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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
Zeggini E, Weedon MN, Lindgren CM, Frayling TM, Elliott KS, Lango H, Timpson NJ, Perry JR, Rayner NW, Freathy RM, Barrett JC, Shields B, Morris AP, Ellard S, Groves CJ, Harries LW, Marchini JL, Owen KR, Knight B, Cardon LR, Walker M, Hitman GA, Morris AD, Doney AS; Wellcome Trust Case Control Consortium (WTCCC); McCarthy MI, Hattersley AT. Zeggini E, et al. Among authors: hattersley at. Science. 2007 Jun 1;316(5829):1336-41. doi: 10.1126/science.1142364. Epub 2007 Apr 26. Science. 2007. PMID: 17463249 Free PMC article.
C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes.
Frayling T, Ellard S, Grove J, Walker M, Hattersley AT. Frayling T, et al. Among authors: hattersley at. Lancet. 1998 Jun 27;351(9120):1933-4. doi: 10.1016/S0140-6736(05)78618-9. Lancet. 1998. PMID: 9654270 No abstract available.
Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes.
Macfarlane WM, Frayling TM, Ellard S, Evans JC, Allen LI, Bulman MP, Ayres S, Shepherd M, Clark P, Millward A, Demaine A, Wilkin T, Docherty K, Hattersley AT. Macfarlane WM, et al. Among authors: hattersley at. J Clin Invest. 1999 Nov;104(9):R33-9. doi: 10.1172/JCI7449. J Clin Invest. 1999. PMID: 10545530 Free PMC article.
848 results