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Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease.
Published in:
Nature Genetics, 2011, v. 43, n. 1, p. 43, doi. 10.1038/ng.733
By:
- Momozawa, Yukihide;
- Mni, Myriam;
- Nakamura, Kayo;
- Coppieters, Wouter;
- Almer, Sven;
- Amininejad, Leila;
- Cleynen, Isabelle;
- Colombel, Jean-Frédéric;
- de Rijk, Peter;
- Dewit, Olivier;
- Finkel, Yigael;
- Gassull, Miquel A.;
- Goossens, Dirk;
- Laukens, Debby;
- Lémann, Marc;
- Libioulle, Cécile;
- O'Morain, Colm;
- Reenaers, Catherine;
- Rutgeerts, Paul;
- Tysk, Curt
Publication type:
Article
Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.
Published in:
Nature Genetics, 2009, v. 41, n. 1, p. 71, doi. 10.1038/ng.285
By:
- Villani, Alexandra-Chloé;
- Lemire, Mathieu;
- Fortin, Geneviève;
- Louis, Edouard;
- Silverberg, Mark S.;
- Collette, Catherine;
- Baba, Nobuyasu;
- Libioulle, Cécile;
- Belaiche, Jacques;
- Bitton, Alain;
- Gaudet, Daniel;
- Cohen, Albert;
- Langelier, Diane;
- Fortin, Paul R.;
- Wither, Joan E.;
- Sarfati, Marika;
- Rutgeerts, Paul;
- Rioux, John D.;
- Vermeire, Severine;
- Hudson, Thomas J.
Publication type:
Article
Evidence for Significant Overlap between Common Risk Variants for Crohn's Disease and Ankylosing Spondylitis.
Published in:
PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0013795
By:
- Laukens, Debby;
- Georges, Michel;
- Libioulle, Cécile;
- Sandor, Cynthia;
- Mni, Myriam;
- Vander Cruyssen, Bert;
- Peeters, Harald;
- Elewaut, Dirk;
- De Vos, Martine
Publication type:
Article
Genetic Variation in the Familial Mediterranean Fever Gene (MEFV) and Risk for Crohn's Disease and Ulcerative Colitis.
Published in:
PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007154
By:
- Villani, Alexandra-Chloé;
- Lemire, Mathieu;
- Louis, Edouard;
- Silverberg, Mark S.;
- Collette, Catherine;
- Fortin, Geneviève;
- Nimmo, Elaine R.;
- Renaud, Yannick;
- Brunet, Sébastien;
- Libioulle, Cécile;
- Belaiche, Jacques;
- Bitton, Alain;
- Gaudet, Daniel;
- Cohen, Albert;
- Langelier, Diane;
- Rioux, John D.;
- Arnott, Ian D. R.;
- Wild, Gary E.;
- Rutgeerts, Paul;
- Satsangi, Jack
Publication type:
Article
Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty.
Published in:
Journal of the Endocrine Society, 2023, v. 7, n. 1, p. 1, doi. 10.1210/jendso/bvac168
By:
- Gernay, Caroline;
- Brachet, Cécile;
- Boros, Emese;
- Tenoutasse, Sylvie;
- Libioulle, Cécile;
- Heinrichs, Claudine
Publication type:
Article
Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4.
Published in:
PLoS Genetics, 2007, v. 3, n. 4, p. e58, doi. 10.1371/journal.pgen.0030058
By:
- Libioulle, Cécile;
- Louis, Edouard;
- Hansoul, Sarah;
- Sandor, Cynthia;
- Farnir, Frédéric;
- Franchimont, Denis;
- Vermeire, Séverine;
- Dewit, Olivier;
- De Vos, Martine;
- Dixon, Anna;
- Demarche, Bruno;
- Gut, Ivo;
- Heath, Simon;
- Foglio, Mario;
- Liming Liang;
- Laukens, Debby;
- Mni, Myriam;
- Zelenika, Diana;
- Van Gossum, André;
- Rutgeerts, Paul
Publication type:
Article
An insertion–deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 24, p. 3008, doi. 10.1093/hmg/ddm259
By:
- Dideberg, Vinciane;
- Kristjansdottir, Gudlaug;
- Milani, Lili;
- Libioulle, Cécile;
- Sigurdsson, Snaevar;
- Louis, Edouard;
- Wiman, Ann-Christin;
- Vermeire, Séverine;
- Rutgeerts, Paul;
- Belaiche, Jacques;
- Franchimont, Denis;
- Van Gossum, André;
- Bours, Vincent;
- Syvänen, Ann-Christine
Publication type:
Article

Found: 7

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease.

Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.

Evidence for Significant Overlap between Common Risk Variants for Crohn's Disease and Ankylosing Spondylitis.

Genetic Variation in the Familial Mediterranean Fever Gene (MEFV) and Risk for Crohn's Disease and Ulcerative Colitis.

Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty.

Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4.

An insertion–deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.