PuSH - Publication Server of Helmholtz Zentrum München

12 Records found.
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1.
Demenais, F.* et al.: Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nat. Genet. 50, 42-53 (2018)
2.
Hara, K.* et al.: Genome-wide association study identifies three novel loci for type 2 diabetes. Hum. Mol. Genet. 23, 239-246 (2014)
3.
Lubitz, S.A.* et al.: Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. J. Am. Coll. Cardiol. 63, 1200-1210 (2014)
4.
Makita, N.* et al.: Novel calmodulin (CALM2) mutations associated with congenital arrhythmia susceptibility. Circ. Cardiovasc. Genet. 7, 466-474 (2014)
5.
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)
6.
Makita, N.* et al.: CALM2 mutations associated with atypical juvenile long QT syndrome. Circulation 128, S:13371 (2013)
7.
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)
8.
Imamura, M.* et al.: A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations. Hum. Mol. Genet. 21, 3042-3049 (2012)
9.
Okada, Y.* et al.: Meta-analysis identifies multiple loci associated with kidney function-related traits in East Asian populations. Nat. Genet. 44, 904-909 (2012)
10.
Okada, Y.* et al.: Common variants at CDKAL1 and KLF9 are associated with body mass index in East Asian populations. Nat. Genet. 44, 302-306 (2012)
11.
Wen, W.* et al.: Meta-analysis identifies common variants associated with body mass index in east Asians. Nat. Genet. 44, 307-311 (2012)
12.
Nalls, M.A.* et al.: Multiple loci are associated with white blood cell phenotypes. PLoS Genet. 7:e1002113 (2011)