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Gregson, J.* et al.: Cardiovascular risk factors are associated with venous thromboembolism. JAMA Cardiol. 4, 163-173 (2019)
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)
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)
Fowkes, F.G.R.* et al.: Development and validation of an ankle brachial index risk model for the prediction of cardiovascular events. Eur. J. Prev. Cardiol. 21, 310-320 (2014)
Lange, L.A.* et al.: Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet. 94, 233-245 (2014)
Emerging Risk Factors Collaboration (Meisinger, C.) et al.: Glycated hemoglobin measurement and prediction of cardiovascular disease. JAMA 311, 1225-1233 (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)
Emerging Risk Factors Collaboration (Döring, A. ; Meisinger, C.) et al.: C-reactive protein, fibrinogen, and cardiovascular disease prediction. N. Engl. J. Med. 367, 1310-1320 (2012)
Franceschini, N.* et al.: Discovery and fine mapping of serum protein loci through transethnic meta-analysis. Am. J. Hum. Genet. 91, 744-753 (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)
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)
Stolk, L.* et al.: Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat. Genet. 44, 260-268 (2012)
Dehghan, A.* et al.: Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 123, 731-738 (2011)
Gieger, C. et al.: New gene functions in megakaryopoiesis and platelet formation. Nature 480, 201-208 (2011)
Nalls, M.A.* et al.: Multiple loci are associated with white blood cell phenotypes. PLoS Genet. 7:e1002113 (2011)
Schunkert, H.* et al.: Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat. Genet. 43, 333-340 (2011)
Wild, P.S.* et al.: A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ. Cardiovasc. Genet. 4, 403-412 (2011)
Eijgelsheim, M.* et al.: Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum. Mol. Genet. 19, 3885-3894 (2010)
Elks, C.E.* et al.: Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat. Genet. 42, 1077-1085 (2010)