Georg Rosenberger

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 · 502 citations

Developmental Biology, Molecular Neuroscience, Brain Development +13

Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Hyung‐Goo Kim, Ingo Kurth, Fei Lan et al. · The American Journal of Human Genetics · 2008 · 330 citations · Full text

Chromatin-remodeling Protein, Chromatin, Developmental Biology +13

WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Hyung‐Goo Kim, Jang-Won Ahn, Ingo Kurth et al. · The American Journal of Human Genetics · 2010 · 192 citations · Full text

Is Mutated, Transcriptional Regulation, Developmental Biology +9

Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome

Isabella Wimplinger, Manuela Morleo, Georg Rosenberger et al. · The American Journal of Human Genetics · 2006 · 161 citations · Full text

Skin Development, Mendelian Disorder, Genetic Disorder +8

Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signaling

Georg Rosenberger · Human Molecular Genetics · 2003 · 120 citations · Full text