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van Setten, J.* et al.: PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. Nat. Commun. 9:2904 (2018)
Christophersen, I.E.* et al.: Fifteen genetic loci associated with the electrocardiographic P wave. Circ. Cardiovasc. Genet. 10:e001667 (2017)
Waldeyer, C.* et al.: Lipoprotein(a) and the risk of cardiovascular disease in the European population: Results from the BiomarCaRE consortium. Eur. Heart J. 38, 2490-2498 (2017)
Zeller, T.* et al.: Transcriptome-wide analysis identifies novel associations with blood pressure. Hypertension 70, 713-750 (2017)
Blankenberg, S.* et al.: Troponin I and cardiovascular risk prediction in the general population: The BiomarCaRE consortium. Eur. Heart J. 37, 2428-2437 (2016)
Ojeda, F.M.* et al.: Comparison of cox model methods in a low-dimensional setting with few events. Geno. Prot. Bioinfo. 14, 235-243 (2016)
Swerdlow, D.I.* et al.: HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: Evidence from genetic analysis and randomised trials. Lancet 385, 351-361 (2015)
Zeller, T.* et al.: Molecular characterization of the NLRC4 expression in relation to interleukin-18 levels. Circ. Cardiovasc. Genet. 8, 717-726 (2015)
Ellis, J.* et al.: Large multiethnic candidate gene study for C-reactive protein levels: Identification of a novel association at CD36 in African Americans. Hum. Genet. 133, 985-995 (2014)
Kraja, A.T.* et al.: Pleiotropic genes for metabolic syndrome and inflammation. Mol. Genet. Metab. 112, 317-338 (2014)
Zeller, T.* et al.: BiomarCaRE: Rationale and design of the European BiomarCaRE project including 300,000 participants from 13 European countries. Eur. J. Epidemiol. 29, 777-790 (2014)
Reiner, A.P.* et al.: Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Hum. Mol. Genet. 22, 3381-3393 (2013)
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)
O'Donnell, C.J.* et al.: Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation 124, 2855-2864 (2012)
Bis, J.C.* et al.: Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nat. Genet. 43, 940-947 (2011)
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)
Schnabel, R.B.* et al.: Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: The National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project. Circ. Cardiovasc. Genet. 4, 557-564 (2011)
Smith, J.G.* et al.: Genome-wide association studies of the PR interval in African Americans. PLoS Genet. 7:e1001304 (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)
Barbalic, M.* et al.: Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Hum. Mol. Genet. 19, 1863-1872 (2010)