PuSH - Publication Server of Helmholtz Zentrum München

55 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
Schlicht, K.* et al.: The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus. Hum. Genet. 138, 375–388 (2019)
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)
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)
Luijk, R.* et al.: Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation. Nat. Commun. 9:3738 (2018)
Parmar, P.* et al.: Association of maternal prenatal smoking GFI1-locus and cardiometabolic phenotypes in 18,212 adults. EBioMedicine 38, 206-216 (2018)
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)
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)
Day, F.R.* et al.: Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat. Genet. 49, 834-841 (2017)
Karlsoon Linner, R.* et al.: An epigenome-wide association study meta-analysis of educational attainment. Mol. Psychiatry 22, 1680-1690 (2017)
Kreiner, E.* et al.: Shared genetic variants suggest common pathways in allergy and autoimmune diseases. J. Allergy Clin. Immunol. 140, 771-781 (2017)
Mandaviya, P.R.* et al.: Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes. PLoS ONE 12:e0182472 (2017)
Wahl, S. et al.: Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity. Nature 541, 81-86 (2017)
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)
Amin, N.* et al.: Genetic variants in RBFOX3 are associated with sleep latency. Eur. J. Hum. Genet. 24, 1488-1495 (2016)
Barban, N.* et al.: Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)
Ehret, G.B.* et al.: The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)
Felix, J.F.* et al.: Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Hum. Mol. Genet. 25, 389-403 (2016)
Gormley, P.* et al.: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 48, 856-866 (2016)
Lu, Y.* et al.: New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Nat. Commun. 7:10495 (2016)
Okbay, A.* et al.: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat. Genet. 48, 624-633 (2016)