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Bentley, A.R.* et al.: Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat. Genet. 51, 636-648 (2019)
de Vries, P.S.* et al.: Multi-ancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions. Am. J. Epidemiol., accepted (2019)
Justice, A.E.* et al.: Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nat. Genet. 51, 452–469 (2019)
Kilpeläinen, T.O.* et al.: Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat. Commun. 10:376 (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)
Feitosa, M.F.* et al.: Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLoS ONE 13:e0198166 (2018)
Gilly, A.* et al.: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Nat. Commun. 9:4674 (2018)
Gilly, A.* et al.: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Nat. Commun. 9:5460 (2018)
Mahajan, A.* et al.: Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat. Genet. 50, 559-571 (2018)
Prins, B.P.* et al.: Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biol. 19:87 (2018)
Sung, Y.J.* et al.: A large-scale multi-ancestry genome-wide study accounting for smoking behavior identifies multiple significant loci for blood pressure. Am. J. Hum. Genet. 102, 375-400 (2018)
Warrington, N.M.* et al.: Maternal and fetal genetic contribution to gestational weight gain. Int. J. Obes. 42, 755-784 (2018)
Warren, H.R.* et al.: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat. Genet. 49, 403-415 (2017)
Felix, J.F.* et al.: Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Hum. Mol. Genet. 25, 389-403 (2016)
Horikoshi, M.* et al.: Genome-wide associations for birth weight and correlations with adult disease. Nature 538, 248-252 (2016)
Artigas, M.S.* et al.: Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Nat. Commun. 6:8658 (2015)
Qi, Q.* et al.: Dietary intake, FTO genetic variants and adiposity: A combined analysis of over 16,000 children and adolescents. Diabetes 64, 2467-2476 (2015)
van der Valk, R.J.* et al.: A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum. Mol. Genet. 24, 1155-1168 (2015)
Wain, L.V.* et al.: Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank. Lancet Resp. Med. 3, 769-781 (2015)
Boraska, V.* et al.: A genome-wide association study of anorexia nervosa. Mol. Psychiatry 19, 1085-1094 (2014)