-
1
-
-
0037308263
-
The genetics of inflammatory bowel disease
-
Bonen DK, Cho JH. The genetics of inflammatory bowel disease. Gastroenterology 2003; 124: 521-536
-
(2003)
Gastroenterology
, vol.124
, pp. 521-536
-
-
Bonen, D.K.1
Cho, J.H.2
-
2
-
-
2442429216
-
Clinical relevance of advances in genetics and pharmacogenetics of IBD
-
Ahmad T, Tamboli CP, Jewell D, Colombel JF. Clinical relevance of advances in genetics and pharmacogenetics of IBD. Gastroenterology 2004; 126: 1533-1549
-
(2004)
Gastroenterology
, vol.126
, pp. 1533-1549
-
-
Ahmad, T.1
Tamboli, C.P.2
Jewell, D.3
Colombel, J.F.4
-
3
-
-
13344259990
-
Mapping of a susceptibility locus for Crohn's disease on chromosome 16
-
Hugot JP, Laurent-Puig P, Gower-Rousseau C, Olson JM, Lee JC, Beaugerie L, Naom I, Dupas JL, Van Gossum A, Orholm M, Bonaiti-Pellie C, Weissenbach J, Mathew CG, Lennard-Jones JE, Cortot A, Colombel JF, Thomas G. Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature 1996; 379: 821-823
-
(1996)
Nature
, vol.379
, pp. 821-823
-
-
Hugot, J.P.1
Laurent-Puig, P.2
Gower-Rousseau, C.3
Olson, J.M.4
Lee, J.C.5
Beaugerie, L.6
Naom, I.7
Dupas, J.L.8
Van Gossum, A.9
Orholm, M.10
Bonaiti-Pellie, C.11
Weissenbach, J.12
Mathew, C.G.13
Lennard-Jones, J.E.14
Cortot, A.15
Colombel, J.F.16
Thomas, G.17
-
4
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
-
Cavanaugh J. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. Am J Hum Genet 2001; 68: 1165-1171
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1165-1171
-
-
Cavanaugh, J.1
-
5
-
-
0034752121
-
Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease
-
Zouali H, Chamaillard M, Lesage S, Cezard JP, Colombel JF, Belaiche J, Almer S, Tysk C, Montague S, Gassull M, Christensen S, Finkel Y, Gower-Rousseau C, Modigliani R, Macry J, Selinger-Leneman H, Thomas G, Hugot JP. Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease. Eur J Hum Genet 2001; 9: 731-742
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 731-742
-
-
Zouali, H.1
Chamaillard, M.2
Lesage, S.3
Cezard, J.P.4
Colombel, J.F.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
Montague, S.9
Gassull, M.10
Christensen, S.11
Finkel, Y.12
Gower-Rousseau, C.13
Modigliani, R.14
Macry, J.15
Selinger-Leneman, H.16
Thomas, G.17
Hugot, J.P.18
-
6
-
-
0034464007
-
Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity
-
Brant SR, Panhuysen CI, Bailey-Wilson JE, Rohal PM, Lee S, Mann J, Ravenhill G, Kirschner BS, Hanauer SB, Cho JH, Bayless TM. Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity. Gastroenterology 2000; 119: 1483-1490
-
(2000)
Gastroenterology
, vol.119
, pp. 1483-1490
-
-
Brant, S.R.1
Panhuysen, C.I.2
Bailey-Wilson, J.E.3
Rohal, P.M.4
Lee, S.5
Mann, J.6
Ravenhill, G.7
Kirschner, B.S.8
Hanauer, S.B.9
Cho, J.H.10
Bayless, T.M.11
-
7
-
-
8444237435
-
Association of NOD2/CARD15 variants with Crohn's disease in a Greek population
-
Gazouli M, Zacharatos P, Mantzaris GJ, Barbatis C, Ikonomopoulos I, Archimandritis AJ, Lukas JC, Papalambros E, Gorgoulis V. Association of NOD2/CARD15 variants with Crohn's disease in a Greek population. Eur J Gastroenterol Hepatol 2004; 16: 1177-1182
-
(2004)
Eur J Gastroenterol Hepatol
, vol.16
, pp. 1177-1182
-
-
Gazouli, M.1
Zacharatos, P.2
Mantzaris, G.J.3
Barbatis, C.4
Ikonomopoulos, I.5
Archimandritis, A.J.6
Lukas, J.C.7
Papalambros, E.8
Gorgoulis, V.9
-
8
-
-
13544276471
-
Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population
-
Gazouli M, Mantzaris G, Kotsinas A, Zacharatos P, Papalambros E, Archimandritis A, Ikonomopoulos J, Gorgoulis VG. Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population. World J Gastroenterol 2005; 11: 681-685
-
(2005)
World J Gastroenterol
, vol.11
, pp. 681-685
-
-
Gazouli, M.1
Mantzaris, G.2
Kotsinas, A.3
Zacharatos, P.4
Papalambros, E.5
Archimandritis, A.6
Ikonomopoulos, J.7
Gorgoulis, V.G.8
-
9
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR, Bayless TM, Kirschner BS, Hanauer SB, Nunez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 2001; 411: 603-606
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
Britton, H.7
Moran, T.8
Karaliuskas, R.9
Duerr, R.H.10
Achkar, J.P.11
Brant, S.R.12
Bayless, T.M.13
Kirschner, B.S.14
Hanauer, S.B.15
Nunez, G.16
Cho, J.H.17
-
10
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 2001; 411: 599-603
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
O'Morain, C.A.9
Gassull, M.10
Binder, V.11
Finkel, Y.12
Cortot, A.13
Modigliani, R.14
Laurent-Puig, P.15
Gower-Rousseau, C.16
Macry, J.17
Colombel, J.F.18
Sahbatou, M.19
Thomas, G.20
more..
