Lehrstuhl für Humangenetik


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

Mutations in IL36RN in patients with generalized pustular psoriasis (2013) Koerber A, Moessner R, Renner R, Sticht H, Wilsmann-Theis D, Schulz P, Sticherling M, et al. Journal article Biallelic SEMA3A defects cause a novel type of syndromic short stature (2013) Hofmann K, Zweier M, Sticht H, Zweier C, Wittmann W, Hoyer J, Uebe S, et al. Journal article Role of α-synuclein in adult neurogenesis and neuronal maturation in the dentate gyrus. (2012) Winner B, Regensburger M, Prots I, Winkler J Journal article α-Synuclein induces alterations in adult neurogenesis in Parkinson disease models via p53-mediated repression of Notch1. (2012) Desplats P, Spencer B, Crews L, Pathel P, Morvinski-Friedmann D, Kosberg K, Roberts S, et al. Journal article LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors. (2012) Winner B, Prots I, Hinkle KM, Yue M, Bahareh B, Dächsel JC, Lincoln SJ, et al. Journal article, Review article Patients with unstable angina pectoris show an increased frequency of the Fc gamma RIIa R131 allele (2012) Raaz-Schrauder D, Ekici AB, Munoz LE, Klinghammer L, Voll RE, Leusen JH, Van De Winkel JG, et al. Journal article Fluoxetine rescues impaired hippocampal neurogenesis in a transgenic A53T synuclein mouse model. (2012) Kohl Z, Winner B, Ubhi K, Rockenstein E, Mante M, Muench M, Barlow C, et al. Journal article Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein (2012) May VEL, Nuber S, Marxreiter F, Riess O, Winner B, Winkler J Journal article Variants in ASB10 are associated with open-angle glaucoma (2012) Pasutto F, Keller KE, Weisschuh N, Sticht H, Samples JR, Yang YF, Zenkel M, et al. Journal article Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta (2012) Tagariello A, Breuer C, Birkner Y, Schmidt S, Koch AM, Cesnjevar R, Rueffer A, et al. Journal article