PuSH - Publication Server of Helmholtz Zentrum München

10 Records found.
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1.
Ashar, F.N.* et al.: A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. Eur. Heart J. 39, 3961-3969 (2018)
2.
Bihlmeyer, N.A.* et al.: ExomeChip-wide analysis of 95 626 individuals identifies 10 novel loci associated with QT and JT intervals. Circ. Genom. Precis. Med. 11:e001758 (2018)
3.
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)
4.
Artigas, M.S.* et al.: Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat. Genet. 43, 1082-1090 (2011)
5.
Eijgelsheim, M.* et al.: Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum. Mol. Genet. 19, 3885-3894 (2010)
6.
Ellinor, P.T.* et al.: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)
7.
Lubitz, S.A.* et al.: Independent susceptibility markers for atrial fibrillation on chromosome 4q25. Circulation 122, 976-984 (2010)
8.
Pfeufer, A. et al.: Genome-wide association study of PR interval. Nat. Genet. 42, 153-159 (2010)
9.
Sotoodehnia, N.* et al.: Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat. Genet. 42, 1068-1076 (2010)
10.
Benjamin, E.J.* et al.: Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet. 41, 879-81 (2009)