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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

Title: Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
Authors: Barrett, Jeffrey Carl; Hansoul, Sarah; Nicolae, DL; Cho, Judy H; Duerr, R H; Rioux, J D; Brant, S R; Silverberg, M S; Taylor, Kent D; Barmada, M. Michael; Bitton, A; Dassopoulos, T; Datta, LW; Green, T; Griffiths, Anne-Marie; Kistner, EO; Murtha, MT; Regueiro, Miguel; Rotter, J I; Schumm, L Philip; Steinhart, A H; Targan, SR; Xavier, Ramnik; NIDDK IBD Genetics Consortium; Libioulle, C; Sandor, Cynthia; Lathrop, Mark; Belaiche, Jacques; Gut, Ivo; Heath, Simon; Laukens, Debby; Mni, Myriam; Rutgeerts, Paul; Van Gossum, André; Zelenika, Diana; Franchimont, Denis; Hugot, JP; De Vos, M; Vermeire, Séverine; Louis, Edouard; Belgian-French IBD Consortium,; Wellcome Trust Case Control Consortium,; Cardon, LR; Anderson, Carl A.; Drummond, H; Nimmo, Elaine R; Ahmad, Tariq; Prescott, NJ; Onnie, CM; Fisher, SA; Marchini, J; Ghori, J; Bumpstead, S; Gwillam, R; Tremelling, M; Delukas, P; Mansfeld, J.; Jewell, D; Satsangi, Jack; Mathew, CG; Parkes, M; Georges, M.; Daly, M J; Dewit, Olivier
Source: Nature genetics, 40 (8
Publication Year: 2008
Collection: DI-fusion : dépôt institutionnel de l'Université libre de Bruxelles (ULB)
Subject Terms: Sciences bio-médicales et agricoles; Crohn Disease -- genetics; Genetic Predisposition to Disease; Genome; Human; Humans; Quantitative Trait Loci
Description: Several risk factors for Crohn's disease have been identified in recent genome-wide association studies. To advance gene discovery further, we combined data from three studies on Crohn's disease (a total of 3,230 cases and 4,829 controls) and carried out replication in 3,664 independent cases with a mixture of population-based and family-based controls. The results strongly confirm 11 previously reported loci and provide genome-wide significant evidence for 21 additional loci, including the regions containing STAT3, JAK2, ICOSLG, CDKAL1 and ITLN1. The expanded molecular understanding of the basis of this disease offers promise for informed therapeutic development. ; Journal Article ; Meta-Analysis ; Research Support, N.I.H. Extramural ; Research Support, Non-U.S. Gov't ; info:eu-repo/semantics/published
Document Type: article in journal/newspaper
File Description: 1 full-text file(s): application/pdf
Language: English
Relation: uri/info:doi/10.1038/ng.175; uri/info:pii/ng.175; uri/info:pmid/18587394; uri/info:scp/48349136889; uri/info:pmcid/PMC2574810; https://dipot.ulb.ac.be/dspace/bitstream/2013/55019/3/PMC2574810.pdf
Availability: https://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/55019; https://dipot.ulb.ac.be/dspace/bitstream/2013/55019/3/PMC2574810.pdf
Accession Number: edsbas.5D5B0C71
Database: BASE