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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
Journal article
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Book chapter / Article in edited volumes
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Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma (2016)
Khor CC, Do T, Jia H, Nakano M, George R, Abu-Amero K, Duvesh R, et al.
Journal article
Dopaminergic lesioning impairs adult hippocampal neurogenesis by distinct modification of α-synuclein (2016)
Schlachetzki J, Grimm T, Schlachetzki Z, Ben Abdallah NMB, Ettle B, Voehringer P, Ferger B, et al.
Journal article
Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency (2016)
Saunier C, Stove SI, Popp B, Gerard B, Blenski M, Ahmew N, De Bie C, et al.
Journal article
Infiltrating T lymphocytes reduce myeloid phagocytosis activity in synucleinopathy model (2016)
Sommer A, Fadler T, Dorfmeister E, Hoffmann AC, Xiang W, Winner B, Prots I
Journal article
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer (2016)
Couch FJ, Kuchenbaecker KB, Michailidou K, Mendoza-Fandino GA, Nord S, Lilyquist J, Olswold C, et al.
Journal article
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies (2016)
Sekula P, Li Y, Stanescu HC, Wuttke M, Ekici AB, Bockenhauer D, Walz G, et al.
Journal article
Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer (2016)
Painter JN, O'Mara TA, Marquart L, Webb PM, Attia J, Medland SE, Cheng T, et al.
Journal article
Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition (2016)
Kuechler A, Czeschik JC, Graf E, Grasshoff U, Hüffmeier U, Busa T, Beck-Woedl S, et al.
Journal article
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly (2016)
Breuss MW, Sultan T, James KN, Rosti RO, Scott E, Musaev D, Furia B, et al.
Journal article, Erratum
Model Testing of PluriTest with Next-Generation Sequencing Data (2016)
Schulze M, Hoja S, Winner B, Winkler J, Edenhofer F, Riemenschneider MJ
Journal article
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