Prof. C. Bezzina PhD publications

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Publications Prof. PhD C. Bezzina

Position
Full Professor
Main activities
Research
Specialisation
Genetics of cardiac disorders
Focus of research

Our group conducts translational research aimed at identifiying genetic risk factors underlying cardiac disorders. Our research focuses on:

- Inherited disorders associated with increased risk of sudden cardiac death in young individuals. This includes the primary electrical disorders (e.g. the Long QT Syndrome, cardiac conduction disease and Brugada Syndrome) and the cardiomyopathies (e.g. hypertrophic cardiomyopathy).

- Risk of sudden cardiac death in the setting of acquired cardiac disease, namely ventricular fibrillation in the setting of acute myocardial ischemia or infarction.

- Congenital heart disease.

 

Besides efforts related to gene discovery, we also conduct functional studies in experimental model systems (e.g., transgenic mice, cardiomyocytes derived from induced pluripotent stem cells) on newly-identified genes or mutations. This allows us to gain insight into the involvement of the given gene or mutation into the pathophysiological mechanism underlying the diseases.

 

In our research we use amongst others the following tools:

Exome sequencing

Genomewide association studies

Expression QTL studies

Transgenesis

Electrophysiological studies (e.g. patch-clamp, optical mapping)
 

2021

  • Harper Andrew R., Goel Anuj, Grace Christopher, Thomson Kate L., Petersen Steffen E., Xu Xiao, Waring Adam, Ormondroyd Elizabeth, Kramer Christopher M., Ho Carolyn Y., Neubauer Stefan, Kolm Paul, Kwong Raymond, Dolman Sarahfaye F., Desvigne-Nickens Patrice, Dimarco John P., Geller Nancy, Kim Dong-Yun, Zhang Cheng, Weintraub William, Abraham Theodore, Anderson Lisa, Appelbaum Evan, Autore Camillo, Berry Colin, Biagini Elena, Bradlow William, Bucciarelli-Ducci Chiara, Chiribiri Amedeo, Choudhury Lubna, Crean Andrew, Dawson Dana, Desai Milind Y., Elstein Eleanor, Flett Andrew, Friedrich Matthias, Heitner Stephen, Helms Adam, Jacoby Daniel L., Kim Han, Kim Bette, Larose Eric, Mahmod Masliza, Mahrholdt Heiko, Maron Martin, McCann Gerry, Michels Michelle, Mohiddin Saidi, Nagueh Sherif, Bezzina Connie R. Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity Nature genetics 2021 [PubMed]
  • Verkerk Arie O., Knottnerus Suzan J. G., Portero Vincent, Bleeker Jeannette C., Ferdinandusse Sacha, Guan Kaomei, IJlst Lodewijk, Visser Gepke, Wanders Ronald J. A., Wijburg Frits A., Bezzina Connie R., Mengarelli Isabella, Houtkooper Riekelt H. Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation Frontiers in pharmacology 2021;11
  • Walsh Roddy, Lahrouchi Najim, Tadros Rafik, Kyndt Florence, Glinge Charlotte, Postema Pieter G., Amin Ahmad S., Nannenberg Eline A., Ware James S., Whiffin Nicola, Mazzarotto Francesco, Škorić-Milosavljević Doris, Krijger Christian, Arbelo Elena, Babuty Dominique, Barajas-Martinez Hector, Beckmann Britt M., Bézieau Stéphane, Bos J. Martijn, Breckpot Jeroen, Campuzano Oscar, Castelletti Silvia, Celen Candan, Clauss Sebastian, Corveleyn Anniek, Crotti Lia, Dagradi Federica, de Asmundis Carlo, Denjoy Isabelle, Dittmann Sven, Ellinor Patrick T., Ortuño Cristina Gil, Giustetto Carla, Gourraud Jean-Baptiste, Hazeki Daisuke, Horie Minoru, Ishikawa Taisuke, Itoh Hideki, Kaneko Yoshiaki, Kanters J. rgen K., Kimoto Hiroki, Kotta Maria-Christina, Krapels Ingrid P. C., Kurabayashi Masahiko, Lazarte Julieta, Leenhardt Antoine, Loeys Bart L., Robyns Tomas, Barc Julien, Bezzina Connie R. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls Genetics in medicine 2021;23 (1):47-58 [PubMed]
  • Mazzarotto Francesco, Hawley Megan H., Beltrami Matteo, Beekman Leander, de Marvao Antonio, McGurk Kathryn A., Statton Ben, Boschi Beatrice, Girolami Francesca, Roberts Angharad M., Lodder Elisabeth M., Allouba Mona, Romeih Soha, Aguib Yasmine, Baksi A. John, Pantazis Antonis, Prasad Sanjay K., Cerbai Elisabetta, Yacoub Magdi H., O’Regan Declan P., Cook Stuart A., Ware James S., Funke Birgit, Olivotto Iacopo, Bezzina Connie R., Barton Paul J. R., Walsh Roddy Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies Genetics in medicine 2021 [PubMed]

