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  • Showing 1-26 of 26 Results
2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.Tajuddin, SM, Schick UM, Eicher JD, Chami N., Giri A., Brody JA, Hill WD, Kacprowski T., Li J., Lyytikäinen LP, Manichaikul A., Mihailov E., O'Donoghue ML, Pankratz N., Pazoki R., Polfus LM, Smith AV, Schurmann C., Vacchi-Suzzi C., Waterworth DM, et al. American journal of human genetics, 2016/06/21, (2016) Read More / View Supplemental Materials
Abstract
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.Eicher, JD, Chami N., Kacprowski T., Nomura A., Chen MH, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N., Polfus L., Schurmann C., Giri A., Brody JA, Lange LA, Manichaikul A., Hill WD, Pazoki R., Elliot P., Evangelou E., et al. American journal of human genetics, 2016/06/21, (2016) Read More / View Supplemental Materials
Abstract
2015
A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh Syndrome.Thompson Legault, J., Strittmatter L., Tardif J., Sharma R., Tremblay-Vaillancourt V., Aubut C., Boucher G., Clish CB, Cyr D., Daneault C., Waters PJ, LSFC Consortium, Vachon L., Morin C., Laprise C., Rioux JD, Mootha VK, and Des Rosiers C. Cell reports, 2015/11/03, Volume 13, Issue 5, p.981-9, (2015) Read More / View Supplemental Materials
Abstract
Ubiquitin Ligase TRIM62 Regulates CARD9-Mediated Anti-fungal Immunity and Intestinal Inflammation.Cao, Z., Conway KL, Heath RJ, Rush JS, Leshchiner ES, Ramirez-Ortiz ZG, Nedelsky NB, Huang H., Ng A., Gardet A., Cheng SC, Shamji AF, Rioux JD, Wijmenga C., Netea MG, Means TK, Daly M. J., and Xavier RJ Immunity, 2015/10/20, Volume 43, Issue 4, p.715-26, (2015) Read More / View Supplemental Materials
Abstract
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study.Cleynen, I., Boucher G., Jostins L., Schumm LP, Zeissig S., Ahmad T., Andersen V., Andrews JM, Annese V., Brand S., Brant SR, Cho JH, Daly M. J., Dubinsky M., Duerr RH, Ferguson LR, Franke A., Gearry RB, Goyette P., Hakonarson H., et al. Lancet (London, England), 2015/10/16, (2015) Read More / View Supplemental Materials
Abstract
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.Winkler, TW, Justice AE, Graff M., Barata L., Feitosa MF, Chu S., Czajkowski J., Esko T., Fall T., Kilpeläinen TO, Lu Y., Mägi R., Mihailov E., Pers TH, Rüeger S., Teumer A., Ehret GB, Ferreira T., Heard-Costa NL, Karjalainen J., et al. PLoS genetics, 2015/10/01, Volume 11, Issue 10, p.e1005378, (2015) Read More / View Supplemental Materials
Abstract
Genetic studies of body mass index yield new insights for obesity biology.Locke, AE, Kahali B., Berndt SI, Justice AE, Pers TH, Day FR, Powell C., Vedantam S., Buchkovich ML, Yang J., Croteau-Chonka DC, Esko T., Fall T., Ferreira T., Gustafsson S., Kutalik Z., Luan J., Mägi R., Randall JC, Winkler TW, et al. Nature, 2015/02/12, Volume 518, Issue 7538, p.197-206, (2015) Read More / View Supplemental Materials
Abstract
High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis.Goyette, P., Boucher G., Mallon D., Ellinghaus E., Jostins L., Huang H., Ripke S., Gusareva ES, Annese V., Hauser SL, Oksenberg JR, Thomsen I., Leslie S., International Inflammatory Bowel Disease Genetics Consortium, Australia and New Zealand IBDGC, Belgium IBD Genetics Consortium, Italian Group for IBD Genetic Consortium, NIDDK Inflammatory Bowel Disease Genetics Consortium, United Kingdom IBDGC, Wellcome Trust Case Control Consortium, et al. Nature genetics, 2015/01/05, (2015) Read More / View Supplemental Materials
