Lehrstuhl für Humangenetik

PHENOTYPE OF VULNERABLE ATHEROSCLEROTIC PLAQUES SHOWS STRONG ASSOCIATION WITH SINGLE NUCLEOTIDE POLYMORPHISM ALLELES OF COMMON RISK VARIANTS FOR CORONARY ARTERY DISEASE (2016) Furtmair R, Kühn C, Koenig C, Ekici AB, Klinghammer L, Achenbach S, Reis A, et al. Conference contribution Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma (2016) Mauri L, Uebe S, Sticht H, Vossmerbaeumer U, Weisschuh N, Manfredini E, Maselli E, et al. Journal article ?-Synuclein-induced myelination deficit defines a novel interventional target for multiple system atrophy (2016) Ettle B, Kerman BE, Valera E, Gillmann C, Schlachetzki J, Reiprich S, Büttner C, et al. Journal article Paradoxical antidepressant effects of alcohol are related to acid sphingomyelinase and its control of sphingolipid homeostasis (2016) Müller C, Kalinichenko L, Tiesel J, Witt M, Stöckl T, Sprenger E, Fuchser J, et al. Journal article Distinct Effects of Chronic Dopaminergic Stimulation on Hippocampal Neurogenesis and Striatal Doublecortin Expression in Adult Mice (2016) Salvi R, Steigleder T, Schlachetzki J, Waldmann E, Schwab S, Winner B, Winkler J, Kohl Z 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 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