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Perry, J.R.* et al.: Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. PLoS Genet. 8:e1002741 (2012)
Voight, B.F.* et al.: The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet. 8:e1002793 (2012)
Zaitlen, N.* et al.: Informed conditioning on clinical covariates increases power in case-control association studies. PLoS Genet. 8:e1003032 (2012)
Allanore, Y.* et al.: Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. PLoS Genet. 7:e1002091 (2011)
Amselem, J.* et al.: Genomic analysis of the necrotrophic fungal pathogens Sclerotinia sclerotiorum and Botrytis cinerea. PLoS Genet. 7:e1002230 (2011)
Böger, C.A.* et al.: Association of eGFR-related loci identified by GWAS with incident CKD and ESRD. PLoS Genet. 7:e1002292 (2011)
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)
IBC 50K CAD Consortium (Klopp, N. ; Baumert, J.J. ; Peters, A. ; Meisinger, C. ; Gieger, C. ; Döring, A. ; Illig, T. ; Meitinger, T. ; Wichmann, H.-E.): Large-scale gene-centric analysis identifies novel variants for coronary artery disease. PLoS Genet. 7:e1002260 (2011)
McKay, J.D.* et al.: A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. PLoS Genet. 7:e1001333 (2011)
Mittelstraß, K. et al.: Discovery of sexual dimorphisms in metabolic and genetic biomarkers. PLoS Genet. 7:e1002215 (2011)
Nalls, M.A.* et al.: Multiple loci are associated with white blood cell phenotypes. PLoS Genet. 7:e1002113 (2011)
Nicholson, G.* et al.: A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection. PLoS Genet. 7:e1002270 (2011)
Ohlsson, C.* et al.: Genetic determinants of serum testosterone concentrations in men. PLoS Genet. 7:e1002313 (2011)
Smith, J.G.* et al.: Genome-wide association studies of the PR interval in African Americans. PLoS Genet. 7:e1001304 (2011)
Speliotes, E.K.* et al.: Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genet. 7:e1001324 (2011)
Surakka, I.* et al.: A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genet. 7:e1002333 (2011)
Winkelmann, J. et al.: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)
Wöhlke, A. et al.: A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. PLoS Genet. 7:e1002304 (2011)
Griciuc, A. et al.: Inactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in Drosophila. PLoS Genet. 6:e1001075 (2010)
Igl, W.* et al.: Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. PLoS Genet. 6:e1000798 (2010)