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Papers authored by Goyette P

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Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.

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International MHC and Autoimmunity Genetics Network, Rioux JD, Goyette P, Vyse TJ, Hammarström L, Fernando MM, Green T, De Jager PL, Foisy S, Wang J, de Bakker PI, Leslie S, McVean G, Padyukov L, Alfredsson L, Annese V,

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Proceedings of the National Academy of Sciences of the United States of America 106(44):18680-5, 2009 Nov 3 - Who cited this? | PubMed ID: 19846760 | Fulltext

Phenotypic and genotypic characteristics of inflammatory bowel disease in French Canadians: comparison with a large North American repository.

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Bhat M, Nguyen GC, Pare P, Lahaie R, Deslandres C, Bernard EJ, Aumais G, Jobin G, Wild G, Cohen A, Langelier D, Brant S, Dassopoulos T, McGovern D, Torres E, Duerr R,

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The American journal of gastroenterology 104(9):2233-40, 2009 Sep - Who cited this? | PubMed ID: 19513023 | Fulltext

Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis.

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Festen EA, Goyette P, Scott R, Annese V, Zhernakova A, Lian J, Lefèbvre C, Brant SR, Cho JH, Silverberg MS, Taylor KD, de Jong DJ, Stokkers PC, McGovern D, Palmieri O, Achkar JP,

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Gut 58(6):799-804, 2009 Jun - Who cited this? | PubMed ID: 19201773 | Fulltext

Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.

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Silverberg MS, Cho JH, Rioux JD, McGovern DP, Wu J, Annese V, Achkar JP, Goyette P, Scott R, Xu W, Barmada MM, Klei L, Daly MJ, Abraham C, Bayless TM, Bossa F,

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Nature genetics 41(6):762, 2009 Jun - Who cited this? | PubMed ID: 19471306 | Fulltext

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.

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Silverberg MS, Cho JH, Rioux JD, McGovern DP, Wu J, Annese V, Achkar JP, Goyette P, Scott R, Xu W, Barmada MM, Klei L, Daly MJ, Abraham C, Bayless TM, Bossa F,

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Nature genetics 41(2):216-20, 2009 Feb - Who cited this? | PubMed ID: 19122664 | Fulltext

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease.

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McCarroll SA, Huett A, Kuballa P, Chilewski SD, Landry A, Goyette P, Zody MC, Hall JL, Brant SR, Cho JH, Duerr RH, Silverberg MS, Taylor KD, Rioux JD, Altshuler D, Daly MJ,

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Nature genetics 40(9):1107-12, 2008 Sep - Who cited this? | PubMed ID: 19165925 | Fulltext

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease.

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McCarroll SA, Huett A, Kuballa P, Chilewski SD, Landry A, Goyette P, Zody MC, Hall JL, Brant SR, Cho JH, Duerr RH, Silverberg MS, Taylor KD, Rioux JD, Altshuler D, Daly MJ,

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Nature genetics, 2008 Aug 24 - Who cited this? | PubMed ID: 18724369 | Fulltext

MAST3: a novel IBD risk factor that modulates TLR4 signaling.

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Labbé C, Goyette P, Lefebvre C, Stevens C, Green T, Tello-Ruiz MK, Cao Z, Landry AL, Stempak J, Annese V, Latiano A, Brant SR, Duerr RH, Taylor KD, Cho JH, Steinhart AH,

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Genes and immunity, 2008 Jul 24 - Who cited this? | PubMed ID: 18650832 | Fulltext

Defining the role of the MHC in autoimmunity: a review and pooled analysis.

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Fernando MM, Stevens CR, Walsh EC, De Jager PL, Goyette P, Plenge RM, Vyse TJ, and Rioux JD

PLoS genetics 4(4), 2008 Apr - Who cited this? | PubMed ID: 18437207 | Fulltext

Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.

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Goyette P, Lefebvre C, Ng A, Brant SR, Cho JH, Duerr RH, Silverberg MS, Taylor KD, Latiano A, Aumais G, Deslandres C, Jobin G, Annese V, Daly MJ, Xavier RJ, and Rioux JD

Mucosal immunology 1(2):131-8, 2008 Mar - Who cited this? | PubMed ID: 19079170 | Fulltext

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.

