PuSH - Publication Server of Helmholtz Zentrum München

22 Records found.
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1.
Justice, A.E.* et al.: Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nat. Genet. 51, 452–469 (2019)
2.
Karasik, D.* et al.: Disentangling the genetics of lean mass. Am. J. Clin. Nutr. 109, 276-287 (2019)
3.
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)
4.
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., accepted (2019)
5.
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)
6.
Li, M.* et al.: SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function. J. Am. Soc. Nephrol. 28, 981-994 (2017)
7.
Zillikens, M.C.* et al.: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat. Commun. 8:80 (2017)
8.
Zillikens, M.C.* et al.: Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat. Commun. 8:1414 (2017)
9.
Barban, N.* et al.: Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)
10.
Winkler, T.W.* et al.: Correction: The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 12:e1006166 (2016)
11.
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat. Genet. 47, 1294-1303 (2015)
12.
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility, and BRCA1-mediated DNA repair. Obstet. Gynecol. 70, 758-762 (2015)
13.
Lunetta, K.L.* et al.: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:7756 (2015)
14.
Lunetta, K.L.* et al.: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:10257 (2015)
15.
Winkler, T.W.* et al.: The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 11:e1005378 (2015)
16.
Perry, J.R.B.* et al.: Parent-of-origin specific allelic associations among 106 genomic1 loci for age at menarche. Nature 514, 92-97 (2014)
17.
Fernández-Rhodes, L.* et al.: Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am. J. Epidemiol. 178, 451-460 (2013)
18.
Vimaleswaran, K.S.* et al.: Causal relationship between obesity and vitamin D status: Bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Med. 10:e1001383 (2013)
19.
Stolk, L.* et al.: Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat. Genet. 44, 260-268 (2012)
20.
Yang, J.* et al.: FTO genotype is associated with phenotypic variability of body mass index. Nature 490, 267-272 (2012)