2020

  • 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]
  • 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.)
  • Knottnerus Suzan J. G., Mengarelli Isabella, Wüst Rob C. I., Baartscheer Antonius, Bleeker Jeannette C., Coronel Ruben, Ferdinandusse Sacha, Guan Kaomei, Ijlst Lodewijk, Li Wener, Luo Xiaojing, Portero Vincent M., Ulbricht Ying, Visser Gepke, Wanders Ronald J. A., Wijburg Frits A., Verkerk Arie O., Houtkooper Riekelt H., Bezzina Connie R. Electrophysiological abnormalities in VLCAD deficient hiPSC-cardiomyocytes can be improved by lowering accumulation of fatty acid oxidation intermediates International journal of molecular sciences 2020;21 (7) [PubMed]
  • Offerhaus Joost A., Bezzina Connie R., Wilde Arthur A. M. Epidemiology of inherited arrhythmias Nature reviews. Cardiology 2020;17 (4):205-215 [PubMed]
  • Glinge Charlotte, Engstrøm Thomas, Midgley Sofie E., Tanck Michael W. T., Madsen Jeppe Ekstrand Halkjær, Pedersen Frants, Jacobsen Mia Ravn, Lodder Elisabeth M., Al-Hussainy Nour R., Stampe Niels Kjær, Trebbien Ramona, Køber Lars, Gerds Thomas, Torp-Pedersen Christian, Fischer Thea K. lsen, Bezzina Connie R., Tfelt-Hansen Jacob, Jabbari Reza Erratum: Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposure (PLoS ONE (2020)15:2(e0226936)Doi: 10.1371/journal.pone.0226936) PLoS ONE 2020;15 (4) [PubMed]
  • Rivaud Mathilde R., Marchal Gerard A., Wolswinkel Rianne, Jansen John A., van der Made Ingeborg, Beekman Leander, Ruiz-Villalba Adrián, Baartscheer Antonius, Rajamani Sridharan, Belardinelli Luiz, van Veen Toon A. B., Basso Cristina, Thiene Gaetano, Creemers Esther E., Bezzina Connie R., Remme Carol Ann Functional modulation of atrio-ventricular conduction by enhanced late sodium current and calcium-dependent mechanisms in Scn5a1798insD/+ mice EP Europace 2020;22 (10):1579-1589 [PubMed]
  • Glinge Charlotte, Lahrouchi Najim, Jabbari Reza, Tfelt-Hansen Jacob, Bezzina Connie R. Genome-wide association studies of cardiac electrical phenotypes Cardiovascular research 2020;116 (9):1620-1634 [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]
  • Walsh Roddy, Bezzina Connie R. Research in understudied populations offers local and global insights into the genetics of hypertrophic cardiomyopathy Polskie archiwum medycyny wewnetrznej 2020;130 (2):76-78 [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]
  • Patel Jyoti, Bezzina Connie R. Scientists on the Spot: The complex inheritance of cardiac disorders Cardiovascular research 2020;116 (1):e11 [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]
  • Glinge Charlotte, Engstrøm Thomas, Midgley Sofie E., Tanck Michael W. T., Halkjær Madsen Jeppe Ekstrand, Pedersen Frants, Jacobsen Mia Ravn, Lodder Elisabeth M., Al-Hussainy Nour R., Stampe Niels Kjær, Trebbien Ramona, Køber Lars, Gerds Thomas, Torp-Pedersen Christian, Fischer Thea K. lsen, Bezzina Connie R., Tfelt-Hansen Jacob, Jabbari Reza Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposure PLoS ONE 2020;15 (2) [PubMed]
  • Glinge Charlotte, Oestergaard Louise, Jabbari Reza, Rossetti Sara, Skals Regitze, Køber Lars, Engstrøm Thomas, Bezzina Connie R., Torp-Pedersen Christian, Gislason Gunnar, Tfelt-Hansen Jacob Sibling history is associated with heart failure after a first myocardial infarction Open heart 2020;7 (1) [PubMed]
  • 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]
  • Walsh Roddy, Tadros Rafik, Bezzina Connie R. When genetic burden reaches threshold European heart journal 2020;41 (39):3849-3855 [PubMed]

