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81.
Smith, J.G.* et al.: Genome-wide association studies of the PR interval in African Americans. PLoS Genet. 7:e1001304 (2011)
82.
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)
83.
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)
84.
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)
85.
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)
86.
Griciuc, A. et al.: Inactivation of VCP/ter94 suppresses retinal pathology caused by misfolded rhodopsin in Drosophila. PLoS Genet. 6:e1001075 (2010)
87.
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)
88.
Ikram, M.K.* et al.: Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet. 6:e1001184 (2010)
89.
Marzi, C. et al.: Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. PLoS Genet. 6:e1001213 (2010)
90.
Meyer, T.E.* et al.: Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six loci influencing serum magnesium levels. PLoS Genet. 6:e1001045 (2010)
91.
Naukkarinen, J.* et al.: Use of genome-wide expression data to mine the 'Gray Zone' of GWA studies leads to novel candidate obesity genes. PLoS Genet. 6, 1-10:e1000976 (2010)
92.
Padmanabhan, S.* et al.: Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. PLoS Genet. 6, 1-11:e1001177 (2010)
93.
Scherag, A.* et al.: Two new loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and German study groups. PLoS Genet. 6:e1000916 (2010)
94.
Segrè, A.V.* et al.: Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. PLoS Genet. 6:e1001058 (2010)
95.
Stark, K.* et al.: Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet. 6:e1001167 (2010)
96.
Blagodatski, A.* et al.: A cis-acting diversification activator both necessary and sufficient for AID-mediated hypermutation. PLoS Genet. 5:e1000332 (2009)
97.
Heid, I.M. et al.: Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: Does heterogeneity of estimates relate to study design? PLoS Genet. 5:e1000694 (2009)
98.
Hicks, A.A.* et al.: Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 5:e1000672 (2009)
99.
Kolz, M. et al.: Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet. 5:e1000504 (2009)
100.
Lindgren, C.M.* et al.: Genome-wide association scan meta-analysis identifies three loci influencing adiposity and fat distribution. PLoS Genet. 5:e1000508 (2009)