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Number of items: 5.
Bibliographic data only
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.