C. Özcelik

Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy

C. Özcelik, Bettina Erdmann, Bernhard Pilz et al. · Proceedings of the National Academy of Sciences · 2002 · 469 citations · Full text

Mutations in the Human Muscle LIM Protein Gene in Families With Hypertrophic Cardiomyopathy

Christian Geier, Andreas Perrot, C. Özcelik et al. · Circulation · 2003 · 249 citations

A role of the cryptic gene in the correct establishment of the left–right axis

Ursula Gaio, Axel Schweickert, Anja Fischer et al. · Current Biology · 1999 · 133 citations · Full text

Developmental Biology, Developmental Genetics, Genetics +11

A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects

Maximilian Posch, Michael Gramlich, Margaret Sunde et al. · Journal of Medical Genetics · 2009 · 131 citations · Full text

Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects

Maximilian Posch, Stephan Waldmüller, Melanie Müller et al. · PLoS ONE · 2011 · 92 citations · Full text

Cardiac Muscle, Cardiomyopathy, Heart Failure +15