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 · 502 citations · Full text

Cardiomyopathy, Heart Failure, Tmem43 Gene +9

Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

Sabine Klaassen, Susanne Probst, Erwin Oechslin et al. · Circulation · 2008 · 447 citations · Full text

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 · 208 citations · Full text

Cardiomyopathy, Genetics, Pathology +5

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

Regenerative Medicine, Cardiac Muscle, Cardiomyopathy +12

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 · 174 citations · Full text

Cardiomyopathy, Heart Failure, Device Therapy +8