2019

  • 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]
  • Cerrone Marina, Remme Carol Ann, Tadros Rafik, Bezzina Connie R., Delmar Mario Beyond the One Gene-One Disease Paradigm Circulation 2019;140 (7):595-610 [PubMed]
  • Vandenwijngaert Sara, Ledsky Clara D., Lahrouchi Najim, Khan Mohsin A. F., Wunderer Florian, Ames Lisa, Honda Toshiyuki, Diener John L., Bezzina Connie R., Buys Emmanuel S., Bloch Donald B., Newton-Cheh Christopher Blood Pressure-Associated Genetic Variants in the Natriuretic Peptide Receptor 1 Gene Modulate Guanylate Cyclase Activity Circulation. Genomic and precision medicine 2019;12 (8):e002472 [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]
  • Casini Simona, Albesa Maxime, Wang Zizun, Portero Vincent, Ross-Kaschitza Daniela, Rougier Jean-S. bastien, Marchal Gerard A., Chung Wendy K., Bezzina Connie R., Abriel Hugues, Remme Carol Ann Functional consequences of the scn5a-p.Y1977n mutation within the py ubiquitylation motif: Discrepancy between hek293 cells and transgenic mice International journal of molecular sciences 2019;20 (20) [PubMed]
  • Škorić-Milosavljević Doris, Tjong Fleur V. Y., Barc Julien, Backx Ad P. C. M., Clur Sally-Ann B., van Spaendonck-Zwarts Karin, Oostra Roelof-Jan, Lahrouchi Najim, Beekman Leander, Bökenkamp Regina, Barge-Schaapveld Daniela Q. C. M., Mulder Barbara J., Lodder Elisabeth M., Bezzina Connie R., Postma Alex V. GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum American journal of medical genetics. Part A 2019;179 (9):1836-1845 [PubMed]
  • Veerman Christiaan C., Mengarelli Isabella, Koopman Charlotte D., Wilders Ronald, van Amersfoorth Shirley C., Bakker Diane, Wolswinkel Rianne, Hababa Mariam, de Boer Teun P., Guan Kaomei, Milnes James, Lodder Elisabeth M., Bakkers Jeroen, Verkerk Arie O., Bezzina Connie R. Genetic variation in GNB5 causes bradycardia by augmenting the cholinergic response via increased acetylcholine-activated potassium current (IK,ACh) Disease models & mechanisms 2019;12 (7) [PubMed]
  • Lahrouchi Najim, George Aman, Ratbi Ilham, Schneider Ronen, Elalaoui Siham C, Moosa Shahida, Bharti Sanita, Sharma Ruchi, Abu-Asab Mones, Onojafe Felix, Adadi Najlae, Lodder Elisabeth M, Laarabi Fatima-Zahra, Lamsyah Yassine, Elorch Hamza, Chebbar Imane, Postma Alex V, Lougaris Vassilios, Plebani Alessandro, Altmueller Janine, Kyrieleis Henriette, Meiner Vardiella, McNeill Helen, Bharti Kapil, Lyonnet Stanislas, Wollnik Bernd, Henrion-Caude Alexandra, Berraho Amina, Hildebrandt Friedhelm, Bezzina Connie R, Brooks Brian P, Sefiani Abdelaziz Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly Nature communications 2019;10 (1):1180 [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.)
  • 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]
  • Bezzina Connie R., Walsh Roddy, Lahrouchi Najim Predicting Risk for Adult-Onset Sudden Cardiac Death in the Population Journal of the American College of Cardiology 2019;74 (21):2635-2637 [PubMed]
  • 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]
  • Page Donna J., Miossec Matthieu J., Williams Simon G., Monaghan Richard M., Fotiou Elisavet, Cordell Heather J., Sutcliffe Louise, Topf Ana, Bourgey Mathieu, Bourque Guillaume, Eveleigh Robert, Dunwoodie Sally L., Winlaw David S., Bhattacharya Shoumo, Breckpot Jeroen, Devriendt Koenraad, Gewillig Marc, Brook J. David, Setchfield Kerry J., Bu'Lock Frances A., O'Sullivan John, Stuart Graham, Bezzina Connie R., Mulder Barbara J. M., Postma Alex V., Bentham James R., Baron Martin, Bhaskar Sanjeev S., Black Graeme C., Newman William G., Hentges Kathryn E., Lathrop G. Mark, Santibanez-Koref Mauro, Keavney Bernard D. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot Circulation research 2019;124 (4):553-563 [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]
  • Montnach Jerome, Agullo-Pascual Esperanza, Tadros Rafik, Bezzina Connie R., Delmar Mario Bioinformatic analysis of a plakophilin-2-dependent transcription network: implications for the mechanisms of arrhythmogenic right ventricular cardiomyopathy in humans and in boxer dogs Europace : European pacing, arrhythmias, and cardiac electrophysiology 2018;20 (3):iii125-iii132 [PubMed]
  • dos Remedios C. G., Lal S. P., Li A., McNamara J., Keogh A., Macdonald P. S., Cooke R., Ehler E., Knöll R., Marston S. B., Stelzer J., Granzier H., Bezzina C., van Dijk S., de Man F., Stienen G. J. M., Odeberg J., Pontén F., Linke W. A., van der Velden J. Correction to: The Sydney Heart Bank: improving translational research while eliminating or reducing the use of animal models of human heart disease (Biophysical Reviews, (2017), 9, 4, (431-441), 10.1007/s12551-017-0305-3) Biophysical Reviews 2018;10 (3):941 [PubMed]
  • Rivaud Mathilde Diversity and complexity of cardiac sodium channel (dys)function: Relevance for arrhythmias in inherited and acquired diseases 2018. ISBN 9789402810233. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Bezzina C. R.; Co-supervisors: Remme C. A., Creemers E. E. J. M.)
  • Rivaud Mathilde R., Baartscheer Antonius, Verkerk Arie O., Beekman Leander, Rajamani Sridharan, Belardinelli Luiz, Bezzina Connie R., Remme Carol Ann Enhanced late sodium current underlies pro-arrhythmic intracellular sodium and calcium dysregulation in murine sodium channelopathy International journal of cardiology 2018;263:54-62 [PubMed]
  • Adriaens M. E., Bezzina C. R. Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits Biophysical Reviews 2018;10 (4):1053-1060 [PubMed]
  • Ma Dongrui, Liu Zhenfeng, Loh Li Jun, Zhao Yongxing, Li Guang, Liew Reginald, Islam Omedul, Wu Jianjun, Chung Ying Ying, Teo Wee Siong, Ching Chi Keong, Tan Boon Yew, Chong Daniel, Ho Kah Leng, Lim Paul, Yong Rita Yu Yin, Panama Brian K., Kaplan Aaron D., Bett Glenna C. L., Ware James, Bezzina Connie R., Verkerk Arie O., Cook Stuart A., Rasmusson Randall L., Wei Heming Identification of an I Na-dependent and I to-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient Scientific reports 2018;8 (1) [PubMed]
  • Adadi Najlae, Radi Fatima Zohra, Lahrouchi Najim, Hara Loubna, Ratbi Ilham, Elalaoui Siham Chafai, Alders Marielle, Zarzur Jamila, Bezzina Connie, Sefiani Abdelaziz Inherited dilated cardiomyopathy in a large moroccan family caused by LMNA mutation Anatolian Journal of Cardiology 2018;20 (1):65-68 [PubMed]
  • Adriaens Michiel E., Lodder Elisabeth M., Moreno-Moral Aida, Silhavý Jan, Heinig Matthias, Glinge Charlotte, Belterman Charly, Wolswinkel Rianne, Petretto Enrico, Pravenec Michal, Remme Carol Ann, Bezzina Connie R. Systems genetics approaches in rat identify novel genes and gene networks associated with cardiac conduction Journal of the American Heart Association 2018;7 (21) [PubMed]

