Independent and population-specific association of risk variants at the IRGM locus with Crohn's diseasePRESCOTT, Natalie J; DOMINY, Katherine M; PARKES, Gareth et al.Human molecular genetics (Print). 2010, Vol 19, Num 9, pp 1828-1839, issn 0964-6906, 12 p.Article

Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNAFRITSCHE, Lars G; LOENHARDT, Thomas; JANSSEN, Andreas et al.Nature genetics. 2008, Vol 40, Num 7, pp 892-896, issn 1061-4036, 5 p.Article

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's diseaseFISHER, Sheila A; TREMELLING, Mark; BARRETT, Jeffrey C et al.Nature genetics. 2008, Vol 40, Num 6, pp 710-712, issn 1061-4036, 3 p.Article

Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairsVAN HEEL, David A; FISHER, Sheila A; KIRBY, Andrew et al.Human molecular genetics (Print). 2004, Vol 13, Num 7, pp 763-770, issn 0964-6906, 8 p.Article

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel diseaseCUTHBERT, Andrew P; FISHER, Sheila A; SCHREIBER, Stefan et al.Gastroenterology (New York, NY. 1943). 2002, Vol 122, Num 4, pp 867-874, issn 0016-5085Article

Association of DLG5 R30Q variant with inflammatory bowel diseaseDALY, Mark J; PEARCE, Alexandra V; COHEN, Albert et al.European journal of human genetics. 2005, Vol 13, Num 7, pp 835-839, issn 1018-4813, 5 p.Article

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD 15 gene in Crohn diseaseMIRZA, Muddassar M; FISHER, Sheila A; SCHREIBER, Stefan et al.American journal of human genetics. 2003, Vol 72, Num 4, pp 1018-1022, issn 0002-9297, 5 p.Article

A decision theory approach to fitness for purpose in analytical measurementFEARN, Tom; FISHER, Sheila A; THOMPSON, Michael et al.Analyst (London. 1877. Print). 2002, Vol 127, Num 6, pp 818-824, issn 0003-2654Article

Searching for Genotype-Phenotype Structure : Using Hierarchical Log-Linear Models in Crohn DiseaseCHAPMAN, Juliet M; ONNIE, Clive M; PRESCOTT, Natalie J et al.American journal of human genetics. 2009, Vol 84, Num 2, pp 178-187, issn 0002-9297, 10 p.Article

Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's diseaseONNIE, Clive M; FISHER, Sheila A; PRESCOTT, Natalie J et al.European journal of gastroenterology & hepatology. 2008, Vol 20, Num 1, pp 37-45, issn 0954-691X, 9 p.Article

Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British populationPEARCE, Alexandra V; FISHER, Sheila A; LEWIS, Cathryn M et al.International journal of colorectal disease (Print). 2007, Vol 22, Num 4, pp 419-424, issn 0179-1958, 6 p.Article

The -174G allele of the interleukin-6 gene confers susceptibility to systemic arthritis in children: A multicenter study using simplex and multiplex juvenile idiopathic arthritis familiesOGILVIE, Emma M; FIFE, Mark S; WOO, Patricia et al.Arthritis and rheumatism. 2003, Vol 48, Num 11, pp 3202-3206, issn 0004-3591, 5 p.Article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseBARRETT, Jeffrey C; HANSOUL, Sarah; BITTON, Alain et al.Nature genetics. 2008, Vol 40, Num 8, pp 955-962, issn 1061-4036, 8 p.Article

Assessment of the contribution of CFH and chromosome 10q26 AMD susceptibility loci in a Russian population isolateFISHER, Sheila A; RIVERA, Andrea; FRITSCHE, Lars G et al.British journal of ophthalmology. 2007, Vol 91, Num 5, pp 576-578, issn 0007-1161, 3 p.Article

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD 15) geneKING, Kathy; BAGNALL, Richard; ROBERTS, Roland G et al.Genomics (San Diego, Calif.). 2007, Vol 90, Num 4, pp 493-501, issn 0888-7543, 9 p.Article

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibilityPARKES, Miles; BARRETT, Jeffrey C; DRUMMOND, Hazel et al.Nature genetics. 2007, Vol 39, Num 7, pp 830-832, issn 1061-4036, 3 p.Article

Relationship between p53 codon 72 polymorphism and susceptibility to sunburn and skin cancerMCGREGOR, Tine M; HARWOOD, Catherine A; LEWIS, Cathryn M et al.Journal of investigative dermatology. 2002, Vol 119, Num 1, pp 84-90, issn 0022-202X, 7 p.Article

Germline Mutation in ATR in Autosomal-Dominant Oropharyngeal Cancer SyndromeTANAKA, Akio; WEINEL, Sarah; YANASE, Yuhki et al.American journal of human genetics. 2012, Vol 90, Num 3, pp 511-517, issn 0002-9297, 7 p.Article

Meta-analysis of genome-wide linkage studies across autoimmune diseasesFORABOSCO, Paola; BOUZIGON, Emmanuelle; NG, Mandy Y et al.European journal of human genetics. 2009, Vol 17, Num 2, pp 236-243, issn 1018-4813, 8 p.Article

Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA methodHERMANOWSKI, Jane; BOUZIGON, Emmanuelle; FORABOSCO, Paola et al.European journal of human genetics. 2007, Vol 15, Num 6, pp 703-710, issn 1018-4813, 8 p.Article

Association of R602W in a protein tyrosine phosphatase gene with a high risk of rheumatoid arthritis in a British population : evidence for an early onset/disease severity effectSTEER, Sophia; LAD, Bhaneeta; GRUMLEY, Janet A et al.Arthritis and rheumatism. 2005, Vol 52, Num 1, pp 358-360, issn 0004-3591, 3 p.Article

Meta-analysis of genome scans of age-related macular degenerationFISHER, Sheila A; ABECASIS, Goncalo R; SCHULTZ, Dennis W et al.Human molecular genetics (Print). 2005, Vol 14, Num 15, pp 2257-2264, issn 0964-6906, 8 p.Article

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease riskRIVERA, Andrea; FISHER, Sheila A; FRITSCHE, Lars G et al.Human molecular genetics (Print). 2005, Vol 14, Num 21, pp 3227-3236, issn 0964-6906, 10 p.Article

Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3KOIVUKOSKI, Liisa; FISHER, Sheila A; RAO, Dabeeru C et al.Human molecular genetics (Print). 2004, Vol 13, Num 19, pp 2325-2332, issn 0964-6906, 8 p.Article