PuSH - Publication Server of Helmholtz Zentrum München

12 Records found.
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1.
Nalls, M.A.* et al.: Genetic comorbidities in Parkinson's disease. Hum. Mol. Genet. 23, 831-841 (2014)
2.
Buck, D.* et al.: Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis. Ann. Neurol. 73, 86-94 (2013)
3.
International Multiple Sclerosis Genetics Consortium (Illig, T. ; Lichtner, P.) et al.: Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45, 1353-1360 (2013)
4.
Mechelli, R.* et al.: A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. PLoS ONE 8:e63300 (2013)
5.
Sabater-Lleal, M.* et al.: Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation 128, 1310-1324 (2013)
6.
Sim, X.* et al.: Genetic loci for retinal arteriolar microcirculation. PLoS ONE 8:e65804 (2013)
7.
Keller, M.F.* et al.: Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum. Mol. Genet. 21, 4996-5009 (2012)
8.
International Stroke Genetics Consortium (Meisinger, C.) & Wellcome Trust Case Control Consortium 2 (WTCCC2): Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat. Genet. 44, 328-333 (2012)
9.
Pattaro, C.* et al.: Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet. 8:e1002584 (2012)
10.
International Parkinson's Disease Genomics Consortium (IPDGC) (Illig, T. ; Lichtner, P.) & Wellcome Trust Case Control Consortium 2 (WTCCC2): A two-stage meta-analysis identifies several new loci for Parkinson's disease. PLoS Genet. 7:e1002142 (2011)
11.
International Multiple Sclerosis Genetics Consortium (Klopp, N. ; Rückert, I.-M. ; Wichmann, H.-E. ; Winkelmann, J.) & Wellcome Trust Case Control Consortium 2 (WTCCC2): Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 476, 214-219 (2011)
12.
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)