N. Hofman PhD publications

2020

• Lieve Krystien V. V., Dusi Veronica, van der Werf Christian, Bos J. Martijn, Lane Conor M., Stokke Mathis Korseberg, Roston Thomas M., Djupsjöbacka Aurora, Wada Yuko, Denjoy Isabelle, Bundgaard Henning, Noguer Ferran Roses I., Semsarian Christopher, Robyns Tomas, Hofman Nynke, Tanck Michael W., van den Berg Maarten P., Kammeraad Janneke A. E., Krahn Andrew D., Clur Sally-Ann B., Sacher Frederic, Till Jan, Skinner Jonathan R., Tfelt-Hansen Jacob, Probst Vincent, Leenhardt Antoine, Horie Minoru, Swan Heikki, Roberts Jason D., Sanatani Shubhayan, Haugaa Kristina H., Schwartz Peter J., Ackerman Michael J., Wilde Arthur A. M. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Circulation. Arrhythmia and electrophysiology 2020;13 (3):e007471 [PubMed]
• Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G., Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L., Mazzanti Andrea, Beckmann Britt M., Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D., Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A., Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M. Ben, Weeke Peter E., Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J., Bos J. Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G., Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A., Veldink Jan H., van den Berg Leonard H., Al-Chalabi Ammar, Shaw Christopher E., Shaw Pamela J., Morrison Karen E., Andersen Peter M., Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C., Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J. Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D., Antzelevitch Charles, Roden Dan M., Saenen Johan, Borggrefe Martin, Odening Katja E., Ellinor Patrick T., Tfelt-Hansen Jacob, Skinner Jonathan R., van den Berg Maarten P., Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R., Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G., Guicheney Pascale, Tan Hanno L., Newton-Cheh Christopher, Ackerman Michael J., Schwartz Peter J., Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A., Tanck Michael W. T., Bezzina Connie R. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome Circulation 2020;142 (4):324-338 [PubMed]

2019

• Blom Lennart J., Visser Marloes, Christiaans Imke, Scholten Marcoen F., Bootsma Marianne, van den Berg Maarten P., Yap Sing-Chien, van der Heijden Jeroen F., Doevendans Pieter A., Loh Peter, Postema Pieter G., Barge-Schaapsveld Daniela Q., Hofman Nynke, Volders Paul G. A., Wilde Arthur A., Hassink Rutger J. Incidence and predictors of implantable cardioverter-defibrillator therapy and its complications in idiopathic ventricular fibrillation patients EP Europace 2019;21 (10):1519-1526 [PubMed]

2018

• Vink Arja Suzanne, Neumann Benjamin, Lieve Krystien V V, Sinner Moritz F, Hofman Nynke, El Kadi Soufiane, Schoenmaker Melissa H A, Slaghekke Hanneke M J, de Jong Jonas S S G, Clur Sally-Ann B, Blom Nico A, Kääb Stefan, Wilde Arthur A M, Postema Pieter G Determination and Interpretation of the QT Interval Circulation 2018;138 (21):2345-2358 [PubMed]

2017

• Vink Arja S., Clur Sally-Ann B., Geskus Ronald B., Blank Andreas C., de Kezel Charlotte C. A., Yoshinaga Masao, Hofman Nynke, Wilde Arthur A. M., Blom Nico A. Effect of Age and Sex on the QTc Interval in Children and Adolescents With Type 1 and 2 Long-QT Syndrome Circulation. Arrhythmia and electrophysiology 2017;10 (4) [PubMed]
• 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]

2016

• Itoh Hideki, Berthet Myriam, Fressart Véronique, Denjoy Isabelle, Maugenre Svetlana, Klug Didier, Mizusawa Yuka, Makiyama Takeru, Hofman Nynke, Stallmeyer Birgit, Zumhagen Sven, Shimizu Wataru, Wilde Arthur A. M., Schulze-Bahr Eric, Horie Minoru, Tezenas du Montcel Sophie, Guicheney Pascale Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction European journal of human genetics 2016;24 (8):1160-1166 [PubMed]
• 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]
• Hofman Nynke, Wilde Arthur A. M. Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal Hearts Cardiac electrophysiology clinics 2016;8 (3):515-523 [PubMed]

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]

2014

• 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]
• van der Werf Christian, Stiekema Lotte, Tan Hanno L., Hofman Nynke, Alders Marielle, van der Wal Allard C., van Langen Irene M., Wilde Arthur A. M. Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up Heart rhythm 2014;11 (10):1728-1732 [PubMed]

