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The role of toll-like receptor variants in acute anterior uveitis.
Pratap DS, Lim LL, Wang JJ, Mackey DA, Kearns LS, Stawell RJ; Wellcome Trust Case Control Consortium 2; Burdon KP, Mitchell P, Craig JE, Hall AJ, Hewitt AW. Pratap DS, et al. Among authors: mitchell p. Mol Vis. 2011;17:2970-7. Epub 2011 Nov 16. Mol Vis. 2011. PMID: 22128242 Free PMC article.
Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye.
Sharma S, Burdon KP, Chidlow G, Klebe S, Crawford A, Dimasi DP, Dave A, Martin S, Javadiyan S, Wood JP, Casson R, Danoy P, Griggs K, Hewitt AW, Landers J, Mitchell P, Mackey DA, Craig JE. Sharma S, et al. Among authors: mitchell p. Invest Ophthalmol Vis Sci. 2012 Jul 24;53(8):4917-25. doi: 10.1167/iovs.11-9047. Invest Ophthalmol Vis Sci. 2012. PMID: 22714896
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
Lu Y, Dimasi DP, Hysi PG, Hewitt AW, Burdon KP, Toh T, Ruddle JB, Li YJ, Mitchell P, Healey PR, Montgomery GW, Hansell N, Spector TD, Martin NG, Young TL, Hammond CJ, Macgregor S, Craig JE, Mackey DA. Lu Y, et al. Among authors: mitchell p. PLoS Genet. 2010 May 13;6(5):e1000947. doi: 10.1371/journal.pgen.1000947. PLoS Genet. 2010. PMID: 20485516 Free PMC article.
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
Burdon KP, Macgregor S, Hewitt AW, Sharma S, Chidlow G, Mills RA, Danoy P, Casson R, Viswanathan AC, Liu JZ, Landers J, Henders AK, Wood J, Souzeau E, Crawford A, Leo P, Wang JJ, Rochtchina E, Nyholt DR, Martin NG, Montgomery GW, Mitchell P, Brown MA, Mackey DA, Craig JE. Burdon KP, et al. Among authors: mitchell p. Nat Genet. 2011 Jun;43(6):574-8. doi: 10.1038/ng.824. Epub 2011 May 1. Nat Genet. 2011. PMID: 21532571
4,346 results