| A sodium-channel mutation causes isolated cardiac conduction disease HL Tan, MTE Bink-Boelkens, CR Bezzina, PC Viswanathan, ... Nature 409 (6823), 1043-1047, 2001 | 454 | 2001 |
| Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death? JH Van Berlo, WG De Voogt, AJ Van Der Kooi, JP Van Tintelen, G Bonne, ... Journal of molecular medicine 83 (1), 79-83, 2005 | 405 | 2005 |
| Risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers: a European cohort study IAW Van Rijsingen, E Arbustini, PM Elliott, J Mogensen, ... Journal of the American College of Cardiology 59 (5), 493-500, 2012 | 370 | 2012 |
| CLINICAL PERSPECTIVE JP van Tintelen, MM Entius, ZA Bhuiyan, R Jongbloed, ACP Wiesfeld, ... Circulation 113 (13), 1650-1658, 2006 | 361 | 2006 |
| Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) AAM Wilde, RJE Jongbloed, PA Doevendans, DR Düren, RNW Hauer, ... Journal of the American College of Cardiology 33 (2), 327-332, 1999 | 316 | 1999 |
| Targeted next‐generation sequencing can replace Sanger sequencing in clinical diagnostics B Sikkema‐Raddatz, LF Johansson, EN de Boer, R Almomani, LG Boven, ... Human mutation 34 (7), 1035-1042, 2013 | 289 | 2013 |
| Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of … PA Van Der Zwaag, IAW Van Rijsingen, A Asimaki, JDH Jongbloed, ... European journal of heart failure 14 (11), 1199-1207, 2012 | 289 | 2012 |
| 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 | 270 | 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 | 269 | 2009 |
| Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy KY van Spaendonck-Zwarts, JP van Tintelen, DJ van Veldhuisen, ... Circulation 121 (20), 2169-2175, 2010 | 255 | 2010 |
| Clinical presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members JA Groeneweg, A Bhonsale, CA James, AS Te Riele, D Dooijes, ... Circulation: Cardiovascular Genetics 8 (3), 437-446, 2015 | 242 | 2015 |
| Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers A Bhonsale, JA Groeneweg, CA James, D Dooijes, C Tichnell, ... European heart journal 36 (14), 847-855, 2015 | 235 | 2015 |
| Expanding spectrum of human RYR2-related disease ZA Bhuiyan, MP van den Berg, JP van Tintelen, MTE Bink-Boelkens, ... Circulation 116 (14), 1569-1576, 2007 | 220 | 2007 |
| 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 | 196 | 2011 |
| 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy JA Towbin, WJ McKenna, DJ Abrams, MJ Ackerman, H Calkins, ... Heart rhythm 16 (11), e301-e372, 2019 | 172 | 2019 |
| Desmin‐related myopathy KY van Spaendonck‐Zwarts, L van Hessem, JDH Jongbloed, ... Clinical genetics 80 (4), 354-366, 2011 | 151 | 2011 |
| Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy KY van Spaendonck-Zwarts, A Posafalvi, MP van den Berg, ... European heart journal 35 (32), 2165-2173, 2014 | 149 | 2014 |
| Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience KY van Spaendonck‐Zwarts, IAW van Rijsingen, MP van den Berg, ... European journal of heart failure 15 (6), 628-636, 2013 | 148 | 2013 |
| Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy … MA Kelly, C Caleshu, A Morales, J Buchan, Z Wolf, SM Harrison, S Cook, ... Genetics in Medicine 20 (3), 351-359, 2018 | 145 | 2018 |
| Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene JP van Tintelen, IC Van Gelder, A Asimaki, AJH Suurmeijer, ACP Wiesfeld, ... Heart Rhythm 6 (11), 1574-1583, 2009 | 145 | 2009 |
J.D.H. JongbloedPrincipal Investigator, clinical laboratoy geneticist, Department of Genetics, University Medical Center Groningen, University oVerified email at umcg.nl
