Institute of Human Genetics


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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Unpublished / Preprint

Publication year

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Abstract

Journal

Comparison of 6q25 breast cancer hits from Asian and European genome wide association studies in the Breast Cancer Association consortium (BCAC) (2012) Hein R, Maranian M, Hopper JL, Kapuscinski MK, Southey MC, Park DJ, Schmidt MK, 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 Percent mammographic density and dense area as risk factors for breast cancer (2012) Rauh C, Hack C, Häberle L, Hein A, Engel A, Schrauder MG, Fasching P, 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 LOXL1 deficiency in the lamina cribrosa as candidate susceptibility factor for a pseudoexfoliation-specific risk of glaucoma (2012) Schlötzer-Schrehardt U, Hammer C, Krysta AW, Hofmann-Rummelt C, Pasutto F, Sasaki T, Kruse F, Zenkel M Journal article Genome-wide association analysis identifies three new breast cancer susceptibility loci (2012) Ghoussaini M, Fletcher O, Michailidou K, Turnbull C, Schmidt MK, Dicks E, Dennis J, 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