Institute of Human Genetics

A Homozygous Mutation in GPT2 Associated with Nonsyndromic Intellectual Disability in a Consanguineous Family from Costa Rica (2017) Lobo-Prada T, Sticht H, Bogantes-Ledezma S, Ekici AB, Uebe S, Reis A, Leal A Journal article EFhd2/Swiprosin-1 is a common genetic determinator for sensation-seeking/low anxiety and alcohol addiction (2017) Mielenz D, Reichel M, Jia T, Quinlan EB, Stöckl T, Mettang M, Zilske D, et al. Journal article, Original article IFN-α/IFN-λ responses to respiratory viruses in paediatric asthma (2017) Bergauer A, Sopel N, Kross B, Vuorinen T, Xepapadaki P, Weiss ST, Blau A, et al. Journal article Blunted transcriptional response to skeletal muscle ischemia in rats with chronic kidney disease: potential role for impaired ischemia-induced angiogenesis (2017) Heiß R, Fahlbusch FB, Jacobi J, Daniel C, Ekici AB, Cordasic N, Amann KU, et al. Journal article High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder (2017) Grünblatt E, Oneda B, Ekici AB, Ball J, Geissler J, Uebe S, Romanos M, et al. Journal article Prenatal androgen receptor activation determines adult alcohol and water drinking in a sex-specific way (2017) Huber S, Zoicas I, Reichel M, Mühle C, Büttner C, Ekici AB, Eulenburg V, et al. Journal article New Therapeutic Approaches in Inflammatory Diseases of the Eye - Targeting Lymphangiogenesis and Cellular Immunity: Research Unit FOR 2240 Presents Itself (2017) Cursiefen C, Bock F, Clahsen T, Regenfuss B, Reis A, Steven P, Heindl LM, et al. Journal article Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants (2017) Tsoi LC, Stuart PE, Tian C, Gudjonsson JE, Das S, Zawistowski M, Ellinghaus E, et al. Journal article Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features (2017) Stankiewicz P, Khan TN, Szafranski P, Slattery L, Streff H, Vetrini F, Bernstein JA, et al. Journal article Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature (2017) Hauer N, Sticht H, Boppudi S, Büttner C, Kraus C, Trautmann U, Zenker M, et al. Journal article