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201.
Ganesh, S.K.* et al.: Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nat. Genet. 41, 1191-1198 (2009)
202.
Ghezzi, D.* et al.: SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy. Nat. Genet. 41, 654-656 (2009)
203.
Gudbjartsson, D.F.* et al.: A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat. Genet. 41, 876-878 (2009)
204.
Gudbjartsson, D.F.* et al.: Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat. Genet. 41, 342-347 (2009)
205.
Hallmayer, J.* et al.: Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nat. Genet. 41, 708-711 (2009)
206.
Harold, D.* et al.: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat. Genet. 41, 1088-1093 (2009)
207.
Kathiresan, S.* et al.: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat. Genet. 41, 334-341 (2009)
208.
Lewis, M.A.* et al.: An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat. Genet. 41, 614-618 (2009)
209.
Newton-Cheh, C.* et al.: Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 41, 666-676 (2009)
210.
Pfeufer, A. et al.: Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat. Genet. 41, 407-414 (2009)
211.
Prokopenko, I.* et al.: Variants in MTNR1B influence fasting glucose levels. Nat. Genet. 41, 77-81 (2009)
212.
Simon-Sanchez, J.* et al.: Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 41, 1308-1314 (2009)
213.
Soranzo, N.* et al.: A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat. Genet. 41, 1182-1190 (2009)
214.
Tregouet, D.A.* et al.: Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat. Genet. 41, 283-285 (2009)
215.
van Es, M.A.* et al.: Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 41, 1083-1087 (2009)
216.
Willer, C.J.* et al.: Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat. Genet. 41, 25-34 (2009)
217.
Döring, A. et al.: SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nat. Genet. 40, 430-436 (2008)
218.
Lettre, G.* et al.: Identification of ten loci associated with height highlights new biological pathways in human growth. Nat. Genet. 40, 584-591 (2008)
219.
Loos, R.J.* et al.: Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat. Genet. 40, 768-775 (2008)
220.
McGowan, K.A. et al.: Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat. Genet. 40, 963-970 (2008)