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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)
Ward-Caviness, C.K. et al.: Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. PLoS ONE 14:e0216222 (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)
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)
Zheng, J.* et al.: LD Hub: A centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. Bioinformatics 33, 272-279 (2017)
Horikoshi, M.* et al.: Genome-wide associations for birth weight and correlations with adult disease. Nature 538, 248-252 (2016)
Simpkin, A.J.* et al.: Prenatal and early life influences on epigenetic age in children: A study of mother-offspring pairs from two cohort studies. Hum. Mol. Genet. 25, 191-201 (2016)
Joshi, P.K.* et al.: Directional dominance on stature and cognition in diverse human populations. Nature 523, 459-462 (2015)
Peyrot, W.J.* et al.: The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects. Mol. Psychiatry 20, 735-743 (2015)
Wood, A.R.* et al.: Defining the role of common variation in the genomic and biological architecture of adult human height. Nat. Genet. 46, 1173-1186 (2014)