PuSH - Publication Server of Helmholtz Zentrum München

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1.
Karlsson Linnér, R.* et al.: Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nat. Genet. 51, 245-257 (2019)
2.
Lee, J.J.* et al.: Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nat. Genet. 52, 1112-1121 (2018)
3.
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)
4.
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)
5.
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)
6.
Ferreira, M.A.* et al.: Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nat. Genet. 49, 1752-1757 (2017)
7.
Kreiner, E.* et al.: Shared genetic variants suggest common pathways in allergy and autoimmune diseases. J. Allergy Clin. Immunol. 140, 771-781 (2017)
8.
Schormair, B. et al.: Identification of novel risk loci for restless legs syndrome: A meta-analysis of genome-wide association studies in individuals of European ancestry: A meta-analysis. Lancet Neurol. 16, 898–907 (2017)
9.
Gormley, P.* et al.: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 48, 856-866 (2016)
10.
Okbay, A.* et al.: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat. Genet. 48, 624-633 (2016)
11.
Okbay, A.* et al.: Genome-wide association study identifies 74 loci associated with educational attainment. Nature 533, 539-542 (2016)
12.
Lunetta, K.L.* et al.: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:7756 (2015)
13.
Lunetta, K.L.* et al.: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:10257 (2015)
14.
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)
15.
Waage, J.E.* et al.: Shared genetic origins of allergy and autoimmune diseases. Allergy 70, 112 (2015)
16.
Waage, J.E.* et al.: A genome-wide association study of allergic rhinitis in 216 361 individuals identifies several novel susceptibility loci and increases knowledge on genetic pathways and cell types involved in disease etiology. Allergy 70, 108 (2015)