrome (types 1-13) European journal of human genetics 2013;21 (10):10.1038/ejhg.2013.28 [PubMed]
  • Bezzina Connie R., Barc Julien, Mizusawa Yuka, Remme Carol Ann, Gourraud Jean-Baptiste, Simonet Floriane, Verkerk Arie O., Schwartz Peter J., Crotti Lia, Dagradi Federica, Guicheney Pascale, Fressart Véronique, Leenhardt Antoine, Antzelevitch Charles, Bartkowiak Susan, Borggrefe Martin, Schimpf Rainer, Schulze-Bahr Eric, Zumhagen Sven, Behr Elijah R., Bastiaenen Rachel, Tfelt-Hansen Jacob, Olesen Morten Salling, Kääb Stefan, Beckmann Britt M., Weeke Peter, Watanabe Hiroshi, Endo Naoto, Minamino Tohru, Horie Minoru, Ohno Seiko, Hasegawa Kanae, Makita Naomasa, Nogami Akihiko, Shimizu Wataru, Aiba Takeshi, Froguel Philippe, Balkau Beverley, Lantieri Olivier, Torchio Margherita, Wiese Cornelia, Weber David, Wolswinkel Rianne, Coronel Ruben, Boukens Bas J., Bézieau Stéphane, Charpentier Eric, Chatel Stéphanie, Despres Aurore, Gros Françoise, Kyndt Florence, Lecointe Simon, Lindenbaum Pierre, Portero Vincent, Violleau Jade, Gessler Manfred, Tan Hanno L., Roden Dan M., Christoffels Vincent M., Le Marec Hervé, Wilde Arthur A., Probst Vincent, Schott Jean-Jacques, Dina Christian, Redon Richard Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death Nature genetics 2013;45 (9):1044-1049 [PubMed]
  • Bezzina Connie R., Barc Julien, Mizusawa Yuka, Remme Carol Ann, Gourraud Jean-Baptiste, Simonet Floriane, Verkerk Arie O., Schwartz Peter J., Crotti Lia, Dagradi Federica, Guicheney Pascale, Fressart Véronique, Leenhardt Antoine, Antzelevitch Charles, Bartkowiak Susan, Schulze-Bahr Eric, Zumhagen Sven, Behr Elijah R., Bastiaenen Rachel, Tfelt-Hansen Jacob, Olesen Morten Salling, Kääb Stefan, Beckmann Britt M., Weeke Peter, Watanabe Hiroshi, Endo Naoto, Minamino Tohru, Horie Minoru, Ohno Seiko, Hasegawa Kanae, Makita Naomasa, Nogami Akihiko, Shimizu Wataru, Aiba Takeshi, Froguel Philippe, Balkau Beverley, Lantieri Olivier, Torchio Margherita, Wiese Cornelia, Weber David, Wolswinkel Rianne, Coronel Ruben, Boukens Bas J., Bézieau Stéphane, Charpentier Eric, Chatel Stéphanie, Despres Aurore, Gros Françoise, Kyndt Florence, Lecointe Simon, Lindenbaum Pierre, Portero Vincent, Violleau Jade, Gessler Manfred, Tan Hanno L., Roden Dan M., Christoffels Vincent M., Le Marec Hervé, Wilde Arthur A., Probst Vincent, Schott Jean-Jacques, Dina Christian, Redon Richard Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death Nature genetics 2013;45 (11):1409 [PubMed]
  • Pazoki Raha, Tanck Michael W. T., Wilde Arthur A. M., Bezzina Connie R. Complex inheritance for susceptibility to sudden cardiac death Current pharmaceutical design 2013;19 (39):6864-6872 [PubMed]
  • Bhuiyan Zahurul A., Al-Shahrani Safar, Al-Aama Jumana, Wilde Arthur A. M., Momenah Tarek S. Congenital long QT syndrome: an update and present perspective in Saudi Arabia Frontiers in pediatrics 2013;1:39 [PubMed]
  • van Rijsingen Ingrid A. W. Dilated cardiomyopathy: translating genetic defects into clinical care. Towards personalized medicine in dilated cardiomyopathy 2013. 177p. ISBN 9789088916199. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Pinto Y. M., Wilde A. A. M.; Co-supervisor: Christiaans I.)
  • Postema Pieter G., Wilde Arthur A. M. Do J waves constitute a syndrome? Journal of electrocardiology 2013;46 (5):461-465 [PubMed]
  • Watanabe Hiroshi, van der Werf Christian, Roses-Noguer Ferran, Adler Arnon, Sumitomo Naokata, Veltmann Christian, Rosso Raphael, Bhuiyan Zahurul A., Bikker Hennie, Kannankeril Prince J., Horie Minoru, Minamino Tohru, Viskin Sami, Knollmann Björn C., Till Jan, Wilde Arthur A. M. Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia Heart rhythm 2013;10 (4):542-547 [PubMed]
  • Gussak Ihor, Antzelevitch Charles, Wilde Arthur A.M., Powell Brian D., Ackerman Michael J., Shen Win Kuang Electrical diseases of the heart: Second edition volume 1: Basic foundations and primary electrical diseasesin: Electrical Diseases of the Heart. Springer-Verlag London Ltd; 2013. p. 1-659, ISBN 9781447148807
  • Gussak Ihor, Antzelevitch Charles, Wilde Arthur A. M., Powell Brian D., Ackerman Michael J., Shen Win-Kuang Electrical Diseases of the Heart. Volume 2: Diagnosis and TreatmentLondon: Springer; 2013. ISBN 9781447149774
  • Nassif Martina, Krul Sébastien P. J., Driessen Antoine H. G., Deneke Thomas, Wilde Arthur A. M., de Bakker Jacques M. T., de Groot Joris R. Electrocardiographic P wave changes after thoracoscopic pulmonary vein isolation for atrial fibrillation Journal of interventional cardiac electrophysiology 2013;37 (3):275-282 [PubMed]
  • van der Werf Christian Epidemiology and clinical aspects of sudden cardiac death in the young 2013. 27p. ISBN 9789461822604. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., van Langen I. M.)
  • Hofman Nynke Evaluation of outcomes of cardiogenetic testing in inherited arrhythmias 2013. 214p. ISBN 9789461822116. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., van Langen I. M.; Co-supervisor: Tan H. L.)
  • Priori Silvia G., Wilde Arthur A., Horie Minoru, Cho Yongkeun, Behr Elijah R., Berul Charles, Blom Nico, Brugada Josep, Chiang Chern-En, Huikuri Heikki, Kannankeril Prince, Krahn Andrew, Leenhardt Antoine, Moss Arthur, Schwartz Peter J., Shimizu Wataru, Tomaselli Gordon, Tracy Cynthia, Ackerman Michael, Belhassen Bernard, Estes N. A. Mark, Fatkin Diane, Kalman Jonathan, Kaufman Elizabeth, Kirchhof Paulus, Schulze-Bahr Eric, Wolpert Christian, Vohra Jitendra, Refaat Marwan, Etheridge Susan P., Campbell Robert M., Martin Edward T., Quek Swee Chye Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes Europace : European pacing, arrhythmias, and cardiac electrophysiology 2013;15 (10):1389-1406 [PubMed]
  • Priori Silvia G., Wilde Arthur A., Horie Minoru, Cho Yongkeun, Behr Elijah R., Berul Charles, Blom Nico, Brugada Josep, Chiang Chern-En, Huikuri Heikki, Kannankeril Prince, Krahn Andrew, Leenhardt Antoine, Moss Arthur, Schwartz Peter J., Shimizu Wataru, Tomaselli Gordon, Tracy Cynthia Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes Heart rhythm 2013;10 (12):e85-108 [PubMed]
  • Krul Sébastien P. J., Berger W. R., Driessen Antoine H. G., Wilde Arthur A. M., de Groot Joris R. Frequentie- en ritmecontrole bij boezemfibrilleren Nederlands tijdschrift voor geneeskunde 2013;157:A5701
  • van Rijsingen Ingrid A. W., Nannenberg Eline A., Arbustini Eloisa, Elliott Perry M., Mogensen Jens, Hermans-van Ast Johanna F., van der Kooi Anneke J., van Tintelen J. Peter, van den Berg Maarten P., Grasso Maurizia, Serio Alessandra, Jenkins Sharon, Rowland Camilla, Richard Pascale, Wilde Arthur A. M., Perrot Andreas, Pankuweit Sabine, Zwinderman Aeilko H., Charron Philippe, Christiaans Imke, Pinto Yigal M. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers European journal of heart failure 2013;15 (4):376-384 [PubMed]
  • van Spaendonck-Zwarts Karin Y., van Rijsingen Ingrid A. W., van den Berg Maarten P., Lekanne Deprez Ronald H., Post Jan G., van Mil Anneke M., Asselbergs Folkert W., Christiaans Imke, van Langen Irene M., Wilde Arthur A. M., de Boer Rudolf A., Jongbloed Jan D. H., Pinto Yigal M., van Tintelen J. Peter Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience European journal of heart failure 2013;15 (6):628-636 [PubMed]
  • Wilde Arthur A. M., Behr Elijah R. Genetic testing for inherited cardiac disease Nature reviews. Cardiology 2013;10 (10):571-583 [PubMed]
  • Behr Elijah R., Ritchie Marylyn D., Tanaka Toshihiro, Kääb Stefan, Crawford Dana C., Nicoletti Paola, Floratos Aris, Sinner Moritz F., Kannankeril Prince J., Wilde Arthur A. M., Bezzina Connie R., Schulze-Bahr Eric, Zumhagen Sven, Guicheney Pascale, Bishopric Nanette H., Marshall Vanessa, Shakir Saad, Dalageorgou Chrysoula, Bevan Steve, Jamshidi Yalda, Bastiaenen Rachel, Myerburg Robert J., Schott Jean-Jacques, Camm A. John, Steinbeck Gerhard, Norris Kris, Altman Russ B., Tatonetti Nicholas P., Jeffery Steve, Kubo Michiaki, Nakamura Yusuke, Shen Yufeng, George Alfred L., Roden Dan M. Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes PLoS ONE 2013;8 (11):e78511 [PubMed]
  • Priori Silvia G., Wilde Arthur A., Horie Minoru, Cho Yongkeun, Behr Elijah R., Berul Charles, Blom Nico, Brugada Josep, Chiang Chern-En, Huikuri Heikki, Kannankeril Prince, Krahn Andrew, Leenhardt Antoine, Moss Arthur, Schwartz Peter J., Shimizu Wataru, Tomaselli Gordon, Tracy Cynthia HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013 Heart rhythm 2013;10 (12):1932-1963 [PubMed]
  • Bhuiyan Zahurul A., Wilde Arthur A. M. IKs in heart and hearing, the ear can do with less than the heart Circulation. Cardiovascular genetics 2013;6 (2):141-143 [PubMed]
  • Schwartz Peter J., Ackerman Michael J., George Alfred L., Wilde Arthur A. M. Impact of genetics on the clinical management of channelopathies Journal of the American College of Cardiology 2013;62 (3):169-180 [PubMed]
  • Viskin Sami, Wilde Arthur A. M., Krahn Andrew D., Zipes Douglas P. Inaccessibility to quinidine therapy is about to get worse Journal of the American College of Cardiology 2013;62 (4):355 [PubMed]
  • de Bie Mihály K., Koopman Marion G., Gaasbeek André, Dekker Friedo W., Maan Arie C., Swenne Cees A., Scherptong Roderick W., van Dessel Pascal F., Wilde Arthur A., Schalij Martin J., Rabelink Ton J., Jukema J. Wouter Incremental prognostic value of an abnormal baseline spatial QRS-T angle in chronic dialysis patients Europace : European pacing, arrhythmias, and cardiac electrophysiology 2013;15 (2):290-296 [PubMed]
  • Amin Ahmad S., Wilde Arthur A. M. Inheritable Potassium Channel Diseasein: Douglas P. Zipes, José Jalife, editors. Cardiac Electrophysiology: From Cell to Bedside. Philadelphia: Elsevier Saunders; 2013. p. 501-509, ISBN 9781455728565
  • Wilde Arthur A. M. Interactieve mechanismen: Verlenging QT-intervalin: C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. Hartman, M. Heringa, J. C. Klaucke, H. Mulder, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2013/2014. Houten: Health Base; 2013. p. 21-23, ISBN 9789074027359
  • van Rijsingen Ingrid A. W., Bakker Annemieke, Azim Donija, Hermans-van Ast Johanna F., van der Kooi Anneke J., van Tintelen J. Peter, van den Berg Maarten P., Christiaans Imke, Lekanne dit Deprez Ronald H., Wilde Arthur A. M., Zwinderman Aeilko H., Meijers Joost C. M., Grootemaat Anita E., Nieuwland Rienk, Pinto Yigal M., Pinto-Sietsma Sara-Joan Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications International journal of cardiology 2013;168 (1):472-477 [PubMed]
  • Wilde Arthur A. M. Lang-QT-intervalsyndroom (LQTS)in: C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. Hartman, M. Heringa, J. C. Klaucke, H. Mulder, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2013/2014. Houten: Health Base; 2013. p. 746-752, ISBN 9789074027359
  • Remme Carol Ann, Wilde Arthur A. M. Late sodium current inhibition in acquired and inherited ventricular (dys)function and arrhythmias Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy 2013;27 (1):91-101 [PubMed]
  • Amin Ahmad S., Pinto Yigal M., Wilde Arthur A. M. Long QT syndrome: beyond the causal mutation Journal of physiology 2013;591 (Part 17):4125-4139 [PubMed]
  • Laksman Zachary W. M., Hamilton Robert M., Chockalingam Priya, Ballantyne Emily, Stephenson Elizabeth A., Gross Gil J., Gula Lorne J., Klein George J., Wilde Arthur A. M., Krahn Andrew D. Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop location Journal of cardiovascular electrophysiology 2013;24 (9):1015-1020 [PubMed]
  • Krul Sébastien P. J., Driessen Antoine H. G., Zwinderman Aeilko H., van Boven Wim J., Wilde Arthur A. M., de Bakker Jacques M. T., de Groot Joris R. Navigating the mini-maze: systematic review of the first results and progress of minimally-invasive surgery in the treatment of atrial fibrillation International journal of cardiology 2013;166 (1):132-140 [PubMed]
  • Wilde A. A. M. Palpitations in a 19-year old man and a slow heart rate at rest Netherlands heart journal 2013;21 (6):310-+
  • Wilde A. A. M. Palpitations in a 19-year-old man, take a second look Netherlands heart journal 2013;21 (4):205-+
  • Wilde A. A. M. Palpitations, once again Netherlands heart journal 2013;21 (1):47-+
  • Wilde A. A. M., de Jong J. S. S. G. Palpitations, should one worry? Netherlands heart journal 2013;21 (3):155-+
  • Mathias Andrew, Moss Arthur J., Lopes Coeli M., Barsheshet Alon, McNitt Scott, Zareba Wojciech, Robinson Jennifer L., Locati Emanuela H., Ackerman Michael J., Benhorin Jesaia, Kaufman Elizabeth S., Platonov Pyotr G., Qi Ming, Shimizu Wataru, Towbin Jeffrey A., Michael Vincent G., Wilde Arthur A. M., Zhang Li, Goldenberg Ilan Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome Heart rhythm 2013;10 (5):720-725 [PubMed]
  • Mizusawa Yuka, Wilde Arthur A. M. QT prolongation and mortality in hospital settings: identifying patients at high risk Mayo Clinic proceedings. Mayo Clinic 2013;88 (4):309-311 [PubMed]
  • Viskin Sami, Wilde Arthur A. M., Guevara-Valdivia Milton E., Daoulah Amin, Krahn Andrew D., Zipes Douglas P., Halkin Amir, Shivkumar Kalyanam, Boyle Noel G., Adler Arnon, Belhassen Bernard, Schapachnik Edgardo, Asrar Farhan, Rosso Raphael, Fadreguilan Erdie C., Veltman Christian, Veerakul G., Marquez Manlio, Juneja Rajnish, Daoulah Amin Naseem, Caorsi Walter Reyes, Cuesta Alejandron, Jensen Henrik Kjaerulf, Hamad Adel Khalifa Sultan, Spears Danna, Lozano Ignacio Fernández, Urda Víctor Castro, Peinado R., Panduranga Prashanth, Emkanjoo Zahra, Bergfeldt Len, Janousek Jan Quinidine, a life-saving medication for Brugada syndrome, is inaccessible in many countries Journal of the American College of Cardiology 2013;61 (23):2383-2387 [PubMed]
  • van der Zwaag P. A., van Rijsingen I. A. W., de Ruiter R., Nannenberg E. A., Groeneweg J. A., Post J. G., Hauer R. N. W., van Gelder I. C., van den Berg M. P., van der Harst P., Wilde A. A. M., van Tintelen J. P. Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy Netherlands heart journal 2013;21 (6):286-293 [PubMed]
  • Nederend Ineke, van der Werf Christian, Wilde Arthur A. M. RyR2 in Cardiac Disordersin: Norbert Weiss, Alexandra Koschak, editors. Pathologies of Calcium Channels. Heidelberg: Springer; 2013. p. 601-614, ISBN 9783642402814
  • Postema Pieter G., Neville Jon, de Jong Jonas S. S. G., Romero Klaus, Wilde Arthur A. M., Woosley Raymond L. Safe drug use in long QT syndrome and Brugada syndrome: comparison of website statistics Europace : European pacing, arrhythmias, and cardiac electrophysiology 2013;15 (7):1042-1049 [PubMed]
  • Wilde Arthur A.M., Ackerman Michael J., Antzelevitch Charles, Gussak Ihor Secondary hereditary and acquired cardiac channelopathies and sudden cardiac deathin: Electrical Diseases of the Heart. Springer-Verlag London Ltd; 2013. p. 1-2, ISBN 9781447149774
  • Pazoki Raha, de Jong Jonas S. S. G., Marsman Roos F., Bruinsma Nienke, Dekker Lukas R. C., Wilde Arthur A. M., Bezzina Connie R., Tanck Michael W. T. SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this condition PLoS ONE 2013;8 (2):e57216 [PubMed]
  • de Jong Jonas S. S. G. Susceptibility to ischemic ventricular fibrillation 2013. 166p. ISBN 9789461084170. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisors: Dekker L. R. C., Bezzina C. R.)
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Tachy-aritmieënin: C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. Hartman, M. Heringa, J. C. Klaucke, H. Mulder, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2013/2014. Houten: Health Base; 2013. p. 703-705, ISBN 9789074027359
  • Smith Tim, Jordaens Luc, Theuns Dominic A. M. J., van Dessel Pascal F., Wilde Arthur A., Hunink M. G. Myriam The cost-effectiveness of primary prophylactic implantable defibrillator therapy in patients with ischaemic or non-ischaemic heart disease: a European analysis European heart journal 2013;34 (3):211-219 [PubMed]
  • Olde Nordkamp Louise R. A., Wilde Arthur A. M., Tijssen Jan G. P., Knops Reinoud E., van Dessel Pascal F. H. M., de Groot Joris R. The ICD for Primary Prevention in Patients With Inherited Cardiac Diseases Indications, Use, and Outcome: A Comparison With Secondary Prevention Circulation. Arrhythmia and electrophysiology 2013;6 (1):91-100 [PubMed]
  • Knops Reinoud E., Olde Nordkamp Louise R. A., de Groot Joris R., Wilde Arthur A. M. Two-incision technique for implantation of the subcutaneous implantable cardioverter-defibrillator Heart rhythm 2013;10 (8):1240-1243 [PubMed]
  • de Groot Joris R., Krul Sébastien P. J., Kroon Sem, Knops Reinoud E., Peters Ron J. G., Wilde Arthur A. M. Unidentified candidates for cardiac resynchronization therapy: guideline adherence in a large academic outpatient clinic in the Netherlands Pacing and clinical electrophysiology 2013;36 (1):69-75 [PubMed]
  • Xiao Ling, Koopmann Tamara T., Ördög Balázs, Postema Pieter G., Verkerk Arie O., Iyer Vivek, Sampson Kevin J., Boink Gerard J. J., Mamarbachi Maya A., Varro Andras, Jordaens Luc, Res Jan, Kass Robert S., Wilde Arthur A., Bezzina C. R., Nattel Stanley Unique cardiac Purkinje fiber transient outward current β-subunit composition: a potential molecular link to idiopathic ventricular fibrillation Circulation research 2013;112 (10):1310-1322 [PubMed]
  • Hummel Yoran M., Wilde Arthur A. M., Voors Adriaan A., Bugatti Silvia, Hillege Hans L., van den Berg Maarten P. Ventricular dysfunction in a family with long QT syndrome type 3 Europace : European pacing, arrhythmias, and cardiac electrophysiology 2013;15 (10):1516-1521 [PubMed]
  • van der Werf Christian, Wilde Arthur A. M. VTs in Catecholaminergic Cardiomyopathy (Catecholaminergic Polymorphic Ventricular Tachycardia)in: Douglas P. Zipes, José Jalife, editors. Cardiac Electrophysiology: From Cell to Bedside. Philadelphia: Elsevier Saunders; 2013. p. 895-902, ISBN 9781455728565
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Wolff-Parkinson-White-syndroom (WPW)in: C. G. Colijn, V. M. Eimermann, J. J. de Gier, J. Hartman, M. Heringa, J. C. Klaucke, H. Mulder, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2013/2014. Houten: Health Base; 2013. p. 881-882, ISBN 9789074027359
  • Hofman Nynke, Tan Hanno L., Alders Mariëlle, Kolder Iris, de Haij Simone, Mannens Marcel M. A. M., Lombardi Maria Paola, Lekanne Deprez Ronald H., van Langen Irene, Wilde Arthur A. M. Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience Circulation 2013;128 (14):1513-1521 [PubMed]

