Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Crohn Disease and SLC22A4[original query] |
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| Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease. Human mutation 2006 Aug 27 (8): 778-85. Fisher Sheila A, Hampe Jochen, Onnie Clive M, Daly Mark J, Curley Christine, Purcell Shaun, Sanderson Jeremy, Mansfield John, Annese Vito, Forbes Alastair, Lewis Cathryn M, Schreiber Stefan, Rioux John D, Mathew Christopher |
| 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 |
| 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 |
| 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 |
Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.
Circulation. Cardiovascular genetics 2009 Apr 2 (2): 134-41. Danik Jacqueline S, Paré Guillaume, Chasman Daniel I, Zee Robert Y L, Kwiatkowski David J, Parker Alex, Miletich Joseph P, Ridker Paul |
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