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410 results

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Page 1
The molecular basis of glutamate formiminotransferase deficiency.
Hilton JF, Christensen KE, Watkins D, Raby BA, Renaud Y, de la Luna S, Estivill X, MacKenzie RE, Hudson TJ, Rosenblatt DS. Hilton JF, et al. Among authors: hudson tj. Hum Mutat. 2003 Jul;22(1):67-73. doi: 10.1002/humu.10236. Hum Mutat. 2003. PMID: 12815595
Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.
Watkins D, Ru M, Hwang HY, Kim CD, Murray A, Philip NS, Kim W, Legakis H, Wai T, Hilton JF, Ge B, Doré C, Hosack A, Wilson A, Gravel RA, Shane B, Hudson TJ, Rosenblatt DS. Watkins D, et al. Among authors: hudson tj. Am J Hum Genet. 2002 Jul;71(1):143-53. doi: 10.1086/341354. Epub 2002 May 30. Am J Hum Genet. 2002. PMID: 12068375 Free PMC article.
Genes to diseases (G2D) computational method to identify asthma candidate genes.
Tremblay K, Lemire M, Potvin C, Tremblay A, Hunninghake GM, Raby BA, Hudson TJ, Perez-Iratxeta C, Andrade-Navarro MA, Laprise C. Tremblay K, et al. Among authors: hudson tj. PLoS One. 2008 Aug 6;3(8):e2907. doi: 10.1371/journal.pone.0002907. PLoS One. 2008. PMID: 18682798 Free PMC article.
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
Engert JC, Lemire M, Faith J, Brisson D, Fujiwara TM, Roslin NM, Brewer CG, Montpetit A, Darmond-Zwaig C, Renaud Y, Doré C, Bailey SD, Verner A, Tremblay G, St-Pierre J, Bétard C, Platko J, Rioux JD, Morgan K, Hudson TJ, Gaudet D. Engert JC, et al. Among authors: hudson tj. Eur J Hum Genet. 2008 Jan;16(1):105-14. doi: 10.1038/sj.ejhg.5201920. Epub 2007 Sep 5. Eur J Hum Genet. 2008. PMID: 17805225
5' flanking variants of resistin are associated with obesity.
Engert JC, Vohl MC, Williams SM, Lepage P, Loredo-Osti JC, Faith J, Doré C, Renaud Y, Burtt NP, Villeneuve A, Hirschhorn JN, Altshuler D, Groop LC, Després JP, Gaudet D, Hudson TJ. Engert JC, et al. Among authors: hudson tj. Diabetes. 2002 May;51(5):1629-34. doi: 10.2337/diabetes.51.5.1629. Diabetes. 2002. PMID: 11978666
Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis.
Villani AC, Lemire M, Louis E, Silverberg MS, Collette C, Fortin G, Nimmo ER, Renaud Y, Brunet S, Libioulle C, Belaiche J, Bitton A, Gaudet D, Cohen A, Langelier D, Rioux JD, Arnott ID, Wild GE, Rutgeerts P, Satsangi J, Vermeire S, Hudson TJ, Franchimont D. Villani AC, et al. Among authors: hudson tj. PLoS One. 2009 Sep 28;4(9):e7154. doi: 10.1371/journal.pone.0007154. PLoS One. 2009. PMID: 19784369 Free PMC article.
Association study between the CX3CR1 gene and asthma.
Tremblay K, Lemire M, Provost V, Pastinen T, Renaud Y, Sandford AJ, Laviolette M, Hudson TJ, Laprise C. Tremblay K, et al. Among authors: hudson tj. Genes Immun. 2006 Dec;7(8):632-9. doi: 10.1038/sj.gene.6364340. Epub 2006 Nov 2. Genes Immun. 2006. PMID: 17082760
410 results