Ellen Schulze-Bahr

Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I

Martin Kruse, Eric Schulze‐Bahr, Valerie A. Corfield et al. · Journal of Clinical Investigation · 2009 · 317 citations · Full text

Cardiac Muscle, Heart Failure, Ion Channel Trpm4 +20

Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

Birgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy et al. · Human Mutation · 2011 · 166 citations

Cardiac Muscle, Heart Failure, Genetics +30

Mutational spectrum in the cardiac transcription factor gene <i>NKX2.5</i> (<i>CSX</i>) associated with congenital heart disease

Birgit Stallmeyer, Hartmut Fenge, Ulrike Nowak‐Göttl et al. · Clinical Genetics · 2010 · 104 citations

Cardiac α-Actin ( <i>ACTC1</i> ) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy

Derk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich et al. · Circulation Genomic and Precision Medicine · 2019 · 54 citations · Full text

A Mutation in the G-Protein Gene <i>GNB2</i> Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction

Birgit Stallmeyer, Johanna Kuß, S. Kotthoff et al. · Circulation Research · 2017 · 50 citations · Full text