2012

  • Makita Naomasa, Seki Akiko, Sumitomo Naokata, Chkourko Halina, Fukuhara Shigetomo, Watanabe Hiroshi, Shimizu Wataru, Bezzina Connie R., Hasdemir Can, Mugishima Hideo, Makiyama Takeru, Baruteau Alban, Baron Estelle, Horie Minoru, Hagiwara Nobuhisa, Wilde Arthur A. M., Probst Vincent, Le Marec Hervé, Roden Dan M., Mochizuki Naoki, Schott Jean-Jacques, Delmar Mario A Connexin40 Mutation Associated With a Malignant Variant of Progressive Familial Heart Block Type I Circulation. Arrhythmia and electrophysiology 2012;5 (1):163-U274 [PubMed]
  • Chockalingam Priya Addressing the diagnostic and therapeutic challenges in inheritable arrythmia syndromes. With emphasis on the pediatric population 2012. 142p. ISBN 9789461821423. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Blom N. A.; Co-supervisor: Clur S. A. B.)
  • Kääb Stefan, Crawford Dana C., Sinner Moritz F., Behr Elijah R., Kannankeril Prince J., Wilde Arthur A. M., Bezzina Connie R., Schulze-Bahr Eric, Guicheney Pascale, Bishopric Nanette H., Myerburg Robert J., Schott Jean-Jacques, Pfeufer Arne, Beckmann Britt-Maria, Martens Eimo, Zhang Taifang, Stallmeyer Birgit, Zumhagen Sven, Denjoy Isabelle, Bardai Abdennasser, van Gelder Isabelle C., Jamshidi Yalda, Dalageorgou Chrysoula, Marshall Vanessa, Jeffery Steve, Shakir Saad, Camm A. John, Steinbeck Gerhard, Perz Siegfried, Lichtner Peter, Meitinger Thomas, Peters Annette, Wichmann H.-Erich, Ingram Christiana, Bradford Yuki, Carter Shannon, Norris Kris, Ritchie Marylyn D., George Alfred L., Roden Dan M. A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes Circulation. Cardiovascular genetics 2012;5 (1):91-99 [PubMed]
  • Chockalingam Priya, Wilde Arthur ARRHYTHMIAS The multifaceted cardiac sodium channel and its clinical implications Heart (British Cardiac Society) 2012;98 (17):1318-1324 [PubMed]
  • Baranchuk Adrian, Nguyen Timothy, Ryu Min Hyung, Femenía Francisco, Zareba Wojciech, Wilde Arthur A. M., Shimizu Wataru, Brugada Pedro, Pérez-Riera Andrés R. Brugada Phenocopy: New Terminology and Proposed Classification Annals of noninvasive electrocardiology 2012;17 (4):299-314 [PubMed]
  • Mizusawa Yuka, Wilde Arthur A. M. Brugada Syndrome Circulation. Arrhythmia and electrophysiology 2012;5 (3):606-616 [PubMed]
  • Mac Gillavry Melvin R., Tan Hanno L., Wilde Arthur A. M. Brugada-syndroomin: H. C. S. van Buren, C. G. Colijn, V. M. Eimermann, J. J. de Gier, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2012/2013. Houten: Boekbinderij Van Hees, Zaltbommel; 2012. p. 830-831, ISBN 9789074027007
  • Davis Richard P., Casini Simona, van den Berg Cathelijne W., Hoekstra Maaike, Remme Carol Ann, Dambrot Cheryl, Salvatori Daniela, Ward-van Oostwaard Dorien, Wilde Arthur A. M., Bezzina Connie R., Verkerk Arie O., Freund Christian, Mummery Christine L. Cardiomyocytes Derived From Pluripotent Stem Cells Recapitulate Electrophysiological Characteristics of an Overlap Syndrome of Cardiac Sodium Channel Disease Circulation 2012;125 (25):3079-+ [PubMed]
  • van der Smagt Jasper J., van der Zwaag Paul A., van Tintelen J. Peter, Cox Moniek G. P. J., Wilde Arthur A. M., van Langen Irene M., Ummels Amber, Hennekam F. A. M., Dooijes Dennis, Gerbens Frans, Bikker Hennie, Hauer Richard N. W., Doevendans Pieter A. Clinical and Genetic Characterization of Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Caused by a Plakophilin-2 Splice Mutation Cardiology 2012;123 (3):181-189 [PubMed]
  • Lodder Elisabeth M., Wilde Arthur A. M. Clinical Assessment of the Pathogenicity of Unknown Variants in Long-QT Syndrome: Does the Pendulum Swing Back? Journal of cardiovascular electrophysiology 2012;23 (6):643-644 [PubMed]
  • Costa Jason, Lopes Coeli M., Barsheshet Alon, Moss Arthur J., Migdalovich Dmitriy, Ouellet Gregory, McNitt Scott, Polonsky Slava, Robinson Jennifer L., Zareba Wojciech, Ackerman Michael J., Benhorin Jesaia, Kaufman Elizabeth S., Platonov Pyotr G., Shimizu Wataru, Towbin Jeffrey A., Vincent G. Michael, Wilde Arthur A. M., Goldenberg Ilan Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndrome Heart rhythm 2012;9 (6):892-898 [PubMed]
  • van der Werf Christian, Nederend Ineke, Hofman Nynke, van Geloven Nan, Ebink Corné, Frohn-Mulder Ingrid M. E., Alings A. Marco W., Bosker Hans A., Bracke Frank A., van den Heuvel Freek, Waalewijn Reinier A., Bikker Hennie, van Tintelen J. Peter, Bhuiyan Zahurul A., van den Berg Maarten P., Wilde Arthur A. M. Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia Disease Penetrance and Expression in Cardiac Ryanodine Receptor Mutation-Carrying Relatives Circulation. Arrhythmia and electrophysiology 2012;5 (4):748-756 [PubMed]
  • Knops R. E., Kooiman K. M., ten Sande J. N., de Groot J. R., Wilde A. A. M. First experience with the wearable cardioverter defibrillator in the Netherlands Netherlands heart journal 2012;20 (2):77-81 [PubMed]
  • Kolder Iris C. R. M. Genetic modifiers in familial cardiac rhythm disorders Ipskamp Drukkers B.V.; 2012. 155p. ISBN 9789461913364. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde Arthur A. M., Zwinderman Aeilco H.; Co-supervisors: Bezzina Connie R., Tanck Michael W. T.)
  • Koyak Zeliha, de Groot Joris R., van Gelder Isabelle C., Bouma Berto J., van Dessel Pascal F. H. M., Budts Werner, van Erven Lieselot, van Dijk Arie P. J., Wilde Arthur A. M., Pieper Petronella G., Sieswerda Gertjan T., Mulder Barbara J. M. Implantable Cardioverter Defibrillator Therapy in Adults With Congenital Heart Disease Who Is at Risk of Shocks? Circulation. Arrhythmia and electrophysiology 2012;5 (1):101-110 [PubMed]
  • Hoekstra Maaike, Mummery Christine L., Wilde Arthur A. M., Bezzina Connie R., Verkerk Arie O. Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythrnias Frontiers in physiology 2012;3:UNSP 346 [PubMed]
  • Hoefen Ryan, Reumann Matthias, Goldenberg Ilan, Moss Arthur J., O-Uchi Jin, Gu Yiping, McNitt Scott, Zareba Wojciech, Jons Christian, Kanters Jorgen K., Platonov Pyotr G., Shimizu Wataru, Wilde Arthur A. M., Rice John Jeremy, Lopes Coeli M. In Silico Cardiac Risk Assessment in Patients With Long QT Syndrome Type 1: Clinical Predictability of Cardiac Models Journal of the American College of Cardiology 2012;60 (21):2182-2191 [PubMed]
  • Wilde Arthur A. M. Interactieve mechanismen: Verlenging QT-intervalin: H. C. S. van Buren, C. G. Colijn, V. M. Eimermann, J. J. de Gier, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2012/2013. Houten: Boekbinderij Van Hees, Zaltbommel; 2012. p. 14-15, ISBN 9789074027007
  • Sarwar Nadeem, Butterworth Adam S., Freitag Daniel F., Gregson John, Willeit Peter, Gorman Donal N., Gao Pei, Saleheen Danish, Rendon Augusto, Nelson Christopher P., Braund Peter S., Hall Alistair S., Chasman Daniel I., Tybjærg-Hansen Anne, Chambers John C., Benjamin Emelia J., Franks Paul W., Clarke Robert, Wilde Arthur A. M., Trip Mieke D., Steri Maristella, Witteman Jacqueline C. M., Qi Lu, van der Schoot C. Ellen, de Faire Ulf, Erdmann Jeanette, Stringham Heather M., Koenig Wolfgang, Rader Daniel J., Melzer David, Reich David, Psaty Bruce M., Kleber Marcus E., Panagiotakos Demosthenes B., Willeit Johann, Wennberg Patrik, Woodward Mark, Adamovic Svetlana, Rimm Eric B., Meade Tom W., Gillum Richard F., Shaffer Jonathan A., Hofman Albert, Onat Altan, Kastelein John J. P., Motazacker Mahdi, de Jong Jonas S. S. G., Dekker Lucas R. C., Tanck Michael, Bezzina Connie R. Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies Lancet 2012;379 (9822):1205-1213 [PubMed]
  • Wilde Arthur A. M. "J-wave syndromes" bring the ATP-sensitive potassium channel back in the spotlight Heart rhythm 2012;9 (4):556-557 [PubMed]
  • Wilde Arthur A. M. Lang-QT-intervalsyndroom (LQTS)in: H. C. S. van Buren, C. G. Colijn, V. M. Eimermann, J. J. de Gier, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2012/2013. Houten: Boekbinderij Van Hees, Zaltbommel; 2012. p. 705-710, ISBN 9789074027007
  • Asselbergs Folkert W., Guo Yiran, van Iperen Erik P. A., Sivapalaratnam Suthesh, Tragante Vinicius, Lanktree Matthew B., Lange Leslie A., Almoguera Berta, Appelman Yolande E., Barnard John, Baumert Jens, Beitelshees Amber L., Bhangale Tushar R., Chen Yii-Der Ida, Gaunt Tom R., Gong Yan, Hopewell Jemma C., Johnson Toby, Kleber Marcus E., Langaee Taimour Y., Li Mingyao, Li Yun R., Liu Kiang, McDonough Caitrin W., Meijs Matthijs F. L., Middelberg Rita P. S., Musunuru Kiran, Nelson Christopher P., O'Connell Jeffery R., Padmanabhan Sandosh, Pankow James S., Pankratz Nathan, Rafelt Suzanne, Rajagopalan Ramakrishnan, Romaine Simon P. R., Schork Nicholas J., Shaffer Jonathan, Shen Haiqing, Smith Erin N., Tischfield Sam E., van der Most Peter J., van Vliet-Ostaptchouk Jana V., Verweij Niek, Chen Wei, Zwinderman A. H., Bezzina Connie R., Trip Mieke D., Wilde Arthur A. M., Hovingh G. Kees, Kastelein John J. P. Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci American journal of human genetics 2012;91 (5):823-838 [PubMed]
  • Chockalingam Priya, Wilde Arthur A. M. Loss-of-Function Sodium Channel Mutations in Infancy A Pattern Unfolds Circulation 2012;125 (1):6-8 [PubMed]
  • Dalal Darshan, de Jong Jonas S. S. G., Tjong Fleur V. Y., Wang Yaping, Bruinsma Nienke, Dekker Lukas R. C., Wilde Arthur A. M. Mild-to-moderate kidney dysfunction and the risk of sudden cardiac death in the setting of acute myocardial infarction Heart rhythm 2012;9 (4):540-545 [PubMed]
  • Amin Ahmad S. Modifiers of phenotype in inheritable arrhythmia syndromes; from bedside to cell Off Page, www.offpage.nl; 2012. 237p. ISBN 9789461821065. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde Arthur A. M., Pinto Yigal M.; Co-supervisor: Tan Hanno L.)
  • Nannenberg Eline A., Sijbrands Eric J. G., Dijksman Lea M., Alders Marielle, van Tintelen J. Peter, Birnie Martijn, van Langen Irene M., Wilde Arthur A. M. Mortality of Inherited Arrhythmia Syndromes Insight Into Their Natural History Circulation. Cardiovascular genetics 2012;5 (2):183-189 [PubMed]
  • Laurent Gabriel, Saal Samuel, Amarouch Mohamed Yassine, Béziau Delphine M., Marsman Roos F. J., Faivre Laurence, Barc Julien, Dina Christian, Bertaux Geraldine, Barthez Olivier, Thauvin-Robinet Christel, Charron Philippe, Fressart Véronique, Maltret Alice, Villain Elisabeth, Baron Estelle, Mérot Jean, Turpault Rodolphe, Coudière Yves, Charpentier Flavien, Schott Jean-Jacques, Loussouarn Gildas, Wilde Arthur A. M., Wolf Jean-Eric, Baró Isabelle, Kyndt Florence, Probst Vincent Multifocal Ectopic Purkinje-Related Premature Contractions A New SCN5A-Related Cardiac Channelopathy Journal of the American College of Cardiology 2012;60 (2):144-156 [PubMed]
  • Brouwer Wessel P., Germans Tjeerd, Head Maaike C., van der Velden Jolanda, Heymans Martijn W., Christiaans Imke, Houweling Arjan C., Wilde Arthur A., van Rossum Albert C. Multiple myocardial crypts on modified long-axis view are a specific finding in pre-hypertrophic HCM mutation carriers European heart journal cardiovascular Imaging 2012;13 (4):292-297 [PubMed]
  • Barsheshet Alon, Goldenberg Ilan, O-Uchi Jin, Moss Arthur J., Jons Christian, Shimizu Wataru, Wilde Arthur A., McNitt Scott, Peterson Derick R., Zareba Wojciech, Robinson Jennifer L., Ackerman Michael J., Cypress Michael, Gray Daniel A., Hofman Nynke, Kanters Jorgen K., Kaufman Elizabeth S., Platonov Pyotr G., Qi Ming, Towbin Jeffrey A., Vincent G. Michael, Lopes Coeli M. Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events Implications for Mutation-Specific Response to beta-Blocker Therapy in Type 1 Long-QT Syndrome Circulation 2012;125 (16):1988-+ [PubMed]
  • Wilde A. A. M., de Jong J. S. S. G. Narrow QRS complexes intervening wide QRS complexes Netherlands heart journal 2012;20 (12):518-+
  • Chockalingam Priya, Crotti Lia, Girardengo Giulia, Johnson Jonathan N., Harris Katy M., van der Heijden Jeroen F., Hauer Richard N. W., Beckmann Britt M., Spazzolini Carla, Rordorf Roberto, Rydberg Annika, Clur Sally-Ann B., Fischer Markus, van den Heuvel Freek, Kääb Stefan, Blom Nico A., Ackerman Michael J., Schwartz Peter J., Wilde Arthur A. M. Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2 Journal of the American College of Cardiology 2012;60 (20):2092-2099 [PubMed]
  • van der Zwaag Paul A., van Rijsingen Ingrid A. W., Asimaki Angeliki, Jongbloed Jan D. H., van Veldhuisen Dirk J., Wiesfeld Ans C. P., Cox Moniek G. P. J., van Lochem Laura T., de Boer Rudolf A., Hofstra Robert M. W., Christiaans Imke, van Spaendonck-Zwarts Karin Y., Lekanne dit Deprez Ronald H., Judge Daniel P., Calkins Hugh, Suurmeijer Albert J. H., Hauer Richard N. W., Saffitz Jeffrey E., Wilde Arthur A. M., van den Berg Maarten P., van Tintelen J. Peter Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy European journal of heart failure 2012;14 (11):1199-1207 [PubMed]
  • Giudicessi John R., Kapplinger Jamie D., Tester David J., Alders Marielle, Salisbury Benjamin A., Wilde Arthur A. M., Ackerman Michael J. Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome Circulation. Cardiovascular genetics 2012;5 (5):519-528 [PubMed]
  • Coronel Ruben, Janse Michiel J., Opthof Tobias, Wilde Arthur A., Taggart Peter Postrepolarization refractoriness in acute ischemia and after antiarrhythmic drug administration: Action potential duration is not always an index of the refractory period Heart rhythm 2012;9 (6):977-982 [PubMed]
  • Olde Nordkamp Louise R. A., Knops Reinoud E., Bardy Gust H., Blaauw Yuri, Boersma Lucas V. A., Bos Johannes S., Delnoy Peter Paul H. M., van Dessel Pascal F. H. M., Driessen Antoine H. G., de Groot Joris R., Herrman Jean Paul R., Jordaens Luc J. L. M., Kooiman Kirsten M., Maass Alexander H., Meine Mathias, Mizusawa Yuka, Molhoek Sander G., van Opstal Jurjen, Tijssen Jan G. P., Wilde Arthur A. M. Rationale and design of the PRAETORIAN trial: A Prospective, RAndomizEd comparison of subcuTaneOus and tRansvenous ImplANtable cardioverter-defibrillator therapy American heart journal 2012;163 (5):753-+ [PubMed]
  • Coronel Ruben, Janse Michiel J., Opthof Tobias, Wilde Arthur A. M., Taggart Peter Reply To the Editor-Postrepolarization Refractoriness in Acute Ischemia and After Antiarrhythmic Drug Administration Heart rhythm 2012;9 (5):E14 [PubMed]
  • van Rijsingen Ingrid A. W., Arbustini Eloisa, Elliott Perry M., Mogensen Jens, Hermans-van Ast Johanna F., van der Kooi Anneke J., van Tintelen J. Peter, van den Berg Maarten P., Pilotto Andrea, Pasotti Michele, Jenkins Sharon, Rowland Camilla, Aslam Uzma, Wilde Arthur A. M., Perrot Andreas, Pankuweit Sabine, Zwinderman Aeilko H., Charron Philippe, Pinto Yigal M. Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers A European Cohort Study Journal of the American College of Cardiology 2012;59 (5):493-500 [PubMed]
  • van Hoorn Frans, Campian Maria E., Spijkerboer Anje, Blom Marieke T., Planken R. Nils, van Rossum Albert C., de Bakker Jacques M. T., Wilde Arthur A. M., Groenink Maarten, Tan Hanno L. SCN5A Mutations in Brugada Syndrome Are Associated with Increased Cardiac Dimensions and Reduced Contractility PLoS ONE 2012;7 (8):e42037 [PubMed]
  • Gallagher James, Huang David T., Wilde Arthur A. M., Rosero Spencer Z. Syncope and Exercise-Related Ventricular Tachycardia Annals of noninvasive electrocardiology 2012;17 (2):146-150 [PubMed]
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Tachy-aritmieënin: H. C. S. van Buren, C. G. Colijn, V. M. Eimermann, J. J. de Gier, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2012/2013. Houten: Boekbinderij Van Hees, Zaltbommel; 2012. p. 663-665, ISBN 9789074027007
  • Bos J. Martijn, Subramaniam Malayannan, Hawse John R., Christiaans Imke, Rajamannan Nalini M., Maleszewski Joseph J., Edwards William D., Wilde Arthur A. M., Spelsberg Thomas C., Ackerman Michael J. TGF beta-inducible early gene-1 (TIEG1) mutations in hypertrophic cardiomyopathy Journal of cellular biochemistry 2012;113 (6):1896-1903 [PubMed]
  • Koopmann Tamara T., Verkerk Arie O., Bezzina Connie R., de Bakker Jacques M. T., Wilde Arthur A. M. The Chemical Compound PTC124 Does Not Affect Cellular Electrophysiology of Cardiac Ventricular Myocytes Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy 2012;26 (1):41-45 [PubMed]
  • Chockalingam Priya, Clur Sally-Ann B., Breur Johannes M. P. J., Kriebel Thomas, Paul Thomas, Rammeloo Lukas A., Wilde Arthur A. M., Blom Nico A. The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children Heart rhythm 2012;9 (12):1986-1992 [PubMed]
  • Olde Nordkamp Louise R. A., Dabiri Abkenari Lara, Boersma Lucas V. A., Maass Alexander H., de Groot Joris R., van Oostrom Antonie J. H. H. M., Theuns Dominic A. M. J., Jordaens Luc J. L. M., Wilde Arthur A. M., Knops Reinoud E. The Entirely Subcutaneous Implantable Cardioverter-Defibrillator Initial Clinical Experience in a Large Dutch Cohort Journal of the American College of Cardiology 2012;60 (19):1933-1939 [PubMed]
  • Adler Arnon, van der Werf Christian, Postema Pieter G., Rosso Raphael, Bhuiyan Zahir A., Kalman Jonathan M., Vohra Jitendra K., Guevara-Valdivia Milton E., Marquez Manlio F., Halkin Amir, Benhorin Jesaia, Antzelevitch Charles, Wilde Arthur A. M., Viskin Sami The phenomenon of "QT stunning": The abnormal QT prolongation provoked by standing persists even as the heart rate returns to normal in patients with long QT syndrome Heart rhythm 2012;9 (6):901-908 [PubMed]
  • Werf Christian van der, Zwinderman Aeilko H., Wilde Arthur A. M. Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developments Europace : European pacing, arrhythmias, and cardiac electrophysiology 2012;14 (2):175-183 [PubMed]
  • van der Werf Christian, Wilde Arthur A. M. Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developments (vol 14, pg 175, 2012) Europace : European pacing, arrhythmias, and cardiac electrophysiology 2012;14 (12):1810
  • Kolder Iris C. R. M., Michels Michelle, Christiaans Imke, ten Cate Folkert J., Majoor-Krakauer Danielle, Danser Alexander H. J., Lekanne Deprez Robert H., Tanck Michael W. T., Wilde Arthur A. M., Bezzina Connie R., Dooijes Dennis The role of renin-angiotensin-aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy European journal of human genetics 2012;20 (10):1071-1077 [PubMed]
  • Opthof T., Janse M. J., Kléber A. G., Wellens H. J. J., Wilde A. A. M., Coronel R. The works of Dirk Durrer (1918-1984) Netherlands heart journal 2012;20 (10):430-433 [PubMed]
  • Krul Sébastien P. J., Driessen Antoine H. G., Wilde Arthur A. M., de Bakker Jacques M. T., de Mol Bas A. J. M., de Groot Joris R. Thoracoscopische behandeling van atriumfibrilleren Nederlands tijdschrift voor geneeskunde 2012;156 (2):A3938 [PubMed]
  • Wilde Arthur A. M., van der Werf Christian Treatment for patients with catecholaminergic polymorphic ventricular tachycardia: are we in need of randomized trials? Journal of electrocardiology 2012;45 (6):739-740 [PubMed]
  • Amin Ahmad S., Giudicessi John R., Tijsen Anke J., Spanjaart Anne M., Reckman Yolan J., Klemens Christine A., Tanck Michael W., Kapplinger Jamie D., Hofman Nynke, Sinner Moritz F., Müller Martina, Wijnen Wino J., Tan Hanno L., Bezzina Connie R., Creemers Esther E., Wilde Arthur A. M., Ackerman Michael J., Pinto Yigal M. Variants in the 3 untranslated region of the KCNQ1-encoded K(v)7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner European heart journal 2012;33 (6):714-723 [PubMed]
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Wolff-Parkinson-White-syndroom (WPW)in: H. C. S. van Buren, C. G. Colijn, V. M. Eimermann, J. J. de Gier, S. W. G. Neutkens, editors. Commentaren Medicatiebewaking 2012/2013. Houten: Boekbinderij Van Hees, Zaltbommel; 2012. p. 832-833, ISBN 9789074027007

