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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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Common genetic determinants of intraocular pressure and primary open-angle glaucoma (2012)
Van Koolwijk LME, Ramdas WD, Ikram MK, Jansonius NM, Pasutto F, Hysi PG, Macgregor S, et al.
Journal article
Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk (2011)
Stevens KN, Garcia-Closas M, Fredericksen Z, Kosel M, Pankratz VS, Hopper JL, Dite GS, et al.
Journal article
Adult neurogenesis and neurite outgrowth are impaired in LRRK2 G2019S mice (2011)
Winner B, Gage FH, Winkler J
Journal article
In vivo demonstration that alpha-synuclein oligomers are toxic. (2011)
Winner B, Jappelli R, Maji SK, Desplats PA, Boyer L, Aigner S, Hetzer C, et al.
Journal article
Breast cancer risk - Genes, environment and clinics Mammakarzinomrisiko - Gene, Umwelt und Klinik (2011)
Fasching P, Ekici AB, Adamietz BR, Wachter DL, Hein A, Bayer CM, Häberle L, et al.
Journal article
Genome-wide association study identifies a common variant associated with risk of endometrial cancer (2011)
Spurdle AB, Thompson DJ, Ahmed S, Ferguson K, Healey CS, O'Mara T, Walker LC, et al.
Journal article
Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: Pooled analysis within the ovarian cancer association consortium (2011)
Lurie G, Wilkens LR, Thompson PJ, Shvetsov YB, Matsuno RK, Carney ME, Palmieri RT, et al.
Journal article
Regulation of Lysyl Oxidase-like 1 (LOXL1) and Elastin-Related Genes by Pathogenic Factors Associated with Pseudoexfoliation Syndrome (2011)
Zenkel M, Krysta A, Pasutto F, Jünemann A, Kruse F, Schlötzer-Schrehardt U
Journal article
Phenotypic variability in a large Czech family with a Dynamin 2-associated Charcot-Marie-Tooth neuropathy (2011)
Haberlova J, Mazanec R, Ridzon P, Barankova L, Nuernberg G, Nuernberg P, Sticht H, et al.
Journal article
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome (2011)
Krumbiegel M, Pasutto F, Schlötzer-Schrehardt U, Uebe S, Zenkel M, Mardin CY, Weisschuh N, et al.
Journal article
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