PuSH - Publication Server of Helmholtz Zentrum München

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61.
Ferreira, M.A.* et al.: Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nat. Genet. 49, 1752-1757 (2017)
62.
Hammerschlag, A.R.* et al.: Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Nat. Genet. 49, 1584-1592 (2017)
63.
Howson, J.M.M.* et al.: Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nat. Genet. 49, 1113-1119 (2017)
64.
Iturbide Martinez De Albeniz, A. & Torres-Padilla, M.E.: Starting embryonic transcription for the first time. Nat. Genet. 49, 820-821 (2017)
65.
Jachowicz, J.W. et al.: LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo. Nat. Genet. 49, 1502–1510 (2017)
66.
Liu, D.J.* et al.: Exome-wide association study of plasma lipids in >300,000 individuals. Nat. Genet. 49, 1758-1766 (2017)
67.
Lu, X.* et al.: Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease. Nat. Genet. 49, 1722–1730 (2017)
68.
McKay, J.D.* et al.: Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nat. Genet. 49, 1126-1132 (2017)
69.
Meehan, T.F.* et al.: Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat. Genet. 49, 1231-1238 (2017)
70.
Melin, B.S.* et al.: Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat. Genet. 49, 789-794 (2017)
71.
Rodriguez-Terrones, D. et al.: A molecular roadmap for the emergence of early-embryonic-like cells in culture. Nat. Genet. 50, 106-119 (2017)
72.
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)
73.
Warren, H.R.* et al.: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat. Genet. 49, 403-415 (2017)
74.
Barban, N.* et al.: Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)
75.
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)
76.
Gormley, P.* et al.: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 48, 856-866 (2016)
77.
Huypens, P. et al.: Epigenetic germline inheritance of diet-induced obesity and insulin resistance. Nat. Genet. 48, 497-499 (2016)
78.
Kenna, K.P.* et al.: NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. Nat. Genet. 48, 1037-1042 (2016)
79.
McCarthy, S.* et al.: A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)
80.
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)