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Unpublished / Preprint

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Abstract

Journal

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