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Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(729)
Research Grants
(48)
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Journal article
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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
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