2011

  • Marsman Roos F., Bardai Abdennasser, Postma Alex V., Res Jan C. J., Koopmann Tamara T., Beekman Leander, van der Wal Allard C., Pinto Yigal M., Lekanne Deprez Ronald H., Wilde Arthur A. M., Jordaens Luc J., Bezzina Connie R. A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death Circulation. Cardiovascular genetics 2011;4 (3):280-287 [PubMed]
  • de Jong Jonas S. S. G., Verkerk Arie O., van Borren Marcel M. G. J., Zakhrabova-Zwiauer Olga M., Nieuwland Rienk, Meijers Joost C. M., Akkerman Jan-Willem N., Wilde Arthur A. M., Tan Hanno L., Dekker Lukas R. C. Activated human platelet products induce proarrhythmic effects in ventricular myocytes Journal of molecular and cellular cardiology 2011;51 (3):347-356 [PubMed]
  • van de Meerakker Judith B. A., van Engelen Klaartje, Mathijssen Inge B., Lekanne dit Deprez Ronald H., Lam Jan, Wilde Arthur A. M., Baars Marieke J. H., Mannens Marcel M. A. M., Mulder Barbara J. M., Moorman Antoon F. M., Postma Alex V. A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q European journal of human genetics 2011;19 (7):820-826 [PubMed]
  • Cox Moniek G. P. J., van der Zwaag Paul A., van der Werf Christian, van der Smagt Jasper J., Noorman Maartje, Bhuiyan Zahir A., Wiesfeld Ans C. P., Volders Paul G. A., van Langen Irene M., Atsma Douwe E., Dooijes Dennis, van den Wijngaard Arthur, Houweling Arjan C., Jongbloed Jan D. H., Jordaens Luc, Cramer Maarten J., Doevendans Pieter A., de Bakker Jacques M. T., Wilde Arthur A. M., van Tintelen J. Peter, Hauer Richard N. W. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study Circulation 2011;123 (23):2690-U87 [PubMed]
  • Opthof T., Wilde A. A. M. Bibliometric data in clinical cardiology revisited. The case of 37 Dutch professors Netherlands heart journal 2011;19 (5):246-255 [PubMed]
  • Schade van Westrum S. M., Hoogerwaard E. M., Dekker L., Standaar T. S., Bakker E., Ippel P. F., Oosterwijk J. C., Majoor-Krakauer D. F., van Essen A. J., Leschot N. J., Wilde A. A. M., de Haan R. J., de Visser M., van der Kooi A. J. Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy Neurology 2011;77 (1):62-66 [PubMed]
  • Hendrix Anneke, Borleffs C. Jan Willem, Vink Aryan, Doevendans Pieter A. F. M., Wilde Arthur A., van Langen Irene M., van der Smagt Jasper J., Bots Michiel L., Mosterd Arend Cardiogenetic screening of first-degree relatives after sudden cardiac death in the young: a population-based approach Europace : European pacing, arrhythmias, and cardiac electrophysiology 2011;13 (5):716-722 [PubMed]
  • Timmer Stefan A. J., Germans Tjeerd, Brouwer Wessel P., Lubberink Mark, van der Velden Jolanda, Wilde Arthur A. M., Christiaans Imke, Lammertsma Adriaan A., Knaapen Paul, van Rossum Albert C. Carriers of the hypertrophic cardiomyopathy MYBPC3 mutation are characterized by reduced myocardial efficiency in the absence of hypertrophy and microvascular dysfunction European journal of heart failure 2011;13 (12):1283-1289 [PubMed]
  • van der Werf Christian, Wilde Arthur A. M. Catecholaminergic polymorphic ventricular tachycardiain: H. F. Baars, J. J. van der Smagt, P. A. F. M. Doevendans, editors. Clinical Cardiogenetics. London: Springer-Verlag; 2011. p. 197-206, ISBN 9781849964708
  • van der Werf Christian, Wilde Arthur A. M. Catecholaminergic polymorphic ventricular tachycardia: important messages from case reports Europace : European pacing, arrhythmias, and cardiac electrophysiology 2011;13 (1):11-13 [PubMed]
  • Pinto Yigal M., Wilde Arthur A. A. M., van Rijsingen Ingrid A. W., Christiaans Imke, Deprez Ronald H. Lekanne, Elliott Perry M. Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14) European journal of human genetics 2011;19 (8):10.1038/ejhg.2010.24 [PubMed]
  • Sy Raymond W., van der Werf Christian, Chattha Ishvinder S., Chockalingam Priya, Adler Arnon, Healey Jeffrey S., Perrin Mark, Gollob Michael H., Skanes Allan C., Yee Raymond, Gula Lorne J., Leong-Sit Peter, Viskin Sami, Klein George J., Wilde Arthur A., Krahn Andrew D. Derivation and validation of a simple exercise-based algorithm for prediction of genetic testing in relatives of LQTS probands Circulation 2011;124 (20):2187-2194 [PubMed]
  • Bhuiyan Zahurul A., Wilde Arthur A. M. Desmosomal mutations across the fence Heart rhythm 2011;8 (8):1222-1223 [PubMed]
  • Kapplinger Jamie D., Landstrom Andrew P., Salisbury Benjamin A., Callis Thomas E., Pollevick Guido D., Tester David J., Cox Moniek G. P. J., Bhuiyan Zahir, Bikker Hennie, Wiesfeld Ans C. P., Hauer Richard N. W., van Tintelen J. Peter, Jongbloed Jan D. H., Calkins Hugh, Judge Daniel P., Wilde Arthur A. M., Ackerman Michael J. Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia-Associated Mutations From Background Genetic Noise Journal of the American College of Cardiology 2011;57 (23):2317-2327 [PubMed]
  • Postema Pieter, de Jong Jonas, Wilde Arthur Drug Use in Brugada Syndrome: Safe or Avoid? Journal of arrhythmia 2011;27
  • Wilde Arthur A. M., Viskin Sami EP testing does not predict cardiac events in Brugada syndrome Heart rhythm 2011;8 (10):1598-1600 [PubMed]
  • Amin Ahmad S., Boink Gerard J. J., Atrafi Florence, Spanjaart Anne M., Asghari-Roodsari Alaleh, Molenaar Remco J., Ruijter Jan M., Wilde Arthur A. M., Tan Hanno L. Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome Europace : European pacing, arrhythmias, and cardiac electrophysiology 2011;13 (7):968-975 [PubMed]
  • Chockalingam Priya, Rammeloo Lukas A., Postema Pieter G., Hruda Jarda, Clur Sally-Ann B., Blom Nico A., Wilde Arthur A. Fever-Induced Life-Threatening Arrhythmias in Children Harboring an SCN5A Mutation Pediatrics 2011;127 (1):E239-E244 [PubMed]
  • van der Werf Christian, Kannankeril Prince J., Sacher Frederic, Krahn Andrew D., Viskin Sami, Leenhardt Antoine, Shimizu Wataru, Sumitomo Naokata, Fish Frank A., Bhuiyan Zahurul A., Willems Albert R., van der Veen Maurits J., Watanabe Hiroshi, Laborderie Julien, Haïssaguerre Michel, Knollmann Björn C., Wilde Arthur A. M. Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Journal of the American College of Cardiology 2011;57 (22):2244-2254 [PubMed]
  • Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2011;19 (Suppl. S):32-37
  • Postema P. G., Christiaans I., Hofman N., Alders M., Koopmann T. T., Bezzina C. R., Loh P., Zeppenfeld K., Volders P. G. A., Wilde A. A. M. Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6 Netherlands heart journal 2011;19 (6):290-296 [PubMed]
  • Marsman R. F. J., Wilde A. A. M., Bezzina C. R. Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study Netherlands heart journal 2011;19 (2):96-100 [PubMed]
  • Smith T., van Dessel P. F., Theuns D. A. M. J., Muskens-Heemskerk A., van Domburg R. T., Wilde A. A., Jordaens L. Health care utilisation after defibrillator implantation for primary prevention according to the guidelines in 2 Dutch academic medical centres Netherlands heart journal 2011;19 (10):405-411 [PubMed]
  • Creemers Esther E., Wilde Arthur A., Pinto Yigal M. Heart failure: advances through genomics Nature reviews. Genetics 2011;12 (5):357-362 [PubMed]
  • Ackerman Michael J., Priori Silvia G., Willems Stephan, Berul Charles, Brugada Ramon, Calkins Hugh, Camm A. John, Ellinor Patrick T., Gollob Michael, Hamilton Robert, Hershberger Ray E., Judge Daniel P., Le Marec Hervè, McKenna William J., Schulze-Bahr Eric, Semsarian Chris, Towbin Jeffrey A., Watkins Hugh, Wilde Arthur, Wolpert Christian, Zipes Douglas P. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) Heart rhythm 2011;8 (8):1308-1339 [PubMed]
  • Ackerman Michael J., Priori Silvia G., Willems Stephan, Berul Charles, Brugada Ramon, Calkins Hugh, Camm A. John, Ellinor Patrick T., Gollob Michael, Hamilton Robert, Hershberger Ray E., Judge Daniel P., Le Marec Hervè, McKenna William J., Schulze-Bahr Eric, Semsarian Chris, Towbin Jeffrey A., Watkins Hugh, Wilde Arthur, Wolpert Christian, Zipes Douglas P., Probst Vincent, Schwartz Peter J., Kääb Stefan, Kirchhof Paulus HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) Europace : European pacing, arrhythmias, and cardiac electrophysiology 2011;13 (8):1077-1109 [PubMed]
  • Arking Dan E., Junttila M. Juhani, Goyette Philippe, Huertas-Vazquez Adriana, Eijgelsheim Mark, Blom Marieke T., Newton-Cheh Christopher, Reinier Kyndaron, Teodorescu Carmen, Uy-Evanado Audrey, Carter-Monroe Naima, Kaikkonen Kari S., Kortelainen Marja-Leena, Boucher Gabrielle, Lagacé Caroline, Moes Anna, Zhao Xiaoqing, Kolodgie Frank, Rivadeneira Fernando, Hofman Albert, Witteman Jacqueline C. M., Uitterlinden André G., Marsman Roos F., Pazoki Raha, Bardai Abdennasser, Koster Rudolph W., Dehghan Abbas, Hwang Shih-Jen, Bhatnagar Pallav, Post Wendy, Hilton Gina, Prineas Ronald J., Li Man, Köttgen Anna, Ehret Georg, Boerwinkle Eric, Coresh Josef, Kao W. H. Linda, Psaty Bruce M., Tomaselli Gordon F., Sotoodehnia Nona, Siscovick David S., Burke Greg L., Marbán Eduardo, Spooner Peter M., Cupples L. Adrienne, Jui Jonathan, Gunson Karen, Kesäniemi Y. Antero, Wilde Arthur A. M., Tardif Jean-Claude, O'Donnell Christopher J., Bezzina Connie R., Virmani Renu, Stricker Bruno H. C. H., Tan Hanno L., Albert Christine M., Chakravarti Aravinda, Rioux John D., Huikuri Heikki V., Chugh Sumeet S. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals PLoS genetics 2011;7 (6):e1002158 [PubMed]
  • Postema Pieter G., van der Werf Christian, Wilde Arthur A. M. Idiopathic ventricular fibrillationin: H. F. Baars, J. J. van der Smagt, P. A. F. M. Doevendans, editors. Clinical Cardiogenetics. London: Springer-Verlag; 2011. p. 229-238, ISBN 9781849964708
  • Bardai Abdennasser, Berdowski Jocelyn, van der Werf Christian, Blom Marieke T., Ceelen Manon, van Langen Irene M., Tijssen Jan G. P., Wilde Arthur A. M., Koster Rudolph W., Tan Hanno L. Incidence, Causes, and Outcomes of Out-of-Hospital Cardiac Arrest in Children A Comprehensive, Prospective, Population-Based Study in the Netherlands Journal of the American College of Cardiology 2011;57 (18):1822-1828 [PubMed]
  • Marsman Roos F., Wilde Arthur A. M., Bezzina Connie R. Inherited cardiac arrhythmia syndromes: role of the sodium channelin: Barbara Cohen-Kligerman, Charles Antzelevitch, Ranjan K. Thakur, Andrea Natale, editors. Basic Science for the Clinical Electrophysiologist. Philadelphia, Pennsylvania: W.B. Saunders Company; 2011. p. 93-112, ISBN 9781455704232
  • Kraaier K., McCracken T., van der Palen J., Wilde A. A. M., Scholten M. F. Is T-wave alternans testing feasible in candidates for prophylactic implantable defibrillators? Netherlands heart journal 2011;19 (1):6-9 [PubMed]
  • van der Wall E. E., de Boer M. J., Doevendans P. A., Wilde A. A., Zijlstra F. Journal metrics for the Netherlands Heart Journal Netherlands heart journal 2011;19 (4):159-161 [PubMed]
  • Butterworth Adam S., Braund Peter S., Farrall Martin, Hardwick Robert J., Saleheen Danish, Peden John F., Soranzo Nicole, Chambers John C., Sivapalaratnam Suthesh, Kleber Marcus E., Keating Brendan, Qasim Atif, Klopp Norman, Erdmann Jeanette, Assimes Themistocles L., Ball Stephen G., Balmforth Anthony J., Barnes Timothy A., Basart Hanneke, Baumert Jens, Bezzina Connie R., Boerwinkle Eric, Boehm Bernhard O., Brocheton Jessy, Bugert Peter, Cambien Francois, Clarke Robert, Codd Veryan, Collins Rory, Couper David, Cupples L. Adrienne, de Jong Jonas S., Diemert Patrick, Ejebe Kenechi, Elbers Clara C., Elliott Paul, Fornage Myriam, Franzosi Maria-Grazia, Frossard Philippe, Garner Stephen, Goel Anuj, Kastelein John J. P., Wilde Arthur A. M., Trip Mieke D., Dekker Lukas R., Henriques José P., Koch Karel T., de Winter Robbert J., Boekholdt S. Matthijs, Maitland-van der Zee Anke-Hilse Large-scale gene-centric analysis identifies novel variants for coronary artery disease PLoS genetics 2011;7 (9):e1002260 [PubMed]
  • Christiaans Imke, Birnie Erwin, Bonsel Gouke J., Mannens Marcel M. A. M., Michels Michelle, Majoor-Krakauer Daniëlle, Dooijes Dennis, van Tintelen J. Peter, van den Berg Maarten P., Volders Paul G. A., Arens Yvonne H., van den Wijngaard Arthur, Atsma Douwe E., Helderman-van den Enden Apollonia T. J. M., Houweling Arjan C., de Boer Karin, van der Smagt Jasper J., Hauer Richard N. W., Marcelis Carlo L. M., Timmermans Janneke, van Langen Irene M., Wilde Arthur A. M. Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy European heart journal 2011;32 (9):1161-1170 [PubMed]
  • Nannenberg Eline A., Michels Michelle, Christiaans Imke, Majoor-Krakauer Danielle, Hoedemaekers Yvonne M., van Tintelen J. Peter, Lombardi M. Paola, ten Cate Folkert J., Schinkel Arend F. L., Tijssen Jan G. P., van Langen Irene M., Wilde Arthur A. M., Sijbrands Eric J. G. Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history Journal of the American College of Cardiology 2011;58 (23):2406-2414 [PubMed]
  • Mizusawa Yuka, Postema Pieter, Wilde Arthur Multiple Clinical Manifestations of a Single SCN5A Mutation Journal of arrhythmia 2011;27
  • Migdalovich Dimitry, Moss Arthur J., Lopes Coeli M., Costa Jason, Ouellet Gregory, Barsheshet Alon, McNitt Scott, Polonsky Slava, Robinson Jennifer L., Zareba Wojciech, Ackerman Michael J., Benhorin Jesaia, Kaufman Elizabeth S., Platonov Pyotr G., Shimizu Wataru, Towbin Jeffrey A., Vincent G. Michael, Wilde Arthur A. M., Goldenberg Ilan Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome Heart rhythm 2011;8 (10):1537-1543 [PubMed]
  • Wilde Arthur A.M. New Therapies Based on New Insights in Inherited Arrhythmia Syndromes Journal of arrhythmia 2011;27 (4):245
  • Opthof T., Wilde A. A. M. One more time: bibliometric analysis of scientific output remains complicated Netherlands heart journal 2011;19 (7-8):359-360 [PubMed]
  • Wilde Arthur A. M., Brugada Ramon Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel Circulation research 2011;108 (7):884-U245 [PubMed]
  • Nof Eyal, Belhassen Bernard, Arad Michael, Bhuiyan Zahurul A., Antzelevitch Charles, Rosso Raphael, Fogelman Rami, Luria David, El-Ani Dalia, Mannens Marcel M. A. M., Viskin Sami, Eldar Michael, Wilde Arthur A. M., Glikson Michael Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor gene Heart rhythm 2011;8 (10):1546-1552 [PubMed]
  • Postema Pieter G., Christiaans Imke, Alders Marielle, Hofman Nynke, Wilde Arthur A. M. Premature plotse dood. Denk aan ernstige familiaire hartritmestoornissen Nederlands tijdschrift voor geneeskunde 2011;155 (39):A3391 [PubMed]
  • Elliott Perry, Baker Robert, Pasquale Ferdinando, Quarta Giovanni, Ebrahim Hatim, Mehta Atul B., Hughes Derralynn A., Anastasakis Aristides, Autore Camillo, Musumeci Maria Beatrice, Frenneaux Michael, Gimeno Juan, Tiina Heliö, Kuusisto Johanna, Aalto-Setäla Katriina, McKeown Pascal, Monserrat Lorenzo, Fernandez Xusto, Pacileo Giuseppe, Limongelli Giuseppe, Rapezzi Claudio, Biagini Elena, ten Cate Folkert J., Wilde Arthur A. M., Pinto Yigal M., Christiaans Imke, Zachara Elisabetta Prevalence of Anderson-Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson-Fabry Disease survey Heart (British Cardiac Society) 2011;97 (23):1957-1960 [PubMed]
  • Scicluna Brendon P., Tanck Michael W. T., Remme Carol Ann, Beekman Leander, Coronel Ruben, Wilde Arthur A. M., Bezzina Connie R. Quantitative trait loci for electrocardiographic parameters and arrhythmia in the mouse Journal of molecular and cellular cardiology 2011;50 (3):380-389 [PubMed]
  • Wilde Arthur A. M., Viskin Sami Rebuttal to EP testing predicts cardiac events in patients with Brugada syndrome Heart rhythm 2011;8 (11):1797 [PubMed]
  • Hofman N., Jongbloed R., Postema P. G., Nannenberg E., Alders M., Wilde A. A. M. Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome Netherlands heart journal 2011;19 (1):10-16 [PubMed]
  • Goldenberg Ilan, Horr Samuel, Moss Arthur J., Lopes Coeli M., Barsheshet Alon, McNitt Scott, Zareba Wojciech, Andrews Mark L., Robinson Jennifer L., Locati Emanuela H., Ackerman Michael J., Benhorin Jesaia, Kaufman Elizabeth S., Napolitano Carlo, Platonov Pyotr G., Priori Silvia G., Qi Ming, Schwartz Peter J., Shimizu Wataru, Towbin Jeffrey A., Vincent G. Michael, Wilde Arthur A. M., Zhang Li Risk for Life-Threatening Cardiac Events in Patients With Genotype-Confirmed Long-QT Syndrome and Normal-Range Corrected QT Intervals Journal of the American College of Cardiology 2011;57 (1):51-59 [PubMed]
  • Deneke Thomas, Chaar Huda, de Groot Joris R., Wilde Arthur A., Lawo Thomas, Mundig Johanna, Bösche Leif, Mügge Andreas, Grewe Peter H. Shift in the pattern of autonomic atrial innervation in subjects with persistent atrial fibrillation Heart rhythm 2011;8 (9):1357-1363 [PubMed]
  • Postema Pieter G., Mosterd Arend, Hofman Nynke, Alders Marielle, Wilde Arthur A. M. Sodium channelopathies: do we really understand what's going on? Journal of cardiovascular electrophysiology 2011;22 (5):590-593 [PubMed]
  • Etheridge Susan P., Bowles Neil E., Arrington Cammon B., Pilcher Thomas, Rope Alan, Wilde Arthur A. M., Alders Marielle, Saarel Elizabeth V., Tavernier Rene, Timothy Katherine W., Tristani-Firouzi Martin Somatic mosaicism contributes to phenotypic variation in Timothy syndrome American journal of medical genetics. Part A 2011;155A (10):2578-2583 [PubMed]
  • Hendrix Anneke Sudden cardiac death in the young: incidence and consequencesUtrecht: Ridderprint BV, Ridderkerk; 2011. 173p. ISBN 9789053353523. [UvA Dissertations Online] Universitair Medisch Centrum Utrecht: Cardiologie. (Supervisors: Doevendans Pieter A. F. M., Wilde Arthur A. M., Bots Michiel L.; Co-supervisor: Mosterd Arend)
  • Wilde Arthur AM SY10-4 Genetics of Ischemic Arrhythmias Journal of arrhythmia 2011;27
  • Scicluna Brendon System-based approach for the identification of novel genes influencing cardiac electrical traits 2011. 190p. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Bezzina C. R.)
  • Christiaans Imke, Wilde Arthur A. M. The never ending story of risk stratification for sudden death in hypertrophic cardiomyopathy American journal of cardiology 2011;107 (12):1871 [PubMed]
  • van Langen Irene, Wilde Arthur A. M. The outpatient clinic for cardiogeneticsin: H. F. Baars, J. J. van der Smagt, P. A. F. M. Doevendans, editors. Clinical Cardiogenetics. London: Springer-Verlag; 2011. p. 413-422, ISBN 9781849964708
  • Christiaans Imke, Wilde Arthur A. M. The patient with hypertrophic cardiomyopathy has a family Heart (British Cardiac Society) 2011;97 (3):262-263 [PubMed]
  • Janssens A. C. J. W., Wilde A. A. M., van Langen I. M. The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease Netherlands heart journal 2011;19 (2):85-88 [PubMed]
  • Birati Edo Y., Belhassen Bernard, Bardai Abdennasser, Wilde Arthur A. M., Viskin Sami The site of origin of torsade de pointes Heart (British Cardiac Society) 2011;97 (20):1650-1654 [PubMed]
  • Krul Sébastien P. J., Driessen Antoine H. G., van Boven Wim J., Linnenbank Andre C., Geuzebroek Guillaume S. C., Jackman Warren M., Wilde Arthur A. M., de Bakker Jacques M. T., de Groot Joris R. Thoracoscopic Video-Assisted Pulmonary Vein Antrum Isolation, Ganglionated Plexus Ablation and Periprocedural Confirmation of Ablation Lesions. First Results of a Hybrid Surgical-Electrophysiological Approach for Atrial Fibrillation Circulation. Arrhythmia and electrophysiology 2011;4 (3):262-270 [PubMed]
  • Jons Christian, O-Uchi Jin, Moss Arthur J., Reumann Matthias, Rice John J., Goldenberg Ilan, Zareba Wojciech, Wilde Arthur A. M., Shimizu Wataru, Kanters Jorgen K., McNitt Scott, Hofman Nynke, Robinson Jennifer L., Lopes Coeli M. B. Use of Mutant-Specific Ion Channel Characteristics for Risk Stratification of Long QT Syndrome Patients Science translational medicine 2011;3 (76):76ra28 [PubMed]

