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Kempf, K.* et al.: Vaspin (SERPINA12) genotypes and risk of type 2 diabetes: Results from the MONICA/KORA studies. Exp. Clin. Endocrinol. Diabet. 118, 184-189 (2010)
Rabstein, S.* et al.: N-acetyltransferase 2, exposure to aromatic and heterocyclic amines, and receptor-defined breast cancer. Eur. J. Cancer Prev. 19, 100-109 (2010)
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)
Justenhoven, C.* et al.: Polymorphic loci of E2F2, CCND1 and CCND3 are associated with HER2 status of breast tumors. Int. J. Cancer 124, 2077-2081 (2009)
Karakas, M.* et al.: Genetic variation in Fcγ receptor IIa and risk of coronary heart disease: Negative results from two large independent populations. BMC Med. Genet. 10:46 (2009)
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)
Justenhoven, C.* et al.: The CYP1B1_1358_GG genotype is associated with estrogen receptor-negative breast cancer. Breast Cancer Res. Treat. 111, 171-177 (2008)
Justenhoven, C.* et al.: Breast cancer: A candidate gene approach across the estrogen metabolic pathway. Breast Cancer Res. Treat. 108, 137-149 (2008)
Lasky-Su, J.* et al.: On the replication of genetic associations: Timing can be everything! Am. J. Hum. Genet. 82, 849-858 (2008)
Müller, M. et al.: Quantifying the contribution of genetic variants for survival phenotypes. Genet. Epidemiol. 32, 574-585 (2008)
Roeber, S.* et al.: Evidence for a pathogenic role of different mutations at codon 188 of PRNP. PLoS ONE 3:e2147 (2008)
Jaremko, M.* et al.: Polymorphism of the DNA repair enzyme XRCC1 is associated with treatment prediction in anthracycline and cyclophosphamide/methotrexate/5-fluorouracil-based chemotherapy of patients with primary invasive breast cancer. Pharmacogenet. Genomics 17, 529-538 (2007)
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)
Rokavec, M.* et al.: A novel polymorphism in the promoter region of ERBB4 is associated with breast and colorectal cancer risk. Clin. Cancer Res. 13, 7506-7514 (2007)
Vollmert, C. et al.: Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians. Am. J. Physiol. Endocrinol. Metab. 292, E836-E844 (2007)
Hinney, A.* et al.: Prevalence, spectrum and functional characterization of Melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany. J. Clin. Endocrinol. Metab. 91, 1761-1769 (2006)
Huth, C. et al.: IL6 gene promoter polymorphisms and type 2 diabetes: Joint analysis of individual participants' data from 21 studies. Diabetes 55, 2915-2921 (2006)
Schoenborn, V.* et al.: The ATGL gene is associated with free fatty acids, triglycerides and type 2 diabetes. Diabetes 55, 1270-1275 (2006)
Vollmert, C. et al.: Significant association of a M129V independent polymorphism in the 5'UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study. J. Med. Genet. 43:e53 (2006)