2017

  • 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]
  • Hoorntje Edgar T., te Rijdt Wouter P., James Cynthia A., Pilichou Kalliopi, Basso Cristina, Judge Daniel P., Bezzina Connie R., van Tintelen J. Peter Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis Cardiovascular research 2017;113 (12):1521-1531 [PubMed]
  • Adadi N., Lahrouchi N., Bouhouch R., Fellat I., Amri R., Alders M., Sefiani A., Bezzina C., Ratbi I. Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report Journal of medical case reports 2017;11 (1) [PubMed]
  • Podliesna Svitlana, Bezzina Connie R., Lodder Elisabeth M. Complex Genetics of Cardiovascular Traits in Mice: F2-Mapping of QTLs and Their Underlying Genes Methods in molecular biology (Clifton, N.J.) 2017;1488:431-454 [PubMed]
  • Tadros Rafik, Coronel Ruben, Bezzina Connie R. Dissecting the Genetic Basis of the ECG as a Means of Understanding Mechanisms of Arrhythmia Circulation. Cardiovascular genetics 2017;10 (4):UNSP e001858 [PubMed]
  • Lahrouchi Najim, Lodder Elisabeth M., Mansouri Maria, Tadros Rafik, Zniber Layla, Adadi Najlae, Clur Sally-Ann B., van Spaendonck-Zwarts Karin Y., Postma Alex V., Sefiani Abdelaziz, Ratbi Ilham, Bezzina Connie R. Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death European journal of human genetics 2017;25 (6):783-787 [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]
  • 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]
  • Lodder Elisabeth M., Verkerk Arie O., Bezzina Connie R. G-Protein beta Subunit Mutations in Sinus Node Dysfunction Circulation research 2017;120 (10):1524-1526 [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)
  • 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.)
  • 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]
  • Heinig Matthias, Adriaens Michiel E., Schafer Sebastian, van Deutekom Hanneke W. M., Lodder Elisabeth M., Ware James S., Schneider Valentin, Felkin Leanne E., Creemers Esther E., Meder Benjamin, Katus Hugo A., Rühle Frank, Stoll Monika, Cambien François, Villard Eric, Charron Philippe, Varro Andras, Bishopric Nanette H., George Alfred L., Dos Remedios Cristobal, Moreno-Moral Aida, Pesce Francesco, Bauerfeind Anja, Rüschendorf Franz, Rintisch Carola, Petretto Enrico, Barton Paul J., Cook Stuart A., Pinto Yigal M., Bezzina Connie R., Hubner Norbert Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy Genome biology 2017;18 (1) [PubMed]
  • Verkerk Arie O., Veerman Christiaan C., Zegers Jan G., Mengarelli Isabella, Bezzina Connie R., Wilders Ronald Patch-Clamp Recording from Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Improving Action Potential Characteristics through Dynamic Clamp International journal of molecular sciences 2017;18 (9) [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]
  • Rivaud Mathilde R., Agullo-Pascual Esperanza, Lin Xianming, Leo-Macias Alejandra, Zhang Mingliang, Rothenberg Eli, Bezzina Connie R., Delmar Mario, Remme Carol Ann Sodium Channel Remodeling in Subcellular Microdomains of Murine Failing Cardiomyocytes Journal of the American Heart Association 2017;6 (12):e007622 [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]
  • 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

