PuSH - Publication Server of Helmholtz Zentrum München

121 Records found.
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61.
Jacquemont, S.* et al.: Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 478, 97-102 (2011)
62.
Lamina, C.* ; Coassin, S.* ; Illig, T. & Kronenberg, F.*: Look beyond one's own nose: Combination of information from publicly available sources reveals an association of GATA4 polymorphisms with plasma triglycerides. Atherosclerosis 219, 698-703 (2011)
63.
Mittelstraß, K. et al.: Discovery of sexual dimorphisms in metabolic and genetic biomarkers. PLoS Genet. 7:e1002215 (2011)
64.
Suhre, K. et al.: A genome-wide association study of metabolic traits in human urine. Nat. Genet. 43, 565-571 (2011)
65.
Suhre, K. et al.: Human metabolic individuality in biomedical and pharmaceutical research. Nature 477, 54-60 (2011)
66.
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)
67.
Yu, Z. et al.: Differences between human plasma and serum metabolite profiles. PLoS ONE 6:e21230 (2011)
68.
Forer, L.* et al.: CONAN: Copy number variation analysis software for genome-wide association studies. BMC Bioinformatics 11:318 (2010)
69.
Heid, I.M. et al.: Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals. Atherosclerosis 208, 412-420 (2010)
70.
Illig, T. et al.: A genome-wide perspective of genetic variation in human metabolism. Nat. Genet. 42, 137-141 (2010)
71.
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)
72.
Lamina, C. et al.: Haplotype misclassification resulting from statistical reconstruction and genotype error, and its impact on association estimates. Ann. Hum. Genet. 74, 452-462 (2010)
73.
Linsel-Nitschke, P.* et al.: Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis 208, 183-189 (2010)
74.
Suhre, K. et al.: Metabolic footprint of diabetes: A multiplatform metabolomics study in an epidemiological setting. PLoS ONE 5:e13953 (2010)
75.
Teslovich, T.M.* et al.: Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466, 707-713 (2010)
76.
Aulchenko, Y.S.* et al.: Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat. Genet. 41, 47-55 (2009)
77.
Boes, E.* ; Coassin, S.* ; Kollerits, B.* ; Heid, I.M. & Kronenberg, F.*: Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: A systematic in-depth review. Exp. Gerontol. 44, 136-160 (2009)
78.
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)
79.
Hersberger, M.* et al.: No association of two functional polymorphisms in human ALOX15 with myocardial infarction. Atherosclerosis 205, 192-196 (2009)
80.
Huth, C. et al.: Joint analysis of individual participants' data from 17 studies on the association of the IL6 variant -174G>C with circulating glucose levels, interleukin-6 levels, and body mass index. Ann. Med. 41, 128-138 (2009)