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121.
McCarthy, S.* et al.: A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)
122.
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)
123.
Pradeepa, M.M.* et al.: Histone H3 globular domain acetylation identifies a new class of enhancers. Nat. Genet. 48, 681-686 (2016)
124.
Surendran, P.* et al.: Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat. Genet. 48, 1151-1161 (2016)
125.
van Rheenen, W.* et al.: Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat. Genet. 48, 1043-1048 (2016)
126.
Witteveen, J.S.* et al.: Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity. Nat. Genet. 48, 877-887 (2016)
127.
Chen, Y.-C.* et al.: Transcriptional regulator PRDM12 is essential for human pain perception. Nat. Genet. 47, 803-808 (2015)
128.
Chen, Y.-C.* et al.: Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception. Nat. Genet. 47, 962 (2015)
129.
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)
130.
Debette, S.* et al.: Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection. Nat. Genet. 47, 78-83 (2015)
131.
Gaulton, K.J.* et al.: Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nat. Genet. 47, 1415-1425 (2015)
132.
Goyette, P.* et al.: High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat. Genet. 47, 172-179 (2015)
133.
Hrabě de Angelis, M. et al.: Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat. Genet. 47, 969-978 (2015)
134.
Kato, N.* et al.: Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat. Genet. 47, 1282-1293 (2015)
135.
Kohl, S.* et al.: Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia. Nat. Genet. 47, 757-765 (2015)
136.
Moutsianas, L.* et al.: Class II HLA interactions modulate genetic risk for multiple sclerosis. Nat. Genet. 47, 1107-1113 (2015)
137.
CARDIoGRAMplusC4D Consortium (Nikpay, M.* ; Goel, A.* ; Won, H.* ; Hall, L.M.* ; Willenborg, C.* ; Kanoni, S.* ; Saleheen, D.* ; Gieger, C. ; Meitinger, T. ; Peters, A. ; Watkins, H.* ; Kathiresan, S.* ; MacPherson, R.*): A comprehensive 1000 genomes–based genome-wide association meta-analysis of coronary artery disease. Nat. Genet. 47, 1121-1130 (2015)
138.
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)
139.
Reincke, M.* et al.: Mutations in the deubiquitinase gene USP8 cause Cushing's disease. Nat. Genet. 47, 31-38 (2015)
140.
Surakka, I.* et al.: The impact of low-frequency and rare variants on lipid levels. Nat. Genet. 47, 589-597 (2015)
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