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Liu, J.* et al.: An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis. Nat. Commun. 10:2581 (2019)
Middeldorp, C.M.* et al.: The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: Design, results and future prospects. Eur. J. Epidemiol. 34, 279-300 (2019)
Warrington, N.M.* et al.: Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nat. Genet. 51, 804-814 (2019)
Wuttke, M.* et al.: A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)
Felix, J.F.* et al.: Cohort profile: Pregnancy and childhood epigenetics (PACE) consortium. Int. J. Epidemiol. 47, 22-23u (2018)
Reese, S.E.* et al.: Epigenome-wide meta-analysis of DNA methylation and childhood asthma. J. Allergy Clin. Immunol. 143, 2062-2074 (2018)
Warrington, N.M.* et al.: Maternal and fetal genetic contribution to gestational weight gain. Int. J. Obes. 42, 755-784 (2018)
Gall, H.* et al.: The Giessen Pulmonary Hypertension Registry: Survival in pulmonary hypertension subgroups. J. Heart Lung Transpl. 36, 957-967 (2017)
Huber, M.B. ; Felix, J.F. ; Vogelmann, M.* & Leidl, R.: Health-related quality of life of the general German population in 2015: Results from the EQ-5D-5L. Int. J. Environ. Res. Public Health 14:426 (2017)
Nolte, I.M.* et al.: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nat. Commun. 8:15805 (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)
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)
Horikoshi, M.* et al.: Genome-wide associations for birth weight and correlations with adult disease. Nature 538, 248-252 (2016)
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)
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
Smith, J.G.* et al.: Discovery of genetic variation on chromosome 5q22 associated with mortality in heart failure. PLoS Genet. 12:e1006034 (2016)
Surendran, P.* et al.: Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)
van der Laan, S.W.* et al.: Cystatin C and cardiovascular disease: A mendelian randomization study. J. Am. Coll. Cardiol. 68, 934-945 (2016)