2010

  • Hofman Nynke, Tan Hanno L., Alders Marielle, van Langen Irene M., Wilde Arthur A. M. Active Cascade Screening in Primary Inherited Arrhythmia Syndromes Does It Lead to Prophylactic Treatment? Journal of the American College of Cardiology 2010;55 (23):2570-2576 [PubMed]
  • Bardy Gust H., Smith Warren M., Hood Margaret A., Crozier Ian G., Melton Iain C., Jordaens Luc, Theuns Dominic, Park Robert E., Wright David J., Connelly Derek T., Fynn Simon P., Murgatroyd Francis D., Sperzel Johannes, Neuzner Jörg, Spitzer Stefan G., Ardashev Andrey V., Oduro Amo, Boersma Lucas, Maass Alexander H., van Gelder Isabelle C., Wilde Arthur A., van Dessel Pascal F., Knops Reinoud E., Barr Craig S., Lupo Pierpaolo, Cappato Riccardo, Grace Andrew A. An Entirely Subcutaneous Implantable Cardioverter-Defibrillator New England journal of medicine 2010;363 (1):36-44 [PubMed]
  • Kapplinger Jamie D., Tester David J., Alders Marielle, Benito Begoña, Berthet Myriam, Brugada Josep, Brugada Pedro, Fressart Véronique, Guerchicoff Alejandra, Harris-Kerr Carole, Kamakura Shiro, Kyndt Florence, Koopmann Tamara T., Miyamoto Yoshihiro, Pfeiffer Ryan, Pollevick Guido D., Probst Vincent, Zumhagen Sven, Vatta Matteo, Towbin Jeffrey A., Shimizu Wataru, Schulze-Bahr Eric, Antzelevitch Charles, Salisbury Benjamin A., Guicheney Pascale, Wilde Arthur A. M., Brugada Ramon, Schott Jean-Jacques, Ackerman Michael J. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing Heart rhythm 2010;7 (1):33-46 [PubMed]
  • Berdowski Jocelyn ARREST - Optimizing out-of-hospital cardiopulmonary resuscitation 2010. 279p. ISBN 9789090257327. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Tijssen J. G. P.; Co-supervisor: Koster R. W.)
  • Cox Moniek G. P. J., van der Smagt Jasper J., Noorman Maartje, Wiesfeld Ans C., Volders Paul G. A., van Langen Irene M., Atsma Douwe E., Dooijes Dennis, Houweling Arjan C., Loh Peter, Jordaens Luc, Arens Yvonne, Cramer Maarten J., Doevendans Pieter A., van Tintelen J. Peter, Wilde Arthur A. M., Hauer Richard N. W. Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteria Circulation. Arrhythmia and electrophysiology 2010;3 (2):126-133 [PubMed]
  • Postema Pieter G., van Dessel Pascal F. H. M., Wilde Arthur A. M. Brugada Syndromein: Dhavendra Kumar, Perry Elliott, editors. Principles and Practice of Clinical Cardiovascular Genetics. New York: Oxford Unitersity Press Inc; 2010. p. 277-290, ISBN 9780195368956
  • Mac Gillavry Melvin R., Tan Hanno L., Wilde Arthur A. M. Brugada-syndroomin: J. J. de Gier, H. C. S. van Buren, V. M. Eimermann, M. Heringa, C. B. Koekoek, M. C. Star, editors. Commentaren Medicatiebewaking 2010/2011. Houten: Boekbinderij Van Hees, Zaltbommel; 2010. p. 732-733, ISBN 9789074027311
  • Amin Ahmad S., Tan Hanno L., Wilde Arthur A. M. Cardiac ion channels in health and disease Heart rhythm 2010;7 (1):117-126 [PubMed]
  • Smith Matthew R., Klotz Laurence, Persson Bo-Eric, Olesen Tine Kold, Wilde Arthur A. M. Cardiovascular Safety of Degarelix: Results From a 12-Month, Comparative, Randomized, Open Label, Parallel Group Phase III Trial in Patients With Prostate Cancer Journal of urology 2010;184 (6):2313-2319 [PubMed]
  • Otten Ellen, Asimaki Angeliki, Maass Alexander, van Langen Irene M., van der Wal Allard, de Jonge Nicolaas, van den Berg Maarten P., Saffitz Jeffrey E., Wilde Arthur A. M., Jongbloed Jan D. H., van Tintelen J. Peter Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks Heart rhythm 2010;7 (8):1058-1064 [PubMed]
  • van der Werf Christian, Hofman Nynke, Tan Hanno L., van Dessel Pascal F., Alders Marielle, van der Wal Allard C., van Langen Irene M., Wilde Arthur A. M. Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: The experience of a tertiary referral center in The Netherlands Heart rhythm 2010;7 (10):1383-1389 [PubMed]
  • de Groot N. M. S., Kirchhof C. J., van Gelder I. C., Meeder J. G., Balk A. H. M. M., Wilde A. A., Simoons M. L. Dronedarone in patients with atrial fibrillation Netherlands heart journal 2010;18 (7-8):370-373 [PubMed]
  • Kraaier Karin, van Dessel Pascal F. H. M., van der Palen Job, Wilde Arthur A. M., Scholten Marcoen F. ECG Quantification of Myocardial Scar Does Not Differ between Primary and Secondary Prevention ICD Recipients with Ischemic Heart Disease Pacing and clinical electrophysiology 2010;33 (2):192-197 [PubMed]
  • Tester David J., Valdivia Carmen, Harris-Kerr Carole, Alders Marielle, Salisbury Benjamin A., Wilde Arthur A. M., Makielski Jonathan C., Ackerman Michael J. Epidemiological, Molecular, and Functional Evidence Suggest A572D-SCN5A Should Not Be Considered An Independent LQT3-Susceptibility Mutation Heart rhythm 2010;7 (7):912-919 [PubMed]
  • Wilde Arthur A. M., Ackerman Michael J. Exercise extreme caution when calling rare genetic variants novel arrhythmia syndrome susceptibility mutations Heart rhythm 2010;7 (12):1883-1885 [PubMed]
  • Amin A. S., Klemens C. A., Verkerk A. O., Meregalli P. G., Asghari-Roodsari A., de Bakker J. M. T., January C. T., Wilde A. A. M., Tan H. L. Fever-triggered ventricular arrhythmias in Brugada syndrome and type 2 long-QT syndrome Netherlands heart journal 2010;18 (3):165-169 [PubMed]
  • Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2010;18 (5):248-254 [PubMed]
  • Postema Pieter G. Further insights into inheritable arrhythmia syndromes. Focus on electrocardiograms 2010. 301p. ISBN 9789090256542. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., de Bakker J. M. T.; Co-supervisors: van Dessel P. F. H. M., Tan H. L.)
  • Bos J. M. Genetic base of hypertrophic cardiomyopathy 2010. 192p. ISBN 9789090249056. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Ackerman M. J.)
  • Hofman Nynke, van Lochem Laura T., Wilde Arthur A. M. Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart Future cardiology 2010;6 (3):395-408 [PubMed]
  • Pazoki Raha, Wilde Arthur A. M., Bezzina Connie R. Genetic Basis of Ventricular Arrhythmias Current cardiovascular risk reports 2010;4 (6):454-460 [PubMed]
  • Hofman Nynke, van Langen Irene, Wilde Arthur A. M. Genetic testing in cardiovascular diseases Current opinion in cardiology 2010;25 (3):243-248 [PubMed]
  • Chambers John C., Zhao Jing, Terracciano Cesare M. N., Bezzina Connie R., Zhang Weihua, Kaba Riyaz, Navaratnarajah Manoraj, Lotlikar Amol, Sehmi Joban S., Kooner Manraj K., Deng Guohong, Siedlecka Urszula, Parasramka Saurabh, El-Hamamsy Ismail, Wass Mark N., Dekker Lukas R. C., de Jong Jonas S. S. G., Sternberg Michael J. E., McKenna William, Severs Nicholas J., de Silva Ranil, Wilde Arthur A. M., Anand Praveen, Yacoub Magdi, Scott James, Elliott Paul, Wood John N., Kooner Jaspal S. Genetic variation in SCN10A influences cardiac conduction Nature genetics 2010;42 (2):149-U80 [PubMed]
  • Bezzina Connie R., Pazoki Raha, Bardai Abdennasser, Marsman Roos F., de Jong Jonas S. S. G., Blom Marieke T., Scicluna Brendon P., Jukema J. Wouter, Bindraban Navin R., Lichtner Peter, Pfeufer Arne, Bishopric Nanette H., Roden Dan M., Meitinger Thomas, Chugh Sumeet S., Myerburg Robert J., Jouven Xavier, Kääb Stefan, Dekker Lukas R. C., Tan Hanno L., Tanck Michael W. T., Wilde Arthur A. M. Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction Nature genetics 2010;42 (8):688-U64 [PubMed]
  • Germans Tjeerd, Russel Iris K., Gotte Marco J. W., Spreeuwenberg Marieke D., Doevendans Pieter A., Pinto Yigal M., van der Geest Rob J., van der Velden Jolanda, Wilde Arthur A. M., van Rossum Albert C. How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonance Journal of cardiovascular magnetic resonance 2010;12 (1):13 [PubMed]
  • Christiaans Imke Hypertrophic cardiomyopathy. Towards an optimal cardiiogenetic strategy 2010. 189p. ISBN 9789090254456. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., van Langen I. M.; Co-supervisors: Bonsel G. J., Birnie E.)
  • Wilde Arthur A. M. Interactiemechanismen: Verlenging QT-intervalin: J. J. de Gier, H. C. S. van Buren, V. M. Eimermann, M. Heringa, C. B. Koekoek, M. C. Star, editors. Commentaren Medicatiebewaking 2010/2011. Houten: Boekbinderij Van Hees, Zaltbommel; 2010. p. 13-14, ISBN 9789074027311
  • Viskin Sami, Belhassen Bernard, Wilde Arthur A. Irreplaceable antiarrhythmic medications are disappearing: the case of quinidine Heart rhythm 2010;7 (6):863 [PubMed]
  • Beckmann Britt Maria, Holinski-Feder Elke, Walter Maggie C., Haserück Nadine, Reithmann Christopher, Hinterseer Martin, Wilde Arthur A., Kääb Stefan Laminopathy presenting as familial atrial fibrillation International journal of cardiology 2010;145 (2):394-396 [PubMed]
  • Wilde Arthur A. M. Lang-QT-intervalsyndroom (LQTS)in: J. J. de Gier, H. C. S. van Buren, V. M. Eimermann, M. Heringa, C. B. Koekoek, M. C. Star, editors. Commentaren Medicatiebewaking 2010/2011. Houten: Boekbinderij Van Hees, Zaltbommel; 2010. p. 617-622, ISBN 9789074027311
  • van Gelder Isabelle C., Groenveld Hessel F., Crijns Harry J. G. M., Tuininga Ype S., Tijssen Jan G. P., Alings A. Marco, Hillege Hans L., Bergsma-Kadijk Johanna A., Cornel Jan H., Kamp Otto, Tukkie Raymond, Bosker Hans A., van Veldhuisen Dirk J., van den Berg Maarten P., van Gelder I. C., Crijns H. J. G. M., Hillege H. L., van den Berg M. P., Tuininga Y. S., Alings A. M., Bosker H. A., Cornel J. H., Kamp O., van Veldhuisen D. J., van der Meer J., Luijckx G., Brügemann J., Wellens H. J., Hauer R. N., Wilde A. A., Groenveld H. F., Janssen M., Tukkie R., Bendermacher P., Olthof H., Robles de Medina R., Kuijer P., Zwart P., Pos L., Peters R., van Stralen R., Buys E., Daniëls M., Kuijper A., van Doorn D., Timmermans A., Hoogslag P., den Hartog F., van Rugge F., Derksen R. Lenient versus strict rate control in patients with atrial fibrillation New England journal of medicine 2010;362 (15):1363-1373 [PubMed]
  • Postema Pieter G., van Dessel Pascal F. H. M., Kors Jan A., Linnenbank Andre C., van Herpen Gerard, Ritsema van Eck Henk J., van Geloven Nan, de Bakker Jacques M. T., Wilde Arthur A. M., Tan Hanno L. Local Depolarization Abnormalities Are the Dominant Pathophysiologic Mechanism for Type 1 Electrocardiogram in Brugada Syndrome A Study of Electrocardiograms, Vectorcardiograms, and Body Surface Potential Maps During Ajmaline Provocation Journal of the American College of Cardiology 2010;55 (8):789-797 [PubMed]
  • Wilde Arthur A. M. Long QT syndrome: A double hit hurts more Heart rhythm 2010;7 (10):1419-1420 [PubMed]
  • Probst V., Veltmann C., Eckardt L., Meregalli P. G., Gaita F., Tan H. L., Babuty D., Sacher F., Giustetto C., Schulze-Bahr E., Borggrefe M., Haissaguerre M., Mabo P., Le Marec H., Wolpert C., Wilde A. A. M. Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome Results From the FINGER Brugada Syndrome Registry Circulation 2010;121 (5):635-643 [PubMed]
  • Hoogendijk Mark G., Potse Mark, Linnenbank André C., Verkerk Arie O., den Ruijter Hester M., van Amersfoorth Shirley C. M., Klaver Eva C., Beekman Leander, Bezzina Connie R., Postema Pieter G., Tan Hanno L., Reimer Annette G., van der Wal Allard C., ten Harkel Arend D. J., Dalinghaus Michiel, Vinet Alain, Wilde Arthur A. M., de Bakker Jacques M. T., Coronel Ruben Mechanism of right precordial ST-segment elevation in structural heart disease: Excitation failure by current-to-load mismatch Heart rhythm 2010;7 (2):238-248 [PubMed]
  • Christiaans Imke, Kok Tjitske M., van Langen Irene M., Birnie Erwin, Bonsel Gouke J., Wilde Arthur A. M., Smets Ellen M. A. Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriers European journal of human genetics 2010;18 (2):251-253 [PubMed]
  • van Bree Maurits D. R., Roos Yvo B. W. E. M., van der Bilt Ivo A. C., Wilde Arthur A. M., Sprengers Marieke E. S., de Gans Koen, Vergouwen Mervyn D. I. Prevalence and Characterization of ECG Abnormalities After Intracerebral Hemorrhage Neurocritical care 2010;12 (1):50-55 [PubMed]
  • Hendrix A., van der Werf C., Bots M. L., Birnie E., van der Smagt J. J., Borleffs C. J. W., Vink A., van Weert H. C., Doevendans P. A. F. M., Wilde A. A. M., Mosterd A., van Langen I. M. Rationale and design of the CAREFUL study : The yield of CARdiogenetic scrEening in First degree relatives of sudden cardiac and UnexpLained death victims <45 years Netherlands heart journal 2010;18 (6):286-290 [PubMed]
  • van der Zwaag P. A., Cox M. G. P. J., van der Werf C., Wiesfeld A. C. P., Jongbloed J. D. H., Dooijes D., Bikker H., Jongbloed R., Suurmeijer A. J. H., van den Berg M. P., Hofstra R. M. W., Hauer R. N. W., Wilde A. A. M., van Tintelen J. P. Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia Netherlands heart journal 2010;18 (12):583-591 [PubMed]
  • Christiaans Imke, van Engelen Klaartje, van Langen Irene M., Birnie Erwin, Bonsel Gouke J., Elliott Perry M., Wilde Arthur A. M. Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers Europace : European pacing, arrhythmias, and cardiac electrophysiology 2010;12 (3):313-321 [PubMed]
  • Verouden Niels J., Haeck Joost D., Koch Karel T., Henriques José P., Baan Jan, van der Schaaf René J., Vis Marije M., Peters Ron J., Wilde Arthur A., Piek Jan J., Tijssen Jan G., de Winter Robbert J. ST-Segment Resolution Prior to Primary Percutaneous Coronary Intervention Is a Poor Indicator of Coronary Artery Patency in Patients with Acute Myocardial Infarction Annals of noninvasive electrocardiology 2010;15 (2):107-115 [PubMed]
  • van der Werf Christian, van Langen Irene M., Wilde Arthur A. M. Sudden Death in the Young What Do We Know About It and How to Prevent? Circulation. Arrhythmia and electrophysiology 2010;3 (1):96-104 [PubMed]
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Tachy-aritmieënin: J. J. de Gier, H. C. S. van Buren, V. M. Eimermann, M. Heringa, C. B. Koekoek, M. C. Star, editors. Commentaren Medicatiebewaking 2010/2011. Houten: Boekbinderij Van Hees, Zaltbommel; 2010. p. 579-581, ISBN 9789074027311
  • Hoogendijk Mark G., Opthof Tobias, Postema Pieter G., Wilde Arthur A. M., de Bakker Jacques M. T., Coronel Ruben The Brugada ECG Pattern A Marker of Channelopathy, Structural Heart Disease, or Neither? Toward a Unifying Mechanism of the Brugada Syndrome Circulation. Arrhythmia and electrophysiology 2010;3 (3):283-290 [PubMed]
  • Kirchhefer Uwe, Wehrmeister Diana, Postma Alex V., Pohlentz Gottfried, Mormann Michael, Kucerova Dana, Müller Frank U., Schmitz Wilhelm, Schulze-Bahr Eric, Wilde Arthur A., Neumann Joachim The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handling Journal of molecular and cellular cardiology 2010;49 (1):95-105 [PubMed]
  • Wilde Arthur A. M., Postema Pieter G., Di Diego José M., Viskin Sami, Morita Hiroshi, Fish Jeffrey M., Antzelevitch Charles The pathophysiological mechanism underlying Brugada syndrome Depolarization versus repolarization Journal of molecular and cellular cardiology 2010;49 (4):543-553 [PubMed]
  • Viskin Sami, Postema Pieter G., Bhuiyan Zahurul A., Rosso Raphael, Kalman Jonathan M., Vohra Jitendra K., Guevara-Valdivia Milton E., Marquez Manlio F., Kogan Evgeni, Belhassen Bernard, Glikson Michael, Strasberg Boris, Antzelevitch Charles, Wilde Arthur A. M. The Response of the QT Interval to the Brief Tachycardia Provoked by Standing A Bedside Test for Diagnosing Long QT Syndrome Journal of the American College of Cardiology 2010;55 (18):1955-1961 [PubMed]
  • Clur Sally-Ann B., Chockalingam Priya, Filippini Luc H., Widyanti Ari P., van Cruijsen Marc, Blom Nico A., Alders Mariel, Hofman Nynke, Wilde Arthur A. M. The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome Pediatric cardiology 2010;31 (4):462-468 [PubMed]
  • Christiaans Imke, Birnie Erwin, van Langen Irene M., van Spaendonck-Zwarts Karin Y., van Tintelen J. Peter, van den Berg Maarten P., Atsma Douwe E., Helderman-van den Enden Apollonia T. J. M., Pinto Yigal M., Hermans-van Ast J. F., Bonsel Gouke J., Wilde Arthur A. M. The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening European heart journal 2010;31 (7):842-848 [PubMed]
  • Leoni Anne-Laure, Gavillet Bruno, Rougier Jean-Sébastien, Marionneau Céline, Probst Vincent, Le Scouarnec Solena, Schott Jean-Jacques, Demolombe Sophie, Bruneval Patrick, Huang Christopher L. H., Colledge William H., Grace Andrew A., Le Marec Hervé, Wilde Arthur A., Mohler Peter J., Escande Denis, Abriel Hugues, Charpentier Flavien Variable Na(v)1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a(+/-) Mouse Model PLoS ONE 2010;5 (2):e9298 [PubMed]
  • Schwartz Peter J., Spazzolini Carla, Priori Silvia G., Crotti Lia, Vicentini Alessandro, Landolina Maurizio, Gasparini Maurizio, Wilde Arthur A. M., Knops Reinoud E., Denjoy Isabelle, Toivonen Lauri, Mönnig Gerold, Al-Fayyadh Majid, Jordaens Luc, Borggrefe Martin, Holmgren Christina, Brugada Pedro, de Roy Luc, Hohnloser Stefan H., Brink Paul A. Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them? Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry Circulation 2010;122 (13):1272-1282 [PubMed]
  • Mac Gillavry Melvin R., Wilde Arthur A. M. Wolff-Parkinson-White-syndroom (WPW)in: J. J. de Gier, H. C. S. van Buren, V. M. Eimermann, M. Heringa, C. B. Koekoek, M. C. Star, editors. Commentaren Medicatiebewaking 2010/2011. Houten: Boekbinderij Van Hees, Zaltbommel; 2010. p. 734-735, ISBN 9789074027311

2009

  • Wilde A. A. M. An irregular heart beat Netherlands heart journal 2009;17 (4):172-+
  • Wilde A. A. M. An unexpected narrow QRS complex-1- Netherlands heart journal 2009;17 (7-8):307
  • Meregalli Paola G. Brugada syndrome. Clinical and pathophysiological aspects 2009. 241p. ISBN 9789490122126. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Tan H. L.)
  • MacGillavry Melvin R., Tan Hanno L., Wilde Arthur A. M. Brugada syndroomin: H. C. S. van Buren, J. J. de Gier, editors. Commentaren Medicatiebewaking 2009/2010. Houten: Health Base; 2009. p. 845-846, ISBN 9789074027304
  • van der Wall E. E., Wilde A. A. M. Case histories: increasing role for major journals Netherlands heart journal 2009;17 (7-8):272-273 [PubMed]
  • Bhuiyan Zahurul A., Al-Shahrani Safar, Al-Khadra Ayman S., Al-Ghamdi Saleh, Al-Khalaf Khalaf, Mannens Marcel M. A. M., Wilde Arthur A. M., Momenah Tarek S. Clinical and Genetic Analysis of Long QT Syndrome in Children from Six Families in Saudi Arabia: Are They Different? Pediatric cardiology 2009;30 (4):490-501 [PubMed]
  • Bhuiyan Zahurul A. Clinical and genetic spectrum of hereditary cardiac arrhythmia syndromes 2009. 327p. ISBN 9789090243184. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Mannens M. M. A. M.)
  • Opthof T., Wilde A. A. M. Comment: Assessment of scientific quality is complicated Netherlands heart journal 2009;17 (12):501-502
  • Bhuiyan Z. A., Momenah T. S., Wilde A. A.M. Congenital primary arrhythmias in childrenin: Heart Disease in Children. Nova Science Publishers Inc.; 2009. p. 1-41, ISBN 9781607415046
  • Wilde Arthur A. M., Pinto Yigal M. Cost-effectiveness of genotyping in inherited arrhythmia syndromes: are we getting value for the money? Circulation. Arrhythmia and electrophysiology 2009;2 (1):1-3 [PubMed]
  • Connolly Stuart J., Ezekowitz Michael D., Yusuf Salim, Eikelboom John, Oldgren Jonas, Parekh Amit, Pogue Janice, Reilly Paul A., Themeles Ellison, Varrone Jeanne, Wang Susan, Alings Marco, Xavier Denis, Zhu Jun, Diaz Rafael, Lewis Basil S., Darius Harald, Diener Hans-Christoph, Joyner Campbell D., Wallentin Lars, Connolly S. J., Ezekowitz M. D., Yusuf S., Eikelboom J., Oldgren J., Parekh A., Reilly P. A., Themeles E., Varrone J., Wang S., Palmcrantz-Graf E., Haehl M., Wallentin L., Alings A. M. W., Amerena J. V., Avezum A., Baumgartner I., Brugada J., Budaj A., Caicedo V., Ceremuzynski L., Chen J. H., Commerford P. J., Dans A. L., Darius H., Di Pasquale G., Diaz R., Cozijnsen L., Postema P. G., Wilde A. A. M. Dabigatran versus warfarin in patients with atrial fibrillation New England journal of medicine 2009;361 (12):1139-1151 [PubMed]
  • Bhuiyan Zahurul A., Jongbloed Jan D. H., van der Smagt Jasper, Lombardi Paola M., Wiesfeld Ans C. P., Nelen Marcel, Schouten Meyke, Jongbloed Roselie, Cox Moniek G. P. J., van Wolferen Marleen, Rodriguez Luz M., van Gelder Isabelle C., Bikker Hennie, Suurmeijer Albert J. H., van den Berg Maarten P., Mannens Marcel M. A. M., Hauer Richard N. W., Wilde Arthur A. M., van Tintelen J. Peter Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients Results From a Multicenter Study Circulation. Cardiovascular genetics 2009;2 (5):418-U22 [PubMed]
  • Postema Pieter G., Wolpert Christian, Amin Ahmad S., Probst Vincent, Borggrefe Martin, Roden Dan M., Priori Silvia G., Tan Hanno L., Hiraoka Masayasu, Brugada Josep, Wilde Arthur A. M. Drugs and Brugada syndrome patients: Review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org) Heart rhythm 2009;6 (9):1335-1341 [PubMed]
  • Viskin Sami, Wilde Arthur A. M., Tan Hanno L., Antzelevitch Charles, Shimizu Wataru, Belhassen Bernard Empiric quinidine therapy for asymptomatic Brugada syndrome: Time for a prospective registry Heart rhythm 2009;6 (3):401-404 [PubMed]
  • Amin Ahmad S., de Groot Elisabeth A. A., Ruijter Jan M., Wilde Arthur A. M., Tan Hanno L. Exercise-Induced ECG Changes in Brugada Syndrome Circulation. Arrhythmia and electrophysiology 2009;2 (5):531-539 [PubMed]
  • Bhuiyan Z. A., Wilde A. A.M. Familial primary arrhythmias: Genes, mechanisms and treatment: Present perspectivein: Heart Disease in Men. Nova Science Publishers Inc.; 2009. p. 3-44, ISBN 9781606922972
  • Watanabe Hiroshi, Chopra Nagesh, Laver Derek, Hwang Hyun Seok, Davies Sean S., Roach Daniel E., Duff Henry J., Roden Dan M., Wilde Arthur A. M., Knollmann Björn C. Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans Nature medicine 2009;15 (4):380-383 [PubMed]
  • Postema P. G., van den Berg M., van Tintelen J. P., van den Heuvel F., Grundeken M., Hofman N., van der Roest W. P., Nannenberg E. A., Krapels I. P. C., Bezzina C. R., Wilde A. Founder mutations in the Netherlands SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide Netherlands heart journal 2009;17 (11):422-428 [PubMed]
  • Remme Carol Ann, Scicluna Brendon P., Verkerk Arie O., Amin Ahmad S., van Brunschot Sandra, Beekman Leander, Deneer Vera H. M., Chevalier Catherine, Oyama Fumitaka, Miyazaki Haruko, Nukina Nobuyuki, Wilders Ronald, Escande Denis, Houlgatte Remi, Wilde Arthur A. M., Tan Hanno L., Veldkamp Marieke W., de Bakker Jacques M. T., Bezzina Connie R. Genetically Determined Differences in Sodium Current Characteristics Modulate Conduction Disease Severity in Mice With Cardiac Sodium Channelopathy Circulation research 2009;104 (11):1283-U112 [PubMed]
  • Olde Nordkamp Louise R. A., Wieling Wouter, Zwinderman Aeilko H., Wilde Arthur A. M., van Dijk Nynke Genetic aspects of vasovagal syncope: a systematic review of current evidence Europace : European pacing, arrhythmias, and cardiac electrophysiology 2009;11 (4):414-420 [PubMed]
  • Christiaans Imke, van Langen Irene M., Birnie Erwin, Bonsel Gouke J., Wilde Arthur A. M., Smets Ellen M. A. Genetic Counseling and Cardiac Care in Predictively Tested Hypertrophic Cardiomyopathy Mutation Carriers: The Patients' Perspective American journal of medical genetics. Part A 2009;149A (7):1444-1451 [PubMed]
  • Kapa Suraj, Tester David J., Salisbury Benjamin A., Harris-Kerr Carole, Pungliya Manish S., Alders Marielle, Wilde Arthur A. M., Ackerman Michael J. Genetic Testing for Long-QT Syndrome Distinguishing Pathogenic Mutations From Benign Variants Circulation 2009;120 (18):1752-U31 [PubMed]
  • Shimizu Wataru, Moss Arthur J., Wilde Arthur A. M., Towbin Jeffrey A., Ackerman Michael J., January Craig T., Tester David J., Zareba Wojciech, Robinson Jennifer L., Qi Ming, Vincent G. Michael, Kaufman Elizabeth S., Hofman Nynke, Noda Takashi, Kamakura Shiro, Miyamoto Yoshihiro, Shah Samit, Amin Vinit, Goldenberg Ilan, Andrews Mark L., McNitt Scott Genotype-Phenotype Aspects of Type 2 Long QT Syndrome Journal of the American College of Cardiology 2009;54 (22):2052-2062 [PubMed]
  • Kirchhof Paulus, Franz Michael R., Bardai Abdennasser, Wilde Arthur M. Giant T-U waves precede torsades de pointes in long QT syndrome: a systematic electrocardiographic analysis in patients with acquired and congenital QT prolongation Journal of the American College of Cardiology 2009;54 (2):143-149 [PubMed]
  • Alders Marielle, Koopmann Tamara T., Christiaans Imke, Postema Pieter G., Beekman Leander, Tanck Michael W. T., Zeppenfeld Katja, Loh Peter, Koch Karel T., Demolombe Sophie, Mannens Marcel M. A. M., Bezzina Connie R., Wilde Arthur A. M. Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation American journal of human genetics 2009;84 (4):468-476 [PubMed]
  • Johnson J. N., Hofman N., Haglund C. M., Cascino G. D., Wilde A. A. M., Ackerman M. J. Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy Neurology 2009;72 (3):224-231 [PubMed]
  • Chockalingam Priya, Clur Sally-Ann B., Reimer Annette G., Blom Nico A., Wilde Arthur A. Idiopathic ventricular fibrillation in two infants, not always idiopathic on follow-up Heart rhythm 2009;6 (10):1501-1503 [PubMed]
  • Postema Pieter G., Ritsema van Eck Henk J., Opthof Tobias, van Herpen Gerard, van Dessel Pascal F. H. M., Priori Silvia G., Wolpert Christian, Borggrefe Martin, Kors Jan A., Wilde Arthur A. M. IK1 modulates the U-wave: insights in a 100-year-old enigma Heart rhythm 2009;6 (3):393-400 [PubMed]
  • van der Bilt I. A. C., Hasan D., Vandertop W. P., Wilde A. A. M., Algra A., Visser F. C., Rinkel G. J. E. Impact of cardiac complications on outcome after aneurysmal subarachnoid hemorrhage A meta-analysis Neurology 2009;72 (7):635-642 [PubMed]
  • Chockalingam Priya, Clur Sally-Ann B., Wilde Arthur A. M., Kuipers Irene, van Woensel Job, Blom Nico A. Implantable cardioverter defibrillator as a bridge to recovery in an infant with cardiac rhabdomyoma European journal of pediatrics 2009;168 (7):863-866 [PubMed]
  • Wilde Arthur A. M., Tan Hanno L. Inheritable potassium channel diseasesin: D. P. Zipes, J. Jalife, editors. Cardiac Electrophysiology; from cell to bedside. Philadelphia: Saunders-Elsevier; 2009. p. 527-534, ISBN 9781416059738
  • Wilde Arthur A. M. Interactiemechanismen: Verlenging QT-interval.in: H. C. S. van Buren, J. J. de Gier, editors. Commentaren Medicatiebewaking 2009/2010. Houten: Health Base; 2009. p. 727-733, ISBN 9789074027304
  • Koopmann Tamara T., Postema Pieter G., Bezzina Connie R., Wilde Arthur A. M. Ion channels involved in genetic cardiac arrhythmiasin: H. Duclohier, editors. Biophysics of Ion Channels and Diseases. Kerala, India: Research Signpost; 2009. p. 113-138
  • van der Wall E. E., de Boer M.-J., Doevendans P. A., Wilde A. A., Zijlstra F. Major achievements in cardiology in the past century: influence on Dutch cardiovascular medicine Netherlands heart journal 2009;17 (4):136-139 [PubMed]
  • Kraaier Karin, Verhorst Patrick M. J., van der Palen Job, van Dessel Pascal F. H. M., Wilde Arthur A. M., Scholten Marcoen F. Microvolt T-wave alternans during exercise and pacing are not comparable Europace : European pacing, arrhythmias, and cardiac electrophysiology 2009;11 (10):1375-1380 [PubMed]
  • Jons Christian, Moss Arthur J., Lopes Coeli M., McNitt Scott, Zareba Wojciech, Goldenberg Ilan, Qi Ming, Wilde Arthur A. M., Shimizu Wataru, Kanters Jorgen K., Towbin Jeffrey A., Ackerman Michael J., Robinson Jennifer L. Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome Journal of cardiovascular electrophysiology 2009;20 (8):859-865 [PubMed]
  • Pilichou Kalliopi, Remme Carol Ann, Basso Cristina, Campian Maria E., Rizzo Stefania, Barnett Phil, Scicluna Brendon P., Bauce Barbara, van den Hoff Maurice J. B., de Bakker Jacques M. T., Tan Hanno L., Valente Marialuisa, Nava Andrea, Wilde Arthur A. M., Moorman Antoon F. M., Thiene Gaetano, Bezzina Connie R. Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy Journal of experimental medicine 2009;206 (8):1787-1802 [PubMed]
  • Pinto Y. M., Wilde A. A.M., Hermans-van Ast J. F., Van Langen I. M., Van Tintelen J. P., Atsma D. E., Arens Y. M., Marcelis C. L., Ten Cate F. J., Vd Smagt J. J., Houweling A. C. National registry for patients and families with a familial heart disease Netherlands heart journal 2009;17 (2):81
  • Cox Moniek G. P. J., van der Smagt Jasper J., Wilde Arthur A. M., Wiesfeld Ans C. P., Atsma Douwe E., Nelen Marcel R., Rodriguez Luz-Maria, Loh Peter, Cramer Maarten J., Doevendans Pieter A., van Tintelen J. Peter, de Bakker Jacques M. T., Hauer Richard N. W. New ECG Criteria in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Circulation. Arrhythmia and electrophysiology 2009;2 (5):524-530 [PubMed]
  • Verouden N. J., Koch K. T., Peters R. J., Henriques J. P., Baan J., van der Schaaf R. J., Vis M. M., Tijssen J. G., Piek J. J., Wellens H. J., Wilde A. A., de Winter R. J. Persistent precordial "hyperacute" T-waves signify proximal left anterior descending artery occlusion Heart (British Cardiac Society) 2009;95 (20):1701-1706 [PubMed]
  • Wilde A. A. M., Simmers T. A. Primary prevention with ICDs, are we on the right track? Netherlands heart journal 2009;17 (3):92-94 [PubMed]
  • de Jong Jonas S. S. G., Marsman Roos F., Henriques José P. S., Koch Karel T., de Winter Robbert J., Tanck Michael W. T., Wilde Arthur A. M., Dekker Lukas R. C. Prognosis among survivors of primary ventricular fibrillation in the percutaneous coronary intervention era American heart journal 2009;158 (3):467-472 [PubMed]
  • Christiaans Imke, van Langen Irene M., Birnie Erwin, Bonsel Gouke J., Wilde Arthur A. M., Smets Ellen M. A. Quality of Life and Psychological Distress in Hypertrophic Cardiomyopathy Mutation Carriers: A Cross-Sectional Cohort Study American journal of medical genetics. Part A 2009;149A (4):602-612 [PubMed]
  • van Tintelen J. P., Wilde A. A. M., Jongbloed J. D. H. Recurrent and founder mutations in inherited cardiac diseases in the Netherlands Netherlands heart journal 2009;17 (11):407-408 [PubMed]
  • Vehmeijer J. T., Christiaans I., van Langen I. M., Birnie E., Bonsel G. J., Smets E. M. A., Wilde A. A. M. Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers Netherlands heart journal 2009;17 (12):464-469 [PubMed]
  • Probst Vincent, Wilde Arthur A. M., Barc Julien, Sacher Frederic, Babuty Dominique, Mabo Philippe, Mansourati Jacques, Le Scouarnec Solena, Kyndt Florence, Le Caignec Cedric, Guicheney Pascale, Gouas Laetitia, Albuisson Juliette, Meregalli Paola G., Le Marec Hervé, Tan Hanno L., Schott Jean-Jacques SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome Circulation. Cardiovascular genetics 2009;2 (6):552-557 [PubMed]
  • Kapplinger Jamie D., Tester David J., Salisbury Benjamin A., Carr Janet L., Harris-Kerr Carole, Pollevick Guido D., Wilde Arthur A. M., Ackerman Michael J. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test Heart rhythm 2009;6 (9):1297-1303 [PubMed]
  • Wieling Wouter, Thijs Roland D., van Dijk N., Wilde Arthur A. M., Benditt David G., van Dijk J. Gert Symptoms and signs of syncope: a review of the link between physiology and clinical clues Brain 2009;132 (Part 10):2630-2642 [PubMed]
  • Wilde A. A. M. Syncope in an old lady Netherlands heart journal 2009;17 (2):77
  • MacGillavry Melvin R., Wilde Arthur A. M. Tachy-aritmie - Algemeenin: H. C. S. van Buren, J. J. de Gier, editors. Commentaren Medicatiebewaking 2009/2010. Houten: Health Base; 2009. p. 685-687, ISBN 9789074027304
  • Groenink Maarten, Wilde Arthur A. M. The "Accordion Sign," a New Tune in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Magnetic Resonance Imaging? Journal of the American College of Cardiology 2009;53 (15):1300-1301 [PubMed]
  • Remme C. A., Verkerk A. O., Hoogaars W. M. H., Aanhaanen W. T. J., Scicluna B. P., Annink C., van den Hoff M. J. B., Wilde A. A. M., van Veen T. A. B., Veldkamp M. W., de Bakker J. M. T., Christoffels V. M., Bezzina C. R. The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium Basic research in cardiology 2009;104 (5):511-522 [PubMed]
  • Opthof T., Wilde A. A. M. The Hirsch-index: a simple, new tool for the assessment of scientific output of individual scientists: The case of Dutch professors in clinical cardiology Netherlands heart journal 2009;17 (4):145-154 [PubMed]
  • van der Werf Christian, van Langen Irene M., Wilde Arthur A. M. The Relationship Between Pre-Participation Screening of Young Competitive Athletes and Family Screening Journal of the American College of Cardiology 2009;53 (24):2309-2309; author reply 2310 [PubMed]
  • Medeiros-Domingo Argelia, Bhuiyan Zahurul A., Tester David J., Hofman Nynke, Bikker Hennie, van Tintelen J. Peter, Mannens Marcel M. A. M., Wilde Arthur A. M., Ackerman Michael J. The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome A Comprehensive Open Reading Frame Mutational Analysis Journal of the American College of Cardiology 2009;54 (22):2065-2074 [PubMed]
  • Kraaier K., Verhorst P. M. J., van Dessel P. F. H. M., Wilde A. A. M., Scholten M. F. Towards a better risk stratification for sudden cardiac death in patients with structural heart disease Netherlands heart journal 2009;17 (3):101-106 [PubMed]
  • Meregalli Paola G., Tan Hanno L., Probst Vincent, Koopmann Tamara T., Tanck Michael W., Bhuiyan Zahurul A., Sacher Frederic, Kyndt Florence, Schott Jean-Jacques, Albuisson J., Mabo Philippe, Bezzina Connie R., Le Marec Herve, Wilde Arthur A. M. Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies Heart rhythm 2009;6 (3):341-348 [PubMed]
  • Colman Nancy, Bakker Annemieke, Linzer Mark, Reitsma Johannes B., Wieling Wouter, Wilde Arthur A. M. Value of history-taking in syncope patients: in whom to suspect long QT syndrome? Europace : European pacing, arrhythmias, and cardiac electrophysiology 2009;11 (7):937-943 [PubMed]
  • Christiaans Imke, Lekanne dit Deprez Ronald H., van Langen Irene M., Wilde Arthur A. M. Ventricular fibrillation in MYH7-related hypertrophic cardiomyopathy before onset of ventricular hypertrophy Heart rhythm 2009;6 (9):1366-1369 [PubMed]
  • Haïssaguerre Michel, Chatel Stéphanie, Sacher Frederic, Weerasooriya Rukshen, Probst Vincent, Loussouarn Gildas, Horlitz Marc, Liersch Ruedige, Schulze-Bahr Eric, Wilde Arthur, Kääb Stefan, Koster Joseph, Rudy Yoram, Le Marec Hervé, Schott Jean Jacques Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel Journal of cardiovascular electrophysiology 2009;20 (1):93-98 [PubMed]
  • MacGillavry Melvin R., Wilde Arthur A. M. WPW syndroom.in: H. C. S. van Buren, J. J. de Gier, editors. Commentaren Medicatiebewaking 2009/2010. Houten: Health Base; 2009. p. 847-848, ISBN 9789074027304