Abstract
2011
Progress towards identifying inflammatory bowel disease susceptibility genes.Rioux, JD Novartis Foundation symposium, 2011/12/08, Volume 263, p.3-11; discussion 11-6, 211-8, (2011) Read More / View Supplemental Materials
Abstract
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.Rivas, MA, Beaudoin M., Gardet A., Stevens C., Sharma Y., Zhang CK, Boucher G., Ripke S., Ellinghaus D., Burtt N., Fennell T., Kirby A., Latiano A., Goyette P., Green T., Halfvarson J., Haritunians T., Korn JM, Kuruvilla F., Lagacé C., et al. Nature genetics, 2011/10/09, Volume 43, Issue 11, p.1066-73, (2011) Read More / View Supplemental Materials
Abstract
2010
LRRK2 is involved in the IFN-gamma response and host response to pathogens.Gardet, A., Benita Y., Li C., Sands BE, Ballester I., Stevens C., Korzenik JR, Rioux JD, Daly M. J., Xavier RJ, and Podolsky DK Journal of immunology (Baltimore, Md. : 1950), 2010/11/01, Volume 185, Issue 9, p.5577-85, (2010) Read More / View Supplemental Materials
Abstract
2008
Autoimmune diseases: insights from genome-wide association studies.Lettre, G., and Rioux JD Human molecular genetics, 2008/10/15, Volume 17, Issue R2, p.R116-21, (2008) Read More / View Supplemental Materials
Abstract
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.Graham, RR, Cotsapas C., Davies L., Hackett R., Lessard CJ, Leon JM, Burtt NP, Guiducci C., Parkin M., Gates C., Plenge RM, Behrens TW, Wither JE, Rioux JD, Fortin PR, Graham DC, Wong AK, Vyse TJ, Daly M. J., Altshuler D., et al. Nature genetics, 2008/09/01, Volume 40, Issue 9, p.1059-61, (2008) Read More / View Supplemental Materials
Abstract
2007
Risk alleles for multiple sclerosis identified by a genomewide study.International Multiple Sclerosis Genetics, Consortium, Hafler DA, Compston A., Sawcer S., Lander E. S., Daly M. J., De Jager PL, de Bakker PI, Gabriel SB, Mirel DB, Ivinson AJ, Pericak-Vance MA, Gregory SG, Rioux JD, McCauley JL, Haines JL, Barcellos LF, Cree B., Oksenberg JR, and Hauser SL The New England journal of medicine, 2007/08/30, Volume 357, Issue 9, p.851-62, (2007) Read More / View Supplemental Materials
Abstract
A second major histocompatibility complex susceptibility locus for multiple sclerosis.Yeo, TW, De Jager PL, Gregory SG, Barcellos LF, Walton A., Goris A., Fenoglio C., Ban M., Taylor CJ, Goodman RS, Walsh E., Wolfish CS, Horton R., Traherne J., Beck S., Trowsdale J., Caillier SJ, Ivinson AJ, Green T., Pobywajlo S., et al. Annals of neurology, 2007/03/01, Volume 61, Issue 3, p.228-36, (2007) Read More / View Supplemental Materials
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2006
A functional candidate screen for coeliac disease genes.Curley, CR, Monsuur AJ, Wapenaar MC, Rioux JD, and Wijmenga C. European journal of human genetics : EJHG, 2006/11/01, Volume 14, Issue 11, p.1215-22, (2006) Read More / View Supplemental Materials
Abstract
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.de Bakker, PI, McVean G., Sabeti PC, Miretti MM, Green T., Marchini J., Ke X., Monsuur AJ, Whittaker P., Delgado M., Morrison J., Richardson A., Walsh EC, Gao X., Galver L., Hart J., Hafler DA, Pericak-Vance M., Todd JA, Daly M. J., et al. Nature genetics, 2006/10/01, Volume 38, Issue 10, p.1166-72, (2006) Read More / View Supplemental Materials
