Cornelia Kraus

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

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation

Anita Rauch, Juliane Hoyer, Sabine Guth et al. · American Journal of Medical Genetics Part A · 2006 · 445 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes

Christian P. Kratz, Lude Franke, Harm Peters et al. · British Journal of Cancer · 2015 · 212 citations · Full text

Medicine, Genetics, Oncology +17

Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression

Markus Zweier, Anne Gregor, Christiane Zweier et al. · Human Mutation · 2010 · 181 citations

Life Sciences, Genetics, Molecular Genetics +16

Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature

Nadine Hauer, Bernt Popp, Schoeller Eva et al. · Genetics in Medicine · 2017 · 147 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17