PuSH - Publication Server of Helmholtz Zentrum München

235 Records found.
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161.
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group (Zhou, K.* ; Bellenguez, C.* ; Spencer, C.C.* ; Bennett, A.J.* ; Coleman, R.L.* ; Tavendale, R.* ; Hawley, S.A.* ; Donnelly, L.A.* ; Schofield, C.* ; Groves, C.J.* ; Burch, L.* ; Carr, F.* ; Strange, A.* ; Freeman, C.* ; Blackwell, J.M.* ; Bramon, E.* ; Brown, M.A.* ; Casas, J.P.* ; Corvin, A.* ; Craddock, N.* ; Deloukas, P.* ; Dronov, S.* ; Duncanson, A.* ; Edkins, S.* ; Gray, E.* ; Hunt, S.* ; Jankowski, J.* ; Langford, C.* ; Markus, H.S.* ; Mathew, C.G.* ; Plomin, R.* ; Rautanen, A.* ; Sawcer, S.J.* ; Samani, N.J.* ; Trembath, R.* ; Viswanathan, A.C.* ; Wood, N.W* ; Harries, L.W.* ; Hattersley, A.T.* ; Doney, A.S.* ; Colhoun, H.* ; Morris, A.D.* ; Sutherland, C.* ; Hardie, D.G.* ; Peltonen, L.* ; McCarthy, M.I.* ; Holman, R.R.* ; Palmer, C.N.* ; Donnelly, P.* ; Pearson, E.R.*) ; Wellcome Trust Case Control Consortium 2 (WTCCC2) (*) & MAGIC Investigators (Grallert, H. ; Gieger, C. ; Meisinger, C. ; Thorand, B. ; Wichmann, H.-E. ; Illig, T.): Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat. Genet. 43, 117-120 (2011)
162.
Anttila, V.* et al.: Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat. Genet. 42, 869-873 (2010)
163.
Bezzina, C.R.* et al.: Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction. Nat. Genet. 42, 688-691 (2010)
164.
Dupuis, J.* et al.: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat. Genet. 42, 105-116 (2010)
165.
Elks, C.E.* et al.: Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat. Genet. 42, 1077-1085 (2010)
166.
Ellinghaus, E.* et al.: Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. Nat. Genet. 42, 991-995 (2010)
167.
Ellinor, P.T.* et al.: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)
168.
Franke, A.* et al.: Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). Nat. Genet. 42, 292-294 (2010)
169.
Freathy, R.M.* et al.: Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nat. Genet. 42, 430-435 (2010)
170.
Haack, T.B. et al.: Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. Nat. Genet. 42, 1131-1134 (2010)
171.
Heid, I.M. et al.: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat. Genet. 42, 949-960 (2010)
172.
Hüffmeier, U.* et al.: Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. Nat. Genet. 42, 996-999 (2010)
173.
Illig, T. et al.: A genome-wide perspective of genetic variation in human metabolism. Nat. Genet. 42, 137-141 (2010)
174.
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)
175.
Liu, J.Z.* et al.: Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat. Genet. 42, 436-440 (2010)
176.
Mangold, E.* et al.: Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat. Genet. 42, 24-26 (2010)
177.
Meindl, A.* et al.: Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat. Genet. 42, 410-414 (2010)
178.
Morelli, G.* et al.: Yersinia pestis genome sequencing identifies patterns of global phylogenetic diversity. Nat. Genet. 42, 1140-1143 (2010)
179.
Pfeufer, A. et al.: Genome-wide association study of PR interval. Nat. Genet. 42, 153-159 (2010)
180.
Repapi, E.* et al.: Genome-wide association study identifies five loci associated with lung function. Nat. Genet. 42, 36-44 (2010)