2008

  • Postema Pieter G., de Jong Jonas S. S. G., van der Bilt Ivo A. C., Wilde Arthur A. M. Accurate electrocardiographic assessment of the QT interval: teach the tangent Heart rhythm 2008;5 (7):1015-1018 [PubMed]
  • Cox Moniek G. P. J., Nelen Marcel R., Wilde Arthur A. M., Wiesfeld Ans C., van der Smagt Jasper J., Loh Peter, Cramer Maarten J., Doevendans Pieter A., van Tintelen J. Peter, de Bakker Jacques M. T., Hauer Richard N. W. Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteria Journal of cardiovascular electrophysiology 2008;19 (8):775-781 [PubMed]
  • Postma Alex V., van de Meerakker Judith B. A., Mathijssen Inge B., Barnett Phil, Christoffels Vincent M., Ilgun Aho, Lam Jan, Wilde Arthur A. M., Lekanne Deprez Ronald H., Moorman Antoon F. M. A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation Circulation research 2008;102 (11):1433-1442 [PubMed]
  • de Winter Robbert J., Verouden Niels J. W., Wellens Hein J. J., Wilde Arthur A. M., Center Of The Academic Medical A New ECG Sign of Proximal LAD Occlusion New England journal of medicine 2008;359 (19):2071-2073 [PubMed]
  • Bhuiyan Zahurul A., Momenah Tarek S., Amin Ahmad S., Al-Khadra Ayman S., Alders Marielle, Wilde Arthur A. M., Mannens Marcel M. A. M. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome Progress in biophysics and molecular biology 2008;98 (2-3):319-327 [PubMed]
  • Sacher Frédéric, Meregalli Paola, Veltmann Christian, Field Michael E., Solnon Aude, Bru Paul, Abbey Sélim, Jaïs Pierre, Tan Hanno L., Wolpert Christian, Lande Gilles, Bertault Valérie, Derval Nicolas, Babuty Dominique, Lacroix Dominique, Boveda Serge, Maury Philippe, Hocini Mélèze, Clémenty Jacques, Mabo Philippe, Lemarec Hervé, Mansourati Jacques, Borggrefe Martin, Wilde Arthur, Haïssaguerre Michel, Probst Vincent Are women with severely symptomatic brugada syndrome different from men? Journal of cardiovascular electrophysiology 2008;19 (11):1181-1185 [PubMed]
  • Postema Pieter G., Wilde Arthur A. M. Arrhythmias in Brugada syndrome: Changing throughout day and season? Heart rhythm 2008;5 (11):1528-1529 [PubMed]
  • Meregalli Paola G., Tan Hanno L., Wilde Arthur A. M. Brugada syndrome: clinical and genetic aspectsin: Ihor Gussak, Charles Antzelevitch, Arthur A. M. Wilde, Paul A. Friedman, Michael J. Ackerman, Win-Kuang Shen, editors. Electrical diseases of the heart. Genetics, mechanisms, treatment, prevention.. London: Springer; 2008. p. 483-499, ISBN 9781846288531
  • Remme Carol Ann, Wilde Arthur A. M., Bezzina Connie R. Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations Trends in cardiovascular medicine 2008;18 (3):78-87 [PubMed]
  • Smits Jeroen P. P., Blom Marieke T., Wilde Arthur A. M., Tan Hanno L. Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview Expert opinion on pharmacotherapy 2008;9 (4):537-549 [PubMed]
  • Wilde Arthur A. M. Channelopathies in children and adults Pacing and clinical electrophysiology 2008;31 Suppl 1 (Suppl. 1):S41-S45 [PubMed]
  • van den Berg M. P., Wilde A. A. M. Deteriorating consciousness and pathognomic ECG: risk of sudden death? Netherlands heart journal 2008;16 (1):33
  • Postema Pieter G., Wilde Arthur A. M. Do patients with long QT syndrome remain at risk for sudden cardiac death after 40 years of age? Nature clinical practice. Cardiovascular medicine 2008;5 (10):602-603 [PubMed]
  • Beckmann Britt M., Wilde Arthur A. M., Kaeaeb Stefan Dual inheritance of sudden death from cardiovascular causes New England journal of medicine 2008;358 (19):2077-2078 [PubMed]
  • Gussak Ihor, Antzelevitch Charles, Wilde Arthur A. M., Friedman Paul A., Ackerman Michael J., Shen Win-Kuang Electrical diseases of the heart. Genetics, mechanisms, treatment, prevention.London: Springer; 2008. ISBN 9781846288531
  • Lemmert Miguel E., de Jong Jonas S. S. G., van Stipdonk Antonius M. W., Crijns Harry J. G. M., Wellens Hein J. J., Krucoff Mitchell W., Dekker Lukas R., Wilde Arthur A. M., Gorgels Anton P. M. Electrocardiographic factors playing a role in ischemic ventricular fibrillation in ST elevation myocardial infarction are related to the culprit artery Heart rhythm 2008;5 (1):71-78 [PubMed]
  • Wilde A. A. M., Tan H. L. Erfelijke aritmiesyndromenin: E. E. van der Wall, F. Van de Werf, F. Zijlstra, editors. Cardiologie. Houten: Bohn Stafleu Van Loghum; 2008. p. 261-267, ISBN 9789031348299
  • Hendriks Karin S. W. H., Hendriks Margriet M. W. B., Birnie Erwin, Grosfeld Frans J. M., Wilde Arthur A. M., van den Bout Jan, Smets Ellen M. A., van Tintelen J. Peter, ten Kroode Herman F. J., van Langen Irene M. Familial disease with a risk of sudden death: a longitudinal study of the psychological consequences of predictive testing for long QT syndrome Heart rhythm 2008;5 (5):719-724 [PubMed]
  • Amin Ahmad S., Meregalli Paola G., Bardai Abdennasser, Wilde Arthur A. M., Tan Hanno L. Fever increases the risk for cardiac arrest in the Brugada syndrome Annals of internal medicine 2008;149 (3):216-218 [PubMed]
  • Amin Ahmad S., Herfst Lucas J., Delisle Brian P., Klemens Christine A., Rook Martin B., Bezzina Connie R., Underkofler Heather A. S., Holzem Katherine M., Ruijter Jan M., Tan Hanno L., January Craig T., Wilde Arthur A. M. Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome Journal of clinical investigation 2008;118 (7):2552-2561 [PubMed]
  • Koopmann Tamara T. Genetic basis of cardiac ion channel diseases 2008. 172p. ISBN 9789090231082. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Moorman A. F. M.; Co-supervisor: Bezzina C. R.)
  • Smets Ellen M. A., Stam Marinka M. H., Meulenkamp Tineke M., van Langen Irene M., Wilde Arthur A. M., Wiegman Albert, de Wert Guido M., Tibben Aad Health-related quality of life of children with a positive carrier status for inherited cardiovascular diseases American journal of medical genetics. Part A 2008;146A (6):700-707 [PubMed]
  • van Dijk Nynke, Boer Kimberly R., Colman Nancy, Bakker Annemieke, Stam Jan, van Grieken Johannes J. M., Wilde Arthur A. M., Linzer Mark, Reitsma Johannes B., Wieling Wouter High diagnostic yield and accuracy of history, physical examination, and ECG in patients with transient loss of consciousness in FAST: The fainting assessment study Journal of cardiovascular electrophysiology 2008;19 (1):48-55 [PubMed]
  • Wilde A. A. M., Hrudova J., Tans J. G. M. Just an ordinary flutter? Netherlands heart journal 2008;16 (2):62-+
  • Wilde Arthur A. M., Bhuiyan Zahurul A., Crotti Lia, Facchini Mario, de Ferrari Gaetano M., Paul Thomas, Ferrandi Chiara, Koolbergen Dave R., Odero Attilio, Schwartz Peter J. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia New England journal of medicine 2008;358 (19):2024-2029 [PubMed]
  • Tan Hanno L., van der Wal Allard C., Campian Maria E., Kruyswijk Hittjo H., ten Hove Jansen Bram, van Doorn Dirk-Jan, Oskam Henk J., Becker Anton E., Wilde Arthur A. M. Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac development Circulation. Arrhythmia and electrophysiology 2008;1 (4):276-281 [PubMed]
  • Germans Tjeerd, Wilde Arthur A. M., van Rossum Albert C. Non-compaction: a distinct cardiomyopathy or non-specific morphological trait? European heart journal 2008;29 (7):949-50; author reply 950-1 [PubMed]
  • Liu Judy F., Goldenberg Ilan, Moss Arthur J., Shimizu Wataru, Wilde Arthur A., Hofman Nynke, McNitt Scott, Zareba Wojciech, Miyamato Yoshihiro, Robinson Jennifer L., Andrews Mark L. Phenotypic variability in Caucasian and Japanese patients with matched LQT1 mutations Annals of noninvasive electrocardiology 2008;13 (3):234-241 [PubMed]
  • Yang P., Koopmann T. T., Pfeufer A., Jalilzadeh S., Schulze-Bahr E., Kääb S., Wilde A. A., Roden D. M., Bezzina C. R. Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity European journal of human genetics 2008;16 (3):350-357 [PubMed]
  • Meulenkamp Tineke M., Tibben Aad, Mollema Eline D., van Langen Irene M., Wiegman Albert, de Wert Guido M., de Beaufort Inez D., Wilde Arthur A. M., Smets Ellen M. A. Predictive Genetic Testing for Cardiovascular Diseases: Impact on Carrier Children American journal of medical genetics. Part A 2008;146A (24):3136-3146 [PubMed]
  • Meregalli P. G., Westendorp I. C. D., Tan H. L., Elsman P., Kok W. E. M., Wilde A. A. M. Pregnancy and the risk of torsades de pointes in congenital long-QT syndrome Netherlands heart journal 2008;16 (12):422-425 [PubMed]
  • Bhuiyan Zahurul A., Momenah Tarek S., Gong Qiuming, Amin Ahmad S., Ghamdi Saleh Al, Carvalho Julene S., Homfray Tessa, Mannens Marcel M. A. M., Zhou Zhengfeng, Wilde Arthur A. M. Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation Heart rhythm 2008;5 (4):553-561 [PubMed]
  • Wilde A. A. M., van Dessel P. F. H. M. Ritmestoornissenin: E. E. van der Wall, F. Van de Werf, F. Zijlstra, editors. Cardiologie. Houten: Bohn Stafleu Van Loghum; 2008. p. 507-510, ISBN 9789031348299
  • Remme Carol Ann, Wilde Arthur A. M. SCN5A overlap syndromes: no end to disease complexity? Europace : European pacing, arrhythmias, and cardiac electrophysiology 2008;10 (11):1253-1255 [PubMed]
  • Postema Pieter G., van Dessel Pascal F. H. M., de Bakker Jacques M. T., Dekker Lukas R. C., Linnenbank Andre C., Hoogendijk Mark G., Coronel Ruben, Tijssen Jan G. P., Wilde Arthur A. M., Tan Hanno L. Slow and discontinuous conduction conspire in Brugada syndrome: a right ventricular mapping and stimulation study Circulation. Arrhythmia and electrophysiology 2008;1 (5):379-386 [PubMed]
  • Watanabe Hiroshi, Koopmann Tamara T., Le Scouarnec Solena, Yang Tao, Ingram Christiana R., Schott Jean-Jacques, Demolombe Sophie, Probst Vincent, Anselme Frederic, Escande Denis, Wiesfeld Ans C. P., Pfeufer Arne, Kääb Stefan, Wichmann H.-Erich, Hasdemir Can, Aizawa Yoshifusa, Wilde Arthur A. M., Roden Dan M., Bezzina Connie R. Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans Journal of clinical investigation 2008;118 (6):2260-2268 [PubMed]
  • Casini Simona, Wilde Arthur A. M., Tan Hanno L. Sodium ion channelopathiesin: Ihor Gussak, Charles Antzelevitch, Arthur A. M. Wilde, Paul A. Friedman, Michael J. Ackerman, Win-Kuang Shen, editors. Electrical diseases of the heart. Genetics, mechanisms, treatment, prevention.. London: Springer; 2008. p. 170-186, ISBN 9781846288531
  • Wilde Arthur A. M., Coronel Ruben The complexity of genotype-phenotype relations associated with loss-of-function sodium channel mutations and the role of in silico studies American journal of physiology. Heart and circulatory physiology 2008;295 (1):H8-H9 [PubMed]
  • Wilde A. A. M. The ECG of a cardiomyopathy 2 Netherlands heart journal 2008;16 (6):221-+
  • Scicluna Brendon P., Wilde Arthur W., Bezzina Connie R. The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why? Journal of cardiovascular electrophysiology 2008;19 (4):445-452 [PubMed]
  • Wilde A. A. M. Too many ventricular extra systoles? Netherlands heart journal 2008;16 (9):315
  • Christiaans Imke, Birnie Erwin, Bonsel Gouke J., Wilde Arthur A. M., van Langen Irene M. Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy European journal of human genetics 2008;16 (10):1201-1207 [PubMed]
  • Wilde A. A. M. Wide complexes intervening regular sinus rhythm 3 Netherlands heart journal 2008;16 (3):102-+
  • Wilde A. A. M. Wide complexes intervening regular sinus rhythm 4 Netherlands heart journal 2008;16 (5):175-+
  • Verouden N. J. W., de Winter F-J., Wilde A. A. M. Wide QRS complexes in the setting of acute myocardial infarction: good news or bad? Netherlands heart journal 2008;16 (4):138-+

