Katharina Schmitt

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

Mutations in <i>GATA4</i>, <i>NKX2.5</i>, <i>CRELD1</i>, and <i>BMP4</i> are infrequently found in patients with congenital cardiac septal defects

Maximilian Posch, Andreas Perrot, Katharina Schmitt et al. · American Journal of Medical Genetics Part A · 2007 · 89 citations

Cardiomyopathy, Genetics, Pathology +10

<i>RMRP</i> gene sequence analysis confirms a cartilage‐hair hypoplasia variant with only skeletal manifestations and reveals a high density of single‐nucleotide polymorphisms

Luisa Bonafé, Katharina Schmitt, Georg Eich et al. · Clinical Genetics · 2002 · 87 citations

Bridge to recovery in children on ventricular assist devices—protocol, predictors of recovery, and long-term follow-up

Oliver Miera, Matthias Germann, My Y. Cho et al. · The Journal of Heart and Lung Transplantation · 2018 · 53 citations

Heart Failure, Device Therapy, Pediatric Heart Disease +9