Franz Rüschendorf

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Louise Metherell, J. Paul Chapple, Sadani N. Cooray et al. · Nature Genetics · 2005 · 444 citations

Mendelian Disorder, Autoimmune Disease, New Interacting Partner +9

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 · 442 citations · Full text

Genetic Testing, Genetics, Pathology +21

G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Sandra M. Pasternack, Ivar von Kügelgen, Khalid Al Aboud et al. · Nature Genetics · 2008 · 406 citations

Molecular Pharmacology, Protein Function, Signal Transduction +12

Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march

Ingo Marenholz, Renate Nickel, Franz Rüschendorf et al. · Journal of Allergy and Clinical Immunology · 2006 · 385 citations · Full text

Biology, Atopic Dermatitis, Genetic Disorder +7

A common variant on chromosome 11q13 is associated with atopic dermatitis

Jorge Esparza-Gordillo, Stephan Weidinger, Regina Fölster‐Holst et al. · Nature Genetics · 2009 · 312 citations

Atopic Dermatitis, Genetics, Skin Allergy +7