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Number of items: 5.

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Barrett, JC; Hansoul, S; Nicolae, DL; Cho, JH; Duerr, RH; Rioux, JD; Brant, SR; Silverberg, MS; Taylor, KD; Barmada, MM; +51 more... Bitton, A; Dassopoulos, T; Datta, LW; Green, T; Griffiths, AM; Kistner, EO; Murtha, MT; Regueiro, MD; Rotter, JI; Schumm, LP; Steinhart, AH; Targan, SR; Xavier, RJ; Libioulle, C; Sandor, C; Lathrop, M; Belaiche, J; Dewit, O; Gut, I; Heath, S; Laukens, D; Mni, M; Rutgeerts, P; van Gossum, A; Zelenika, D; Franchimont, D; Hugot, JP; de Vos, M; Vermeire, S; Louis, E; Cardon, LR; Anderson, CA; Drummond, H; Nimmo, E; Ahmad, T; Prescott, NJ; Onnie, CM; Fisher, SA; Marchini, J; Ghori, J; Bumpstead, S; Gwilliam, R; Tremelling, M; Deloukas, P; Mansfield, J; Jewell, D; Satsangi, J; Mathew, CG; Parkes, M; Georges, M; Daly, MJ; (2008) Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet, 40 (8). pp. 955-62. ISSN 1061-4036 DOI: https://doi.org/10.1038/ng.175 Full text not available from this repository.

Fisher, SA; Tremelling, M; Anderson, CA; Gwilliam, R; Bumpstead, S; Prescott, NJ; Nimmo, ER; Massey, D; Berzuini, C; Johnson, C; +26 more... Barrett, JC; Cummings, FR; Drummond, H; Lees, CW; Onnie, CM; Hanson, CE; Blaszczyk, K; Inouye, M; Ewels, P; Ravindrarajah, R; Keniry, A; Hunt, S; Carter, M; Watkins, N; Ouwehand, W; Lewis, CM; Cardon, L; Lobo, A; Forbes, A; Sanderson, J; Jewell, DP; Mansfield, JC; Deloukas, P; Mathew, CG; Parkes, M; Satsangi, J; (2008) Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. Nat Genet, 40 (6). pp. 710-2. ISSN 1061-4036 DOI: https://doi.org/10.1038/ng.145 Full text not available from this repository.

Hampe, J; Franke, A; Rosenstiel, P; Till, A; Teuber, M; Huse, K; Albrecht, M; Mayr, G; de la Vega, FM; Briggs, J; +11 more... Gunther, S; Prescott, NJ; Onnie, CM; Hasler, R; Sipos, B; Folsch, UR; Lengauer, T; Platzer, M; Mathew, CG; Krawczak, M; Schreiber, S; (2007) A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet, 39 (2). pp. 207-11. ISSN 1061-4036 DOI: https://doi.org/10.1038/ng1954 Full text not available from this repository.

Imielinski, M; Baldassano, RN; Griffiths, A; Russell, RK; Annese, V; Dubinsky, M; Kugathasan, S; Bradfield, JP; Walters, TD; Sleiman, P; +101 more... Kim, CE; Muise, A; Wang, K; Glessner, JT; Saeed, S; Zhang, H; Frackelton, EC; Hou, C; Flory, JH; Otieno, G; Chiavacci, RM; Grundmeier, R; Castro, M; Latiano, A; Dallapiccola, B; Stempak, J; Abrams, DJ; Taylor, K; McGovern, D; Silber, G; Wrobel, I; Quiros, A; Barrett, JC; Hansoul, S; Nicolae, DL; Cho, JH; Duerr, RH; Rioux, JD; Brant, SR; Silverberg, MS; Taylor, KD; Barmuda, MM; Bitton, A; Dassopoulos, T; Datta, LW; Green, T; Griffiths, AM; Kistner, EO; Murtha, MT; Regueiro, MD; Rotter, JI; Schumm, LP; Steinhart, AH; Targan, SR; Xavier, RJ; Libioulle, C; Sandor, C; Lathrop, M; Belaiche, J; Dewit, O; Gut, I; Heath, S; Laukens, D; Mni, M; Rutgeerts, P; van Gossum, A; Zelenika, D; Franchimont, D; Hugot, JP; de Vos, M; Vermeire, S; Louis, E; Cardon, LR; Anderson, CA; Drummond, H; Nimmo, E; Ahmad, T; Prescott, NJ; Onnie, CM; Fisher, SA; Marchini, J; Ghori, J; Bumpstead, S; Gwillam, R; Tremelling, M; Delukas, P; Mansfield, J; Jewell, D; Satsangi, J; Mathew, CG; Parkes, M; Georges, M; Daly, MJ; Heyman, MB; Ferry, GD; Kirschner, B; Lee, J; Essers, J; Grand, R; Stephens, M; Levine, A; Piccoli, D; van Limbergen, J; Cucchiara, S; Monos, DS; Guthery, SS; Denson, L; Wilson, DC; Grant, SF; Daly, M; Hakonarson, H; (2009) Common variants at five new loci associated with early-onset inflammatory bowel disease. Nat Genet, 41 (12). pp. 1335-40. ISSN 1061-4036 DOI: https://doi.org/10.1038/ng.489 Full text not available from this repository.

McGregor, L; Makela, V; Darling, SM; Vrontou, S; Chalepakis, G; Roberts, C; Smart, N; Rutland, P; Prescott, N; Hopkins, J; +15 more... Bentley, E; Shaw, A; Roberts, E; Mueller, R; Jadeja, S; Philip, N; Nelson, J; Francannet, C; Perez-Aytes, A; Megarbane, A; Kerr, B; Wainwright, B; Woolf, AS; Winter, RM; Scambler, PJ; (2003) Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat Genet, 34 (2). pp. 203-8. ISSN 1061-4036 DOI: https://doi.org/10.1038/ng1142 Full text not available from this repository.

This list was generated on Thu Jul 25 12:04:04 2019 BST.