Lepage P - Search Results

1

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: lepage p. 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

2

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: lepage p. Nat Genet. 2000 Feb;24(2):120-5. doi: 10.1038/72769. Nat Genet. 2000. PMID: 10655055

3

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: lepage p. J Lipid Res. 2000 Jun;41(6):945-52. J Lipid Res. 2000. PMID: 10828087 Free article.

4

Complete nucleotide sequence and genomic structure of the human NRAMP1 gene region on chromosome region 2q35.

Marquet S, Lepage P, Hudson TJ, Musser JM, Schurr E. Marquet S, et al. Among authors: lepage p. Mamm Genome. 2000 Sep;11(9):755-62. doi: 10.1007/s003350010151. Mamm Genome. 2000. PMID: 10967134

5

A distal upstream enhancer from the myelin basic protein gene regulates expression in myelin-forming schwann cells.

Forghani R, Garofalo L, Foran DR, Farhadi HF, Lepage P, Hudson TJ, Tretjakoff I, Valera P, Peterson A. Forghani R, et al. Among authors: lepage p. J Neurosci. 2001 Jun 1;21(11):3780-7. doi: 10.1523/JNEUROSCI.21-11-03780.2001. J Neurosci. 2001. PMID: 11356866 Free PMC article.

6

Haplotype mapping indicates two independent origins for the Cmv1s susceptibility allele to cytomegalovirus infection and refines its localization within the Ly49 cluster.

Lee SH, Gitas J, Zafer A, Lepage P, Hudson TJ, Belouchi A, Vidal SM. Lee SH, et al. Among authors: lepage p. Immunogenetics. 2001 Aug;53(6):501-5. doi: 10.1007/s002510100359. Immunogenetics. 2001. PMID: 11685461 No abstract available.

7

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: lepage p. Diabetes. 2002 May;51(5):1629-34. doi: 10.2337/diabetes.51.5.1629. Diabetes. 2002. PMID: 11978666

8

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.

Mootha VK, Lepage P, Miller K, Bunkenborg J, Reich M, Hjerrild M, Delmonte T, Villeneuve A, Sladek R, Xu F, Mitchell GA, Morin C, Mann M, Hudson TJ, Robinson B, Rioux JD, Lander ES. Mootha VK, et al. Among authors: lepage p. Proc Natl Acad Sci U S A. 2003 Jan 21;100(2):605-10. doi: 10.1073/pnas.242716699. Epub 2003 Jan 14. Proc Natl Acad Sci U S A. 2003. PMID: 12529507 Free PMC article.

9

A survey of genetic and epigenetic variation affecting human gene expression.

Pastinen T, Sladek R, Gurd S, Sammak A, Ge B, Lepage P, Lavergne K, Villeneuve A, Gaudin T, Brändström H, Beck A, Verner A, Kingsley J, Harmsen E, Labuda D, Morgan K, Vohl MC, Naumova AK, Sinnett D, Hudson TJ. Pastinen T, et al. Among authors: lepage p. Physiol Genomics. 2004 Jan 15;16(2):184-93. doi: 10.1152/physiolgenomics.00163.2003. Physiol Genomics. 2004. PMID: 14583597

10

A combinatorial network of evolutionarily conserved myelin basic protein regulatory sequences confers distinct glial-specific phenotypes.

Farhadi HF, Lepage P, Forghani R, Friedman HC, Orfali W, Jasmin L, Miller W, Hudson TJ, Peterson AC. Farhadi HF, et al. Among authors: lepage p. J Neurosci. 2003 Nov 12;23(32):10214-23. doi: 10.1523/JNEUROSCI.23-32-10214.2003. J Neurosci. 2003. PMID: 14614079 Free PMC article.

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