PuSH - Publication Server of Helmholtz Zentrum München

32 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
Kunkle, B.W.* et al.: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nat. Genet. 51, 414-430 (2019)
Warrington, N.M.* et al.: Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nat. Genet. 51, 804-814 (2019)
Roselli, C.* et al.: Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50, 1225–1233 (2018)
Christophersen, I.E.* et al.: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)
Day, F.R.* et al.: Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat. Genet. 49, 834-841 (2017)
Direk, N.* et al.: An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biol. Psychiatry 82, 322-329 (2017)
Weng, L.C.* et al.: Genetic interactions with age, sex, body mass index, and hypertension in relation to atrial fibrillation: The AFGen Consortium. Sci. Rep. 7:11303 (2017)
Chen, B.H.* et al.: DNA methylation-based measures of biological age: Meta-analysis predicting time to death. Aging 8, 1844-1865 (2016)
Jun, G.* et al.: A novel Alzheimer disease locus located near the gene encoding tau protein. Mol. Psychiatry 21, 108–117 (2016)
Lin, H.* et al.: Gene-gene interaction analyses for atrial fibrillation. Sci. Rep. 6:35371 (2016)
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat. Genet. 47, 1294-1303 (2015)
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility, and BRCA1-mediated DNA repair. Obstet. Gynecol. 70, 758-762 (2015)
Lunetta, K.L.* et al.: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:7756 (2015)
Lubitz, S.A.* et al.: Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. J. Am. Coll. Cardiol. 63, 1200-1210 (2014)
Lüneburg, N.* et al.: Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. Circ. Cardiovasc. Genet. 7, 864-872 (2014)
Perry, J.R.B.* et al.: Parent-of-origin specific allelic associations among 106 genomic1 loci for age at menarche. Nature 514, 92-97 (2014)
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
Fernández-Rhodes, L.* et al.: Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am. J. Epidemiol. 178, 451-460 (2013)
Hek, K.* et al.: A genome-wide association study of depressive symptoms. Biol. Psychiatry 73, 667-678 (2013)