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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
Hunt KA, Mistry V, Bockett NA, Ahmad T, Ban M, Barker JN, Barrett JC, Blackburn H, Brand O, Burren O, Capon F, Compston A, Gough SC, Jostins L, Kong Y, Lee JC, Lek M, MacArthur DG, Mansfield JC, Mathew CG, Mein CA, Mirza M, Nutland S, Onengut-Gumuscu S, Papouli E, Parkes M, Rich SS, Sawcer S, Satsangi J, Simmonds MJ, Trembath RC, Walker NM, Wozniak E, Todd JA, Simpson MA, Plagnol V, van Heel DA. Hunt KA, et al. Nature. 2013 Jun 13;498(7453):232-5. doi: 10.1038/nature12170. Epub 2013 May 22. Nature. 2013. PMID: 23698362 Free PMC article.
A common CTLA4 haplotype associated with coeliac disease.
Hunt KA, McGovern DP, Kumar PJ, Ghosh S, Travis SP, Walters JR, Jewell DP, Playford RJ, van Heel DA. Hunt KA, et al. Eur J Hum Genet. 2005 Apr;13(4):440-4. doi: 10.1038/sj.ejhg.5201357. Eur J Hum Genet. 2005. PMID: 15657618
Genetics in coeliac disease.
van Heel DA, Hunt K, Greco L, Wijmenga C. van Heel DA, et al. Best Pract Res Clin Gastroenterol. 2005 Jun;19(3):323-39. doi: 10.1016/j.bpg.2005.01.001. Best Pract Res Clin Gastroenterol. 2005. PMID: 15925839 Review.
Genetic variation in myosin IXB is associated with ulcerative colitis.
van Bodegraven AA, Curley CR, Hunt KA, Monsuur AJ, Linskens RK, Onnie CM, Crusius JB, Annese V, Latiano A, Silverberg MS, Bitton A, Fisher SA, Steinhart AH, Forbes A, Sanderson J, Prescott NJ, Strachan DP, Playford RJ, Mathew CG, Wijmenga C, Daly MJ, Rioux JD, van Heel DA. van Bodegraven AA, et al. Among authors: hunt ka. Gastroenterology. 2006 Dec;131(6):1768-74. doi: 10.1053/j.gastro.2006.09.011. Epub 2006 Sep 8. Gastroenterology. 2006. PMID: 17087940
130 results