  • van der Harst Pim, van Setten Jessica, Verweij Niek, Vogler Georg, Franke Lude, Maurano Matthew T., Wang Xinchen, Mateo Leach Irene, Eijgelsheim Mark, Sotoodehnia Nona, Hayward Caroline, Sorice Rossella, Meirelles Osorio, Lyytikäinen Leo-Pekka, Polašek Ozren, Tanaka Toshiko, Arking Dan E., Ulivi Sheila, Trompet Stella, Müller-Nurasyid Martina, Smith Albert V., Dörr Marcus, Kerr Kathleen F., Magnani Jared W., del Greco M Fabiola, Zhang Weihua, Nolte Ilja M., Silva Claudia T., Padmanabhan Sandosh, Tragante Vinicius, Esko Tõnu, Abecasis Gonçalo R., Adriaens Michiel E., Andersen Karl, Barnett Phil, Bis Joshua C., Bodmer Rolf, Buckley Brendan M., Campbell Harry, Cannon Megan V., Chakravarti Aravinda, Chen Lin Y., Delitala Alessandro, Devereux Richard B., Doevendans Pieter A., Dominiczak Anna F., Ferrucci Luigi, Ford Ian, Gieger Christian, Harris Tamara B., Haugen Eric, Heinig Matthias, Hernandez Dena G., Hillege Hans L., Hirschhorn Joel N., Hofman Albert, Hubner Norbert, Hwang Shih-Jen, Iorio Annamaria, Kähönen Mika, Kellis Manolis, Kolcic Ivana, Kooner Ishminder K., Kooner Jaspal S., Kors Jan A., Lakatta Edward G., Lage Kasper, Launer Lenore J., Levy Daniel, Lundby Alicia, Macfarlane Peter W., May Dalit, Meitinger Thomas, Metspalu Andres, Nappo Stefania, Naitza Silvia, Neph Shane, Nord Alex S., Nutile Teresa, Okin Peter M., Olsen Jesper V., Oostra Ben A., Penninger Josef M., Pennacchio Len A., Pers Tune H., Perz Siegfried, Peters Annette, Pinto Yigal M., Pfeufer Arne, Pilia Maria Grazia, Pramstaller Peter P., Prins Bram P., Raitakari Olli T., Raychaudhuri Soumya, Rice Ken M., Rossin Elizabeth J., Rotter Jerome I., Schafer Sebastian, Schlessinger David, Schmidt Carsten O., Sehmi Jobanpreet, Silljé Herman H. W., Sinagra Gianfranco, Sinner Moritz F., Slowikowski Kamil, Soliman Elsayed Z., Spector Timothy D., Spiering Wilko, Stamatoyannopoulos John A., Stolk Ronald P., Strauch Konstantin, Tan Sian-Tsung, Tarasov Kirill V., Trinh Bosco, Uitterlinden Andre G., van den Boogaard Malou, van Duijn Cornelia M., van Gilst Wiek H., Viikari Jorma S., Visscher Peter M., Vitart Veronique, Völker Uwe, Waldenberger Melanie, Weichenberger Christian X., Westra Harm-Jan, Wijmenga Cisca, Wolffenbuttel Bruce H., Yang Jian, Bezzina Connie R., Munroe Patricia B., Snieder Harold, Wright Alan F., Rudan Igor, Boyer Laurie A., Asselbergs Folkert W., van Veldhuisen Dirk J., Stricker Bruno H., Psaty Bruce M., Ciullo Marina, Sanna Serena, Lehtimäki Terho, Wilson James F., Bandinelli Stefania, Alonso Alvaro, Gasparini Paolo, Jukema J. Wouter, Kääb Stefan, Gudnason Vilmundur, Felix Stephan B., Heckbert Susan R., de Boer Rudolf A., Newton-Cheh Christopher, Hicks Andrew A., Chambers John C., Jamshidi Yalda, Visel Axel, Christoffels Vincent M., Isaacs Aaron, Samani Nilesh J., de Bakker Paul I. W. 52 Genetic Loci Influencing Myocardial Mass Journal of the American College of Cardiology 2016;68 (13):1435-1448 [PubMed]
  • Lahrouchi N., Bezzina C. R. Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role? Netherlands heart journal 2016;24 (1):11-15 [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]
  • 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]
  • 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.)
  • Postma Alex V., Bezzina Connie R., Christoffels Vincent M. Genetics of congenital heart disease: the contribution of the noncoding regulatory genome Journal of human genetics 2016;61 (1):13-19 [PubMed]
  • Nicod Jérôme, Davies Robert W., Cai Na, Hassett Carl, Goodstadt Leo, Cosgrove Cormac, Yee Benjamin K., Lionikaite Vikte, McIntyre Rebecca E., Remme Carol Ann, Lodder Elisabeth M., Gregory Jennifer S., Hough Tertius, Joynson Russell, Phelps Hayley, Nell Barbara, Rowe Clare, Wood Joe, Walling Alison, Bopp Nasrin, Bhomra Amarjit, Hernandez-Pliego Polinka, Callebert Jacques, Aspden Richard M., Talbot Nick P., Robbins Peter A., Harrison Mark, Fray Martin, Launay Jean-Marie, Pinto Yigal M., Blizard David A., Bezzina Connie R., Adams David J., Franken Paul, Weaver Tom, Wells Sara, Brown Steve D. M., Potter Paul K., Klenerman Paul, Lionikas Arimantas, Mott Richard, Flint Jonathan Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing Nature genetics 2016;48 (8):912-918 [PubMed]
  • Creemers Esther E., Bawazeer Amira, Ugalde Alejandro P., van Deutekom Hanneke W. M., van der Made Ingeborg, de Groot Nina E., Adriaens Michiel E., Cook Stuart A., Bezzina Connie R., Hubner Norbert, van der Velden Jolanda, Elkon Ran, Agami Reuven, Pinto Yigal M. Genome-Wide Polyadenylation Maps Reveal Dynamic mRNA 3'-End Formation in the Failing Human Heart Circulation research 2016;118 (3):433-438 [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]
  • Lahrouchi Najim, Behr Elijah R., Bezzina Connie R. Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death Cases Frontiers in cardiovascular medicine 2016;3:13 [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]
  • 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]
  • 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]
  • 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]
  • Bezzina Connie R., Lahrouchi Najim, Priori Silvia G. Genetics of sudden cardiac death Circulation research 2015;116 (12):1919-1936 [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]
  • 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.)
  • Milano Annalisa, Lodder Elisabeth M., Bezzina Connie R. TNNI3K in cardiovascular disease and prospects for therapy Journal of molecular and cellular cardiology 2015;82:167-173 [PubMed]
  • Milano Annalisa Understanding cardiac electrical phenotypes in the genomic era 2015. 164p. ISBN 9789462951044. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Bezzina C. R.; Co-supervisor: Lodder E. M.)

