PuSH - Publikationsserver des Helmholtz Zentrums München

Zeitschriften-Browsing

274 Datensätze gefunden.
Zum Exportieren der Ergebnisse bitte einloggen.
▮◀ ◀◀ 1 ... 2 ... 3 ... 4 ... 5 ... 6 ... 7 ... 8 ... 9 ... 10 ... 11 ... 12 ... 13 ... 14 ... ▶▶ ▶▮
Alle Publikationen dieser Seite in den Korb legen
61.
Kunkle, B.W.* et al.: Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2). Nat. Genet. 51, 1423-1424 (2019)
62.
Lane, J.M.* et al.: Biological and clinical insights from genetics of insomnia symptoms. Nat. Genet. 51, 387-393 (2019)
63.
Maccaferri, M.* et al.: Durum wheat genome highlights past domestication signatures and future improvement targets. Nat. Genet. 51, 885–895 (2019)
64.
Malik, R.* et al.: Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3). Nat. Genet. (2019)
65.
Pont, C.* et al.: Tracing the ancestry of modern bread wheats. Nat. Genet. 51, 905-911 (2019)
66.
Sakornsakolpat, P.* et al.: Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. Nat. Genet. 51, 494-505 (2019)
67.
Satizabal, C.L.* et al.: Genetic architecture of subcortical brain structures in 38,851 individuals. Nat. Genet. 51, 1624-1636 (2019)
68.
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)
69.
Shrine, N.* et al.: Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (Nature Genetics, (2019), 51, 3, (481-493), 10.1038/s41588-018-0321-7). Nat. Genet., DOI: 10.1038/s41588-019-0438-3 (2019)
70.
Tachmazidou, I.* et al.: Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Nat. Genet. 51, 230-236 (2019)
71.
Tin, A.* et al.: Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nat. Genet. 51, 1459-1474 (2019)
72.
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)
73.
Watson, H.J.* et al.: Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat. Genet. 51, 1207-1214 (2019)
74.
Wuttke, M.* et al.: A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)
75.
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)
76.
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)
77.
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., DOI: 10.1038/s41588-018-0297-3 (2018)
78.
Fernandes-Rosa, F.L.* et al.: A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism. Nat. Genet. 50, 355-361 (2018)
79.
Klarin, D.* et al.: Genetics of blood lipids among similar to 300,000 multi-ethnic participants of the Million Veteran Program. Nat. Genet. 50, 1514-1523 (2018)
80.
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)
▮◀ ◀◀ 1 ... 2 ... 3 ... 4 ... 5 ... 6 ... 7 ... 8 ... 9 ... 10 ... 11 ... 12 ... 13 ... 14 ... ▶▶ ▶▮