2007

  • Wilde A. A. M., Blom N. A. Abnormal repolarisation, spot diagnosis? Netherlands heart journal 2007;15 (3):114-+
  • Wilde A. A. M. An abnormal ECG? Netherlands heart journal 2007;15 (12):426-+
  • Wilde Arthur A. M. An irregular rhythm at older age. Rhythm puzzle Netherlands heart journal 2007;15 (4):157-166
  • Bhuiyan Zahurul A., Hamdan Mohamed A., Shamsi Eman T. A., Postma Alex V., Mannens Marcel M. A. M., Wilde Arthur A. M., Al-Gazali Lihadh A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22 Journal of cardiovascular electrophysiology 2007;18 (10):1060-1066 [PubMed]
  • Wilde A. A. M., Langendijk P. Antiarrhythmic drugs, patients, and the pharmaceutical industry: value for patients, physicians, pharmacists or shareholders? Netherlands heart journal 2007;15 (4):127-128 [PubMed]
  • Wilde Arthur A. M. Arrhythmias and the electrocardiogram in inherited arrhythmia disorders Journal of electrocardiology 2007;40 (Suppl. 1):S7-S8
  • Otterspoor L. C., Reichert C. L. A., Cramer M. J. M., Bhuiyan Z. A., Wilde A. A. M., Hauer R. N. W. Arrhythmogenic right ventricular cardiomyopathy: asymptomatic to life threatening as illustrated by the cases of two sisters Netherlands heart journal 2007;15 (10):348-353 [PubMed]
  • Langendijk P., de Bruin Marieke, Tan H. L., Wilde A. A. M. Bewaking van QT-tijdverlenging. Hoe groot het risico is en hoe apothekers het kunnen beperken Pharmaceutisch Weekblad 2007;142 (17):30-34
  • Erol-Yilmaz Ayten, Atasever Bektas, Mathura Keshen, Lindeboom Jerome, Wilde Arthur, Ince Can, Tukkie Raymond Cardiac resynchronization improves microcirculation Journal of cardiac failure 2007;13 (2):95-99 [PubMed]
  • Kodde J., Hofman N., Reichert C. L. A., van Langen I. M., Wilde A. A. M. Cardiogenetic counselling in a non-university hospital Netherlands heart journal 2007;15 (12):412-414 [PubMed]
  • Casini Simona, Tan Hanno L., Bhuiyan Zahurul A., Bezzina Connie R., Barnett Phil, Cerbai Elisabetta, Mugelli Alessandro, Wilde Arthur A. M., Veldkamp Marieke W. Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation Cardiovascular research 2007;76 (3):418-429 [PubMed]
  • Probst Vincent, Denjoy Isabelle, Meregalli Paola G., Amirault Jean-Christophe, Sacher Frederic, Mansourati Jacques, Babuty Dominique, Villain Elisabeth, Victor Jacques, Schott Jean-Jacques, Lupoglazoff Jean-Marc, Mabo Philippe, Veltmann Christian, Jesel Laurence, Chevalier Philippe, Clur Sally-Ann B., Haissaguerre Michel, Wolpert Christian, Le Marec Herve, Wilde Arthur A. M. Clinical aspects and prognosis of Brugada syndrome in children Circulation 2007;115 (15):2042-2048 [PubMed]
  • Moss Arthur J., Shimizu Wataru, Wilde Arthur A. M., Towbin Jeffrey A., Zareba Wojciech, Robinson Jennifer L., Qi Ming, Vincent G. Michael, Ackerman Michael J., Kaufman Elizabeth S., Hofman Nynke, Seth Rahul, Kamakura Shiro, Miyamoto Yoshihiro, Goldenberg Ilan, Andrews Mark L., McNitt Scott Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene Circulation 2007;115 (19):2481-2489 [PubMed]
  • Borleffs C. J. W., Wilde A. A. M., Cramer M. J. M., Wever E., Mosterd A. Clinical implementation of guidelines for cardioverter defibrillator implantation: lost in translation? Netherlands heart journal 2007;15 (4):129-132 [PubMed]
  • Akkerhuis J. M., Baars H. F., Marcelis C. L. M., Akkerhuis K. M., Wilde A. A. M. Congenitaal lange-QT-tijdsyndroom: oorzaak van recidiverende wegrakingen en plotse dood op jonge leeftijd Nederlands tijdschrift voor geneeskunde 2007;151 (43):2357-2364 [PubMed]
  • Hofman Nynke, Tan Hanno L., Clur Sally-Ann, Alders Mariel, van Langen Irene M., Wilde Arthur A. M. Contribution of inherited heart disease to sudden cardiac death in childhood Pediatrics 2007;120 (4):e967-e973 [PubMed]
  • Antzelevitch Charles, Wilde Arthur, Eckardt Lars, Hiraoka Masayasu, Corrado Domenico Diagnostic and genetic aspects of the Brugada and other inherited arrhythmias syndromes Journal of electrocardiology 2007;40 (1 Suppl. S):S11-S14 [PubMed]
  • Hofman Nynke, Wilde Arthur A. M., Tan Hanno L. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European heart journal 2007;28 (11):1399 [PubMed]
  • Hofman Nynke, Wilde Arthur A. M., Kääb Stefan, van Langen Irene M., Tanck Michael W. T., Mannens Marcel M. A. M., Hinterseer Martin, Beckmann Britt-Maria, Tan Hanno L. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European heart journal 2007;28 (5):575-580 [PubMed]
  • Remme C. A., Verkerk A. O., Wilde A. A. M., Veldkamp M. W., de Bakker J. M. T., Bezzina C. R. Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation Netherlands heart journal 2007;15 (6):235-238 [PubMed]
  • Ritsema van Eck Henk J. , Postema Pieter G., van Herpen Gerard, Wilde Arthur A. M., Kors Jan A. Dynamic changes of the TU complex in the electrocardiogram Journal of electrocardiology 2007;40 (1 Suppl. S):S22-S25
  • Nannenberg E. A., Wilde A. A. M., van Langen I. M. Een familie met een aantal malen plotselinge hartdoodin: N. J. Leschot, D. L. Willems, editors. Probleemgeoriënteerd denken in de genetica in klinisch en ethisch perspectief. Utrecht: De Tijdstroom; 2007. p. 267-276, ISBN 9789058981073
  • Koopmann Tamara T., Beekman Leander, Alders Marielle, Meregalli Paola G., Mannens Marcel M. A. M., Moorman Antoon F. M., Wilde Arthur A. M., Bezzina Connie R. Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort Heart rhythm 2007;4 (6):752-755 [PubMed]
  • Bhuiyan Zahurul A., van den Berg Maarten P., van Tintelen J. Peter, Bink-Boelkens Margreet T. E., Wiesfeld Ans C. P., Alders Marielle, Postma Alex V., van Langen Irene, Mannens Marcel M. A. M., Wilde Arthur A. M. Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features Circulation 2007;116 (14):1569-1576 [PubMed]
  • Panhuyzen-Goedkoop N. M., Dekker L. R. C., Wilde A. A. M. Five years of palpitations Netherlands heart journal 2007;15 (6):231+242-+
  • Bökenkamp Regina, Wilde Arthur A., Schalij Martin J., Blom Nico A. Flecainide for recurrent malignant ventricular arrhythmias in two siblings with Andersen-Tawil syndrome Heart rhythm 2007;4 (4):508-511 [PubMed]
  • Bezzina Connie R., Wilde Arthur A. M. Genetic basis for cardiac arrhythmiasin: James T. Willerson, J.N. Cohn, Hein J. J. Wellens, D. R. Holmes, editors. Cardiovascular Medicine. London: Springer-Verlag; 2007. p. 2577-2598
  • Hofman N., Postema P. G., van Langen I. M., Nannenberg E. A., Alders M., Jongbloed R., Smeets H. J. M., Wilde A. A. M. Genetische identificatie van patiënten en families met lange-QT-syndroom: grote regionale verschillen in de resultaten van 10 jaar Nederlands tijdschrift voor geneeskunde 2007;151 (11):644-648 [PubMed]
  • van Tintelen J. Peter, Hofstra Robert M. W., Katerberg Hilga, Rossenbacker Tom, Wiesfeld Ans C. P., Sarvaas Gideon J. du Marchie, Wilde Arthur A. M., van Langen Irene M., Nannenberg Eline A., van der Kooi Anneke J., Kraak Marian, van Gelder Isabelle C., van Veldhuisen Dirk Jan, Vos Yvonne, van den Berg Maarten P. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics American heart journal 2007;154 (6):1130 1130-9-1139 [PubMed]
  • Wilde Arthur A. M., Tan Hanno L. Inherited arrhythmia syndromes Circulation journal 2007;71 Suppl A:A12-A19 [PubMed]
  • de Bruin Marie L., Langendijk Pim N. J., Koopmans Richard P., Wilde Arthur A. M., Leufkens Hubert G. M., Hoes Arno W. In-hospital cardiac arrest is associated with use of non-antiarrhythmic QTc-prolonging drugs British journal of clinical pharmacology 2007;63 (2):216-223 [PubMed]
  • Udo E. O., Baars H. F., Winter J. B., Wilde A. A. M. Not just any ICD device in patients with long-QT syndrome Netherlands heart journal 2007;15 (12):418-421 [PubMed]
  • Borleffs C. J. W., Wilde A. A. M., Bots M. L., Kruyt E., Mosterd A. Obductie redt levens. Onwetendheid over erfelijke hartafwijking maakt onnodig slachtoffers Medisch contact 2007;45:1851-1854
  • Leschot N. J., Wilde A. A. M. Optimale behandeling met bètablokkers bij chronisch hartfalen mogelijk afhankelijk van de genetische achtergrond van de patiënt Nederlands tijdschrift voor geneeskunde 2007;151 (29):1610-1611 [PubMed]
  • Wilde Arthur A. M., Idzerda H.H.D. Palpitations after a MAZE procedure. Rhythm puzzle Netherlands heart journal 2007;15 (2):72-82
  • Wilde A. A. M., Cuppen M., Smeets J. L. R. M. Palpitations all the time Netherlands heart journal 2007;15 (5):198+203-+
  • Mulder B. J. M., de Winter R. J., Wilde A. A. M. Percutaneous pulmonary valve replacement: a new development in the lifetime strategy for patients with congenital heart disease Netherlands heart journal 2007;15 (1):3-4 [PubMed]
  • Krediet C. T.P., Wilde A. A.M., Halliwill J. R., Wieling Wouter Post-Exercise Vasovagal Syncopein: Syncope Cases. Blackwell Publishing; 2007. p. 46-48, ISBN 9781405151092
  • Germans Tjeerd, Dijkmans Pieter A., Wilde Arthur A. M., Kamp Otto, van Rossum Albert C. Prominent crypt formation in the inferoseptum of a hypertrophic cardiomyopathy mutation carrier mimics noncompaction cardiomyopathy Circulation 2007;115 (22):E610-E611 [PubMed]
  • Paul Matthias, Gerss Joachim, Schulze-Bahr Eric, Wichter Thomas, Vahlhaus Christian, Wilde Arthur A. M., Breithardt Günter, Eckardt Lars Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data European heart journal 2007;28 (17):2126-2133 [PubMed]
  • Germans T., Wilde A. A. M., van Echteld C. J. A., Kamp O., Pinto Y. M., van Rossum A. C. Structural abnormalities of the left ventricle in hypertrophic cardiomyopathy mutation carriers detectable before the development of hypertrophy Netherlands heart journal 2007;15 (4):161-163 [PubMed]
  • Nannenberg Eline A., Wilde Arthur A. M. Syncope bij patiënt met een familieanamnese voor plotselinge dood.in: G. K. Hovingh, G. A. Somsen, editors. Probleemgeoriënteerd denken in de cardiologie. Utrecht: De Tijdstroom; 2007. p. 109-122, ISBN 9789058981080
  • Crotti Lia, Spazzolini Carla, Schwartz Peter J., Shimizu Wataru, Denjoy Isabelle, Schulze-Bahr Eric, Zaklyazminskaya Elena V., Swan Heikki, Ackerman Michael J., Moss Arthur J., Wilde Arthur A. M., Horie Minoru, Brink Paul A., Insolia Roberto, de Ferrari Gaetano M., Crimi Gabriele The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: Toward a mutation-specific risk stratification Circulation 2007;116 (21):2366-2375 [PubMed]
  • Wilde Arthur A. M., Wieling Wouter Vasovagal syncope or ventricular fibrillation. Your diagnosis better be accurate Clinical autonomic research 2007;17 (4):203-205 [PubMed]
  • Wilde Arthur A. M. Wide complexes intervening regular sinus rhythm 2. Imaging in cardiology. Rhythm puzzle Netherlands heart journal 2007;15 (1):33-39

2006

  • Schoonderwoerd Bas A., Wiesfeld Ans C. P., Wilde Arthur A. M., van den Heuvel Freek, van Tintelen J. Peter, van den Berg Maarten P., van Veldhuisen Dirk J., van Gelder Isabelle C. A family with Andersen-Tawil syndrome and dilated cardiomyopathy Heart rhythm 2006;3 (11):1346-1350 [PubMed]
  • Wilde A. A. M., Bakker R. H. A narrow QRS complex tachycardia sensitive to Isoptin Netherlands heart journal 2006;14 (7-8):268-279
  • Wilde A. A. M., Peters R. H. J. And what about the ECG? Netherlands heart journal 2006;14 (9):315-319
  • Wilde A. A. M. An old lady with chest pain Netherlands heart journal 2006;14 (4):154-159
  • Wilde A. A. M., Dekker L. R. C. A pre-excited wide QRS complex: is that all there is? Netherlands heart journal 2006;14 (3):108-118
  • Kannankeril Prince J., Bhuiyan Zahurul A., Darbar Dawood, Mannens Marcel M. A. M., Wilde Arthur A. M., Roden Dan M. Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family Heart rhythm 2006;3 (8):939-944 [PubMed]
  • Wilde Arthur A. M., Langendijk Pim N. J. Brugada syndrome and the use of anesthetics Heart rhythm 2006;3 (9):1079-1081 [PubMed]
  • Bezzina Connie R., Shimizu Wataru, Yang Ping, Koopmann Tamara T., Tanck Michael W. T., Miyamoto Yoshihiro, Kamakura Shiro, Roden Dan M., Wilde Arthur A. M. Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction Circulation 2006;113 (3):338-344 [PubMed]
  • van Langen Irene M., Wilde Arthur A. M. Con: Newborn screening to prevent sudden cardiac death? Heart rhythm 2006;3 (11):1356-1359 [PubMed]
  • Meregalli Paola G., Ruijter Jan M., Hofman Nynke, Bezzina Connie R., Wilde Arthur A. M., Tan Hanno L. Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndrome Journal of cardiovascular electrophysiology 2006;17 (8):857-864 [PubMed]
  • van den Berg Maarten P., Haaksma Jaap, Veeger Nic J. G. M., Wilde Arthur A. M. Diurnal variation of ventricular repolarization in a large family with LQT3-Brugada syndrome characterized by nocturnal sudden death Heart rhythm 2006;3 (3):290-295 [PubMed]
  • van Langen I. M., Wilde A. A. M. ECG screening of newborns to avoid sudden infant death syndrome? Netherlands heart journal 2006;14 (2):43-45
  • Dekker Lukas R. C., Bezzina Connie R., Henriques José P. S., Tanck Michael W., Koch Karel T., Alings Marco W., Arnold Alfred E. R., de Boer Menko-Jan, Gorgels Anton P. M., Michels H. Rolf, Verkerk Agnes, Verheugt Freek W. A., Zijlstra Felix, Wilde Arthur A. M. Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients Circulation 2006;114 (11):1140-1145 [PubMed]
  • Imboden Medea, Swan Heikki, Denjoy Isabelle, van Langen Irene Marijke, Latinen-Forsblom Päivi Johanna, Napolitano Carlo, Fressart Véronique, Breithardt Guenter, Berthet Myriam, Priori Silvia, Hainque Bernard, Wilde Arthur Arnold Maria, Schulze-Bahr Eric, Feingold Josué, Guicheney Pascale Female predominance and transmission distortion in the long-QT syndrome New England journal of medicine 2006;355 (26):2744-2751 [PubMed]
  • Wieling W., Krediet C. T. P., Wilde A. A. M. Flush after syncope: not always an arrhythmia Journal of cardiovascular electrophysiology 2006;17 (7):804-805 [PubMed]
  • Hermans J. F., Christiaans I., van Tintelen J. P., Wilde A. A. M., Pinto Y. M. GENCOR: a national registry for patients and families suffering from a familial heart disease in the Netherlands Netherlands heart journal 2006;14 (7-8):272-276 [PubMed]
  • Tan Hanno L., Bardai Abdennasser, Shimizu Wataru, Moss Arthur J., Schulze-Bahr Eric, Noda Takashi, Wilde Arthur A. M. Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implications Circulation 2006;114 (20):2096-2103 [PubMed]
  • van Laar I. M. B. H., van Langen I. M., Cohen-Overbeek T. E., Wilde A. A. M., Govaerts L. C. P., ten Harkel A. D. J. Het Jervell-Lange-Nielsen-syndroom: klinische presentatie bij een zuigeling Tijdschrift voor kindergeneeskunde 2006;74 (3):114-ev
  • Marcelis C. L. M., Wilde A. A. M. Het lange QT-syndroom: een cardiale ionkanaalziekte Tijdschrift voor kindergeneeskunde 2006;74 (2):71-76
  • Wilde A. A. M. Interactiemechanismen: verlenging QT-intervalin: J. J. de Gier, H. C. S. van Buren, editors. Commentaren Medicatiebewaking 2006/2007. Houten: Health Base; 2006. p. 16-ev, ISBN 9789074027267
  • Darbar D., Yang T., Roden D. M., Churchwell K., Wilde A. A. M. Letter regarding article by Darbar et al, "Unmasking of Brugada syndrome by lithium" - Response Circulation 2006;113 (10):E408
  • Coronel R., Casini S., Koopmann T. T., Verkerk A. O., de Groot J. R., Bezzina C. R., Veldkamp M. W., Linnenbank A. C., Tan H. L., Wilde A. A. M., de Bakker J. M. T., Wilms-Schopman F. J. G., Bhuiyan Z., van der Wal A. C., Brugada P. Letters regarding article by Coronel et al, "Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: A combined electrophysiological, genetic, histopathologic, and computational study" - Response Circulation 2006;113 (16):E726-E727
  • Koopmann Tamara T., Alders Marielle, Jongbloed Roselie J., Guerrero Silvia, Mannens Marcel M. A. M., Wilde Arthur A. M., Bezzina Connie R. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies Heart rhythm 2006;3 (1):52-55 [PubMed]
  • Wilde A. A. M., Simmers T. A. Long QT syndrome revealed by exercisein: R. García-Civera, G. Barón-Esquivias, J. J. Blanc, M. Brignole, A. Moya i Mitjans, R. Ruiz-Granell, W. Wieling, editors. Syncope cases. Malden, MA: Blackwell Futura; 2006. p. 170-171, ISBN 9781405151092
  • Langendijk P. N. J., Wilde A. A. M. Medicatie voor aandachtstekort-hyperactiviteitstoornis (ADHD) en het risico op cardiovasculaire sterfte Nederlands tijdschrift voor geneeskunde 2006;150 (31):1713-1714 [PubMed]
  • Groenink M., Wilde A. A. M. Moet je altijd een MRI doen na een 'aborted sudden death'? Cardiologen vademecum 2006;9 (10)
  • van der Wall E. E., de Boer M.-J., Doevendans P. A., Wilde A. A. M., Zijlstra F. Netherlands Heart Journal: accepted into PubMed Central! Netherlands heart journal 2006;14 (12):403-404 [PubMed]
  • Remme Carol Ann, Verkerk Arie O., Nuyens Dieter, van Ginneken Antoni C. G., van Brunschot Sandra, Belterman Charly N. W., Wilders Ronald, van Roon Marian A., Tan Hanno L., Wilde Arthur A. M., Carmeliet Peter, de Bakker Jacques M. T., Veldkamp Marieke W., Bezzina Connie R. Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD Circulation 2006;114 (24):2584-2594 [PubMed]
  • Wilde A. A. M., Dekker L. R. C. Palpitations again, have a close look Netherlands heart journal 2006;14 (11):393-399
  • Wilde A. A. M. Palpitations and dizziness in a 65-year-old man Netherlands heart journal 2006;14 (5):189-203
  • van Tintelen J. Peter, Entius Mark M., Bhuiyan Zahurul A., Jongbloed Roselie, Wiesfeld Ans C. P., Wilde Arthur A. M., van der Smagt Jasper, Boven Ludolf G., Mannens Marcel M. A. M., van Langen Irene M., Hofstra Robert M. W., Otterspoor Luuk C., Doevendans Pieter A. F. M., Rodriguez Luz-Maria, van Gelder Isabelle C., Hauer Richard N. W. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy Circulation 2006;113 (13):1650-1658 [PubMed]
  • Christiaans I., van Langen I. M., Wilde A. A. M. Plotselinge dood op jonge leeftijd. De noodzaak van obductie en erfelijkheidsonderzoek Medisch contact 2006;61 (31-32):1253-ev
  • van der Bilt I. A. C., Hasan D., Rinkel G. J. E., Wilde A. A. M., Visser F. C. Rationale of the SEAS study Netherlands heart journal 2006;14 (11):366-ev
  • van der Bilt I. A. C., Hasan D., Rinkel G. J. E., Wilde A. A. M., Visser F. C. Rationale of the SEAS study: Serial Echocardiography After Subarachnoid haemorrhage, a prospective national, multicentre, multidisciplinary, cohort study to evaluate cardiac abnormalities following intracranial haemorrhage Netherlands heart journal 2006;14 (11):366-371 [PubMed]
  • Darbar Dawood, Yang Tao, Roden Dan M., Churchwell Keith, Wilde Arthur A.M. Response [4] Unmasking of Brugada Syndrome by Lithium Circulation 2006;113 (10):e408
  • Wilde A. A. M., Tan H. L. Should I be worried? Netherlands heart journal 2006;14 (1):33-39
  • Wilde Arthur A. M. Spontaneous electrocardiographic fluctuations in Brugada syndrome: does it matter? European heart journal 2006;27 (21):2493-2494 [PubMed]
  • Germans Tjeerd, Wilde Arthur A. M., Dijkmans Pieter A., Chai Wenxia, Kamp Otto, Pinto Yigal M., van Rossum Albert C. Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations Journal of the American College of Cardiology 2006;48 (12):2518-2523 [PubMed]
  • Benditt D. G., Wieling Wouter, Olshansky Brian, Abe Haruhiko, Alboni Paolo, Andresen Dietrich, Axelrod Felicia B., Bennaroch Eduardo, Bergfeldt Lennart, Blanc Jean Jacques, Brignole Michele, Camm A. John, Chelimsky Thomas, Cortelli Pietro, Van Dijk J. Gert, Van Dijk Nynke, Esler Murray, Fitzpatrick Adam, Fouad-Tarazi Fetnat, Freeman Roy, Goldstein Mary Ann, Grubb Blair, Herweg Bengt, Hilz Max J., Jacob Giris, Jardine David, Jordan Jens, Joyner Michael J., Kapoor Wishwa, Kaufmann Horacio, Kenny Rose Anne, Krahn Andrew, Lau Chu Pak, Levine Benjamin D., Van Lieshout Johannes J., Lipsitz Lewis, Low Philip, Lurie Keith G., Malik Marek, Mathias Christopher J., Moya Angel, Raj Satish R., Raviele Antonio, Saksena Sanjeev, Sarasin Francois P., Saul Philip J., Schondorf Ronald, Senard Jean Michel, Sheldon Robert, Shen Win Kuang, Sra Jasbir, Stephenson John, Stewart Julian M., Sutton Richard, Tanaka Hidetaka, Theodorakis George, Thijs Roland D., Ungar Andrea, Wilde A. A.M. The ACCF/AHA scientific statement on syncope: A document in need of thoughtful revision Clinical autonomic research 2006;16 (6):363-368 [PubMed]
  • van den Berg M. P., Haaksma J., Wilde A. A. M. T-wave alternans in a patient with long-QT syndrome type 3 Netherlands heart journal 2006;14 (4):152-153
  • Koopmann Tamara T., Bezzina Connie R., Wilde Arthur A. M. Voltage-gated sodium channels: action players with many faces Annals of medicine 2006;38 (7):472-482 [PubMed]
  • van Langen I. M., Christiaans I., Wilde A. A. M. Wanneer moet je denken aan genetische analysis (met obductiie) bij plotse dood in de familie? Cardiologen vademecum 2006;9 (8)
  • Wilde A. A. M. Wide complexes intervening regular sinus rhythm Netherlands heart journal 2006;14 (12):436-442

