Hudson TJ - Search Results

1

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.

2

Mapping common regulatory variants to human haplotypes.

Pastinen T, Ge B, Gurd S, Gaudin T, Dore C, Lemire M, Lepage P, Harmsen E, Hudson TJ. Pastinen T, et al. Among authors: hudson tj. Hum Mol Genet. 2005 Dec 15;14(24):3963-71. doi: 10.1093/hmg/ddi420. Epub 2005 Nov 21. Hum Mol Genet. 2005. PMID: 16301213

3

Influence of human genome polymorphism on gene expression.

Pastinen T, Ge B, Hudson TJ. Pastinen T, et al. Among authors: hudson tj. Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R9-16. doi: 10.1093/hmg/ddl044. Hum Mol Genet. 2006. PMID: 16651375 Review.

4

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

5

Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria.

Dobson CM, Wai T, Leclerc D, Kadir H, Narang M, Lerner-Ellis JP, Hudson TJ, Rosenblatt DS, Gravel RA. Dobson CM, et al. Among authors: hudson tj. Hum Mol Genet. 2002 Dec 15;11(26):3361-9. doi: 10.1093/hmg/11.26.3361. Hum Mol Genet. 2002. PMID: 12471062

6

Microarray analysis of brain RNA in mice with methylenetetrahydrofolate reductase deficiency and hyperhomocysteinemia.

Chen Z, Ge B, Hudson TJ, Rozen R. Chen Z, et al. Among authors: hudson tj. Brain Res Gene Expr Patterns. 2002 Jan;1(2):89-93. doi: 10.1016/s1567-133x(01)00018-7. Brain Res Gene Expr Patterns. 2002. PMID: 15018804

7

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.

Engert JC, Bérubé P, Mercier J, Doré C, Lepage P, Ge B, Bouchard JP, Mathieu J, Melançon SB, Schalling M, Lander ES, Morgan K, Hudson TJ, Richter A. Engert JC, et al. Among authors: hudson tj. Nat Genet. 2000 Feb;24(2):120-5. doi: 10.1038/72769. Nat Genet. 2000. PMID: 10655055

8

Survey of allelic expression using EST mining.

Ge B, Gurd S, Gaudin T, Dore C, Lepage P, Harmsen E, Hudson TJ, Pastinen T. Ge B, et al. Among authors: hudson tj. Genome Res. 2005 Nov;15(11):1584-91. doi: 10.1101/gr.4023805. Genome Res. 2005. PMID: 16251468 Free PMC article.

9

Toward further mapping of the association between the IL2RA locus and type 1 diabetes.

Qu HQ, Montpetit A, Ge B, Hudson TJ, Polychronakos C. Qu HQ, et al. Among authors: hudson tj. Diabetes. 2007 Apr;56(4):1174-6. doi: 10.2337/db06-1555. Diabetes. 2007. PMID: 17395754

10

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

Richter A, Rioux JD, Bouchard JP, Mercier J, Mathieu J, Ge B, Poirier J, Julien D, Gyapay G, Weissenbach J, Hudson TJ, Melançon SB, Morgan K. Richter A, et al. Among authors: hudson tj. Am J Hum Genet. 1999 Mar;64(3):768-75. doi: 10.1086/302274. Am J Hum Genet. 1999. PMID: 10053011 Free PMC article.

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