PuSH - Publication Server of Helmholtz Zentrum München

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1.
Flannick, J.* et al.: Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature 570, 71-76 (2019)
2.
Yu, B.* et al.: The Consortium of Metabolomics Studies (COMETS): Metabolomics in 47 Prospective Cohort Studies. Am. J. Epidemiol. 188, 991-1012 (2019)
3.
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)
4.
Wild, P.S.* et al.: Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. J. Clin. Invest. 127, 1798-1812 (2017)
5.
Ehret, G.B.* et al.: The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)
6.
Smith, J.G.* et al.: Discovery of genetic variation on chromosome 5q22 associated with mortality in heart failure. PLoS Genet. 12:e1006034 (2016)
7.
Surendran, P.* et al.: Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)
8.
Huan, T.* et al.: A meta-analysis of gene expression signatures of blood pressure and hypertension. PLoS Genet. 11:e1005035 (2015)
9.
Jansen, H.* et al.: Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis 241, 419-426 (2015)
10.
Kaess, B.M.* et al.: Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community. J. Am. Heart Assoc. 4:e001544 (2015)
11.
Lieb, W.* et al.: Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes. Circ. Cardiovasc. Genet. 8, 131-140 (2015)
12.
Würtz, P.* et al.: Metabolite profiling and cardiovascular event risk: A prospective study of three population-based cohorts. Circulation 131, 774-785 (2015)
13.
Ganesh, S.K.* et al.: Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am. J. Hum. Genet. 95, 49-65 (2014)
14.
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)
15.
Simino, J.* et al.: Gene-age interactions in blood pressure regulation: A large-scale investigation with the CHARGE, Global BPgen, and ICBP consortia. Am. J. Hum. Genet. 95, 24-38 (2014)
16.
Tragante, V.* et al.: Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. Am. J. Hum. Genet. 94, 349-360 (2014)
17.
Ho, J.E.* et al.: Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. J. Clin. Invest. 123, 4208-4218 (2013)
18.
Lieb, W.* et al.: Genetic predisposition to higher blood pressure increases coronary artery disease risk. Hypertension 61, 995-1001 (2013)
19.
Coviello, A.D.* et al.: A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple loci implicated in sex steroid hormone regulation. PLoS Genet. 8:e1002805 (2012)
20.
Grallert, H. et al.: Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: Meta-analysis of genome-wide association studies from five community-based studies. Eur. Heart J. 33, 238-251 (2012)