Rioux JD - Search Results

1

Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension.

Hamet P, Merlo E, Seda O, Broeckel U, Tremblay J, Kaldunski M, Gaudet D, Bouchard G, Deslauriers B, Gagnon F, Antoniol G, Pausová Z, Labuda M, Jomphe M, Gossard F, Tremblay G, Kirova R, Tonellato P, Orlov SN, Pintos J, Platko J, Hudson TJ, Rioux JD, Kotchen TA, Cowley AW Jr. Hamet P, et al. Among authors: rioux jd. Am J Hum Genet. 2005 May;76(5):815-32. doi: 10.1086/430133. Epub 2005 Mar 30. Am J Hum Genet. 2005. PMID: 15800845 Free PMC article.

2

Genomewide scan of multiple sclerosis in Finnish multiplex families.

Kuokkanen S, Gschwend M, Rioux JD, Daly MJ, Terwilliger JD, Tienari PJ, Wikström J, Palo J, Stein LD, Hudson TJ, Lander ES, Peltonen L. Kuokkanen S, et al. Among authors: rioux jd. Am J Hum Genet. 1997 Dec;61(6):1379-87. doi: 10.1086/301637. Am J Hum Genet. 1997. PMID: 9399895 Free PMC article.

3

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.

4

Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16.

Rioux JD, Daly MJ, Green T, Stone V, Lander ES, Hudson TJ, Steinhart AH, Bull S, Cohen Z, Greenberg G, Griffiths A, McLeod R, Silverberg M, Williams CN, Siminovitch KA. Rioux JD, et al. Gastroenterology. 1998 Nov;115(5):1062-5. doi: 10.1016/s0016-5085(98)70074-5. Gastroenterology. 1998. PMID: 9797358

5

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: rioux jd. Am J Hum Genet. 1999 Mar;64(3):768-75. doi: 10.1086/302274. Am J Hum Genet. 1999. PMID: 10053011 Free PMC article.

6

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: rioux jd. Genomics. 1999 Dec 1;62(2):156-64. doi: 10.1006/geno.1999.6003. Genomics. 1999. PMID: 10610707

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. Among authors: rioux jd. 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. 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

Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.

Pajukanta P, Cargill M, Viitanen L, Nuotio I, Kareinen A, Perola M, Terwilliger JD, Kempas E, Daly M, Lilja H, Rioux JD, Brettin T, Viikari JS, Rönnemaa T, Laakso M, Lander ES, Peltonen L. Pajukanta P, et al. Among authors: rioux jd. Am J Hum Genet. 2000 Dec;67(6):1481-93. doi: 10.1086/316902. Epub 2000 Nov 13. Am J Hum Genet. 2000. PMID: 11078477 Free PMC article.

10

A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16.

Lee N, Daly MJ, Delmonte T, Lander ES, Xu F, Hudson TJ, Mitchell GA, Morin CC, Robinson BH, Rioux JD. Lee N, et al. Among authors: rioux jd. Am J Hum Genet. 2001 Feb;68(2):397-409. doi: 10.1086/318197. Epub 2001 Jan 10. Am J Hum Genet. 2001. PMID: 11156535 Free PMC article.

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