Martin Zenker

Germline KRAS mutations cause Noonan syndrome

Suzanne Schubbert, Martin Zenker, Sara L. Rowe et al. · Nature Genetics · 2006 · 740 citations

Life Sciences, Genetics, Molecular Genetics +9

Identifying facial phenotypes of genetic disorders using deep learning

Yaron Gurovich, Yair Hanani, Omri Bar et al. · Nature Medicine · 2018 · 732 citations

Medicine, Genetics, Molecular Genetics +16

A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome

Carolin E. Sadowski, Svjetlana Lovric, Shazia Ashraf et al. · Journal of the American Society of Nephrology · 2014 · 655 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Sabine Endele, Georg Rosenberger, Kirsten Geider et al. · Nature Genetics · 2010 · 509 citations

Life Sciences, Genetics, Neuroscience +16

Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

Martin Zenker, Thomas Aigner, Olaf Wendler et al. · Human Molecular Genetics · 2004 · 499 citations

Medicine, Genetics, Molecular Genetics +17