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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)
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)
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)
Pappa, I.* et al.: A genome-wide approach to children's aggressive behavior: The EAGLE consortium. Am. J. Med. Genet. B 171, 562-572 (2016)
Artigas, M.S.* et al.: Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Nat. Commun. 6:8658 (2015)
Li, Q.* et al.: Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: The CREAM consortium. Hum. Genet. 134, 131-146 (2015)
Paternoster, L.* et al.: Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nat. Genet. 47, 1449-1456 (2015)
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)
Hoggart, C.J.* et al.: Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index. PLoS Genet. 10, 1-12:e1004508 (2014)
van der Valk, R.J.* et al.: Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants. J. Allergy Clin. Immunol. 134, 46-55 (2014)
Bønnelykke, K.* et al.: Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Nat. Genet. 45, 902-906 (2013)
Cheng, C.Y.* et al.: Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am. J. Hum. Genet. 93, 264-277 (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)
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
Evans, D.M.* et al.: Mining the human phenome using allelic scores that index biological intermediates. PLoS Genet. 9:e1003919 (2013)
Horikoshi, M.* et al.: New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nat. Genet. 45, 76-82 (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)
Bradfield, J.P.* et al.: A genome-wide association meta-analysis identifies new childhood obesity loci. Nat. Genet. 44, 526-531 (2012)
Paternoster, L.* et al.: Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nat. Genet. 44, 187-192 (2012)
Taal, H.R.* et al.: Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat. Genet. 44, 532-538 (2012)