PuSH - Publication Server of Helmholtz Zentrum München

39 Records found.
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21.
Lieb, W.* et al.: Genetic predisposition to higher blood pressure increases coronary artery disease risk. Hypertension 61, 995-1001 (2013)
22.
Sinner, M.F.* et al.: A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern. Heart Rhythm 9, 1627-1634 (2012)
23.
Voight, B.F.* et al.: The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet. 8:e1002793 (2012)
24.
Johnson, T.* et al.: Blood pressure loci identified with a gene-centric array. Am. J. Hum. Genet. 89, 688-700 (2011)
25.
Min, J.L.* et al.: The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits. PLoS ONE 6:e22070 (2011)
26.
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)
27.
Smith, J.G.* et al.: Genome-wide association studies of the PR interval in African Americans. PLoS Genet. 7:e1001304 (2011)
28.
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)
29.
Eijgelsheim, M.* et al.: Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum. Mol. Genet. 19, 3885-3894 (2010)
30.
Ellinor, P.T.* et al.: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)
31.
Padmanabhan, S.* et al.: Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. PLoS Genet. 6, 1-11:e1001177 (2010)
32.
Pfeufer, A. et al.: Genome-wide association study of PR interval. Nat. Genet. 42, 153-159 (2010)
33.
Sotoodehnia, N.* et al.: Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat. Genet. 42, 1068-1076 (2010)
34.
Benjamin, E.J.* et al.: Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet. 41, 879-81 (2009)
35.
Body, S.C.* et al.: Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery. Circ. Cardiovasc. Genet. 2, 499-506 (2009)
36.
Kääb, S.* et al.: Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur. Heart J. 30, 813-819 (2009)
37.
Newton-Cheh, C.* et al.: Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 41, 666-676 (2009)
38.
Nolte, I.M.* et al.: Common genetic variation near the Phospholamban gene is associated with cardiac repolarisation: Meta-analysis of three genome-wide association studies. PLoS ONE 4:e6138 (2009)
39.
Arking, D.E.* et al.: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006)