PuSH - Publication Server of Helmholtz Zentrum München

111 Records found.
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1.
Imboden, M.* et al.: Epigenome-wide association study of lung function level and its change. Eur. Respir. J., accepted (2019)
2.
Shrine, N.* et al.: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet. 51, 481-493 (2019)
3.
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)
4.
Evangelou, E.* et al.: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat. Genet. 50, 1412-1425 (2018)
5.
Evangelou, E.* et al.: Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x). Nat. Genet., accepted (2018)
6.
Jiang, X.* et al.: Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat. Commun. 9:260 (2018)
7.
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)
8.
Reese, S.E.* et al.: Epigenome-wide meta-analysis of DNA methylation and childhood asthma. J. Allergy Clin. Immunol., accepted (2018)
9.
Waage, J.* et al.: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat. Genet. 50, 1072–1080 (2018)
10.
Waage, J.* et al.: Author correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat. Genet. 50:1343 (2018)
11.
Warrington, N.M.* et al.: Maternal and fetal genetic contribution to gestational weight gain. Int. J. Obes. 42, 755-784 (2018)
12.
Aschard, H.* et al.: Evidence for large-scale gene-by-smoking interaction effects on pulmonary function. Int. J. Epidemiol. 46, 894-904 (2017)
13.
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)
14.
Justice, A.E.* et al.: Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nat. Commun. 8:14977 (2017)
15.
Kreiner, E.* et al.: Shared genetic variants suggest common pathways in allergy and autoimmune diseases. J. Allergy Clin. Immunol. 140, 771-781 (2017)
16.
Poobalasingam, T.* et al.: Heterozygous Vangl2Looptail mice reveal novel roles for the planar cell polarity pathway in adult lung homeostasis and repair. Dis. Model. Mech. 10, 409-423 (2017)
17.
Wain, L.V.* et al.: Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nat. Genet. 49, 416-425 (2017)
18.
Wain, L.V.* et al.: Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney. Hypertension 70, e4-e19 (2017)
19.
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)
20.
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)