2014

  • van den Boogaard Malou, Smemo Scott, Burnicka-Turek Ozanna, Arnolds David E., van de Werken Harmen J. G., Klous Petra, McKean David, Muehlschlegel Jochen D., Moosmann Julia, Toka Okan, Yang Xinan H., Koopmann Tamara T., Adriaens Michiel E., Bezzina Connie R., de Laat Wouter, Seidman Christine, Seidman J. G., Christoffels Vincent M., Nobrega Marcelo A., Barnett Phil, Moskowitz Ivan P. A common genetic variant within SCN10A modulates cardiac SCN5A expression Journal of clinical investigation 2014;124 (4):1844-1852 [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]
  • Bezzina Connie R. Common genetic variation and risk for sudden cardiac death in acquired cardiac disease Heart rhythm 2014;11 (4):653-654 [PubMed]
  • 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]
  • Mizusawa Yuka, Bezzina Connie R. Early repolarization pattern: its ECG characteristics, arrhythmogeneity and heritability Journal of interventional cardiac electrophysiology 2014;39 (3):185-192 [PubMed]
  • Tragante Vinicius, Barnes Michael R., Ganesh Santhi K., Lanktree Matthew B., Guo Wei, Franceschini Nora, Smith Erin N., Johnson Toby, Holmes Michael V., Padmanabhan Sandosh, Karczewski Konrad J., Almoguera Berta, Barnard John, Baumert Jens, Chang Yen-Pei Christy, Elbers Clara C., Farrall Martin, Fischer Mary E., Gaunt Tom R., Gho Johannes M. I. H., Gieger Christian, Goel Anuj, Gong Yan, Isaacs Aaron, Kleber Marcus E., Mateo Leach Irene, McDonough Caitrin W., Meijs Matthijs F. L., Melander Olle, Nelson Christopher P., Nolte Ilja M., Pankratz Nathan, Price Tom S., Shaffer Jonathan, Shah Sonia, Tomaszewski Maciej, van der Most Peter J., van Iperen Erik P. A., Vonk Judith M., Witkowska Kate, Wong Caroline O. L., Zhang Li, Beitelshees Amber L., Berenson Gerald S., Bhatt Deepak L., Brown Morris, Burt Amber, Cooper-DeHoff Rhonda M., Connell John M., Cruickshanks Karen J., Curtis Sean P., Davey-Smith George, Delles Christian, Gansevoort Ron T., Guo Xiuqing, Haiqing Shen, Hastie Claire E., Hofker Marten H., Hovingh G. Kees, Kim Daniel S., Kirkland Susan A., Klein Barbara E., Klein Ronald, Li Yun R., Maiwald Steffi, Newton-Cheh Christopher, O'Brien Eoin T., Onland-Moret N. Charlotte, Palmas Walter, Parsa Afshin, Penninx Brenda W., Pettinger Mary, Vasan Ramachandran S., Ranchalis Jane E., M Ridker Paul, Rose Lynda M., Sever Peter, Shimbo Daichi, Steele Laura, Stolk Ronald P., Thorand Barbara, Trip Mieke D., van Duijn Cornelia M., Verschuren W. Monique, Wijmenga Cisca, Wyatt Sharon, Young J. Hunter, Zwinderman Aeilko H., Bezzina Connie R., Boerwinkle Eric, Casas Juan P., Caulfield Mark J., Chakravarti Aravinda, Chasman Daniel I., Davidson Karina W., Doevendans Pieter A., Dominiczak Anna F., FitzGerald Garret A., Gums John G., Fornage Myriam, Hakonarson Hakon, Halder Indrani, Hillege Hans L., Illig Thomas, Jarvik Gail P., Johnson Julie A., Kastelein John J. P., Koenig Wolfgang, Kumari Meena, März Winfried, Murray Sarah S., O'Connell Jeffery R., Oldehinkel Albertine J., Pankow James S., Rader Daniel J., Redline Susan, Reilly Muredach P., Schadt Eric E., Kottke-Marchant Kandice, Snieder Harold, Snyder Michael, Stanton Alice V., Tobin Martin D., Uitterlinden André G., van der Harst Pim, van der Schouw Yvonne T., Samani Nilesh J., Watkins Hugh, Johnson Andrew D., Reiner Alex P., Zhu Xiaofeng, de Bakker Paul I. W., Levy Daniel, Asselbergs Folkert W., Munroe Patricia B., Keating Brendan J. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci American journal of human genetics 2014;94 (3):349-360 [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.)
  • Marsman Roos F., Tan Hanno L., Bezzina Connie R. Genetics of sudden cardiac death caused by ventricular arrhythmias Nature reviews. Cardiology 2014;11 (2):96-111 [PubMed]
  • Koopmann Tamara T., Adriaens Michiel E., Moerland Perry D., Marsman Roos F., Westerveld Margriet L., Lal Sean, Zhang Taifang, Simmons Christine Q., Baczko Istvan, Dos Remedios Cristobal, Bishopric Nanette H., Varro Andras, George Alfred L., Lodder Elisabeth M., Bezzina Connie R. Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart PLoS ONE 2014;9 (5):e97380 [PubMed]
  • Lodder Elisabeth M., Bezzina Connie R. Genomics of cardiac electrical function Briefings in functional genomics 2014;13 (1):39-50 [PubMed]
  • 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]
  • Lodder Elisabeth M., Scicluna Brendon P., Beekman Leander, Arends Danny, Moerland Perry D., Tanck Michael W. T., Adriaens Michiel E., Bezzina Connie R. Integrative genomic approach identifies multiple genes involved in cardiac collagen deposition Circulation. Cardiovascular genetics 2014;7 (6):790-798 [PubMed]
  • Shy Diana, Gillet Ludovic, Ogrodnik Jakob, Albesa Maxime, Verkerk Arie O., Wolswinkel Rianne, Rougier Jean-Sébastien, Barc Julien, Essers Maria C., Syam Ninda, Marsman Roos F., van Mil Anneke M., Rotman Samuel, Redon Richard, Bezzina Connie R., Remme Carol Ann, Abriel Hugues PDZ domain-binding motif regulates cardiomyocyte compartment-specific NaV1.5 channel expression and function Circulation 2014;130 (2):147-160 [PubMed]

