Jörg‐Detlef Drenckhahn

Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene

Nancy D. Merner, Kathy Hodgkinson, Annika Haywood et al. · The American Journal of Human Genetics · 2008 · 509 citations · Full text

Medicine, Cardiology, Genetics +10

Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

Sabine Klaassen, Susanne Probst, Erwin Oechslin et al. · Circulation · 2008 · 451 citations · Full text

Medicine, Cardiology, Genetics +16

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

Anne-Karin Arndt, Sebastian Schäfer, Jörg‐Detlef Drenckhahn et al. · The American Journal of Human Genetics · 2013 · 210 citations · Full text

Medicine, Genetics, Molecular Genetics +11

Compensatory Growth of Healthy Cardiac Cells in the Presence of Diseased Cells Restores Tissue Homeostasis during Heart Development

Jörg‐Detlef Drenckhahn, Quenten Schwarz, Stephen P. Gray et al. · Developmental Cell · 2008 · 177 citations · Full text

Life Sciences, Cell Biology, Developmental Biology +17

The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)

Kathy Hodgkinson, Patrick S. Parfrey, Anne S. Bassett et al. · Journal of the American College of Cardiology · 2005 · 175 citations · Full text

Medicine, Cardiology, Internal Medicine +12