Hudson TJ - Search Results

1

Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics Study.

Anand SS, Xie C, Paré G, Montpetit A, Rangarajan S, McQueen MJ, Cordell HJ, Keavney B, Yusuf S, Hudson TJ, Engert JC; INTERHEART Investigators. Anand SS, et al. Among authors: hudson tj. Circ Cardiovasc Genet. 2009 Feb;2(1):16-25. doi: 10.1161/CIRCGENETICS.108.813709. Epub 2009 Jan 23. Circ Cardiovasc Genet. 2009. PMID: 20031563

2

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease.

Clee SM, Zwinderman AH, Engert JC, Zwarts KY, Molhuizen HO, Roomp K, Jukema JW, van Wijland M, van Dam M, Hudson TJ, Brooks-Wilson A, Genest J Jr, Kastelein JJ, Hayden MR. Clee SM, et al. Among authors: hudson tj. Circulation. 2001 Mar 6;103(9):1198-205. doi: 10.1161/01.cir.103.9.1198. Circulation. 2001. PMID: 11238261

3

ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels.

Zwarts KY, Clee SM, Zwinderman AH, Engert JC, Singaraja R, Loubser O, James E, Roomp K, Hudson TJ, Jukema JW, Kastelein JJ, Hayden MR. Zwarts KY, et al. Among authors: hudson tj. Clin Genet. 2002 Feb;61(2):115-25. doi: 10.1034/j.1399-0004.2002.610206.x. Clin Genet. 2002. PMID: 11940086

4

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

5

Susceptibility to leprosy is associated with PARK2 and PACRG.

Mira MT, Alcaïs A, Nguyen VT, Moraes MO, Di Flumeri C, Vu HT, Mai CP, Nguyen TH, Nguyen NB, Pham XK, Sarno EN, Alter A, Montpetit A, Moraes ME, Moraes JR, Doré C, Gallant CJ, Lepage P, Verner A, Van De Vosse E, Hudson TJ, Abel L, Schurr E. Mira MT, et al. Among authors: hudson tj. Nature. 2004 Feb 12;427(6975):636-40. doi: 10.1038/nature02326. Epub 2004 Jan 25. Nature. 2004. PMID: 14737177 Free article.

6

Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy.

Poon AH, Laprise C, Lemire M, Montpetit A, Sinnett D, Schurr E, Hudson TJ. Poon AH, et al. Among authors: hudson tj. Am J Respir Crit Care Med. 2004 Nov 1;170(9):967-73. doi: 10.1164/rccm.200403-412OC. Epub 2004 Jul 28. Am J Respir Crit Care Med. 2004. PMID: 15282199

7

An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.

Saba TG, Montpetit A, Verner A, Rioux P, Hudson TJ, Drouin R, Drouin CA. Saba TG, et al. Among authors: hudson tj. Hum Genet. 2005 Feb;116(3):167-71. doi: 10.1007/s00439-004-1193-8. Epub 2004 Nov 25. Hum Genet. 2005. PMID: 15668823

8

Human resistin gene polymorphism is associated with visceral obesity and fasting and oral glucose stimulated C-peptide in the Québec Family Study.

Bouchard L, Weisnagel SJ, Engert JC, Hudson TJ, Bouchard C, Vohl MC, Pérusse L. Bouchard L, et al. Among authors: hudson tj. J Endocrinol Invest. 2004 Dec;27(11):1003-9. doi: 10.1007/BF03345301. J Endocrinol Invest. 2004. PMID: 15754730

9

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis.

Lincoln MR, Montpetit A, Cader MZ, Saarela J, Dyment DA, Tiislar M, Ferretti V, Tienari PJ, Sadovnick AD, Peltonen L, Ebers GC, Hudson TJ. Lincoln MR, et al. Among authors: hudson tj. Nat Genet. 2005 Oct;37(10):1108-12. doi: 10.1038/ng1647. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186814 Free article.

10

An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population.

Montpetit A, Nelis M, Laflamme P, Magi R, Ke X, Remm M, Cardon L, Hudson TJ, Metspalu A. Montpetit A, et al. Among authors: hudson tj. PLoS Genet. 2006 Mar;2(3):e27. doi: 10.1371/journal.pgen.0020027. Epub 2006 Mar 10. PLoS Genet. 2006. PMID: 16532062 Free PMC article.

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