Paths to understanding the genetic basis of autoimmune diseaseRIOUX, John D; ABBAS, Abul K.Nature (London). 2005, Vol 435, Num 7042, pp 584-589, issn 0028-0836, 6 p.Article

Autophagy as an important process in gut homeostasis and Crohn's disease pathogenesisXAVIER, Ramnik J; HUETT, Alan; RIOUX, John D et al.Gut. 2008, Vol 57, Num 6, pp 717-720, issn 0017-5749, 4 p.Article

GWA studies : rewriting the story of IBDBUDARF, Marcia L; LABBE, Catherine; DAVID, Geneviève et al.Trends in genetics (Regular ed.). 2009, Vol 25, Num 3, pp 137-146, issn 0168-9525, 10 p.Article

Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in EuropeansMORRIS, David L; TAYLOR, Kimberly E; PONS-ESTEL, Bernardo A et al.American journal of human genetics. 2012, Vol 91, Num 5, pp 778-793, issn 0002-9297, 16 p.Article

Common variants in the NLRP3 region contribute to Crohn's disease susceptibilityVILLANI, Mexandra-Chloé; LEMIRE, Mathieu; GAUDET, Daniel et al.Nature genetics. 2009, Vol 41, Num 1, pp 71-76, issn 1061-4036, 6 p.Article

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisRIOUX, John D; XAVIER, Ramnik J; SHUGART, Yin Yao et al.Nature genetics. 2007, Vol 39, Num 5, pp 596-604, issn 1061-4036, 9 p.Article

Haplotype analysis of tumour necrosis factor receptor genes in 1p36 : no evidence for association with systemic lupus erythematosusCHADHA, Sapna; MILLER, Katie; FARWELL, Lisa et al.European journal of human genetics. 2006, Vol 14, Num 1, pp 69-78, issn 1018-4813, 10 p.Article

Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 lociRIOUX, John D; KARINEN, Hannele; KOSMA, Veli-Matti et al.American journal of medical genetics. 2004, Vol 130A, Num 4, pp 345-350, issn 0148-7299, 6 p.Article

Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairsVAN HEEL, David A; FISHER, Sheila A; KIRBY, Andrew et al.Human molecular genetics (Print). 2004, Vol 13, Num 7, pp 763-770, issn 0964-6906, 8 p.Article

High-resolution haplotype structure in the human genomeDALY, Mark J; RIOUX, John D; SCHAFFNER, Stephen F et al.Nature genetics. 2001, Vol 29, Num 2, pp 229-232, issn 1061-4036Article

Occupational and environmental exposures and risk of systemic lupus erythematosus: silica, sunlight, solventsCOOPER, Glinda S; WITHER, Joan; BERNATSKY, Sasha et al.Rheumatology (Oxford. Print). 2010, Vol 49, Num 11, pp 2172-2180, issn 1462-0324, 9 p.Article

A functional candidate screen for coeliac disease genesCURLEY, Christine R; MONSUUR, Alienke J; WAPENAAR, Martin C et al.European journal of human genetics. 2006, Vol 14, Num 11, pp 1215-1222, issn 1018-4813, 8 p.Article

Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19TELLO-RUIZ, Marcela Karey; CURLEY, Christine; WEDEMEYER, Neils et al.European journal of human genetics. 2006, Vol 14, Num 6, pp 780-790, issn 1018-4813, 11 p.Article

A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder populationLAITINEN, Tarja; DALY, Mark J; LAITINEN, Lauri A et al.Nature genetics. 2001, Vol 28, Num 1, pp 87-91, issn 1061-4036Article

Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult heightHIRSCHHORN, Joel N; LINDGREN, Cecilia M; GAUDET, Daniel et al.American journal of human genetics. 2001, Vol 69, Num 1, pp 106-116, issn 0002-9297Article

A second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthmaKAUPPI, Paula; LINDBLAD-TOH, Kerstin; SEVON, Petteri et al.Genomics (San Diego, Calif.). 2001, Vol 77, Num 1-2, pp 35-42, issn 0888-7543Article

Pooled DNA Resequencing of 68 Myocardial Infarction Candidate Genes in French CanadiansBEAUDOIN, Melissa; SIN LO, Ken; N'DIAYE, Amidou et al.Circulation. Cardiovascular genetics (Print). 2012, Vol 5, Num 5, pp 547-554, issn 1942-325X, 8 p.Article

Variation Within DNA Repair Pathway Genes and Risk of Multiple SclerosisBRIGGS, Farren B. S; GOLDSTEIN, Benjamin A; OKSENBERG, Jorge R et al.American journal of epidemiology. 2010, Vol 172, Num 2, pp 217-224, issn 0002-9262, 8 p.Article

Molecular pathogenesis of inflammatory bowel disease : Genotypes, phenotypes and personalized medicineGOYETTEI, Philippe; LABBE, Catherine; TRINH, Truc T et al.Annals of medicine (Helsinki). 2007, Vol 39, Num 3, pp 177-199, issn 0785-3890, 23 p.Article

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosisDE JAGER, Philip L; SAWCER, Stephen; RIOUX, John D et al.European journal of human genetics. 2006, Vol 14, Num 3, pp 317-321, issn 1018-4813, 5 p.Article

Genetic variation in toll-like receptor 9 and susceptibility to systemic lupus erythematosusDE JAGER, Philip L; RICHARDSON, Angela; VYSE, Tim J et al.Arthritis and rheumatism. 2006, Vol 54, Num 4, pp 1279-1282, issn 0004-3591, 4 p.Article

Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families : Increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid diseaseHUI WU; CANTOR, Rita M; JULKUNEN, Heikki et al.Arthritis and rheumatism. 2005, Vol 52, Num 8, pp 2396-2402, issn 0004-3591, 7 p.Article

IBD5 is a general risk factor for inflammatory bowel disease: Replication of association with Crohn disease and identification of a novel association with ulcerative colitisGIALLOURAKIS, Cosmas; STOLL, Monika; MILLER, Katie et al.American journal of human genetics. 2003, Vol 73, Num 1, pp 205-211, issn 0002-9297, 7 p.Article

CARD15 genetic variation in a Quebec population: Prevalence, genotype-phenotype relationship, and haplotype structureVERMEIRE, Severine; WILD, Gary; DALY, Mark J et al.American journal of human genetics. 2002, Vol 71, Num 1, pp 74-83, issn 0002-9297Article

Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individualsBRIGGS, Farren B. S; BARTLETT, Selena E; HAFLER, David A et al.Human molecular genetics (Print). 2010, Vol 19, Num 21, pp 4286-4295, issn 0964-6906, 10 p.Article