A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defectsMaximilian Posch, C. Özcelik, Georges Nemer et al.|Journal of Medical Genetics|2009Cited by 131
Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal DefectsMaximilian Posch, C. Özcelik, Katharina Schmitt et al.|PLoS ONE|2011Cited by 93
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 defectsMaximilian Posch, Felix Berger, Christian Geier et al.|American Journal of Medical Genetics Part A|2007Cited by 89