Hudson TJ - Search Results

1

Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.

Villani AC, Lemire M, Fortin G, Louis E, Silverberg MS, Collette C, Baba N, Libioulle C, Belaiche J, Bitton A, Gaudet D, Cohen A, Langelier D, Fortin PR, Wither JE, Sarfati M, Rutgeerts P, Rioux JD, Vermeire S, Hudson TJ, Franchimont D. Villani AC, et al. Among authors: hudson tj. Nat Genet. 2009 Jan;41(1):71-6. doi: 10.1038/ng.285. Epub 2008 Dec 21. Nat Genet. 2009. PMID: 19098911 Free PMC article.

2

Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.

Rioux JD, Stone VA, Daly MJ, Cargill M, Green T, Nguyen H, Nutman T, Zimmerman PA, Tucker MA, Hudson T, Goldstein AM, Lander E, Lin AY. Rioux JD, et al. Am J Hum Genet. 1998 Oct;63(4):1086-94. doi: 10.1086/302053. Am J Hum Genet. 1998. PMID: 9758611 Free PMC article.

3

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.

4

Procedure to protect confidentiality of familial data in community genetics and genomic research.

Gaudet D, Arsenault S, Bélanger C, Hudson T, Perron P, Bernard M, Hamet P. Gaudet D, et al. Clin Genet. 1999 Apr;55(4):259-64. doi: 10.1034/j.1399-0004.1999.550408.x. Clin Genet. 1999. PMID: 10361987

5

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.

Engert JC, Doré C, Mercier J, Ge B, Bétard C, Rioux JD, Owen C, Bérubé P, Devon K, Birren B, Melançon SB, Morgan K, Hudson TJ, Richter A. Engert JC, et al. Among authors: hudson tj. Genomics. 1999 Dec 1;62(2):156-64. doi: 10.1006/geno.1999.6003. Genomics. 1999. PMID: 10610707

6

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

7

Glycerol as a correlate of impaired glucose tolerance: dissection of a complex system by use of a simple genetic trait.

Gaudet D, Arsenault S, Pérusse L, Vohl MC, St-Pierre J, Bergeron J, Després JP, Dewar K, Daly MJ, Hudson T, Rioux JD. Gaudet D, et al. Am J Hum Genet. 2000 May;66(5):1558-68. doi: 10.1086/302903. Epub 2000 Mar 27. Am J Hum Genet. 2000. PMID: 10736265 Free PMC article.

8

Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.

Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, McLeod RS, Griffiths AM, Green T, Brettin TS, Stone V, Bull SB, Bitton A, Williams CN, Greenberg GR, Cohen Z, Lander ES, Hudson TJ, Siminovitch KA. Rioux JD, et al. Among authors: hudson tj. Am J Hum Genet. 2000 Jun;66(6):1863-70. doi: 10.1086/302913. Epub 2000 Apr 21. Am J Hum Genet. 2000. PMID: 10777714 Free PMC article.

9

Molecular scanning of the human PPARa gene: association of the L162v mutation with hyperapobetalipoproteinemia.

Vohl MC, Lepage P, Gaudet D, Brewer CG, Bétard C, Perron P, Houde G, Cellier C, Faith JM, Després JP, Morgan K, Hudson TJ. Vohl MC, et al. Among authors: hudson tj. J Lipid Res. 2000 Jun;41(6):945-52. J Lipid Res. 2000. PMID: 10828087 Free article.

10

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.

Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, Vohl MC, Nemesh J, Lane CR, Schaffner SF, Bolk S, Brewer C, Tuomi T, Gaudet D, Hudson TJ, Daly M, Groop L, Lander ES. Altshuler D, et al. Among authors: hudson tj. Nat Genet. 2000 Sep;26(1):76-80. doi: 10.1038/79216. Nat Genet. 2000. PMID: 10973253

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