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161.
Hollingworth, P.* et al.: Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat. Genet. 43, 429-436 (2011)
162.
Hu, T.T.* et al.: The Arabidopsis lyrata genome sequence and the basis of rapid genome size change. Nat. Genet. 43, 476-481 (2011)
163.
Kilpeläinen, T.O.* et al.: Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Nat. Genet. 43, 753-760 (2011)
164.
Kornum, B.R.* et al.: Common variants in P2RY11 are associated with narcolepsy. Nat. Genet. 43, 66-71 (2011)
165.
Melum, E.* et al.: Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. Nat. Genet. 43, 17-19 (2011)
166.
Purdue, M.P.* et al.: Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. Nat. Genet. 43, 60-65 (2011)
167.
Schunkert, H.* et al.: Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat. Genet. 43, 333-340 (2011)
168.
Small, K.S.* et al.: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes. Nat. Genet. 43, 561-564 (2011)
169.
Suhre, K. et al.: A genome-wide association study of metabolic traits in human urine. Nat. Genet. 43, 565-571 (2011)
170.
Wain, L.V.* et al.: Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat. Genet. 43, 1005-1011 (2011)
171.
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)
172.
Anttila, V.* et al.: Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat. Genet. 42, 869-873 (2010)
173.
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)
174.
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)
175.
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)
176.
Ellinghaus, E.* et al.: Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. Nat. Genet. 42, 991-995 (2010)
177.
Ellinor, P.T.* et al.: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)
178.
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)
179.
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)
180.
Haack, T.B. et al.: Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. Nat. Genet. 42, 1131-1134 (2010)