PuSH - Publication Server of Helmholtz Zentrum München

9 Records found.
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1.
Liu, J.* et al.: An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis. Nat. Commun. 10:2581 (2019)
2.
Timmers, P.R.* et al.: Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. eLife 8:e39856 (2019)
3.
Ward-Caviness, C.K. et al.: DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis. Blood 132, 1842-1850 (2018)
4.
Xue, A.* et al.: Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Nat. Commun. 9:2941 (2018)
5.
Ferreira, M.A.* et al.: Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nat. Genet. 49, 1752-1757 (2017)
6.
Nolte, I.M.* et al.: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nat. Commun. 8:15805 (2017)
7.
Ried, J.S. et al.: A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nat. Commun. 7:13357 (2016)
8.
Baumert, J.J. et al.: No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: Results from meta-analyses of 80,607 subjects. PLoS ONE 9:e111156 (2014)
9.
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)