Institute of Human Genetics

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 Hyperandrogenemia and high prolactin in congenital utero-vaginal aplasia patients (2017) Oppelt P, Mueller A, Stephan L, Dittrich R, Lermann J, Büttner C, Ekici AB, et al. Journal article GSK3ss-Dependent Dysregulation of Neurodevelopment in SPG11-Patient Induced Pluripotent Stem Cell Model (2016) Mishra HK, Prots I, Havlicek S, Kohl Z, Pérez-Brangulí F, Börstler T, Anneser L, et al. Journal article KNOCK-OUT OF THE HUMAN ENDOGENOUS RETROVIRUS ERV3 USING CRISPR/CAS9 TECHNOLOGY (2016) Hübner H, Fahlbusch FB, Ekici AB, Vasileiou G, Beckmann M, Strick R, Rübner M Conference contribution PHENOTYPE OF VULNERABLE ATHEROSCLEROTIC PLAQUES SHOWS STRONG ASSOCIATION WITH SINGLE NUCLEOTIDE POLYMORPHISM ALLELES OF COMMON RISK VARIANTS FOR CORONARY ARTERY DISEASE (2016) Furtmair R, Kühn C, Koenig C, Ekici AB, Klinghammer L, Achenbach S, Reis A, et al. Conference contribution Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma (2016) Mauri L, Uebe S, Sticht H, Vossmerbaeumer U, Weisschuh N, Manfredini E, Maselli E, et al. Journal article