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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)
Demenais, F.* et al.: Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nat. Genet. 50, 42-53 (2018)
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)
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)
Middeldorp, C.M.* et al.: A Genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts. J. Am. Acad. Child Adolesc. Psychiatry 55, 896-905.e6 (2016)
van der Valk, R.J.* et al.: A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum. Mol. Genet. 24, 1155-1168 (2015)
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)
Verhoeven, V.J.M.* et al.: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat. Genet. 45, 314-318 (2013)
Boraska, V.* et al.: Genome-wide meta-analysis of common variant differences between men and women. Hum. Mol. Genet. 21, 4805-4815 (2012)
Ikram, M.A.* et al.: Common variants at 6q22 and 17q21 are associated with intracranial volume. Nat. Genet. 44, 539-544 (2012)
Taal, H.R.* et al.: Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat. Genet. 44, 532-538 (2012)