Mansfield JC - Search Results

1

Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.

Prescott NJ, Lehne B, Stone K, Lee JC, Taylor K, Knight J, Papouli E, Mirza MM, Simpson MA, Spain SL, Lu G, Fraternali F, Bumpstead SJ, Gray E, Amar A, Bye H, Green P, Chung-Faye G, Hayee B, Pollok R, Satsangi J, Parkes M, Barrett JC, Mansfield JC, Sanderson J, Lewis CM, Weale ME, Schlitt T, Mathew CG; UK IBD Genetics Consortium. Prescott NJ, et al. Among authors: mansfield jc. PLoS Genet. 2015 Feb 11;11(2):e1004955. doi: 10.1371/journal.pgen.1004955. eCollection 2015 Feb. PLoS Genet. 2015. PMID: 25671699 Free PMC article.

2

The CC chemokine receptor 5 delta32 mutation is not associated with inflammatory bowel disease (IBD) in NE England.

Craggs A, Welfare M, Donaldson PT, Mansfield JC. Craggs A, et al. Among authors: mansfield jc. Genes Immun. 2001 Apr;2(2):114-6. doi: 10.1038/sj.gene.6363735. Genes Immun. 2001. PMID: 11393656

3

Role of polymorphisms in the interleukin-10 gene in determining disease susceptibility and phenotype in inflamatory bowel disease.

Aithal GP, Craggs A, Day CP, Welfare M, Daly AK, Mansfield JC, Hudson M. Aithal GP, et al. Among authors: mansfield jc. Dig Dis Sci. 2001 Jul;46(7):1520-5. doi: 10.1023/a:1010604307776. Dig Dis Sci. 2001. PMID: 11478505

4

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Cuthbert AP, Fisher SA, Mirza MM, King K, Hampe J, Croucher PJ, Mascheretti S, Sanderson J, Forbes A, Mansfield J, Schreiber S, Lewis CM, Mathew CG. Cuthbert AP, et al. Gastroenterology. 2002 Apr;122(4):867-74. doi: 10.1053/gast.2002.32415. Gastroenterology. 2002. PMID: 11910337

5

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

Mirza MM, Fisher SA, King K, Cuthbert AP, Hampe J, Sanderson J, Mansfield J, Donaldson P, Macpherson AJ, Forbes A, Schreiber S, Lewis CM, Mathew CG. Mirza MM, et al. Am J Hum Genet. 2003 Apr;72(4):1018-22. doi: 10.1086/373880. Epub 2003 Mar 3. Am J Hum Genet. 2003. PMID: 12618963 Free PMC article.

6

Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease.

King K, Moody A, Fisher SA, Mirza MM, Cuthbert AP, Hampe J, Sutherland-Craggs A, Sanderson J, MacPherson AJ, Forbes A, Mansfield J, Schreiber S, Lewis CM, Mathew CG. King K, et al. Eur J Immunogenet. 2003 Jun;30(3):187-90. doi: 10.1046/j.1365-2370.2003.00387.x. Eur J Immunogenet. 2003. PMID: 12786995

7

Genetic variation at the chromosome 16 chemokine gene cluster: development of a strategy for association studies in complex disease.

Fisher SA, Moody A, Mirza MM, Cuthbert AP, Hampe J, Macpherson A, Sanderson J, Forbes A, Mansfield J, Schreiber S, Lewis CM, Mathew CG. Fisher SA, et al. Ann Hum Genet. 2003 Sep;67(Pt 5):377-90. doi: 10.1046/j.1469-1809.2003.00040.x. Ann Hum Genet. 2003. PMID: 12940913

8

Association of DLG5 R30Q variant with inflammatory bowel disease.

Daly MJ, Pearce AV, Farwell L, Fisher SA, Latiano A, Prescott NJ, Forbes A, Mansfield J, Sanderson J, Langelier D, Cohen A, Bitton A, Wild G, Lewis CM, Annese V, Mathew CG, Rioux JD. Daly MJ, et al. Eur J Hum Genet. 2005 Jul;13(7):835-9. doi: 10.1038/sj.ejhg.5201403. Eur J Hum Genet. 2005. PMID: 15841097

9

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

King K, Sheikh MF, Cuthbert AP, Fisher SA, Onnie CM, Mirza MM, Pattni RC, Sanderson J, Forbes A, Mansfield J, Lewis CM, Roberts RG, Mathew CG. King K, et al. Hum Mutat. 2006 Jan;27(1):44-54. doi: 10.1002/humu.20264. Hum Mutat. 2006. PMID: 16278823

10

Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.

Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG. Fisher SA, et al. Hum Mutat. 2006 Aug;27(8):778-85. doi: 10.1002/humu.20358. Hum Mutat. 2006. PMID: 16835882

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