New links to the pathogenesis of Crohn disease provided by genome-wide association scansMATHEW, Christopher G.Nature reviews. Genetics (Print). 2008, Vol 9, Num 1, pp 9-14, issn 1471-0056, 6 p.Article

Genetics of inflammatory bowel disease: progress and prospectsMATHEW, Christopher G; LEWIS, Cathryn M.Human molecular genetics (Print). 2004, Vol 13, pp R161-R168, issn 0964-6906, NS1Article

Mutation of the RAD51C gene in a Fanconi anemia― like disorderVAZ, Fiona; HANENBERG, Helmut; FRATERNALI, Franca et al.Nature genetics. 2010, Vol 42, Num 5, pp 406-409, issn 1061-4036, 4 p.Article

Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibilityFRANKE, Andre; BALSCHUN, Tobias; SINA, Christian et al.Nature genetics. 2008, Vol 40, Num 11, pp 1319-1323, issn 1061-4036, 5 p.Article

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1HAMPE, Jochen; FRANKE, Andre; GÜNTHER, Simone et al.Nature genetics. 2007, Vol 39, Num 2, pp 207-211, issn 1061-4036, 5 p.Article

Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemiaTISCHKOWITZ, Marc; AMEZIANE, Najim; WAISFISZ, Quinten et al.British journal of haematology. 2003, Vol 123, Num 3, pp 469-471, issn 0007-1048, 3 p.Article

Association of complementation group and mutation type with clinical outcome in fanconi anemiaFAIVRE, Laurence; GUARDIOLA, Philippe; VAN WEEL-SIPMAN, Margreet et al.Blood. 2000, Vol 96, Num 13, pp 4064-4070, issn 0006-4971Article

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

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

Genetic variation in DLG5 is associated with inflammatory bowel diseaseSTOLL, Monika; CORNELIUSSEN, Brit; NIKOLAUS, Susanna et al.Nature genetics. 2004, Vol 36, Num 5, pp 476-480, issn 1061-4036, 5 p.Article

Isolation of a cDNA representing the Fanconi anemia complementation group E geneDE WINTER, Johan P; LEVEILLE, France; LIGHTFOOT, Jeff et al.American journal of human genetics. 2000, Vol 67, Num 5, pp 1306-1308, issn 0002-9297Article

Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African populationBYE, Hannah; PRESCOTT, Natalie J; LEWIS, Cathryn M et al.Carcinogenesis (New York. Print). 2012, Vol 33, Num 11, pp 2155-2161, issn 0143-3334, 7 p.Article

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

Recruiting first-degree relatives for prevention research : a comparison of clinician and proband-led methods of Contact in Crohn's diseaseREID, Erin P; FORBES, Alastair; SANDERSON, Jeremy et al.European journal of human genetics. 2006, Vol 14, Num 12, pp 1263-1268, issn 1018-4813, 6 p.Article

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypesLEVITUS, Marieke; ROOIMANS, Martin A; JOENJE, Hans et al.Blood. 2004, Vol 103, Num 7, pp 2498-2503, issn 0006-4971, 6 p.Article

Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1HUSSAIN, Shobbir; WITT, Emily; HUBER, Pia A. J et al.Human molecular genetics (Print). 2003, Vol 12, Num 19, pp 2503-2510, issn 0964-6906, 8 p.Article

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's diseaseALDHOUS, Marian C; ABU BAKAR, Suhaili; PRESCOTT, Natalie J et al.Human molecular genetics (Print). 2010, Vol 19, Num 24, pp 4930-4938, issn 0964-6906, 9 p.Article

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancerREID, Sarah; SCHINDLER, Detlev; WURM, Melanie et al.Nature genetics. 2007, Vol 39, Num 2, pp 162-164, issn 1061-4036, 3 p.Article

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

Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease. CommentaryVAN HEEL, David A; GHOSH, Subrata; FOXWELL, Brian M. J et al.Lancet (British edition). 2005, Vol 365, Num 9473, pp 1752-1754, issn 0140-6736, 6 p.Article

A common Fanconi anemia mutation in black populations of sub-Saharan AfricaMORGAN, Neil V; ESSOP, Fahmida; DIGWEED, Martin et al.Blood. 2005, Vol 105, Num 9, pp 3542-3544, issn 0006-4971, 3 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