2013

• Hofman Nynke Evaluation of outcomes of cardiogenetic testing in inherited arrhythmias 2013. 214p. ISBN 9789461822116. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Wilde A. A. M., van Langen I. M.; Co-supervisor: Tan H. L.)
• Mook Olaf R. F., Haagmans Martin A., Soucy Jean-François, van de Meerakker Judith B. A., Baas Frank, Jakobs Marja E., Hofman Nynke, Christiaans Imke, Lekanne Deprez Ronald H., Mannens Marcel M. A. M. Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics Journal of medical genetics 2013;50 (9):614-626 [PubMed]
• Hofman Nynke, Tan Hanno L., Alders Mariëlle, Kolder Iris, de Haij Simone, Mannens Marcel M. A. M., Lombardi Maria Paola, Lekanne Deprez Ronald H., van Langen Irene, Wilde Arthur A. M. Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience Circulation 2013;128 (14):1513-1521 [PubMed]

2012

• van der Werf Christian, Nederend Ineke, Hofman Nynke, van Geloven Nan, Ebink Corné, Frohn-Mulder Ingrid M. E., Alings A. Marco W., Bosker Hans A., Bracke Frank A., van den Heuvel Freek, Waalewijn Reinier A., Bikker Hennie, van Tintelen J. Peter, Bhuiyan Zahurul A., van den Berg Maarten P., Wilde Arthur A. M. Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia Disease Penetrance and Expression in Cardiac Ryanodine Receptor Mutation-Carrying Relatives Circulation. Arrhythmia and electrophysiology 2012;5 (4):748-756 [PubMed]
• Barsheshet Alon, Goldenberg Ilan, O-Uchi Jin, Moss Arthur J., Jons Christian, Shimizu Wataru, Wilde Arthur A., McNitt Scott, Peterson Derick R., Zareba Wojciech, Robinson Jennifer L., Ackerman Michael J., Cypress Michael, Gray Daniel A., Hofman Nynke, Kanters Jorgen K., Kaufman Elizabeth S., Platonov Pyotr G., Qi Ming, Towbin Jeffrey A., Vincent G. Michael, Lopes Coeli M. Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events Implications for Mutation-Specific Response to beta-Blocker Therapy in Type 1 Long-QT Syndrome Circulation 2012;125 (16):1988-+ [PubMed]
• 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

• 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]
• Postema Pieter G., Christiaans Imke, Alders Marielle, Hofman Nynke, Wilde Arthur A. M. Premature plotse dood. Denk aan ernstige familiaire hartritmestoornissen Nederlands tijdschrift voor geneeskunde 2011;155 (39):A3391 [PubMed]
• Hofman N., Jongbloed R., Postema P. G., Nannenberg E., Alders M., Wilde A. A. M. Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome Netherlands heart journal 2011;19 (1):10-16 [PubMed]
• Postema Pieter G., Mosterd Arend, Hofman Nynke, Alders Marielle, Wilde Arthur A. M. Sodium channelopathies: do we really understand what's going on? Journal of cardiovascular electrophysiology 2011;22 (5):590-593 [PubMed]
• Jons Christian, O-Uchi Jin, Moss Arthur J., Reumann Matthias, Rice John J., Goldenberg Ilan, Zareba Wojciech, Wilde Arthur A. M., Shimizu Wataru, Kanters Jorgen K., McNitt Scott, Hofman Nynke, Robinson Jennifer L., Lopes Coeli M. B. Use of Mutant-Specific Ion Channel Characteristics for Risk Stratification of Long QT Syndrome Patients Science translational medicine 2011;3 (76):76ra28 [PubMed]

2010

• Hofman Nynke, Tan Hanno L., Alders Marielle, van Langen Irene M., Wilde Arthur A. M. Active Cascade Screening in Primary Inherited Arrhythmia Syndromes Does It Lead to Prophylactic Treatment? Journal of the American College of Cardiology 2010;55 (23):2570-2576 [PubMed]
• van der Werf Christian, Hofman Nynke, Tan Hanno L., van Dessel Pascal F., Alders Marielle, van der Wal Allard C., van Langen Irene M., Wilde Arthur A. M. Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: The experience of a tertiary referral center in The Netherlands Heart rhythm 2010;7 (10):1383-1389 [PubMed]
• Hofman Nynke, van Lochem Laura T., Wilde Arthur A. M. Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart Future cardiology 2010;6 (3):395-408 [PubMed]
• Hofman Nynke, van Langen Irene, Wilde Arthur A. M. Genetic testing in cardiovascular diseases Current opinion in cardiology 2010;25 (3):243-248 [PubMed]
• Clur Sally-Ann B., Chockalingam Priya, Filippini Luc H., Widyanti Ari P., van Cruijsen Marc, Blom Nico A., Alders Mariel, Hofman Nynke, Wilde Arthur A. M. The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome Pediatric cardiology 2010;31 (4):462-468 [PubMed]

