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Saleheen, D.* et al.: Loss of cardioprotective effects at the ADAMTS7 locus as a result of gene-smoking interactions. Circulation 135, 2336-2353 (2017)
Stitziel, N.O.* et al.: Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease. N. Engl. J. Med. 374, 1134-1144 (2016)
Stitziel, N.O.* et al.: Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease (vol 374, pg 1134, 2016). N. Engl. J. Med. 374, 1898-1898 (2016)
Jansen, H.* et al.: Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis 241, 419-426 (2015)
Nelson, C.P.* et al.: Genetically determined height and coronary artery disease. N. Engl. J. Med. 372, 1608-1618 (2015)
Dichgans, M.* et al.: Shared genetic susceptibility to ischemic stroke and coronary artery disease: A genome-wide analysis of common variants. Stroke 45, 24-36 (2014)
Dick, K.J.* et al.: DNA methylation and body-mass index: A genome-wide analysis. Lancet 383, 1990-1998 (2014)
Codd, V.* et al.: Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013)
Deloukas, P.* et al.: Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
Lieb, W.* et al.: Genetic predisposition to higher blood pressure increases coronary artery disease risk. Hypertension 61, 995-1001 (2013)
Minelli, C.* et al.: Importance of different types of prior knowledge in selecting genome-wide findings for follow-up. Genet. Epidemiol. 37, 205-213 (2013)
Pichler, I.* et al.: Serum iron levels and the risk of Parkinson disease: A mendelian randomization study. PLoS Med. 10, 4270-4276:e1001462 (2013)
Thompson, J.R.* et al.: SNP prioritization using a Bayesian probability of association. Genet. Epidemiol. 37, 214-221 (2013)
Hartz, S.M.* et al.: Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. JAMA psychiatry 69, 854-860 (2012)
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)
Reilly, M.P.* et al.: Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies. Lancet 377, 383-392 (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)
Allen, H.L.* et al.: Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467, 832-838 (2010)