Abstract
Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.Tello-Ruiz, MK, Curley C., DelMonte T., Giallourakis C., Kirby A., Miller K., Wild G., Cohen A., Langelier D., Latiano A., Wedemeyer N., Lander E., Schreiber S., Annese V., Daly M. J., and Rioux JD European journal of human genetics : EJHG, 2006/06/01, Volume 14, Issue 6, p.780-90, (2006) Read More / View Supplemental Materials
Abstract
2005
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4.Plenge, RM, Padyukov L., Remmers EF, Purcell S., Lee AT, Karlson EW, Wolfe F., Kastner DL, Alfredsson L., Altshuler D., Gregersen PK, Klareskog L., and Rioux JD American journal of human genetics, 2005/12/01, Volume 77, Issue 6, p.1044-60, (2005) Read More / View Supplemental Materials
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The promise and perils of interpreting genetic associations in Crohn's disease.Trinh, TT, and Rioux JD Gut, 2005/10/01, Volume 54, Issue 10, p.1354-7, (2005) Read More / View Supplemental Materials
A high-density screen for linkage in multiple sclerosis.Sawcer, S., Ban M., Maranian M., Yeo TW, Compston A., Kirby A., Daly M. J., De Jager PL, Walsh E., Lander E. S., Rioux JD, Hafler DA, Ivinson A., Rimmler J., Gregory SG, Schmidt S., Pericak-Vance MA, Akesson E., Hillert J., Datta P., et al. American journal of human genetics, 2005/09/01, Volume 77, Issue 3, p.454-67, (2005) Read More / View Supplemental Materials
Abstract
Association of DLG5 R30Q variant with inflammatory bowel disease.Daly, M. J., Pearce AV, Farwell L., Fisher SA, Latiano A., Prescott NJ, Forbes A., Mansfield J., Sanderson J., Langelier D., Cohen A., Bitton A., Wild G., Lewis CM, Annese V., Mathew CG, and Rioux JD European journal of human genetics : EJHG, 2005/07/01, Volume 13, Issue 7, p.835-9, (2005) Read More / View Supplemental Materials
Abstract
Paths to understanding the genetic basis of autoimmune disease.Rioux, JD, and Abbas AK Nature, 2005/06/02, Volume 435, Issue 7042, p.584-9, (2005) Read More / View Supplemental Materials
Abstract
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.Miretti, MM, Walsh EC, Ke X., Delgado M., Griffiths M., Hunt S., Morrison J., Whittaker P., Lander E. S., Cardon LR, Bentley DR, Rioux JD, Beck S., and Deloukas P. American journal of human genetics, 2005/04/01, Volume 76, Issue 4, p.634-46, (2005) Read More / View Supplemental Materials
Abstract
2004
Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci.Rioux, JD, Karinen H., Kocher K., McMahon SG, Kärkkäinen P., Janatuinen E., Heikkinen M., Julkunen R., Pihlajamäki J., Naukkarinen A., Kosma VM, Daly M. J., Lander E. S., and Laakso M. American journal of medical genetics. Part A, 2004/11/01, Volume 130A, Issue 4, p.345-50, (2004) Read More / View Supplemental Materials
Abstract
Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.Sawcer, SJ, Maranian M., Singlehurst S., Yeo T., Compston A., Daly M. J., De Jager PL, Gabriel S., Hafler DA, Ivinson AJ, Lander E. S., Rioux JD, Walsh E., Gregory SG, Schmidt S., Pericak-Vance MA, Barcellos L., Hauser SL, Oksenberg JR, Kenealy SJ, et al. Human molecular genetics, 2004/09/01, Volume 13, Issue 17, p.1943-9, (2004) Read More / View Supplemental Materials
Abstract
  • Showing 1-26 of 26 Results