2009

• 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]
• Shimizu Wataru, Moss Arthur J., Wilde Arthur A. M., Towbin Jeffrey A., Ackerman Michael J., January Craig T., Tester David J., Zareba Wojciech, Robinson Jennifer L., Qi Ming, Vincent G. Michael, Kaufman Elizabeth S., Hofman Nynke, Noda Takashi, Kamakura Shiro, Miyamoto Yoshihiro, Shah Samit, Amin Vinit, Goldenberg Ilan, Andrews Mark L., McNitt Scott Genotype-Phenotype Aspects of Type 2 Long QT Syndrome Journal of the American College of Cardiology 2009;54 (22):2052-2062 [PubMed]
• Johnson J. N., Hofman N., Haglund C. M., Cascino G. D., Wilde A. A. M., Ackerman M. J. Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy Neurology 2009;72 (3):224-231 [PubMed]
• Medeiros-Domingo Argelia, Bhuiyan Zahurul A., Tester David J., Hofman Nynke, Bikker Hennie, van Tintelen J. Peter, Mannens Marcel M. A. M., Wilde Arthur A. M., Ackerman Michael J. The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome A Comprehensive Open Reading Frame Mutational Analysis Journal of the American College of Cardiology 2009;54 (22):2065-2074 [PubMed]

2008

• Liu Judy F., Goldenberg Ilan, Moss Arthur J., Shimizu Wataru, Wilde Arthur A., Hofman Nynke, McNitt Scott, Zareba Wojciech, Miyamato Yoshihiro, Robinson Jennifer L., Andrews Mark L. Phenotypic variability in Caucasian and Japanese patients with matched LQT1 mutations Annals of noninvasive electrocardiology 2008;13 (3):234-241 [PubMed]

2007

• Kodde J., Hofman N., Reichert C. L. A., van Langen I. M., Wilde A. A. M. Cardiogenetic counselling in a non-university hospital Netherlands heart journal 2007;15 (12):412-414 [PubMed]
• Moss Arthur J., Shimizu Wataru, Wilde Arthur A. M., Towbin Jeffrey A., Zareba Wojciech, Robinson Jennifer L., Qi Ming, Vincent G. Michael, Ackerman Michael J., Kaufman Elizabeth S., Hofman Nynke, Seth Rahul, Kamakura Shiro, Miyamoto Yoshihiro, Goldenberg Ilan, Andrews Mark L., McNitt Scott Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene Circulation 2007;115 (19):2481-2489 [PubMed]
• Hofman Nynke, Tan Hanno L., Clur Sally-Ann, Alders Mariel, van Langen Irene M., Wilde Arthur A. M. Contribution of inherited heart disease to sudden cardiac death in childhood Pediatrics 2007;120 (4):e967-e973 [PubMed]
• Hofman Nynke, Wilde Arthur A. M., Tan Hanno L. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European heart journal 2007;28 (11):1399 [PubMed]
• Hofman Nynke, Wilde Arthur A. M., Kääb Stefan, van Langen Irene M., Tanck Michael W. T., Mannens Marcel M. A. M., Hinterseer Martin, Beckmann Britt-Maria, Tan Hanno L. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European heart journal 2007;28 (5):575-580 [PubMed]
• Hofman N., Postema P. G., van Langen I. M., Nannenberg E. A., Alders M., Jongbloed R., Smeets H. J. M., Wilde A. A. M. Genetische identificatie van patiënten en families met lange-QT-syndroom: grote regionale verschillen in de resultaten van 10 jaar Nederlands tijdschrift voor geneeskunde 2007;151 (11):644-648 [PubMed]

2006

• 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]

2005

• van Langen I. M., Birnie E., Schuurman E., Tan H. L., Hofman N., Bonsel G. J., Wilde A. A. M. Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey Clinical genetics 2005;68 (4):360-368 [PubMed]
• Tan Hanno L., Hofman Nynke, van Langen Irene M., van der Wal Allard C., Wilde Arthur A. M. Sudden unexplained death - Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives Circulation 2005;112 (2):207-213 [PubMed]

2004

• van Langen I. M., Hofman N., Tan H. L., Wilde A. A. M. Family and population strategies for screening and counselling of inherited cardiac arrhythmias Annals of medicine 2004;36 (Suppl. 1):116-124 [PubMed]