Fisher S - Search Results

1

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.

Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, Frenzel H, King K, Hasselmeyer A, MacPherson AJ, Bridger S, van Deventer S, Forbes A, Nikolaus S, Lennard-Jones JE, Foelsch UR, Krawczak M, Lewis C, Schreiber S, Mathew CG. Hampe J, et al. Among authors: fisher s. Lancet. 2001 Jun 16;357(9272):1925-8. doi: 10.1016/S0140-6736(00)05063-7. Lancet. 2001. PMID: 11425413

2

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. Among authors: fisher sa. Gastroenterology. 2002 Apr;122(4):867-74. doi: 10.1053/gast.2002.32415. Gastroenterology. 2002. PMID: 11910337

3

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6.

Fisher SA, Hampe J, Macpherson AJ, Forbes A, Lennard-Jones JE, Schreiber S, Curran ME, Mathew CG, Lewis CM. Fisher SA, et al. Eur J Hum Genet. 2002 Apr;10(4):259-65. doi: 10.1038/sj.ejhg.5200792. Eur J Hum Genet. 2002. PMID: 12032734

4

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. Among authors: fisher sa. 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.

5

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

6

Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.

Pearce AV, Fisher SA, Prescott NJ, Onnie CM, Pattni R, Green P, Forbes A, Mansfield J, Sanderson J, Schreiber S, Lewis CM, Mathew CG. Pearce AV, et al. Among authors: fisher sa. Int J Colorectal Dis. 2007 Apr;22(4):419-24. doi: 10.1007/s00384-006-0151-4. Epub 2006 May 31. Int J Colorectal Dis. 2007. PMID: 16944184

7

A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.

Prescott NJ, Fisher SA, Franke A, Hampe J, Onnie CM, Soars D, Bagnall R, Mirza MM, Sanderson J, Forbes A, Mansfield JC, Lewis CM, Schreiber S, Mathew CG. Prescott NJ, et al. Among authors: fisher sa. Gastroenterology. 2007 May;132(5):1665-71. doi: 10.1053/j.gastro.2007.03.034. Epub 2007 Mar 24. Gastroenterology. 2007. PMID: 17484864

8

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

King K, Bagnall R, Fisher SA, Sheikh F, Cuthbert A, Tan S, Mundy NI, Rosenstiel P, Schreiber S, Mathew CG, Roberts RG. King K, et al. Among authors: fisher sa. Genomics. 2007 Oct;90(4):493-501. doi: 10.1016/j.ygeno.2007.07.009. Epub 2007 Aug 24. Genomics. 2007. PMID: 17719742 Free article.

9

Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.

Onnie CM, Fisher SA, Prescott NJ, Mirza MM, Green P, Sanderson J, Forbes A, Lewis CM, Mathew CG. Onnie CM, et al. Eur J Gastroenterol Hepatol. 2008 Jan;20(1):37-45. doi: 10.1097/MEG.0b013e3282f1622b. Eur J Gastroenterol Hepatol. 2008. PMID: 18090989

OBJECTIVES: Genetic variants at the CARD15 and IBD5 loci are strongly associated with Crohn's disease (CD), but evidence of the effect of these variants on the clinical expression of CD is conflicting and has often been hampered by small sample sizes. ...Allele frequencies …

OBJECTIVES: Genetic variants at the CARD15 and IBD5 loci are strongly associated with Crohn's disease (CD), but evidence of the effec …

10

Power of genetic association studies in the presence of linkage disequilibrium and allelic heterogeneity.

Fisher SA, Lewis CM. Fisher SA, et al. Hum Hered. 2008;66(4):210-22. doi: 10.1159/000143404. Epub 2008 Jul 9. Hum Hered. 2008. PMID: 18612206 Free PMC article.

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