2005

  • Smits Jeroen P. P., Koopmann Tamara T., Wilders Ronald, Veldkamp Marieke W., Opthof Tobias, Bhuiyan Zahir A., Mannens Marcel M. A. M., Balser Jeffrey R., Tan Hanno L., Bezzina Connie R., Wilde Arthur A. M. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families Journal of molecular and cellular cardiology 2005;38 (6):969-981 [PubMed]
  • Hendriks K. S. W. H., van Langen I. M., van Tintelen J. P., Grosfeld F. J. M., Wilde A. A. M., ten Kroode H. F. J. An extended family suddenly confronted with a life-threatening hereditary arrhythmia Netherlands heart journal 2005;13 (9):295-299 [PubMed]
  • Wilde A. A. M. Brugada syndrome: diagnostic criteriain: C. Antzelevitch, P. Brugada, J. Brugada, R. Brugada, editors. The Brugada syndrome: from bench to bedside. New Delhi: Gopsons Paper Ltd; 2005. p. 78-86
  • Antzelevitch C., Brugada P., Borggrefe M., Brugada J., Brugada R., Corrado D., Gussak I., Le Marec H., Nademanee K., Perez Riera A. R., Tan H. [=Hanno L.], Shimizu W., Schulze-Bahr E., Wilde A. A. M. Brugada syndrome: overviewin: C. Antzelevitch, P. Brugada, J. Brugada, R. Brugada, editors. The Brugada syndrome: from bench to bedside. Malden, MA: Blackwell Futura; 2005. p. 1-22
  • Antzelevitch Charles, Brugada Pedro, Borggrefe Martin, Brugada Josep, Brugada Ramon, Corrado Domenico, Gussak Ihor, LeMarec Herve, Nademanee Koonlawee, Perez Riera Andres Ricardo, Shimizu Wataru, Schulze-Bahr Eric, Tan Hanno, Wilde Arthur Brugada syndrome: report of the second consensus conference Heart rhythm 2005;2 (4):429-440 [PubMed]
  • Antzelevitch Charles, Brugada Pedro, Borggrefe Martin, Brugada Josep, Brugada Ramon, Corrado Domenico, Gussak Ihor, LeMarec Herve, Nademanee Koonlawee, Perez Riera Andres Ricardo, Shimizu Wataru, Schulze-Bahr Eric, Tan Hanno, Wilde Arthur Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association Circulation 2005;111 (5):659-670 [PubMed]
  • Hendriks Karin S. W. H., Grosfeld F. J. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M., van den Bout J., ten Kroode H. F. J. Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for Long QT Syndrome American journal of medical genetics. Part A 2005;138A (2):107-112 [PubMed]
  • Erol-Yilmaz Ayten, Verberne Hein J., Schrama Tim A., Hrudova Jana, de Winter Robbert J., van Eck-Smit Berthe L. F., de Bruin Rianne, Bax Jeroen J., Schalij Martin J., Wilde Arthur A., Tukkie Raymond Cardiac resynchronization induces favorable neurohumoral changes Pacing and clinical electrophysiology 2005;28 (4):304-310 [PubMed]
  • Postma A. V., Denjoy I., Kamblock J., Alders M., Lupoglazoff J.-M., Vaksmann G., Dubosq-Bidot L., Sebillon P., Mannens M. M. A. M., Guicheney P., Wilde A. A. M. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients Journal of medical genetics 2005;42 (11):863-870 [PubMed]
  • Denjoy I., Postma Alex V., Lupoglazoff Jean-Marc, Vaksman G., Kamblock J., Leenhardt A., Wilde Arthur A. M. Catecholaminergic ventricular tachycardia in children. Archives des maladies du coeur et des vaisseaux 2005;98:506-512
  • van Langen I. M. Clinical genetic care in diseases predisposing to sudden cardiac death 2005. 218p. ISBN 9789090196800. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Bonsel G. J.; Co-supervisors: Birnie E., Leschot N. J.)
  • Beaufort-Krol Gertie C. M., van den Berg Maarten P., Wilde Arthur A. M., van Tintelen J. Peter, Viersma Jan Willem, Bezzina Connie R., Bink-Boelkens Margreet Th E. Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood Journal of the American College of Cardiology 2005;46 (2):331-337 [PubMed]
  • Tieleman Robert G., van Gelder Isabelle C., Bosker Hans A., Kingma Tsjerk, Wilde Arthur A. M., Kirchhof Charles J. H. J., Bennekers Johan H., Bracke Frank A. L. E., Veeger Nic J. G. M., Haaksma Jaap, Allessie Maurits A., Crijns Harry J. G. M. Does flecainide regain its antiarrhythmic activity after electrical cardioversion of persistent atrial fibrillation? Heart rhythm 2005;2 (3):223-230 [PubMed]
  • ten Harkel Arend D. J., Witsenburg Maarten, de Jong Peter L., Jordaens Luc, Wijman Marjolein, Wilde Arthur A. M. Efficacy of an implantable cardioverter-defibrillator in a neonate with LQT3 associated arrhythmias Europace : European pacing, arrhythmias, and cardiac electrophysiology 2005;7 (1):77-84 [PubMed]
  • Wilde A. A. M. Erfelijk bepaalde hartritmestoornissenin: A. P. M. Gorgels, J. L. R. M. Smeets, editors. Leerboek Elektrocardiologie. S.l.: Bohn Stafleu Van Loghum Healthcare Communications; 2005. p. 117-131
  • Hendriks K. S. W. H. Familial arrhythmia. Psychological impact of genetic testing 2005. 161p. ISBN 9789090197081. [UvA Dissertations Online] University of Amsterdam. (Supervisors: van den Bout J., Wilde A. A. M.; Co-supervisor: ten Kroode H. F. J.)
  • van Langen I., Wilde A. A. M. Genen en kansen; preventie van topsportleedin: I. van Hilvoorde, B. Pasveer, editors. Beter dan Goed. Over genetica en de toekomst van topsport. Diemen: Veen Magazines; 2005. p. 26-43, ISBN 9789085710271
  • Wilde A. A. M. Genetics of arrhythmias. Mapping the substrate in the genesin: N. M. van Hemel, F. E. E. Vermeulen, J. M. T. de Bakker, editors. Exclusion or Targetting?. Nieuwegein: Grafische Producties Budde-Elinkwijk; 2005. p. 85-94, ISBN 9789090191843
  • Wilde Arthur A. M., Bezzina Connie R. Genetics of cardiac arrhythmias Heart (British Cardiac Society) 2005;91 (10):1352-1358 [PubMed]
  • Smits J. P. P., Wilde A. A. M. Genotype-phenotype relationship in the Brugada syndromein: C. Antzelevitch, P. Brugada, J. Brugada, R. Brugada, editors. The Brugada syndrome: from bench to bedside. Malden, MA: Blackwell Futura; 2005. p. 140-148
  • Paulussen Aimée D. C., Raes Adam, Jongbloed Roselie J., Gilissen Ron A. H. J., Wilde Arthur A. M., Snyders Dirk J., Smeets Hubert J. M., Aerssens Jeroen HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency Cardiovascular research 2005;67 (3):467-475 [PubMed]
  • Hendriks Karin S. W. H., Grosfeld F. J. M., Wilde A. A. M., van den Bout J., van Langen I. M., van Tintelen J. P., ten Kroode H. F. J. High distress in parents whose children undergo predictive testing for long QT syndrome Community genetics 2005;8 (2):103-113 [PubMed]
  • Erol-Yilmaz Ayten, Schrama Tim A., Tanka Jutta Schroeder, Tijssen Jan G., Wilde Arthur A., Tukkie Raymond Individual optimization of pacing sensors improves exercise capacity without influencing quality of life Pacing and clinical electrophysiology 2005;28 (1):17-24 [PubMed]
  • Wilde Arthur A. M., Dekker Lukas R. C. Is there a genetic basis for malignant ventricular arrhythmias? Heart rhythm 2005;2 (10):1145-1147 [PubMed]
  • Wilde A. A. M., Simmers T. A. It's not what you think it is Netherlands heart journal 2005;13 (6):244-249
  • Wilde A. A. M., Kok W. E. M. Lang-QT-intervalsyndroom (LQTS)in: J. J. de Gier, H. C. S. van Buren, editors. Commentaren Medicatiebewaking 2005/2006. Houten: Stichting Health Base; 2005. p. 574-580
  • Groenewegen W. A., Wilde A. A. M. Letter regarding article by McNair et al, "SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia" Circulation 2005;112 (1):E9-e9; author reply 10 [PubMed]
  • Eckardt Lars, Probst Vincent, Smits Jeroen P. P., Bahr Eric Schulze, Wolpert Christian, Schimpf Rainer, Wichter Thomas, Boisseau Pierre, Heinecke Achim, Breithardt Günter, Borggrefe Martin, LeMarec Herve, Böcker Dirk, Wilde Arthur A. M. Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome Circulation 2005;111 (3):257-263 [PubMed]
  • Smits Jeroen P. P., Veldkamp Marieke W., Wilde Arthur A. M. Mechanisms of inherited cardiac conduction disease Europace : European pacing, arrhythmias, and cardiac electrophysiology 2005;7 (2):122-137 [PubMed]
  • Bezzina C. R., Wilde A. A. M. Molecular, genetic and clinical aspects of arrhythmia disordersin: M. Hiraoka, S. Ogawa, I. Kodoma, H. Inoue, H. Kasanuki, T. Katoh, editors. Advances in Electrocardiology 2004. Proceedings of the 31st International Congress on Electrocardiology, Kyoto, Japan. divers: World Scientific; 2005. p. 297-310
  • Amin A. S., Verkerk A. O., Bhuiyan Z. A., Wilde A. A. M., Tan H. L. Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties Acta physiologica Scandinavica 2005;185 (4):291-301 [PubMed]
  • Simmers T. A., Wilde A. A. M. Now you see it, now you don't Netherlands heart journal 2005;13 (5):195-202
  • Meregalli Paola G., Wilde Arthur A. M., Tan Hanno L. Pathophysiological mechanisms of Brugada syndrome: Depolarization disorder, repolarization disorder, or more? Cardiovascular research 2005;67 (3):367-378 [PubMed]
  • Wilde A. A. M. Patïent profiteert met het verstrijken der jaren steeds meer van een geïmplanteerde defibrillator Nederlands tijdschrift voor geneeskunde 2005;149 (10):550
  • Wilde A. A. M., van Langen I. M., Mannens M. M. A. M., Waalewijn R. A., Maes A. Plotseling overlijden op jonge leeftijd en het belang van moleculair-pathologisch onderzoek Nederlands tijdschrift voor geneeskunde 2005;149 (29):1601-1604 [PubMed]
  • van Langen I. M., Birnie E., Schuurman E., Tan H. L., Hofman N., Bonsel G. J., Wilde A. A. M. Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey Clinical genetics 2005;68 (4):360-368 [PubMed]
  • Coronel Ruben, Casini Simona, Koopmann Tamara T., Wilms-Schopman Francien J. G., Verkerk Arie O., de Groot Joris R., Bhuiyan Zahurul, Bezzina Connie R., Veldkamp Marieke W., Linnenbank André C., van der Wal Allard C., Tan Hanno L., Brugada Pedro, Wilde Arthur A. M., de Bakker Jacques M. T. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome - A combined electrophysiological, genetic, histopathologic, and computational study Circulation 2005;112 (18):2769-2777 [PubMed]
  • Simmers T. A., Wilde A. A. M. Right you are Netherlands heart journal 2005;13 (12):466-483
  • Verkerk Arie O., Wilders Ronald, Schulze-Bahr Eric, Beekman Leander, Bhuiyan Zahurul A., Bertrand Jessica, Eckardt Lars, Lin Dongxin, Borggrefe Martin, Breithardt Günter, Mannens Marcel M. A. M., Tan Hanno L., Wilde Arthur A. M., Bezzina Connie R. Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome Cardiovascular research 2005;68 (3):441-453 [PubMed]
  • Yilmaz A. Studies on cardiac pacing.Emphasis on pacemakers sensors and cardiac resynchronization therapy 2005. 200p. ISBN 9789090191089. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Tukkie R.)
  • Smits Jeroen P. P., Veldkamp Marieke W., Bezzina Connie R., Bhuiyan Zahir A., Wedekind Horst, Schulze-Bahr Eric, Wilde Arthur A. M. Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome Cardiovascular research 2005;67 (3):459-466 [PubMed]
  • Tan Hanno L., Hofman Nynke, van Langen Irene M., van der Wal Allard C., Wilde Arthur A. M. Sudden unexplained death - Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives Circulation 2005;112 (2):207-213 [PubMed]
  • Krediet C. T. Paul, Wilde Arthur A. M., Halliwill John R., Wieling Wouter Syncope during exercise, documented with continuous blood pressure monitoring during ergometer testing Clinical autonomic research 2005;15 (1):59-62 [PubMed]
  • Lo-A-Njoe Shirley M., Wilde Arthur A., van Erven Lieselot, Blom Nico A. Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy Heart rhythm 2005;2 (12):1365-1368 [PubMed]
  • Denjoy I., Postma A. V., Lupoglazoff J. M., Vaksman G., Kamblock J., Leenhardt A., Wilde A. A., Guicheney P. Tachycardies ventriculaires catécholergiques chez l'enfant Archives des maladies du coeur et des vaisseaux 2005;98 (5):506-512 [PubMed]
  • Wilde Arthur A. M., van den Berg Maarten P. Ten years of genes in inherited arrhythmia syndromes: an example of what we have learned from patients, electrocardiograms, and computers Journal of electrocardiology 2005;38 (4 Suppl):145-149 [PubMed]
  • Wilde A. A. M., Pinto Y. M. The ECG of a (cardio)myopathy? Netherlands heart journal 2005;13 (10):373-383
  • Simmers T. A., Wilde A. A. M. The ions have it Netherlands heart journal 2005;13 (11):428-433
  • Bezzina Connie R., Wilde Arthur A. M., Roden Dan M. The molecular genetics of arrhythmias Cardiovascular research 2005;67 (3):343-346 [PubMed]
  • Darbar Dawood, Yang Tao, Churchwell Keith, Wilde Arthur A. M., Roden Dan M. Unmasking of Brugada syndrome by lithium Circulation 2005;112 (11):1527-1531 [PubMed]
  • Wilde A. A. M., van den Brink R. B. Where do the extras come from? Netherlands heart journal 2005;13 (2):67-83

2004

  • Wilde A. A. M., Tan H. L. A fainting lady with some extrasystoles Netherlands heart journal 2004;12 (2):73-89
  • Nollen G. J. Anatomical and functional evaluation of the cardiovascular system in Marfan syndrome 2004. 143p. ISBN 9789090182124. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., van der Wall E. E.; Co-supervisor: Mulder B. J. M.)
  • Colman N., Wieling W., Wilde A. A. M. A patient with recurrent syncope and ST-elevation on the electrocardiogram Europace : European pacing, arrhythmias, and cardiac electrophysiology 2004;6 (4):296-300 [PubMed]
  • van Alem A. P. Arrest 4: Out-of-hospital resuscication with automated external defribillators 2004. 207p. ISBN 9789090178509. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Tijssen J. G. P.; Co-supervisors: Koster R. W., de Vos R.)
  • van den Berg M. P., Tulleken J. E., Wilde A. A. M. 'Brugada ECG' elicited by imipramine overdose Netherlands heart journal 2004;12 (9):404-406
  • Tukkie Raymond, Sogaard Peter, Vleugels Jim, de Groot Irma K. L. M., Wilde Arthur A. M., Tan Hanno L. Delay in right ventricular activation contributes to Brugada syndrome Circulation 2004;109 (10):1272-1277 [PubMed]
  • Erol-Yilmaz Ayten, Tukkie Raymond, de Boo Job, Schrama Tim, Wilde Arthur Direct comparison of a contractility and activity pacemaker sensor during treadmill exercise testing Pacing and clinical electrophysiology 2004;27 (11):1493-1499 [PubMed]
  • Krediet C. T. Paul, Wilde Arthur A. M., Wieling Wouter, Halliwill John R. Exercise related syncope, when it's not the heart Clinical autonomic research 2004;14 (Suppl. 1):25-36 [PubMed]
  • van Langen I. M., Hofman N., Tan H. L., Wilde A. A. M. Family and population strategies for screening and counselling of inherited cardiac arrhythmias Annals of medicine 2004;36 (Suppl. 1):116-124 [PubMed]
  • Tan H. L., Tukkie R., Vleugels J., de Groot I. K. L. M., Wilde A. A. M., Sogaard P. Further confirmation that a conduction disturbance underlies the electrocardiographic pattern of the so-called Brugada syndrome - Response Circulation 2004;110 (5):E53
  • van Langen I. M., Wilde A. A. M. Genetische aspectenin: J. N. Keeman, P. W. de Leeuw, J. A. Mazel, F. G. Zitman, editors. Het medisch jaar 2004. Houten: Bohn Stafleu Van Loghum; 2004. p. 58-66
  • Wilde A. A. M., Simmers T. A. I think a niece of mine was referred to a neurologist Netherlands heart journal 2004;12 (6):302-319
  • Wilde A. A. M., Simmers T. A. Just one collapse during soccer Netherlands heart journal 2004;12 (7-8):355-377
  • Wilde A. A. M. Lang-QT-intervalsyndroom (LQTS)in: H. C. S. van Buren, J. J. de Gier, J. Andeweg, null e.a., editors. Commentaren Medicatiebewaking 2004/2005. Houtem: Health Base; 2004. p. 543-549
  • Bellocq Chloé, van Ginneken Antoni C. G., Bezzina Connie R., Alders Mariel, Escande Denis, Mannens Marcel M. A. M., Baró Isabelle, Wilde Arthur A. M. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome Circulation 2004;109 (20):2394-2397 [PubMed]
  • Tukkie R., Rienks R., Wilde A. A. M. Nightly phenomena, day time work? Netherlands heart journal 2004;12 (11):510-511
  • Wilde A. A. M., Tan H. One to one, one to two, two to one? What is the rhythm? Netherlands heart journal 2004;12 (3):123-138
  • Simmers T. A., Wilde A. A. M. Out of the frying pan and into the fire Netherlands heart journal 2004;12 (5):234-253
  • Simmers T. A., Tukkie R., Dekker L. R. C., Wilde A. A. M. Primary prevention: prime time?: ICD trials (and tribulations) Netherlands heart journal 2004;12 (6):261-264
  • Hoogsteen J. M., Bennekers J. H., van der Wall E. E., van Hemel N. M., Wilde A. A. M., Crijns H. J. G. M., Gorgels A. P. M., Smeets J. L. R. M., Hauer R. N. W., Jordaens J. L. M., Schalij M. J. Recommendations and cardiological evaluation of athletes with arrhythmias Netherlands heart journal 2004;12 (5):214-222
  • Hoogsteen J. M., Bennekers J. H., van der Wall E. E., van Hemel N. M., Wilde A. A. M., Crijns H. J. G. M., Gorgels A. P. M., Smeets J. L. R. M., Hauer R. N. W., Jordaens J. L. M., Schalij M. J. Recommendations and cardiological evaluation of athletes with arrhythmias Netherlands heart journal 2004;12 (4):157-164
  • Hoogsteen J., Bennekers J. H., van der Wall E. E., van Hemel N. M., Wilde A. A. M., Crijns H. J. G. M., Gorgels A. P. M., Smeets J. L. R. M., Hauer R. N. W., Jordaens J. L. M., Schalij M. J. Recommendations and cardiological evaluation of athletes with arrhythmias: Part 1 Netherlands heart journal 2004;12 (4):157-164 [PubMed]
  • Hoogsteen J., Bennekers J. H., van der Wall E. E., van Hemel N. M., Wilde A. A. M., Crijns H. J. G. M., Gorgels A. P. M., Smeets J. L. R. M., Hauer R. N. W., Jordaens J. L. M., Schalij M. J. Recommendations and cardiological evaluation of athletes with arrhythmias: Part 2 Netherlands heart journal 2004;12 (5):214-222 [PubMed]
  • Smits J. P. P. The clinical and electrophysiological spectrum of cardiac sodium channel mutations 2004. 220p. ISBN 9789090181646. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Jongsma H. J.; Co-supervisor: Veldkamp M. W.)
  • Wilde A. A. M., Pinto Y. M. Therapie van hypertrofische cardiomyopathiein: J. N. Keeman, P. W. de Leeuw, J. A. Mazel, F. G. Zitman, editors. Het medisch jaar 2004. Houten: Bohn Stafleu Van Loghum; 2004. p. 53-66

2003

  • Groenewegen W. Antoinette, Firouzi Mehran, Bezzina Connie R., Vliex Saskia, van Langen Irene M., Sandkuijl Lodewijk, Smits Jeroen P. P., Hulsbeek Miriam, Rook Martin B., Jongsma Habo J., Wilde Arthur A. M. A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill Circulation research 2003;92 (1):14-22 [PubMed]
  • Bezzina Connie R., Verkerk Arie O., Busjahn Andreas, Jeron Andreas, Erdmann Jeanette, Koopmann Tamara T., Bhuiyan Zahurul A., Wilders Ronald, Mannens Marcel M. A. M., Tan Hanno L., Luft Friedrich C., Schunkert Heribert, Wilde Arthur A. M. A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization Cardiovascular research 2003;59 (1):27-36 [PubMed]
  • Simmers T. A., Wilde A. A. M. A long RP supraventricular tachycardia Netherlands heart journal 2003;11 (6):274-286 [PubMed]
  • Groenewegen W. Antoinette, Bezzina Connie R., van Tintelen J. Peter, Hoorntje Theo M., Mannens Marcel M. A. M., Wilde Arthur A. M., Jongsma Habo J., Rook Martin B. A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics Cardiovascular research 2003;57 (4):1072-1078 [PubMed]
  • Wilders R., Veldkamp M. W., Baartscheer A., Zegers J. G., Bezzina C. R., Wilde A. A. M. Bradycardia in LQT3 patients: Insights from 0D modelsin: A. Anonymous, editors. Engineering in Medicine and Biology Society, 2003. S.l.: s.n.; 2003. p. 32-35, ISBN 9780780377899
  • Simmers T. A., Wilde A. A. M. Carotid sinus clues Netherlands heart journal 2003;11 (4):175-194 [PubMed]
  • Simmers T. A., Tukkie R., Wilde A. A. M. COMPANION - a friend indeed Netherlands heart journal 2003;11 (9):333-336
  • Bezzina Connie R., Rook Martin B., Groenewegen W. Antoinette, Herfst Lucas J., van der Wal Allard C., Lam Jan, Jongsma Habo J., Wilde Arthur A. M., Mannens Marcel M. A. M. Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system Circulation research 2003;92 (2):159-168 [PubMed]
  • Veldkamp Marieke W., Wilders Ronald, Baartscheer Antonius, Zegers Jan G., Bezzina Connie R., Wilde Arthur A. M. Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families Circulation research 2003;92 (9):976-983 [PubMed]
  • Brouwer Jan, van den Berg Maarten P., Grobbee Diederick E., Haaksma Jaap, Wilde Arthur A. M. Diagnostic performance of various QTc interval formulas in a large family with long QT syndrome type 3: Bazett's formula not so bad after all Annals of noninvasive electrocardiology 2003;8 (4):269-274 [PubMed]
  • Tan Hanno L., Bezzina Connie R., Smits Jeroen P. P., Verkerk Arie O., Wilde Arthur A. M. Genetic control of sodium channel function Cardiovascular research 2003;57 (4):961-973 [PubMed]
  • Tan H. L., Bezzina C. R., Smits J. P. P., Verkerk A. O., Wilde A. A. M. Genetic control of sodium channel function (vol 57, pg 961, 2003) Cardiovascular research 2003;59 (3):799-802
  • van Langen I. M., Birnie E., Leschot N. J., Bonsel G. J., Wilde A. A. M. Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era? European heart journal 2003;24 (6):562-568 [PubMed]
  • Postma A. V. Genetics aspects of cardiac arrythmia syndromes 2003. 162p. ISBN 9789090170916. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisors: Moorman A. F. M., Mannens M. M. A. M.)
  • Wilde A. A. M., Simmers T. A. I don't know what it is, but it doesn't feel right Netherlands heart journal 2003;11 (7-8):317-330 [PubMed]
  • Wieling W., Ganzeboom K. S., Krediet C. T. P., Grundmeijer H. G. L. M., Wilde A. A. M., van Dijk J. G. Initiële diagnostische strategie bij wegrakingen: het belang van de anamnese Nederlands tijdschrift voor geneeskunde 2003;147 (18):849-854 [PubMed]
  • Bezzina C. R., Wilde A. A. M. Ion channel disease as a cause of the Brugada syndrome; molecular and genetic aspectsin: I. Gussak, editors. Contemporary cardiology: cardiac repolarization: bridging basic and clinical science. Totowa NJ: Humana Press Inc; 2003. p. 187-200
  • Wilde A. A. M. Lang-QT-intervalsyndroom (LQTS)in: J. J. de Gier, H. C. S. van Buren, editors. Commentaren Medicatiebewaking 2003/2004. Houten: Stichting Health Base; 2003. p. 493-498, ISBN 9789074027229
  • Herfst Lucas J., Potet Franck, Bezzina Connie R., Groenewegen W. Antoinette, Le Marec Hervé, Hoorntje Theo M., Demolombe Sophie, Baró Isabelle, Escande Denis, Jongsma Habo J., Wilde Arthur A. M., Rook Martin B. Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects Journal of molecular and cellular cardiology 2003;35 (5):549-557 [PubMed]
  • Wilde Arthur A. M., Pfaffendorf Martin [QT-Zeit-Verlangerung durch Arzneistoffe] Medizinische Monatsschrift fur Pharmazeuten 2003;26 (1):4-10 [PubMed]
  • Dekker L. R. C., Wilde A. A. M. Recent breakthroughs in the genetics of atrial fibrillation Netherlands heart journal 2003;11 (10):385-386
  • Wilde Arthur A. M., Tan Hanno L. Relation between basic and clinical electrophysiologic characteristics in Brugada syndrome: Facts or fiction? Journal of cardiovascular electrophysiology 2003;14 (4):412-414 [PubMed]
  • Simmers T. A., Wilde A. A. M. Rhythm puzzle Netherlands heart journal 2003;11 (4):175
  • Simmers T. A., Wilde A. A. M. Rhythm puzzle: A long RP Supraventricular tachycardia Netherlands heart journal 2003;11 (6):274
  • Wilde A. A. M., Simmers T. A. Rhythm puzzle: I don't know what it is, but it doesn't feel right Netherlands heart journal 2003;11 (7):317
  • Simmers T. A., Wilde A. A. M. Rhythm puzzle: the av-node revisited Netherlands heart journal 2003;11 (11):474-475
  • Tukkie R., Wilde A. A. M. TDI-Echocardiography: A new screening tool for long QT syndrome? European journal of echocardiography 2003;4 (3):157-158 [PubMed]
  • Alders Marielle, Jongbloed Roselie, Deelen Wout, van den Wijngaard Arthur, Doevendans Pieter, ten Cate Folkert, Regitz-Zagrosek Vera, Vosberg Hans Peter, van Langen Irene, Wilde Arthur, Dooijes Dennis, Mannens Marcel The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands European heart journal 2003;24 (20):1848-1853 [PubMed]
  • Simmers T. A., Wilde A. A. M. The AV-node revisited Netherlands heart journal 2003;11 (11):474-490 [PubMed]
  • Wilde A. A. M., Antzelevitch C., Borggrefe M., Brugada J., Brugada P., Brugada R., Towbin J. A., Corrado D., Hauer R. N. W., Kass R. S., Nademanee K., Priori S. G. The Brugada Numbers (reply to letter) Circulation 2003;107 (18):122
  • Wilde A. A. M., Antzelevitch C. The continuing story: The aetiology of Brugada syndrome: functional or structural basis? European heart journal 2003;24 (22):2072-2073
  • van Langen I. M., Birnie E., Alders M., Jongbloed R. J., Le Marec H., Wilde A. A. M. The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome Journal of medical genetics 2003;40 (2):141-145 [PubMed]
  • Wilde A. A. M., Tan H. L. Untitled - Reply Journal of cardiovascular electrophysiology 2003;14 (11):1258

2002

  • Postma Alex V., Denjoy Isabelle, Hoorntje Theo M., Lupoglazoff Jean-Marc, Da Costa Antoine, Sebillon Pascale, Mannens Marcel M. A. M., Wilde Arthur A. M., Guicheney Pascale Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia Circulation research 2002;91 (8):E21-E26 [PubMed]
  • Tan Hanno L., Kupershmidt Sabina, Zhang Rong, Stepanovic Svetlana, Roden Dan M., Wilde Arthur A. M., Anderson Mark E., Balser Jeffrey R. A calcium sensor in the sodium channel modulates cardiac excitability Nature 2002;415 (6870):442-447 [PubMed]
  • van den Berg M. P., Viersma J. W., Beaufort-Krol G. C. M., Bink-Boelkens M. Th E., Bezzina C. R., Veldkamp M. W., Brouwer J., Haaksma J., van Tintelen J. P., van Langen I. M., Wouda A. A., Wilde A. A. M. A large family characterised by nocturnal sudden death Netherlands heart journal 2002;10 (7-8):304-312 [PubMed]
  • van Langen I. M., van Oel C. J., Bonsel G. J., Wilde A. A. M., Mollema E., Leschot N. J. Balancerend tussen de medische voordelen en de maatschappelijke neveneffecten van genetische diagnostiek bij zeldzame catastrofale aandoeningen: het voorbeeld van familiaire plotselinge doodin: De zin en onzin van genetische screening. S.l.: Nationaal regie-orgaan genomics; 2002. p. 26-56
  • Wilde A. A. M., Remme C. A., Derksen R., Wever E. F. D., Hauer R. N. W. Brugada syndrome European heart journal 2002;23 (8):675-676 [PubMed]
  • Smits J. P. P., Wilde Arthur A. M. Brugada syndrome: in search of a genotype-phenotype relationship Auf der Suche nach "Genotype-Phenotype"-Verhältnissen in das Brugada-Syndrom Herzschrittmachertherapie & Elektrophysiologie 2002;13 (3):142-148 [PubMed]
  • Smits J. P. P., Wilde A. A. M. Brugada syndrome: in search of genotype-phenotype relationship Herzschrittmachertherapie & Elektrophysiologie 2002;13:142-148
  • Postma A. V., Wilde A. A. M. Catecholaminergic polymorphic ventricular tachycardia: A reviewin: M. J. Schalij, M. J. Janse, A. T. Oosterom, H. J. J. Wellens, E. E. van der Wall, editors. Einthoven 2002: 100 years of electrocardiography. Leiden: The Einthoven Foundation; 2002. p. 505-513
  • Neffke J. G. J., Tulevski I. I., van der Wall E. E., Wilde A. A. M., van Veldhuisen D. J., Dodge-Khatami A., Mulder B. J. M. ECG determinants in adult patients with chronic right ventricular pressure overload caused by congenital heart disease: relation with plasma neurohormones and MRI parameters Heart (British Cardiac Society) 2002;88 (3):266-270 [PubMed]
  • Wilde A. A. M., Tan H. L., Bezzina C. R. Familial primary arrhythmia syndromes: Nice to know or need to know Netherlands heart journal 2002;10 (5):225-228
  • Conrath Chantal E., Wilde Arthur A. M., Jongbloed Rosalie J. E., Alders Mariëlle, van Langen Irene M., van Tintelen J. Peter, Doevendans Pieter A., Opthof Tobias Gender differences in the long QT syndrome: effects of beta-adrenoceptor blockade Cardiovascular research 2002;53 (3):770-776 [PubMed]
  • Wilde A. A. M. Geneesmiddelen en het lange QT-interval Geneesmiddelenbulletin 2002;36 (3):27-32
  • Wilde A. A. M., van Langen I. M., Doevendans P. A. F. M. Genetica van aandoeningen van de hartspierin: J. R. T. C. Roelandt, K. I. Lie, H. J. J. Wellens, F. van der Werf, editors. Cardiologie. Houten: Bohn Stafleu Van Loghum; 2002. p. 59-64
  • Smits Jeroen P. P., Eckardt Lars, Probst Vincent, Bezzina Connie R., Schott Jean Jacques, Remme Carol Ann, Haverkamp Wilhelm, Breithardt Günter, Escande Denis, Schulze-Bahr Eric, Lemarec Hervé, Wilde Arthur A. M. Genotype-phenotype relationship in Brugada syndrome: Electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients Journal of the American College of Cardiology 2002;40 (2):350-356 [PubMed]
  • ten Harkel A. D. J., Lubbers L. J., Hoorntje T. H., Blom N. A., van Langen I. M., Sreeram N., Wilde A. A. M. Het lange-QT-tijdsyndroom bij kinderen Tijdschrift voor kindergeneeskunde 2002;70 (2):50-56
  • van Dockum W. G., Doevendans P. A. F. M., van Rossum A. C., Wilde A. A. M. Hypertrofische cardiomyopathie: een genetisch overdraagbare hartziekte Nederlands tijdschrift voor geneeskunde 2002;146 (15):705-712 [PubMed]
  • Wilde Arthur A. M. Is there a role for implantable cardioverter defibrillators in long QT syndrome? Journal of cardiovascular electrophysiology 2002;13 (1 Suppl):S110-S113 [PubMed]
  • Doevendans P. A. F. M., Wilde A. A. M. Moleculaire cardiologiein: J. R. T. C. Roelandt, K. I. Lie, H. J. J. Wellens, F. van der Werf, editors. Cardiologie. Houten: Bohn Stafleu Van Loghum; 2002. p. 31-40
  • Wilde A. A. M., Antzelevitch C., Borggrefe M., Brugada J., Brugada R., Brugada P., Corrado D., Hauer R. N. W., Kass R. S., Nademanee K., Priori S. G., Towbin J. A. Proposed diagnostic criteria for the Brugada syndrome European heart journal 2002;23 (21):1648-1654 [PubMed]
  • Wilde Arthur A. M., Antzelevitch Charles, Borggrefe Martin, Brugada Josep, Brugada Ramón, Brugada Pedro, Corrado Domenico, Hauer Richard N. W., Kass Robert S., Nademanee Koonlawee, Priori Silvia G., Towbin Jeffrey A. Proposed diagnostic criteria for the Brugada syndrome - Consensus report Circulation 2002;106 (19):2514-2519 [PubMed]
  • Erol-Yilmaz A., Tukkie R., Schrama T. A. M., Romkes H. J., Wilde A. A. M. Reversed remodelling of dilated left sided cardiomyopathy after upgrading from VVIR to VVIR biventricular pacing Europace : European pacing, arrhythmias, and cardiac electrophysiology 2002;4 (4):445-449 [PubMed]
  • Remme C. A. The ATP-sensitive potassium channel in the heart. Functional, electrophysiological and molecular aspects 2002. 207p. ISBN 9789090155982. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., Moorman A. F. M.)
  • Tan Hanno L., Wilde Arthur A. M. Understanding torsade de pointes: A bridge to tailored drug therapy? Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy 2002;16 (2):87-88 [PubMed]