2013

  • Zumhagen Sven, Veldkamp Marieke W., Stallmeyer Birgit, Baartscheer Antonius, Eckardt Lars, Paul Matthias, Remme Carol Ann, Bhuiyan Zahurul A., Bezzina Connie R., Schulze-Bahr Eric A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome PLoS ONE 2013;8 (6):e67963 [PubMed]
  • Lodder Elisabeth M., Bezzina Connie R. Arrhythmogenic right ventricular cardiomyopathy: growing evidence for complex inheritance Circulation. Cardiovascular genetics 2013;6 (6):525-527 [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]
  • Guo Yiran, Lanktree Matthew B., Taylor Kira C., Hakonarson Hakon, Lange Leslie A., Keating Brendan J., Fairfax Benjamin P., Elbers Clara C., Barnard John, Farrall Martin, Padmanabhan Sandosh, Baumert Jens, Castillo Berta A., Gaunt Tom R., Gong Yan, Rajagopalan Ramakrishnan, Romaine Simon P. R., Kumari Meena, Rafelt Suzanne, Smith Erin N., Li Yun R., Sivapalaratnam Suthesh, van Iperen Erik P. A., Speliotes Elizabeth K., Toskala Elina, Zhang Li, Ochs-Balcom Heather M., Bhangale Tushar R., Chandrupatla Hareesh R., Drenos Fotios, Gieger Christian, Gupta Jayanta, Johnson Toby, Kleber Marcus E., Makino Seiko, Mangino Massimo, Meng Yan, Nelson Christopher P., Pankow James S., Pankratz Nathan, Price Tom S., Shaffer Jonathan, Bezzina Connie R., Chen Wei, de Jong Jonas S., Zafarmand Mohammad H., Zwinderman Aeilko H., Hovingh Kees G., Kastelein John J. P., Trip Mieke D. Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals Human molecular genetics 2013;22 (1):184-201 [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]
  • Cordell Heather J., Bentham Jamie, Topf Ana, Zelenika Diana, Heath Simon, Mamasoula Chrysovalanto, Cosgrove Catherine, Blue Gillian, Granados-Riveron Javier, Setchfield Kerry, Thornborough Chris, Breckpot Jeroen, Soemedi Rachel, Martin Ruairidh, Rahman Thahira J., Hall Darroch, van Engelen Klaartje, Moorman Antoon F. M., Zwinderman Aelko H., Barnett Phil, Koopmann Tamara T., Adriaens Michiel E., Varro Andras, George Alfred L., Dos Remedios Christobal, Bishopric Nanette H., Bezzina Connie R., O'Sullivan John, Gewillig Marc, Bu'lock Frances A., Winlaw David, Bhattacharya Shoumo, Devriendt Koen, Brook J. David, Mulder Barbara J. M., Mital Seema, Postma Alex V., Lathrop G. Mark, Farrall Martin, Goodship Judith A., Keavney Bernard D. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 Nature genetics 2013;45 (7):822-824 [PubMed]
  • Boukens Bas J., Sylva Marc, de Gier-de Vries Corrie, Remme Carol Ann, Bezzina Connie R., Christoffels Vincent M., Coronel Ruben Reduced sodium channel function unmasks residual embryonic slow conduction in the adult right ventricular outflow tract Circulation research 2013;113 (2):137-141 [PubMed]
  • 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]
  • Bardai Abdennasser, Amin Ahmad S., Blom Marieke T., Bezzina Connie R., Berdowski Jocelyn, Langendijk Pim N. J., Beekman Leander, Klemens Christine A., Souverein Patrick C., Koster Rudolph W., de Boer Anthonius, Tan Hanno L. Sudden cardiac arrest associated with use of a non-cardiac drug that reduces cardiac excitability: evidence from bench, bedside, and community European heart journal 2013;34 (20):1506-1516 [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.)
  • 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]

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]
  • 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]
  • 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]
  • Kolder Iris C. R. M., Tanck Michael W. T., Bezzina Connie R. Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death Journal of molecular and cellular cardiology 2012;52 (3):620-629 [PubMed]
  • Lodder Elisabeth M., Scicluna Brendon P., Milano Annalisa, Sun Albert Y., Tang Hao, Remme Carol Ann, Moerland Perry D., Tanck Michael W. T., Pitt Geoffrey S., Marchuk Douglas A., Bezzina Connie R. Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction PLoS genetics 2012;8 (12):e1003113 [PubMed]
  • Verkerk Arie O., Remme Carol Ann, Schumacher Cees A., Scicluna Brendon P., Wolswinkel Rianne, de Jonge Berend, Bezzina Connie R., Veldkamp Marieke W. Functional Na(V)1.8 Channels in Intracardiac Neurons The Link Between SCN10A and Cardiac Electrophysiology Circulation research 2012;111 (3):333-343 [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.)
  • van den Boogaard Malou, Wong L. Y. Elaine, Tessadori Federico, Bakker Martijn L., Dreizehnter Lisa K., Wakker Vincent, Bezzina Connie R., 't Hoen Peter A. C., Bakkers Jeroen, Barnett Phil, Christoffels Vincent M. Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer Journal of clinical investigation 2012;122 (7):2519-2530 [PubMed]
  • Clarke Robert, Bennett Derrick A., Parish Sarah, Verhoef Petra, Dötsch-Klerk Mariska, Lathrop Mark, Xu Peng, Nordestgaard Børge G., Holm Hilma, Hopewell Jemma C., Saleheen Danish, Tanaka Toshihiro, Anand Sonia S., Chambers John C., Kleber Marcus E., Ouwehand Willem H., Yamada Yoshiji, Elbers Clara, Peters Bas, Stewart Alexandre F. R., Reilly Muredach M., Thorand Barbara, Yusuf Salim, Engert James C., Assimes Themistocles L., Kooner Jaspal, Danesh John, Watkins Hugh, Samani Nilesh J., Collins Rory, Peto Richard, Holm H., Thorsteinsdottir U., Gretarsdottir S., Gulcher J. R., Thorgeirsson G., Andersen K., Stefansson K., Parish S., Bennett D. A., Clarke R., Peto R., Sleight P., Collins R., Hopewell J. C., Watkins H., Kastelein J. J., Trip M. D., Bezzina C. R., Maitland-van der Zee A. H. Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias PLoS medicine 2012;9 (2):e1001177 [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]
  • Rizzo Stefania, Lodder Elisabeth M., Verkerk Arie O., Wolswinkel Rianne, Beekman Leander, Pilichou Kalliopi, Basso Cristina, Remme Carol Ann, Thiene Gaetano, Bezzina Connie R. Intercalated disc abnormalities, reduced Na+ current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes Cardiovascular research 2012;95 (4):409-418 [PubMed]
  • 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]
  • 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]
  • 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]
  • 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]
  • 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]

