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Page 1
Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample.
Heid IM, Lamina C, Küchenhoff H, Fischer G, Klopp N, Kolz M, Grallert H, Vollmert C, Wagner S, Huth C, Müller J, Müller M, Hunt SC, Peters A, Paulweber B, Wichmann HE, Kronenberg F, Illig T. Heid IM, et al. Among authors: huth c. Am J Epidemiol. 2008 Oct 15;168(8):878-89. doi: 10.1093/aje/kwn208. Epub 2008 Sep 12. Am J Epidemiol. 2008. PMID: 18791193 Free PMC article.
Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians.
Vollmert C, Hahn S, Lamina C, Huth C, Kolz M, Schöpfer-Wendels A, Mann K, Bongardt F, Mueller JC, Kronenberg F, Wichmann HE, Herder C, Holle R, Löwel H, Illig T, Janssen OE; KORA group. Vollmert C, et al. Among authors: huth c. Am J Physiol Endocrinol Metab. 2007 Mar;292(3):E836-44. doi: 10.1152/ajpendo.00584.2005. Epub 2006 Nov 14. Am J Physiol Endocrinol Metab. 2007. PMID: 17106059 Free article.
APOA5 variants and metabolic syndrome in Caucasians.
Grallert H, Sedlmeier EM, Huth C, Kolz M, Heid IM, Meisinger C, Herder C, Strassburger K, Gehringer A, Haak M, Giani G, Kronenberg F, Wichmann HE, Adamski J, Paulweber B, Illig T, Rathmann W. Grallert H, et al. Among authors: huth c. J Lipid Res. 2007 Dec;48(12):2614-21. doi: 10.1194/jlr.M700011-JLR200. Epub 2007 Sep 3. J Lipid Res. 2007. PMID: 17768309 Free article.
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.
Huth C, Illig T, Herder C, Gieger C, Grallert H, Vollmert C, Rathmann W, Hamid YH, Pedersen O, Hansen T, Thorand B, Meisinger C, Doring A, Klopp N, Gohlke H, Lieb W, Hengstenberg C, Lyssenko V, Groop L, Ireland H, Stephens JW, Wernstedt Asterholm I, Jansson JO, Boeing H, Mohlig M, Stringham HM, Boehnke M, Tuomilehto J, Fernandez-Real JM, Lopez-Bermejo A, Gallart L, Vendrell J, Humphries SE, Kronenberg F, Wichmann HE, Heid IM. Huth C, et al. Ann Med. 2009;41(2):128-38. doi: 10.1080/07853890802337037. Ann Med. 2009. PMID: 18752089 Free PMC article.
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study.
Bauer A, Zierer A, Gieger C, Büyüközkan M, Müller-Nurasyid M, Grallert H, Meisinger C, Strauch K, Prokisch H, Roden M, Peters A, Krumsiek J, Herder C, Koenig W, Thorand B, Huth C. Bauer A, et al. Among authors: huth c. Genet Epidemiol. 2021 Sep;45(6):633-650. doi: 10.1002/gepi.22389. Epub 2021 Jun 3. Genet Epidemiol. 2021. PMID: 34082474
Genetic variants in the leukemia-associated Rho guanine nucleotide exchange factor (ARHGEF12) gene are not associated with T2DM and related parameters in Caucasians (KORA study).
Holzapfel C, Klopp N, Grallert H, Huth C, Gieger C, Meisinger C, Strassburger K, Giani G, Wichmann HE, Laumen H, Hauner H, Herder C, Rathmann W, Illig T. Holzapfel C, et al. Among authors: huth c. Eur J Endocrinol. 2007 Sep;157(3):R1-5. doi: 10.1530/EJE-07-0297. Eur J Endocrinol. 2007. PMID: 17766704
236 results