Ans C.P. Wiesfeld

Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members

Judith A. Groeneweg, Aditya Bhonsale, Cynthia A. James et al. · Circulation Cardiovascular Genetics · 2015 · 470 citations · Full text

Phospholamban R14del Mutation in Patients Diagnosed with Dilated Cardiomyopathy or Arrhythmogenic Right Ventricular Cardiomyopathy: Evidence Supporting the Concept of Arrhythmogenic Cardiomyopathy

Paul A. van der Zwaag, Ingrid A.W. van Rijsingen, Angeliki Asimaki et al. · European Journal of Heart Failure · 2012 · 452 citations · Full text

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

Hiroshi Watanabe, Tamara T. Koopmann, Solena Le Scouarnec et al. · Journal of Clinical Investigation · 2008 · 432 citations · Full text

Cardiac Muscle, Channelopathies, Ventricular Fibrillation +15

Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

J. Peter van Tintelen, Mark M. Entius, Zahurul A. Bhuiyan et al. · Circulation · 2006 · 353 citations

Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

Jamie D. Kapplinger, Andrew P. Landstrom, Benjamin A. Salisbury et al. · Journal of the American College of Cardiology · 2011 · 301 citations · Full text

Cardiomyopathy, Heart Failure, Genetic Disorder +6