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]
  • Pilichou Kalliopi, Bezzina Connie R., Thiene Gaetano, Basso Cristina Arrhythmogenic cardiomyopathy: transgenic animal models provide novel insights into disease pathobiology Circulation. Cardiovascular genetics 2011;4 (3):318-326 [PubMed]
  • Postma Alex V., Christoffels Vincent M., Bezzina Connie R. Developmental aspects of cardiac arrhythmogenesis Cardiovascular research 2011;91 (2):243-251 [PubMed]
  • 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]
  • 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]
  • 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
  • van den Berg Maarten P., Bezzina Connie R. KCND3 mutations in Brugada syndrome: the plot thickens Heart rhythm 2011;8 (7):1033-1035 [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]
  • 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]
  • 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.)

2010

  • Remme Carol Ann, Bezzina Connie R. Cardiac desmosomal (dys)function and myocyte viability Cell cycle (Georgetown, Tex.) 2010;9 (7):1246-1252 [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]
  • Koopmann Tamara T., Bezzina Connie R. Genetics of lone atrial fibrillation Europace : European pacing, arrhythmias, and cardiac electrophysiology 2010;12 (10):1351-1352 [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]
  • Horn Denise, Kapeller Johannes, Rivera-Brugués Núria, Moog Ute, Lorenz-Depiereux Bettina, Eck Sebastian, Hempel Maja, Wagenstaller Janine, Gawthrope Alex, Monaco Anthony P., Bonin Michael, Riess Olaf, Wohlleber Eva, Illig Thomas, Bezzina Connie R., Franke Andre, Spranger Stephanie, Villavicencio-Lorini Pablo, Seifert Wenke, Rosenfeld Jochen, Klopocki Eva, Rappold Gudrun A., Strom Tim M. Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits Human mutation 2010;31 (11):E1851-E1860 [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]
  • Remme Carol Ann, Bezzina Connie R. Sodium Channel (Dys)Function and Cardiac Arrhythmias Cardiovascular therapeutics 2010;28 (5):287-294 [PubMed]
  • Casini Simona, Tan Hanno L., Demirayak Ilker, Remme Carol Ann, Amin Ahmad S., Scicluna Brendon P., Chatyan Houssine, Ruijter Jan M., Bezzina Connie R., van Ginneken Antoni C. G., Veldkamp Marieke W. Tubulin polymerization modifies cardiac sodium channel expression and gating Cardiovascular research 2010;85 (4):691-700 [PubMed]

2009

  • Stein Mèra, van Veen Toon A. B., Remme Carol Ann, Boulaksil Mohamed, Noorman Maartje, van Stuijvenberg Leonie, van der Nagel Roel, Bezzina Connie R., Hauer Richard N. W., de Bakker Jacques M. T., van Rijen Harold V. M. Combined reduction of intercellular coupling and membrane excitability differentially affects transverse and longitudinal cardiac conduction Cardiovascular research 2009;83 (1):52-60 [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]
  • 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]
  • 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
  • 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]
  • 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]
  • 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]

2008

  • 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]
  • Bezzina Connie R., Remme Carol Ann Dilated cardiomyopathy due to sodium channel dysfunction: what is the connection? Circulation. Arrhythmia and electrophysiology 2008;1 (2):80-82 [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.)
  • Bezzina Connie R. Genetics of cardiomyopathy and channelopathy Heart and metabolism : management of the coronary patient 2008;41:5-10
  • 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]
  • 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]
  • 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]

2007

  • 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]
  • 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]
  • 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]
  • 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
  • Remme Carol Ann, Bezzina Connie R. Genetic modulation of cardiac repolarization reserve - Editorial commentary Heart rhythm 2007;4 (5):608-610 [PubMed]

2006

  • 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]
  • 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]
  • 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]
  • 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]
  • 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]
  • Firouzi Mehran, Kok Bart, Spiering Wilko, Busjahn Andreas, Bezzina Connie R., Ruijter Jan M., Koeleman Bobby P. C., Schipper Maria, Groenewegen W. Antoinette, Jongsma Habo J., de Leeuw Peter W. Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men Journal of hypertension 2006;24 (2):325-330 [PubMed]
  • 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]

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]
  • 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]
  • Wilde Arthur A. M., Bezzina Connie R. Genetics of cardiac arrhythmias Heart (British Cardiac Society) 2005;91 (10):1352-1358 [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
  • 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]
  • 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]
  • 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]
  • Bezzina Connie R., Wilde Arthur A. M., Roden Dan M. The molecular genetics of arrhythmias Cardiovascular research 2005;67 (3):343-346 [PubMed]

2004

  • 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]

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]
  • 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
  • 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]
  • 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
  • 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
  • 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]

2002

  • 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]
  • 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
  • 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]
  • Bezzina Connie R., Tan Hanno L. Pharmacological rescue of mutant ion channels Cardiovascular research 2002;55 (2):229-232 [PubMed]

2001

  • 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]
  • 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]
  • 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]

2000

  • 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]
  • 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]

1999

  • 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]
  • 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]
  • 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]

1998

  • Alshinawi C., Scerri C., Galdies R., Aquilina A., Felice A. E. Two new missense mutations (P134T and A244V) in the coagulation factor VII gene Human mutation 1998;11 (Suppl. 1):S189-S191 [PubMed]

1996

  • Felice A. E., Alshinawi C. Polymerase chain Reaction in molecular biotechnology; appropriate technology for developing countries World journal of microbiology & biotechnology 1996;12 (5):467-471 [PubMed]