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11 Records found.
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1.
Ji, Y.* et al.: Genome-wide and abdominal MRI data provide evidence that a genetically determined favorable adiposity phenotype is characterized by lower ectopic liver fat and lower risk of type 2 diabetes, heart disease, and hypertension. Diabetes 68, 207-219 (2019)
2.
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)
3.
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)
4.
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)
5.
Macé, A.* et al.: CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nat. Commun. 8:744 (2017)
6.
Horikoshi, M.* et al.: Genome-wide associations for birth weight and correlations with adult disease. Nature 538, 248-252 (2016)
7.
Wood, A.R.* et al.: Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively. Diabetologia 59, 1214-1221 (2016)
8.
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)
9.
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)
10.
Lunetta, K.L.* et al.: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:7756 (2015)
11.
Lunetta, K.L.* et al.: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:10257 (2015)