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Timmers, P.R.* et al.: Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. eLife 8:e39856 (2019)
Xue, A.* et al.: Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Nat. Commun. 9:2941 (2018)
Kettunen, J.* et al.: Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Nat. Commun. 7:11122 (2016)
Vogt, S. et al.: Characterization of the metabolic profile associated with serum 25-hydroxyvitamin D: A cross-sectional analysis in population-based data. Int. J. Epidemiol. 45, 1469-1481 (2016)
Peters, M.J.* et al.: The transcriptional landscape of age in human peripheral blood. Nat. Commun. 6:8570 (2015)
Surakka, I.* et al.: The impact of low-frequency and rare variants on lipid levels. Nat. Genet. 47, 589-597 (2015)
Westra, H.J.* et al.: Cell specific eQTL analysis without sorting cells. PLoS Genet. 11:e1005223 (2015)
Würtz, P.* et al.: Metabolite profiling and cardiovascular event risk: A prospective study of three population-based cohorts. Circulation 131, 774-785 (2015)
Herder, C.* et al.: Genetic determinants of circulating interleukin-1 receptor antagonist levels and their association with glycemic traits. Diabetes 63, 4343-4359 (2014)
Global Lipids Genetics Consortium et al.: Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274-1283 (2013)
Codd, V.* et al.: Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013)
Cousminer, D.L.* et al.: Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Hum. Mol. Genet. 22, 2735-2747 (2013)
Do, R.* et al.: Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat. Genet. 45, 1345-1352 (2013)
Fall, T.* et al.: The role of adiposity in cardiometabolic traits: A mendelian randomization analysis. PLoS Med. 10:e1001474 (2013)
Mäkelä, K.M.* et al.: Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium. Circ. Cardiovasc. Genet. 6, 73-81 (2013)
Westra, H.J.* et al.: Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat. Genet. 45, 1238-1243 (2013)
Coviello, A.D.* et al.: A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple loci implicated in sex steroid hormone regulation. PLoS Genet. 8:e1002805 (2012)
Dehghan, A.* et al.: Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 123, 731-738 (2011)
Heid, I.M. et al.: Corrigendum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat. Genet. 43, 1164 (2011)
Winkelmann, J. et al.: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)