PuSH - Publication Server of Helmholtz Zentrum München

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1.
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)
2.
Locke, A.E.* et al.: Genetic studies of body mass index yield new insights for obesity biology. Nature 518, 197-206 (2015)
3.
Shungin, D.* et al.: New genetic loci link adipose and insulin biology to body fat distribution. Nature 518, 187-196 (2015)
4.
Holmes, M.V.* et al.: Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA(2))-V isoenzyme in coronary heart disease modified mendelian randomization analysis using PLA2G5 expression levels. Circ. Cardiovasc. Genet. 7, 144-150 (2014)
5.
Wood, A.R.* et al.: Defining the role of common variation in the genomic and biological architecture of adult human height. Nat. Genet. 46, 1173-1186 (2014)
6.
Deloukas, P.* et al.: Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)
7.
Sabater-Lleal, M.* et al.: Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation 128, 1310-1324 (2013)
8.
Billings, L.K.* et al.: Impact of common variation in bone-related genes on type 2 diabetes and related traits. Diabetes 61, 2176-2186 (2012)
9.
Huang, J.* et al.: Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood 120, 4873-4881 (2012)
10.
Scott, R.A.* et al.: Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat. Genet. 44, 991-1005 (2012)
11.
Bown, M.J.* et al.: Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. Am. J. Hum. Genet. 89, 619-627 (2011)
12.
Strawbridge, R.J.* et al.: Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes 60, 2624-2634 (2011)