Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 37, 2007, Pages 14747-14752

  Raelson, John V ^a   Little, Randall D ^a   Ruether, Andreas ^b   Fournier, Hélène ^a   Paquin, Bruno ^a   Van Eerdewegh, Paul ^a   Bradley, W E C ^c   Croteau, Pascal ^a   Nguyen Huu, Quynh ^a   Segal, Jonathan ^a   Debrus, Sophie ^a   Allard, René ^a   Rosenstiel, Philip ^b   Franke, Andre ^b   Jacobs, Gunnar ^b   Nikolaus, Susanna ^b   Vidal, Jean Michel ^a   Szego, Peter ^d   Laplante, Nathalie ^a   Clark, Hilary F ^e   Paulussen, Renéj ^a   Hooper, John W ^a   Keith, Tim P ^a   Belouchi, Abdelmajid ^a   Schreiber, Stefan ^b   more..

^a Genizon BioSciences Inc   (Canada)

^b UNIVERSITY OF KIEL   (Germany)

^c NOTRE DAME HOSPITAL   (Canada)

^d MCGILL UNIVERSITY   (Canada)

^e GENENTECH INC   (United States)

Author keywords

Complex disease; Haplotype; IL23R

Indexed keywords

ALLELE; ARTICLE; CANADA; CAUCASIAN; CHROMOSOME 3P; CHROMOSOME 4P; CONTROLLED STUDY; CROHN DISEASE; GENE; GENE IDENTIFICATION; GENE LOCUS; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GERMANY; HAPLOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; IBD5 GENE; IMMUNE RESPONSE; IMMUNOHISTOCHEMISTRY; NOD2 GENE; POPULATION GENETICS; PRIORITY JOURNAL; VALIDATION PROCESS;

ALLELES; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 3; CHROMOSOMES, HUMAN, PAIR 4; CROHN DISEASE; FOUNDER EFFECT; FRANCE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; GENOME, HUMAN; HAPLOTYPES; HUMANS; NOD2 SIGNALING ADAPTOR PROTEIN; PHYSICAL CHROMOSOME MAPPING; QUEBEC; RECEPTORS, INTERLEUKIN; REPRODUCIBILITY OF RESULTS; RISK FACTORS;

EID: 35548958718     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0706645104     Document Type: Article

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