2001

  • Tan H. L., Spekhorst H. H., Peters R. J., Wilde A. A. Adenosine induced ventricular arrhythmias in the emergency room Pacing and clinical electrophysiology 2001;24 (4 Part 1):450-455 [PubMed]
  • Brundel B. J., van Gelder I. C., Henning R. H., Tuinenburg A. E., Wietses M., Grandjean J. G., Wilde A. A., van Gilst W. H., Crijns H. J. Alterations in potassium channel gene expression in atria of patients with persistent and paroxysmal atrial fibrillation: differential regulation of protein and mRNA levels for K+ channels Journal of the American College of Cardiology 2001;37 (3):926-932 [PubMed]
  • Tan H. L., Bink-Boelkens M. T., Bezzina C. R., Viswanathan P. C., Beaufort-Krol G. C., van Tintelen P. J., van den Berg M. P., Wilde A. A., Balser J. R. A sodium-channel mutation causes isolated cardiac conduction disease Nature 2001;409 (6823):1043-1047 [PubMed]
  • Bezzina C. R., Rook M. B., Wilde A. A. Cardiac sodium channel and inherited arrhythmia syndromes Cardiovascular research 2001;49 (2):257-271 [PubMed]
  • Doevendans P. A., Wilde A. A. Cardiovascular geneticsDordrecht: Kluwer Academic Publishers; 2001.
  • Wedekind H., Smits J. P., Schulze-Bahr E., Arnold R., Veldkamp M. W., Bajanowski T., Borggrefe M., Brinkmann B., Warnecke I., Funke H., Bhuiyan Z. A., Wilde A. A., Breithardt G., Haverkamp W. De novo mutation in the SCN5A gene associated with early onset of sudden infant death Circulation 2001;104 (10):1158-1164 [PubMed]
  • Remme C. A., Wever E. F., Wilde A. A., Derksen R., Hauer R. N. Diagnosis and long-term follow-up of the Brugada syndrome in patients with idiopathic ventricular fibrillation European heart journal 2001;22 (5):400-409 [PubMed]
  • Viswanathan P. C., Bezzina C. R., George A. L., Roden D. M., Wilde A. A., Balser J. R. Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes Circulation 2001;104 (10):1200-1205 [PubMed]
  • Schwartz P. J., Priori S. G., Spazzolini C., Moss A. J., Vincent G. M., Napolitano C., Denjoy I., Guicheney P., Breithardt G., Keating M. T., Towbin J. A., Beggs A. H., Brink P., Wilde A. A. M., Toivonen L., Zareba W., Robinson J. L., Timothy K. W., Corfield V., Wattanasirichaigoon D., Corbett C., Haverkamp W., Schulze-Bahr E., Lehmann M. H., Schwartz K., Coumel P., Bloise R. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias Circulation 2001;103 (1):89-95 [PubMed]
  • Remme C. A., Schumacher C. A., de Jong J. W., Fiolet J. W., de Groot J. R., Coronel R., Wilde A. A. K(ATP) channel opening during ischemia: effects on myocardial noradrenaline release and ventricular arrhythmias Journal of cardiovascular pharmacology 2001;38 (3):406-416 [PubMed]
  • Coumel P., Wilde A. A. Learning from mistakes: the case of clinical electrophysiology: a perspective on evidence-based rhythmology Circulation 2001;104 (7):845-847 [PubMed]
  • Wilde A. A., Escande D. LQT genotype-phenotype relationships: patients and patches Cardiovascular research 2001;51 (4):627-629 [PubMed]
  • van den Berg M. P., Wilde A. A., Viersma T. J. W., Brouwer J., Haaksma J., van der Hout A. H., Stolte-Dijkstra I., Bezzina C. R., van Langen I. M., Beaufort-Krol G. C., Cornel J. H., Crijns H. J. Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome Journal of cardiovascular electrophysiology 2001;12 (6):630-636 [PubMed]
  • Dekker L. R. C., Wilde A. A. M. Primary ventricular fibrillation in acute myocardial infarction: an inherited disease? Netherlands heart journal 2001;9 (6):213-215 [PubMed]
  • Alings M., Dekker L., Sadée A., Wilde A. Quinidine induced electrocardiographic normalization in two patients with Brugada syndrome Pacing and clinical electrophysiology 2001;24 (9 Part 1):1420-1422 [PubMed]
  • Demolombe S., Lande G., Charpentier F., van Roon M. A., van den Hoff M. J., Toumaniantz G., Baro I., Guihard G., Le Berre N., Corbier A., de Bakker Jacques, Opthof T., Wilde A., Moorman A. F., Escande D. Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation Cardiovascular research 2001;50 (2):314-327 [PubMed]
  • Demolombe S., Lande G., Charpentier F., van Roon M. A., van den Hoff Maurice J. B., Toumaniantz G., Baro I., Guihard G., Le Berre N., Corbier A., Bakker J., Opthof T., Wilde Arthur A. M., Moorman Antonius F. M. Transgenic mice overexpressing human KvLQT1 dominant negative isoform. Part I: phenotypic characterization. Cardiovascular research 2001;50:314-327

2000

  • Wilde A. A. M., Mannens M. M. A. M., Alders M., van der Lip K., Hoorntje T. M., Sreeram N., van Tintelen P., van der Wal A. A knockout may not always be a knockout - Response Circulation 2000;102 (18):E122-E122
  • Wilde A. A., Priori S. G. Brugada syndrome and sudden death European heart journal 2000;21 (17):1483-1484 [PubMed]
  • van Langen I. M., Wilde A. A. De waarheid na de dood; obducties als kwaliteitsinstrument serieus nemen Nederlands tijdschrift voor geneeskunde 2000;144 (9):451 [PubMed]
  • Postma A. V., Bezzina C. R., de Vries J. F., Wilde A. A., Moorman A. F., Mannens M. M. Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3 Human genetics 2000;106 (6):614-619 [PubMed]
  • Hoogerwaard E. M., Ginjaar H. B., Wilde A. A., Leschot N. J., de Voogt W. G., de Visser M. Het hartzeer van een spierdystrofie Nederlands tijdschrift voor geneeskunde 2000;144 (46):2181-2184 [PubMed]
  • ten Kroode H. F., van Langen I. M., Hendriks K. S., van Tintelen J. P., Grosfeld F. J., Wilde A. A. Het lang-QT-intervalsyndroom en erfelijkheidsonderzoek: psychische reacties in drie generaties van een familie Nederlands tijdschrift voor geneeskunde 2000;144 (21):995-999 [PubMed]
  • Remme C. A., Wilde A. A. KATP channel openers, myocardial ischemia, and arrhythmias--should the electrophysiologist worry? Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy 2000;14 (1):17-22 [PubMed]
  • Wilde A. A., Roden D. M. Predicting the long-QT genotype from clinical data: from sense to science Circulation 2000;102 (23):2796-2798 [PubMed]
  • van der Wouw P. A., Brauns A. C., Bailey S. E., Powers J. E., Wilde A. A. Premature ventricular contractions during triggered imaging with ultrasound contrast Journal of the American Society of Echocardiography 2000;13 (4):288-294 [PubMed]
  • Tan Han L., Wilde Arthur A. M. Proarrhythmia related to sodium channel blockade II: postulated mechanisms of Brugada syndrome and their possible involvement in class 1C drug-induced ventricular arrhythmias during ischemia. Cardiac Electrophysiology Reviews 2000;4:217-221
  • Veldkamp M. W., Viswanathan P. C., Bezzina C., Baartscheer A., Wilde A. A., Balser J. R. Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel Circulation research 2000;86 (9):E91-E97 [PubMed]
  • Wilde A. A., van Langen I. M. Van gen naar ziekte; ionkanaaleiwitten en het lange-QT-intervalsyndroom Nederlands tijdschrift voor geneeskunde 2000;144 (46):2205-2207 [PubMed]
  • Wilde A. A., Veldkamp M. W. What we can learn from individual resuscitated patients Cardiovascular research 2000;46 (1):14-16 [PubMed]

1999

  • Remme C. A., Wilde A. A. A new, sympathetic look at KATP channels in the heart Cardiovascular research 1999;43 (1):17-19 [PubMed]
  • Bezzina C., Veldkamp M. W., van den Berg M. P., Postma A. V., Rook M. B., Viersma J. W., van Langen I. M., Tan-Sindhunata G., Bink-Boelkens M. T., van der Hout A. H., Mannens M. M., Wilde A. A. A single Na(+) channel mutation causing both long-QT and Brugada syndromes Circulation research 1999;85 (12):1206-1213 [PubMed]
  • Wilde A. A., Jongbloed R. J., Doevendans P. A., Düren D. R., Hauer R. N., van Langen I. M., van Tintelen J. P., Smeets H. J., Meyer H., Geelen J. L. Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) Journal of the American College of Cardiology 1999;33 (2):327-332 [PubMed]
  • Alings M., Wilde A. "Brugada" syndrome: clinical data and suggested pathophysiological mechanism Circulation 1999;99 (5):666-673 [PubMed]
  • Schott J. J., Alshinawi C., Kyndt F., Probst V., Hoorntje T. M., Hulsbeek M., Wilde A. A., Escande D., Mannens M. M., Le Marec H. Cardiac conduction defects associate with mutations in SCN5A Nature genetics 1999;23 (1):20-21 [PubMed]
  • Hoogerwaard E. M., van der Wouw P. A., Wilde A. A., Bakker E., Ippel P. F., Oosterwijk J. C., Majoor-Krakauer D. F., van Essen A. J., Leschot N. J., de Visser M. Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy Neuromuscular disorders 1999;9 (5):347-351 [PubMed]
  • Roden D. M., Wilde A. A. Drug-induced J point elevation: a marker for genetic risk of sudden death or ECG curiosity? Journal of cardiovascular electrophysiology 1999;10 (2):219-223 [PubMed]
  • Priori S. G., Barhanin J., Hauer R. N., Haverkamp W., Jongsma H. J., Kleber A. G., McKenna W. J., Roden D. M., Rudy Y., Schwartz K., Schwartz P. J., Towbin J. A., Wilde A. A. M. Genetic and molecular basis of cardiac arrhythmias: impact on clinical management part III Circulation 1999;99 (5):674-681 [PubMed]
  • Priori S. G., Barhanin J., Hauer R. N., Haverkamp W., Jongsma H. J., Kleber A. G., McKenna W. J., Roden D. M., Rudy Y., Schwartz K., Schwartz P. J., Towbin J. A., Wilde A. M. Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II Circulation 1999;99 (4):518-528 [PubMed]
  • Priori S. G., Barhanin J., Hauer R. N., Haverkamp W., Jongsma H. J., Kleber A. G., McKenna W. J., Roden D. M., Rudy Y., Schwartz K., Schwartz P. J., Towbin J. A., Wilde A. Genetic and molecular basis of cardiac arrhythmias; impact on clinical management. Study group on molecular basis of arrhythmias of the working group on arrhythmias of the european society of cardiology European heart journal 1999;20 (3):174-195 [PubMed]
  • Hoorntje T., Alders M., van Tintelen P., van der Lip K., Sreeram N., van der Wal A., Mannens M., Wilde A. Homozygous premature truncation of the HERG protein : the human HERG knockout Circulation 1999;100 (12):1264-1267 [PubMed]
  • Rook M. B., Bezzina Alshinawi C., Groenewegen W. A., van Gelder I. C., van Ginneken A. C., Jongsma H. J., Mannens M. M., Wilde A. A. Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome Cardiovascular research 1999;44 (3):507-517 [PubMed]
  • Wittkampf F. H., Wever E. F., Derksen R., Wilde A. A., Ramanna H., Hauer R. N., Robles de Medina E. O. LocaLisa: new technique for real-time 3-dimensional localization of regular intracardiac electrodes Circulation 1999;99 (10):1312-1317 [PubMed]
  • Tan H. L., Alings M., van Olden R. W., Wilde A. A. Long-term (subacute) potassium treatment in congenital HERG-related long QT syndrome (LQTS2) Journal of cardiovascular electrophysiology 1999;10 (2):229-233 [PubMed]
  • Jongbloed R. J., Wilde A. A., Geelen J. L., Doevendans P., Schaap C., van Langen I., van Tintelen J. P., Cobben J. M., Beaufort-Krol G. C., Geraedts J. P., Smeets H. J. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families Human mutation 1999;13 (4):301-310 [PubMed]
  • Wilde A. A., van Langen I. M., van Tintelen J. P., Hauer R. N. Presymptomatisch onderzoek na plotselinge hartdood in de familie Nederlands tijdschrift voor geneeskunde 1999;143 (32):1643-1648 [PubMed]
  • Hoogerwaard E. M., Bakker E., Ippel P. F., Oosterwijk J. C., Majoor-Krakauer D. F., Leschot N. J., van Essen A. J., Brunner H. G., van der Wouw P. A., Wilde A. A., de Visser M. Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study Lancet 1999;353 (9170):2116-2119 [PubMed]
  • Wilde A. A. M., Düren D. Sudden cardiac death, RBBB, and right precordial ST-segment elevation Circulation 1999;99 (5):722-723 [PubMed]

1998

  • Demolombe S., Baró I., Péréon Y., Bliek J., Mohammad-Panah R., Pollard H., Morid S., Mannens M., Wilde A., Barhanin J., Charpentier F., Escande D. A dominant negative isoform of the long QT syndrome 1 gene product Journal of biological chemistry 1998;273 (12):6837-6843 [PubMed]
  • Schotborgh C. E., Wilde Arthur A. M. ATP-sensitive potassium channel openers and blockers in the cardiovascular system: physiology, pharmacology and clinical effects.in: Seminars in Cardiothoracic and Cardiovascular Anesthesia. 1998. p. 243-255
  • Janse M. J., Wilde A. A. Molecular mechanisms of arrhythmias Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology 1998;17 (Suppl. 2):II41-II46 [PubMed]
  • van Langen I. M., Wilde A. A., Mannens M. A. Plotselinge dood bij jonge mensen door aritmogene rechterventrikeldysplasie Nederlands tijdschrift voor geneeskunde 1998;142 (13):739-740 [PubMed]
  • Wilde Arthur A. M. Proarrhythmia related to sodium channel blockade: mechanisms, monitoring, prevention and management. Cardiac Electrophysiology Review 1998;2:136-141
  • Tan H. L., Wilde A. A., Peters R. J. Suppression of torsades de pointes by atropine Heart (British Cardiac Society) 1998;79 (1):99-100 [PubMed]
  • Tan H. L., Wilde A. A. T wave alternans after sotalol: evidence for increased sensitivity to sotalol after conversion from atrial fibrillation to sinus rhythm Heart (British Cardiac Society) 1998;80 (3):303-306 [PubMed]

1997

  • Wilde A. A. ATP and the role of IK.ATP during acute myocardial ischemia: controversies revive Cardiovascular research 1997;35 (2):181-183 [PubMed]
  • Hoogerwaard E. M., de Voogt W. G., Wilde A. A., van der Wouw P. A., Bakker E., van Ommen G. J., de Visser M. Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period Journal of neurology 1997;244 (10):657-663 [PubMed]
  • Creanza M., van Dam-Koopman I. M., Wilde A. A., Robles de Medina E. O. Het aangeboren lange-QT-tijdsyndroom Nederlands tijdschrift voor geneeskunde 1997;141 (19):926-931 [PubMed]
  • Wilde A. A., Mannens M. M. Iatrogene collaps; is die te voorkomen? Nederlands tijdschrift voor geneeskunde 1997;141 (16):796-797 [PubMed]
  • Wilde A. A., Veldkamp M. W. Ion channels, the QT interval, and arrhythmias Pacing and clinical electrophysiology 1997;20 (8 Part 2):2048-2051 [PubMed]
  • Mannens M., Wilde A. KVLQT1, the rhythm of imprinting Nature genetics 1997;15 (2):113-115 [PubMed]
  • Wilde A. A., Düren D. R., Hauer R. N., deBakker J. M., Bakker P. F., Becker A. E., Janse M. J. Mitral valve prolapse and ventricular arrhythmias: observations in a patient with a 20-year history Journal of cardiovascular electrophysiology 1997;8 (3):307-316 [PubMed]
  • Schotborgh C. E., Wilde A. A. Sulfonylurea derivatives in cardiovascular research and in cardiovascular patients Cardiovascular research 1997;34 (1):73-80 [PubMed]
  • van den Berg M. H., Wilde A. A., Robles de Medina E. O., Meyer H., Geelen J. L., Jongbloed R. J., Wellens H. J., Geraedts J. P. The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene Human genetics 1997;100 (3-4):356-361 [PubMed]

1996

  • Wilde A. A. ATP-sensitive potassium channels, transmural ischemia and the ECG implications for the non-insulin dependent diabetic patient? Cardiovascular research 1996;31 (5):688-690 [PubMed]

1995

  • Wilde A. A., Aksnes G. Myocardial potassium loss and cell depolarisation in ischaemia and hypoxia Cardiovascular research 1995;29 (1):1-15 [PubMed]

1994

  • Wilde A. A., Janse M. J. Electrophysiological effects of ATP sensitive potassium channel modulation: implications for arrhythmogenesis Cardiovascular research 1994;28 (1):16-24 [PubMed]
  • Wilde A. A. K+ ATP-channel opening and arrhythmogenesis Journal of cardiovascular pharmacology 1994;24 (Suppl. 4):S35-S40 [PubMed]
  • Wilde A. A., Veldkamp M. W., van Ginneken A. C., Opthof T. Phentolamine blocks ATP sensitive potassium channels in cardiac ventricular cells Cardiovascular research 1994;28 (6):847-850 [PubMed]

1993

  • Wilde A. A. Het ATP-gevoelige kaliumkanaal: functie en de mogelijkheden van farmacologische beïnvloeding Nederlands tijdschrift voor geneeskunde 1993;137 (22):1086-1090 [PubMed]
  • Wilde A. A. Role of ATP-sensitive K+ channel current in ischemic arrhythmias Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy 1993;7 (Suppl. 3):521-526 [PubMed]
  • von Kaenel W. E., Bloomfield E. L., Amaranath L., Wilde A. A. Vancomycin does not enhance hypotension under anesthesia Anesthesia and analgesia 1993;76 (4):809-811 [PubMed]

1992

  • Wilde A. A. KATP channel opening and cardioprotection Cardiovascular research 1992;26 (11):1156-1157 [PubMed]
  • de Jong F., Opthof T., Wilde A. A., Janse M. J., Charles R., Lamers W. H., Moorman A. F. Persisting zones of slow impulse conduction in developing chicken hearts Circulation research 1992;71 (2):240-250 [PubMed]

1991

  • Wilde A. A., Kléber A. G. Effect of norepinephrine and heart rate on intracellular sodium activity and membrane potential in beating guinea pig ventricular muscle Circulation research 1991;68 (5):1482-1489 [PubMed]
  • Tranum-Jensen J., Wilde A. A., Vermeulen J. T., Janse M. J. Morphology of electrophysiologically identified junctions between Purkinje fibers and ventricular muscle in rabbit and pig hearts Circulation research 1991;69 (2):429-437 [PubMed]
  • Wilde Arthur A. M., Schumacher Clemens A., Fiolet Johannes W. T. Opening and blocking the ATP-sensitive K+ channel and K+ accumulation in the isolated ischemic rabbit heart. New Trends in Arrhythmias 1991;VII:49-54
  • Hauer R. N., de Bakker J. M., de Wilde Arthur A. M., Straks W., Vermeulen J. T., Janse M. J. Ventricular tachycardia after in vivo DC shock ablation in dogs. Electrophysiologic and histologic correlation Circulation 1991;84 (1):267-278 [PubMed]

1990

  • Sanchis J., Opthof Tobias, Wilde Arthur A. M., Janse Michiel J. Mutual electronic interaction between the rabbit sinoatrial and atrioventricular node. Journal of cardiovascular electrophysiology 1990;1:318-326
  • Wilde A. A., Escande D., Schumacher C. A., Thuringer D., Mestre M., Fiolet J. W., Janse M. J. Potassium accumulation in the globally ischemic mammalian heart. A role for the ATP-sensitive potassium channel Circulation research 1990;67 (4):835-843 [PubMed]
  • de Jong F., Opthof Tobias, Wilde Arthur A. M., Janse Michiel J, Lamers Wouter H., Moorman Antonius F. M. Subpopulations of cardiomyocytes in the embryonic chicken heart. Annals of the New York Academy of Sciences 1990;588:354-356
  • de Bakker J. M., Coronel R., Tasseron S., Wilde A. A., Opthof T., Janse M. J., van Capelle F. J., Becker A. E., Jambroes G. Ventricular tachycardia in the infarcted, Langendorff-perfused human heart: role of the arrangement of surviving cardiac fibers Journal of the American College of Cardiology 1990;15 (7):1594-1607 [PubMed]

1989

  • Wilde A. A., Escande D., Schumacher C. A., Thuringer D., Mestre M., Fiolet J. W. Glibenclamide inhibition of ATP-sensitive K+ channels and ischemia-induced K+ accumulation in the mammalian heart Pflugers Archiv 1989;414 (Suppl. 1):S176 [PubMed]

1988

  • Wilde A. A., Peters R. J., Janse M. J. Catecholamine release and potassium accumulation in the isolated globally ischemic rabbit heart Journal of molecular and cellular cardiology 1988;20 (10):887-896 [PubMed]
  • Janse Michiel J., Wilms-Schopman Francisca J. G., Opthof Tobias, Vermeulen J. T., Wilde Arthur A. M. Characteristics of ventricular fibrillation induced by acute myocardial ischemia. New Trends in Arrhythmias 1988;I-II:251
  • de Bakker J. M., van Capelle F. J., Janse M. J., Wilde A. A., Coronel R., Becker A. E., Dingemans K. P., van Hemel N. M., Hauer R. N. Reentry as a cause of ventricular tachycardia in patients with chronic ischemic heart disease: electrophysiologic and anatomic correlation Circulation 1988;77 (3):589-606 [PubMed]

1986

  • Kléber A. G., Janse M. J., Wilms-Schopmann F. J., Wilde A. A., Coronel R. Changes in conduction velocity during acute ischemia in ventricular myocardium of the isolated porcine heart Circulation 1986;73 (1):189-198 [PubMed]
  • Kleber A. G., Wilde A. A. Regulation of intracellular sodium ions in acute reversible myocardial ischemia--a perspective Journal of molecular and cellular cardiology 1986;18 (Suppl. 4):27-30 [PubMed]
  • Wilde A. A., Kléber A. G. The combined effects of hypoxia, high K+, and acidosis on the intracellular sodium activity and resting potential in guinea pig papillary muscle Circulation research 1986;58 (2):249-256 [PubMed]
  • Wilensky R. L., Tranum-Jensen J., Coronel R., Wilde A. A., Fiolet J. W., Janse M. J. The subendocardial border zone during acute ischemia of the rabbit heart: an electrophysiologic, metabolic, and morphologic correlative study Circulation 1986;74 (5):1137-1146 [PubMed]

1984

  • Kodama I., Wilde Arthur A. M., Janse Michiel J, Durrer D., Yamada K. Combined effects of hypoxia, hyperkalemia and acidosis on membrane action potential and excitabil¬ity of guinea-pig ventricular muscle. Journal of molecular and cellular cardiology 1984;16:247-259