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Rioux JD, Xavier RJ, Taylor KD, Silverberg MS, Goyette P, Huett A, Green T, Kuballa P, Barmada MM, Datta LW, Shugart YY, Griffiths AM, Targan SR, Ippoliti AF, Bernard EJ, Mei L,

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Nature genetics 39(5):596-604, 2007 May - Who cited this? | PubMed ID: 17435756 | Fulltext

Molecular pathogenesis of inflammatory bowel disease: genotypes, phenotypes and personalized medicine.

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Goyette P, Labbé C, Trinh TT, Xavier RJ, and Rioux JD

Annals of medicine 39(3):177-99, 2007 - Who cited this? | PubMed ID: 17457716 | Fulltext

RARgamma acts as a tumor suppressor in mouse keratinocytes.

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Chen CF, Goyette P, and Lohnes D

Oncogene 23(31):5350-9, 2004 Jul 8 - Who cited this? | PubMed ID: 15094780 | Fulltext

Multiple transcription start sites and alternative splicing in the methylenetetrahydrofolate reductase gene result in two enzyme isoforms.

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Tran P, Leclerc D, Chan M, Pai A, Hiou-Tim F, Wu Q, Goyette P, Artigas C, Milos R, and Rozen R

Mammalian genome : official journal of the International Mammalian Genome Society 13(9):483-92, 2002 Sep - Who cited this? | PubMed ID: 12370778 | Fulltext

Regulation of gli activity by all-trans retinoic acid in mouse keratinocytes.

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Goyette P, Allan D, Peschard P, Chen CF, Wang W, and Lohnes D

Cancer research 60(19):5386-9, 2000 Oct 1 - Who cited this? | PubMed ID: 11034076 | Fulltext

Characterization of retinoic acid receptor-deficient keratinocytes.

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Goyette P, Feng Chen C, Wang W, Seguin F, and Lohnes D

The Journal of biological chemistry 275(22):16497-505, 2000 Jun 2 - Who cited this? | PubMed ID: 10748128 | Fulltext

The thermolabile variant 677C-->T can further reduce activity when expressed in cis with severe mutations for human methylenetetrahydrofolate reductase.

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Goyette P and Rozen R

Human mutation 16(2):132-8, 2000 - Who cited this? | PubMed ID: 10923034 | Fulltext

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR).

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Goyette P, Pai A, Milos R, Frosst P, Tran P, Chen Z, Chan M, and Rozen R

Mammalian genome : official journal of the International Mammalian Genome Society 9(8):652-6, 1998 Aug - Who cited this? | PubMed ID: 9680386 | Fulltext

Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene.

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Goyette P, Rosenblatt D, and Rozen R

Journal of inherited metabolic disease 21(6):690-1, 1998 Aug - Who cited this? | PubMed ID: 9762613 | Fulltext

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.

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Christensen B, Frosst P, Lussier-Cacan S, Selhub J, Goyette P, Rosenblatt DS, Genest J, and Rozen R

Arteriosclerosis, thrombosis, and vascular biology 17(3):569-73, 1997 Mar - Who cited this? | PubMed ID: 9102178 | Fulltext

Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.

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Goyette P, Christensen B, Rosenblatt DS, and Rozen R

American journal of human genetics 59(6):1268, 1996 Dec - Who cited this? | PubMed ID: 8940272 | Fulltext

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

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Leclerc D, Campeau E, Goyette P, Adjalla CE, Christensen B, Ross M, Eydoux P, Rosenblatt DS, Rozen R, and Gravel RA

Human molecular genetics 5(12):1867-74, 1996 Dec - Who cited this? | PubMed ID: 8968737 | Fulltext

In-line microwave blood warming of in-date human packed red blood cells.

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Pappas CG, Paddock H, Goyette P, Grabowy R, Connolly RJ, and Schwaitzberg SD

Critical care medicine 23(7):1243-50, 1995 Jul - Who cited this? | PubMed ID: 7600834 | Fulltext

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.

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Goyette P, Frosst P, Rosenblatt DS, and Rozen R

American journal of human genetics 56(5):1052, 1995 May - Who cited this? | PubMed ID: 7726158 | Fulltext

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.

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Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, and van den Heuvel LP

Nature genetics 10(1):111-3, 1995 May - Who cited this? | PubMed ID: 7647779 | Fulltext

Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification.

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Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, and Rozen R

Nature genetics 7(4):551, 1994 Aug - Who cited this? | PubMed ID: 7951330 | Fulltext

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.

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Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, and Rozen R

Nature genetics 7(2):195-200, 1994 Jun - Who cited this? | PubMed ID: 7920641 | Fulltext

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