Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: Crohn Disease and CARD15[original query] |
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CARD15 genotype and phenotype analysis in 55 pediatric patients with Crohn disease from Saxony, Germany. Journal of pediatric gastroenterology and nutrition 2003 Oct 37 (4): 492-7. Sun Liping, Roesler Joachim, Rösen-Wolff Angela, Winkler Ulf, Koch Rainer, Thürigen Anett, Henker Job |
Interaction of polymorphisms in the CARD15 and CD14 genes in patients with Crohn disease. Scandinavian journal of gastroenterology 2003 Aug 38 (8): 834-6. Klein W, Tromm A, Griga T, Folwaczny C, Hocke M, Eitner K, Marx M, Duerig N, Epplen J |
CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis. American journal of human genetics 2003 Sep 73 (3): 677-81. Rahman P, Bartlett S, Siannis F, Pellett F J, Farewell V T, Peddle L, Schentag C T, Alderdice C A, Hamilton S, Khraishi M, Tobin Y, Hefferton D, Gladman D |
Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease. American journal of human genetics 2003 Apr 72 (4): 1018-22. Mirza Muddassar M, Fisher Sheila A, King Kathy, Cuthbert Andrew P, Hampe Jochen, Sanderson Jeremy, Mansfield John, Donaldson Peter, Macpherson Andrew J S, Forbes Alastair, Schreiber Stefan, Lewis Cathryn M, Mathew Christopher |
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population. The Journal of investigative dermatology 2004 May 122 (5): 1106-7. Giardina Emiliano, Novelli Giuseppe, Costanzo Antonio, Nisticò Steven, Bulli Cristina, Sinibaldi Cecilia, Sorgi Maria Laura, Chimenti Sergio, Pallone Francesco, Taccari Egisto, Borgiani Pao |
Genetic variation in DLG5 is associated with inflammatory bowel disease. Nature genetics 2004 May 36 (5): 476-80. Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S |
Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation. Blood 2004 Aug 104 (3): 889-94. Holler E, Rogler G, Herfarth H, Brenmoehl J, Wild PJ, Hahn J, Eissner G, Schölmerich J, Andreesen R |
Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease. Scandinavian journal of gastroenterology 2003 Dec 38 (12): 1235-40. Mendoza J L, Murillo L S, Fernández L, Peña A S, Lana R, Urcelay E, Cruz-Santamaría D M, de la Concha E G, Díaz-Rubio M, García-Paredes |
Influence of CARD15 mutations on disease activity and response to therapy in 65 pediatric Crohn patients from Saxony, Germany. Journal of pediatric gastroenterology and nutrition 2005 Jul 41 (1): 27-32. Roesler Joachim, Thürigen Anett, Sun Liping, Koch Rainer, Winkler Ulf, Laass Martin W, Gahr Manfred, Rösen-Wolff Angela, Henker Job |
CARD15 mutations are rare in Swedish pediatric Crohn disease. Journal of pediatric gastroenterology and nutrition 2005 Apr 40 (4): 456-60. Ideström Maja, Rubio Carlos, Granath Fredrik, Finkel Yigael, Hugot J |
Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15. Human mutation 2006 Jan 27 (1): 44-54. King Kathy, Sheikh Mohammed F, Cuthbert Andrew P, Fisher Sheila A, Onnie Clive M, Mirza Muddassar M, Pattni Reenal C, Sanderson Jeremy, Forbes Alastair, Mansfield John, Lewis Cathryn M, Roberts Roland G, Mathew Christopher |
Ileal lymphonodular hyperplasia is not associated with NOD2/CARD15 mutations. Journal of pediatric gastroenterology and nutrition 2006 Jul 43 (1): 30-4. Shaoul Ron, Eliakim Rami, Tamir Ada, Karban Am |
Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases. BMC medical genetics 2006 7 (): 20. Smyth Deborah J, Howson Joanna M M, Payne Felicity, Maier Lisa M, Bailey Rebecca, Holland Kieran, Lowe Christopher E, Cooper Jason D, Hulme John S, Vella Adrian, Dahlman Ingrid, Lam Alex C, Nutland Sarah, Walker Neil M, Twells Rebecca C J, Todd John |
Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations. European journal of human genetics : EJHG 2006 Apr 14 (4): 459-68. Medici Valentina, Mascheretti Silvia, Croucher Peter J P, Stoll Monika, Hampe Jochen, Grebe Jochen, Sturniolo Giacomo C, Solberg Camilla, Jahnsen Jorgen, Moum Bjorn, Schreiber Stefan, Vatn Morten |
DLG5 variants contribute to Crohn disease risk in a Canadian population. Human mutation 2006 Apr 27 (4): 353-8. Newman William G, Gu Xiangjun, Wintle Richard F, Liu Xiangdong, van Oene Mark, Amos Christopher I, Siminovitch Katherine |
Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men. Human genetics 2006 Apr 119 (3): 305-11. Friedrichs Frauke, Brescianini Sonia, Annese Vito, Latiano Anna, Berger Klaus, Kugathasan Subra, Broeckel Ulrich, Nikolaus Susanna, Daly Mark J, Schreiber Stefan, Rioux John D, Stoll Moni |
Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn disease. Journal of medical genetics 2007 Nov 44 (11): 689-94. Lewis C M, Whitwell S C L, Forbes A, Sanderson J, Mathew C G, Marteau T |
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
PLoS genetics 2007 Apr 3 (4): e58. Libioulle Cécile, Louis Edouard, Hansoul Sarah, Sandor Cynthia, Farnir Frédéric, Franchimont Denis, Vermeire Séverine, Dewit Olivier, de Vos Martine, Dixon Anna, Demarche Bruno, Gut Ivo, Heath Simon, Foglio Mario, Liang Liming, Laukens Debby, Mni Myriam, Zelenika Diana, Van Gossum André, Rutgeerts Paul, Belaiche Jacques, Lathrop Mark, Georges Mich |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
Nature genetics 2007 May 39 (5): 596-604. Rioux John D, Xavier Ramnik J, Taylor Kent D, Silverberg Mark S, Goyette Philippe, Huett Alan, Green Todd, Kuballa Petric, Barmada M Michael, Datta Lisa Wu, Shugart Yin Yao, Griffiths Anne M, Targan Stephan R, Ippoliti Andrew F, Bernard Edmond-Jean, Mei Ling, Nicolae Dan L, Regueiro Miguel, Schumm L Philip, Steinhart A Hillary, Rotter Jerome I, Duerr Richard H, Cho Judy H, Daly Mark J, Brant Steven |
Evaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn disease. Journal of pediatric gastroenterology and nutrition 2007 Oct 45 (4): 405-8. Leshinsky-Silver Esther, Karban Amir, Dalal Ilan, Eliakim Rami, Shirin Haim, Tzofi Tzipi, Boaz Mona, Levine Ar |
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nature genetics 2007 Feb 39 (2): 207-11. Hampe Jochen, Franke Andre, Rosenstiel Philip, Till Andreas, Teuber Markus, Huse Klaus, Albrecht Mario, Mayr Gabriele, De La Vega Francisco M, Briggs Jason, Günther Simone, Prescott Natalie J, Onnie Clive M, Häsler Robert, Sipos Bence, Fölsch Ulrich R, Lengauer Thomas, Platzer Matthias, Mathew Christopher G, Krawczak Michael, Schreiber Stef |
Frequency and clinical correlations of granulomas in children with Crohn disease. Journal of pediatric gastroenterology and nutrition 2008 Apr 46 (4): 392-8. De Matos Vera, Russo Pierre A, Cohen Aaron B, Mamula Petar, Baldassano Robert N, Piccoli David |
Association of IL23R p.381Gln and ATG16L1 p.197Ala with Crohn disease in the Czech population. Journal of pediatric gastroenterology and nutrition 2009 Jul . Dusatkova P, Hradsky O, Lenicek M, Bronsky J, Nevoral J, Kotalova R, Bajerova K, Vitek L, Lukas M, Cinek O |
Polymorphisms in the IBD5 locus are associated with Crohn disease in pediatric Ashkenazi Jewish patients. Journal of pediatric gastroenterology and nutrition 2009 May 48 (5): 531-7. Tomer Gitit, Wetzler Graciela, Keddache Mehdi, Denson Lee |
Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer. BMC gastroenterology 2009 9 (1): 79. Möckelmann Nikolaus, von Schönfels Witigo, Buch Stephan, von Kampen Oliver, Sipos Bence, Egberts Jan Hendrik, Rosenstiel Philip, Franke Andre, Brosch Mario, Hinz Sebastian, Röder Christian, Kalthoff Holger, Fölsch Ulrich R, Krawczak Michael, Schreiber Stefan, Bröring Clemens Dieter, Tepel Jürgen, Schafmayer Clemens, Hampe Joch |
NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease. Journal of pediatric surgery 2010 Aug 45 (8): 1591-7. Lacher Martin, Helmbrecht Johanna, Schroepf Sebastian, Koletzko Sibylle, Ballauff Antje, Classen Martin, Uhlig Holm, Hubertus Jochen, Hartl Dominik, Lohse Peter, von Schweinitz Dietrich, Kappler Rola |
Three common CARD15 mutations are not responsible for the pathogenesis of Crohn's disease in Iranians. Hepato-gastroenterology 0 57 (98): 275-82. Teimoori-Toolabi Ladan, Vahedi Homayoun, Mollahajian Hamid, Kamali Esmat, Hajizadeh-Sikaroodi Shohreh, Zeinali Sirous, Tabrizian Tahmineh, Olfati Golrokh, Rashtak Shahrooz, Malekzadeh Fatemeh, Ghoddosi Alireza, Malekzadeh Re |
Penetrance of NOD2/CARD15 genetic variants in the general population. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2010 Apr 182 (7): 661-5. Yazdanyar Shiva, Kamstrup Pia R, Tybjaerg-Hansen Anne, Nordestgaard Børge |
Low mannose-binding lectin (MBL) is associated with paediatric inflammatory bowel diseases and ileal involvement in patients with Crohn disease. Journal of Crohn's & colitis 2013 Mar 7 (2): 134-41. Kovacs Marta, Papp Maria, Lakatos Peter Laszlo, Jacobsen Silvia, Nemes Eva, Polgar Marianne, Solyom Eniko, Bodi Piroska, Horvath Agnes, Molnar Kriszta, Szabo Doloresz, Cseh Aron, Muller Katalin Eszter, Dezsofi Antal, Arato Andras, Veres Gab |
NOD2 polymorphisms may direct a Crohn's disease phenotype in patients with Very EarlyOnset Inflammatory Bowel Disease. Journal of pediatric gastroenterology and nutrition 2023 5 . Ashleigh Watson, Lisa Forbes Satter, Ashley Reiland Sauceda, Richard Kellermayer, Lina B Kar |
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