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81.
Ikram, M.K.* et al.: Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet. 6:e1001184 (2010)
82.
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)
83.
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)
84.
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)
85.
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)
86.
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)
87.
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)
88.
Stark, K.* et al.: Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet. 6:e1001167 (2010)
89.
Blagodatski, A.* et al.: A cis-acting diversification activator both necessary and sufficient for AID-mediated hypermutation. PLoS Genet. 5:e1000332 (2009)
90.
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)
91.
Hicks, A.A.* et al.: Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 5:e1000672 (2009)
92.
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)
93.
Lindgren, C.M.* et al.: Genome-wide association scan meta-analysis identifies three loci influencing adiposity and fat distribution. PLoS Genet. 5:e1000508 (2009)
94.
Richards, J.B.* et al.: A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. PLoS Genet. 5:e1000768 (2009)
95.
Gieger, C. et al.: Genetics meets metabolomics: A genome-wide association study of metabolite profiles in human serum. PLoS Genet. 4:e1000282 (2008)
96.
Hertzano, R.* et al.: A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells. PLoS Genet. 4:e1000207 (2008)
97.
Lisse, T.S. et al.: ER stress-mediated apoptosis in a new mouse model of Osteogenesis imperfecta. PLoS Genet. 4:e7 (2008)
98.
Spiden, S.L.* et al.: The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. PLoS Genet. 4:e1000238 (2008)
99.
Weidinger, S. et al.: Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. PLoS Genet. 4:e1000166 (2008)
100.
Lyon, H.N.* et al.: The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts. PLoS Genet. 3, 0627-0633:e61 (2007)