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Kollerits, B.* et al.: Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein b-containing lipoproteins. Hum. Mol. Genet. 18, 4669-4676 (2009)
Boes, E.* et al.: INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolism. Obesity 16, 827-833 (2008)
Brandstatter, A.* et al.: Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI. Diabetes Care 31, 1662-1667 (2008)
Döring, A. et al.: SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nat. Genet. 40, 430-436 (2008)
Gieger, C. et al.: Genetics meets metabolomics: A genome-wide association study of metabolite profiles in human serum. PLoS Genet. 4:e1000282 (2008)
Heid, I.M. et al.: Estimating the Single Nucleotide Polymorphism Genotype Misclassification From Routine Double Measurements in a Large Epidemiologic Sample. Am. J. Epidemiol. 168, 878-889 (2008)
Heid, I.M. et al.: Association of the MC4R V103I polymorphism with the metabolic syndrome: The KORA Study. Obesity 16, 369-376 (2008)
Heid, I.M. et al.: Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. Circ. Cardiovasc. Genet. 1, 10-20 (2008)
Kollerits, B.* et al.: Intermittent claudication in the Erfurt Male Cohort (ERFORT) Study: its determinants and the impact on mortality. A population-based prospective cohort study with 30 years of follow-up. Atherosclerosis 198, 214-222 (2008)
Lasky-Su, J.* et al.: On the replication of genetic associations: Timing can be everything! Am. J. Hum. Genet. 82, 849-858 (2008)
Lingenhel, A.* et al.: Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease. Exp. Gerontol. 43, 1102-1107 (2008)
Linsel-Nitschke, P.* et al.: Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study. PLoS ONE 3:e2986 (2008)
Müller, M. et al.: Quantifying the contribution of genetic variants for survival phenotypes. Genet. Epidemiol. 32, 574-585 (2008)
Pichler, M.* et al.: Association of the melanocortin-4 receptor V103I polymorphism with dietary intake in severely obese persons. Am. J. Clin. Nutr. 88, 797-800 (2008)
Rosenberger, A.* et al.: Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years. BMC Cancer 8:60 (2008)
Sauter, W. et al.: Matrix metalloproteinase 1 (MMP1) is associated with early-onset lung cancer. Cancer Epidemiol. Biomarkers Prev. 17, 1127-1135 (2008)
Broedl, U.C.* et al.: Apolipoprotein A-IV is an independent predictor of disease activity in patients with inflammatory bowel disease. Inflamm. Bowel Dis. 13, 391-397 (2007)
Frischmann, M.E.* et al.: In vivo turnover study demonstrates diminished clearance of lipoprotein(a) in hemodialysis patients. Kidney Int. 71, 1036-1043 (2007)
Grallert, H. et al.: APOA5 variants and metabolic syndrome in Caucasians. J. Lipid Res. 48, 2614-2621 (2007)
Kollerits, B.* ; Fliser, D.* ; Heid, I.M. ; Ritz, E.* & Kronenberg, F.*: Gender-specific association of adiponectin as a predictor of progression of chronic kidney disease: The Mild to Moderate Kidney Disease Study. Kidney Int. 71, 1279-1286 (2007)