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Malik, R.* et al.: Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3). Nat. Genet. (2019)
Ward-Caviness, C.K. et al.: Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. PLoS ONE 14:e0216222 (2019)
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)
Nolte, I.M.* et al.: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nat. Commun. 8:15805 (2017)
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)
de Vries, P.S.* et al.: A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Hum. Mol. Genet. 25, 358-370 (2016)
Smith, J.G.* et al.: Discovery of genetic variation on chromosome 5q22 associated with mortality in heart failure. PLoS Genet. 12:e1006034 (2016)
Interleukin 1 Genetics Consortium et al.: Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A mendelian randomisation analysis. Lancet Diabet. Endocrinol. 3, 243-253 (2015)
Huffman, J.E.* et al.: Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood 126, e19-e29 (2015)
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)
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)
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)
Sim, X.* et al.: Genetic loci for retinal arteriolar microcirculation. PLoS ONE 8:e65804 (2013)
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)
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)
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)
Manning, A.K.* et al.: A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat. Genet. 44, 659-669 (2012)
Gieger, C. et al.: New gene functions in megakaryopoiesis and platelet formation. Nature 480, 201-208 (2011)
Smith, N.L.* et al.: Genetic predictors of fibrin D-dimer levels in healthy adults. Circulation 123, 1864-1872 (2011)
Wain, L.V.* et al.: Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat. Genet. 43, 1005-1011 (2011)