| Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and … R Coronel, S Casini, TT Koopmann, FJG Wilms-Schopman, AO Verkerk, ... Circulation 112 (18), 2769-2777, 2005 | 524 | 2005 |
| Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia AAM Wilde, ZA Bhuiyan, L Crotti, M Facchini, GM De Ferrari, T Paul, ... New England Journal of Medicine 358 (19), 2024-2029, 2008 | 436 | 2008 |
| Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy JP van Tintelen, MM Entius, ZA Bhuiyan, R Jongbloed, ACP Wiesfeld, ... Circulation 113 (13), 1650-1658, 2006 | 430 | 2006 |
| Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia C van der Werf, PJ Kannankeril, F Sacher, AD Krahn, S Viskin, ... Journal of the American College of Cardiology 57 (22), 2244-2254, 2011 | 419 | 2011 |
| The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular … A Medeiros-Domingo, ZA Bhuiyan, DJ Tester, N Hofman, H Bikker, ... Journal of the American College of Cardiology 54 (22), 2065-2074, 2009 | 373 | 2009 |
| Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia–associated mutations from background genetic noise JD Kapplinger, AP Landstrom, BA Salisbury, TE Callis, GD Pollevick, ... Journal of the American College of Cardiology 57 (23), 2317-2327, 2011 | 337 | 2011 |
| Expanding Spectrum of Human RYR2-Related Disease: New Electrocardiographic, Structural, and Genetic Features ZA Bhuiyan, MP van den Berg, JP van Tintelen, MTE Bink-Boelkens, ... Circulation 116 (14), 1569-1576, 2007 | 273 | 2007 |
| The response of the QT interval to the brief tachycardia provoked by standing: a bedside test for diagnosing long QT syndrome S Viskin, PG Postema, ZA Bhuiyan, R Rosso, JM Kalman, JK Vohra, ... Journal of the American College of Cardiology 55 (18), 1955-1961, 2010 | 264 | 2010 |
| A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families JPP Smits, TT Koopmann, R Wilders, MW Veldkamp, T Opthof, ... Journal of molecular and cellular cardiology 38 (6), 969-981, 2005 | 261 | 2005 |
| Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies PG Meregalli, HL Tan, V Probst, TT Koopmann, MW Tanck, ZA Bhuiyan, ... Heart Rhythm 6 (3), 341-348, 2009 | 253 | 2009 |
| Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right … MGPJ Cox, PA van der Zwaag, C van der Werf, JJ van der Smagt, ... Circulation 123 (23), 2690-2700, 2011 | 235 | 2011 |
| De Novo Mutation in the SCN5A Gene Associated With Early Onset of Sudden Infant Death H Wedekind, JPP Smits, E Schulze-Bahr, R Arnold, MW Veldkamp, ... Circulation 104 (10), 1158-1164, 2001 | 231 | 2001 |
| A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization CR Bezzina, AO Verkerk, A Busjahn, A Jeron, J Erdmann, TT Koopmann, ... Cardiovascular research 59 (1), 27-36, 2003 | 214 | 2003 |
| Novel calmodulin mutations associated with congenital arrhythmia susceptibility N Makita, N Yagihara, L Crotti, CN Johnson, BM Beckmann, MS Roh, ... Circulation: Cardiovascular Genetics 7 (4), 466-474, 2014 | 210 | 2014 |
| A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence RF Marsman, J Barc, L Beekman, M Alders, D Dooijes, ... Journal of the American College of Cardiology 63 (3), 259-266, 2014 | 185 | 2014 |
| Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: Disease penetrance and expression in cardiac ryanodine receptor mutation–carrying relatives C van der Werf, I Nederend, N Hofman, N van Geloven, C Ebink, ... Circulation: Arrhythmia and Electrophysiology 5 (4), 748-756, 2012 | 179 | 2012 |
| Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience ZA Bhuiyan, M Klein, P Hammond, A van Haeringen, MMAM Mannens, ... Journal of medical genetics 43 (7), 568-575, 2006 | 178 | 2006 |
| Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry L Crotti, C Spazzolini, DJ Tester, A Ghidoni, AE Baruteau, BM Beckmann, ... European heart journal 40 (35), 2964-2975, 2019 | 137 | 2019 |
| Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair MG Vrouwe, E Elghalbzouri-Maghrani, M Meijers, P Schouten, ... Human molecular genetics 16 (12), 1478-1487, 2007 | 130 | 2007 |
| TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT HD Devalla, R Gélinas, EH Aburawi, A Beqqali, P Goyette, C Freund, ... EMBO molecular medicine 8 (12), 1390-1408, 2016 | 115 | 2016 |
