PuSH - Publication Server of Helmholtz Zentrum München

21 Records found.
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1.
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)
2.
de Vries, P.S.* et al.: Multi-ancestry Genome-Wide Association study of lipid levels incorporating gene-alcohol interactions. Am. J. Epidemiol. 188, 1033-1054 (2019)
3.
Karasik, D.* et al.: Disentangling the genetics of lean mass. Am. J. Clin. Nutr. 109, 276-287 (2019)
4.
Kilpeläinen, T.O.* et al.: Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat. Commun. 10:376 (2019)
5.
Sung, Y.J.* et al.: A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum. Mol. Genet., accepted (2019)
6.
Jiang, X.* et al.: Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat. Commun. 9:260 (2018)
7.
Ligthart, S.* et al.: Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. Am. J. Hum. Genet. 103, 691-706 (2018)
8.
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)
9.
Zillikens, M.C.* et al.: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat. Commun. 8:80 (2017)
10.
Zillikens, M.C.* et al.: Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat. Commun. 8:1414 (2017)
11.
Smith, J.G.* et al.: Discovery of genetic variation on chromosome 5q22 associated with mortality in heart failure. PLoS Genet. 12:e1006034 (2016)
12.
Loth, D.W.* et al.: Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat. Genet. 46, 669-677 (2014)
13.
Tang, W.* et al.: Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. PLoS ONE 9:e100776 (2014)
14.
Vimaleswaran, K.S.* et al.: Association of vitamin D status with arterial blood pressure and hypertension risk: A mendelian randomisation study. Lancet Diabet. Endocrinol. 2, 719-729 (2014)
15.
Hancock, D.B.* et al.: Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. PLoS Genet. 8:e1003098 (2013)
16.
Vimaleswaran, K.S.* et al.: Causal relationship between obesity and vitamin D status: Bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Med. 10:e1001383 (2013)
17.
Fox, C.S.* et al.: Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. PLoS Genet. 8:e1002695 (2012)
18.
Murabito, J.M.* et al.: Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circ. Cardiovasc. Genet. 5, 100-112 (2012)
19.
Artigas, M.S.* et al.: Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat. Genet. 43, 1082-1090 (2011)
20.
Kanoni, S.* et al.: Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: A 14-cohort meta-analysis. Diabetes 60, 2407-2416 (2011)