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9 Records found.
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1.
Roselli, C.* et al.: Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50, 1225–1233 (2018)
2.
Esslinger, U.B.* et al.: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy. PLoS ONE 12:e0172995 (2017)
3.
Wild, P.S.* et al.: Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. J. Clin. Invest. 127, 1798-1812 (2017)
4.
Keenan, T.* et al.: Causal assessment of serum urate levels in cardiometabolic diseases through a mendelian randomization study. J. Am. Coll. Cardiol. 67, 407-416 (2016)
5.
Smith, J.G.* et al.: Discovery of genetic variation on chromosome 5q22 associated with mortality in heart failure. PLoS Genet. 12:e1006034 (2016)
6.
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
7.
Kapoor, A.* et al.: An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval. Am. J. Hum. Genet. 94, 854-869 (2014)
8.
Saxena, R.* et al.: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am. J. Hum. Genet. 90, 410-425 (2012)
9.
Lanktree, M.B.* et al.: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height. Am. J. Hum. Genet. 88, 6-18 (2011)