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428 related items for PubMed ID: 18047539

  • 1. Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.
    Amre DK, Mack D, Israel D, Morgan K, Lambrette P, Law L, Grimard G, Deslandres C, Krupoves A, Bucionis V, Costea I, Bissonauth V, Feguery H, D'Souza S, Levy E, Seidman EG.
    Am J Gastroenterol; 2008 Mar; 103(3):615-20. PubMed ID: 18047539
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  • 2. Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.
    Török HP, Glas J, Endres I, Tonenchi L, Teshome MY, Wetzke M, Klein W, Lohse P, Ochsenkühn T, Folwaczny M, Göke B, Folwaczny C, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Jul; 104(7):1723-33. PubMed ID: 19455129
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  • 3. Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease.
    Amre DK, Mack DR, Morgan K, Israel D, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Deslandres C, Levy E, Seidman EG.
    Aliment Pharmacol Ther; 2009 May 01; 29(9):1025-31. PubMed ID: 19210299
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  • 6. Evaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn disease.
    Leshinsky-Silver E, Karban A, Dalal I, Eliakim R, Shirin H, Tzofi T, Boaz M, Levine A.
    J Pediatr Gastroenterol Nutr; 2007 Oct 01; 45(4):405-8. PubMed ID: 18030204
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  • 7. The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
    Glas J, Konrad A, Schmechel S, Dambacher J, Seiderer J, Schroff F, Wetzke M, Roeske D, Török HP, Tonenchi L, Pfennig S, Haller D, Griga T, Klein W, Epplen JT, Folwaczny C, Lohse P, Göke B, Ochsenkühn T, Mussack T, Folwaczny M, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2008 Mar 01; 103(3):682-91. PubMed ID: 18162085
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  • 8. Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.
    Hradsky O, Lenicek M, Dusatkova P, Bronsky J, Nevoral J, Valtrova V, Kotalova R, Szitanyi P, Petro R, Starzykova V, Bortlik M, Vitek L, Lukas M, Cinek O.
    Tissue Antigens; 2008 Jun 01; 71(6):538-47. PubMed ID: 18489434
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  • 9. IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease.
    Dubinsky MC, Wang D, Picornell Y, Wrobel I, Katzir L, Quiros A, Dutridge D, Wahbeh G, Silber G, Bahar R, Mengesha E, Targan SR, Taylor KD, Rotter JI, Western Regional Research Alliance for Pediatric IBD.
    Inflamm Bowel Dis; 2007 May 01; 13(5):511-5. PubMed ID: 17309073
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  • 12. NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.
    Tomer G, Ceballos C, Concepcion E, Benkov KJ.
    Am J Gastroenterol; 2003 Nov 01; 98(11):2479-84. PubMed ID: 14638352
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  • 13. Tumor necrosis factor receptor gene polymorphisms in Crohn's disease: association with clinical phenotypes.
    Waschke KA, Villani AC, Vermeire S, Dufresne L, Chen TC, Bitton A, Cohen A, Thomson AB, Wild GE.
    Am J Gastroenterol; 2005 May 01; 100(5):1126-33. PubMed ID: 15842589
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  • 14. rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.
    Glas J, Seiderer J, Pasciuto G, Tillack C, Diegelmann J, Pfennig S, Konrad A, Schmechel S, Wetzke M, Török HP, Stallhofer J, Jürgens M, Griga T, Klein W, Epplen JT, Schiemann U, Mussack T, Lohse P, Göke B, Ochsenkühn T, Folwaczny M, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Mar 01; 104(3):665-72. PubMed ID: 19262523
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  • 15. Investigation of NOD1/CARD4 variation in inflammatory bowel disease using a haplotype-tagging strategy.
    Van Limbergen J, Nimmo ER, Russell RK, Drummond HE, Smith L, Anderson NH, Davies G, Arnott ID, Wilson DC, Satsangi J.
    Hum Mol Genet; 2007 Sep 15; 16(18):2175-86. PubMed ID: 17613538
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  • 16. Association of interleukin 23 receptor variants with psoriatic arthritis.
    Rahman P, Inman RD, Maksymowych WP, Reeve JP, Peddle L, Gladman DD.
    J Rheumatol; 2009 Jan 15; 36(1):137-40. PubMed ID: 19040306
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  • 17. DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's disease.
    Biank V, Friedrichs F, Babusukumar U, Wang T, Stoll M, Broeckel U, Kugathasan S.
    Am J Gastroenterol; 2007 Feb 15; 102(2):391-8. PubMed ID: 17156146
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  • 18. Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians.
    Juyal G, Amre D, Midha V, Sood A, Seidman E, Thelma BK.
    Aliment Pharmacol Ther; 2007 Nov 15; 26(10):1325-32. PubMed ID: 17892524
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