PuSH - Publication Server of Helmholtz Zentrum München

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1.
Ligthart, S.* et al.: Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. Am. J. Hum. Genet. 103, 691-706 (2018)
2.
Lin, H.* et al.: Common and rare coding genetic variation underlying the electrocardiographic PR interval. Circ. Genom. Precis. Med. 11:e002037 (2018)
3.
Roselli, C.* et al.: Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50, 1225–1233 (2018)
4.
van Setten, J.* et al.: PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. Nat. Commun. 9:2904 (2018)
5.
Christophersen, I.E.* et al.: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)
6.
Christophersen, I.E.* et al.: Fifteen genetic loci associated with the electrocardiographic P wave. Circ. Cardiovasc. Genet. 10:e001667 (2017)
7.
Weng, L.C.* et al.: Genetic interactions with age, sex, body mass index, and hypertension in relation to atrial fibrillation: The AFGen Consortium. Sci. Rep. 7:11303 (2017)
8.
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)
9.
Huan, T.* et al.: A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. Hum. Mol. Genet. 25, 4611-4623 (2016)
10.
Lin, H.* et al.: Gene-gene interaction analyses for atrial fibrillation. Sci. Rep. 6:35371 (2016)
11.
Zeller, T.* et al.: Molecular characterization of the NLRC4 expression in relation to interleukin-18 levels. Circ. Cardiovasc. Genet. 8, 717-726 (2015)
12.
Ellis, J.* et al.: Large multiethnic candidate gene study for C-reactive protein levels: Identification of a novel association at CD36 in African Americans. Hum. Genet. 133, 985-995 (2014)
13.
Kraja, A.T.* et al.: Pleiotropic genes for metabolic syndrome and inflammation. Mol. Genet. Metab. 112, 317-338 (2014)
14.
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)
15.
Lüneburg, N.* et al.: Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. Circ. Cardiovasc. Genet. 7, 864-872 (2014)
16.
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)
17.
Hek, K.* et al.: A genome-wide association study of depressive symptoms. Biol. Psychiatry 73, 667-678 (2013)
18.
Reiner, A.P.* et al.: Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Hum. Mol. Genet. 22, 3381-3393 (2013)
19.
Emerging Risk Factors Collaboration (Döring, A. ; Meisinger, C.) et al.: C-reactive protein, fibrinogen, and cardiovascular disease prediction. N. Engl. J. Med. 367, 1310-1320 (2012)
20.
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)