-
11
-
-
0035897904
-
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
-
Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, Frenzel H, King K, Hasselmeyer A, MacPherson AJ, Bridger S, van Deventer S, Forbes A, Nikolaus S, Lennard-Jones JE, Foelsch UR, Krawczak M, Lewis C, Schreiber S, Mathew CG. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 2001; 357: 1925-1928
-
(2001)
Lancet
, vol.357
, pp. 1925-1928
-
-
Hampe, J.1
Cuthbert, A.2
Croucher, P.J.3
Mirza, M.M.4
Mascheretti, S.5
Fisher, S.6
Frenzel, H.7
King, K.8
Hasselmeyer, A.9
MacPherson, A.J.10
Bridger, S.11
van Deventer, S.12
Forbes, A.13
Nikolaus, S.14
Lennard-Jones, J.E.15
Foelsch, U.R.16
Krawczak, M.17
Lewis, C.18
Schreiber, S.19
Mathew, C.G.20
more..
-
12
-
-
2442585704
-
Functional variants of OCTN cation transporter genes are associated with Crohn disease
-
Peltekova VD, Wintle RF, Rubin LA, Amos CI, Huang Q, Gu X, Newman B, Van Oene M, Cescon D, Greenberg G, Griffiths AM, St George-Hyslop PH, Siminovitch KA. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat Genet 2004; 36: 471-475
-
(2004)
Nat Genet
, vol.36
, pp. 471-475
-
-
Peltekova, V.D.1
Wintle, R.F.2
Rubin, L.A.3
Amos, C.I.4
Huang, Q.5
Gu, X.6
Newman, B.7
Van Oene, M.8
Cescon, D.9
Greenberg, G.10
Griffiths, A.M.11
St George-Hyslop, P.H.12
Siminovitch, K.A.13
-
13
-
-
2442519456
-
Genetic variation in DLG5 is associated with inflammatory bowel disease
-
Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S. Genetic variation in DLG5 is associated with inflammatory bowel disease. Nat Genet 2004; 36: 476-480
-
(2004)
Nat Genet
, vol.36
, pp. 476-480
-
-
Stoll, M.1
Corneliussen, B.2
Costello, C.M.3
Waetzig, G.H.4
Mellgard, B.5
Koch, W.A.6
Rosenstiel, P.7
Albrecht, M.8
Croucher, P.J.9
Seegert, D.10
Nikolaus, S.11
Hampe, J.12
Lengauer, T.13
Pierrou, S.14
Foelsch, U.R.15
Mathew, C.G.16
Lagerstrom-Fermer, M.17
Schreiber, S.18
-
14
-
-
0026415351
-
Inflammatory bowel disease 2
-
Podolsky DK. Inflammatory bowel disease 2. N Engl J Med 1991; 325: 928-937
-
(1991)
N Engl J Med
, vol.325
, pp. 928-937
-
-
Podolsky, D.K.1
-
16
-
-
2442674327
-
Genome scan analyses and positional cloning strategy in IBD: Successes and limitations
-
Wild GE, Rioux JD. Genome scan analyses and positional cloning strategy in IBD: successes and limitations. Best Pract Res Clin Gastroenterol 2004; 18: 541-553
-
(2004)
Best Pract Res Clin Gastroenterol
, vol.18
, pp. 541-553
-
-
Wild, G.E.1
Rioux, J.D.2
-
17
-
-
0034842137
-
Carnitine transport by organic cation transporters and systemic carnitine deficiency
-
Lahjouji K, Mitchell GA, Qureshi IA. Carnitine transport by organic cation transporters and systemic carnitine deficiency. Mol Genet Metab 2001; 73: 287-297
-
(2001)
Mol Genet Metab
, vol.73
, pp. 287-297
-
-
Lahjouji, K.1
Mitchell, G.A.2
Qureshi, I.A.3
-
18
-
-
0023013994
-
Metabolic induction of experimental ulcerative colitis by inhibition of fatty acid oxidation
-
Roediger WE, Nance S. Metabolic induction of experimental ulcerative colitis by inhibition of fatty acid oxidation. Br J Exp Pathol 1986; 67: 773-782
-
(1986)
Br J Exp Pathol
, vol.67
, pp. 773-782
-
-
Roediger, W.E.1
Nance, S.2
-
19
-
-
0038389762
-
IBD5 is a general risk factor for inflammatory bowel disease: Replication of association with Crohn disease and identification of a novel association with ulcerative colitis
-
Giallourakis C, Stoll M, Miller K, Hampe J, Lander ES, Daly MJ, Schreiber S, Rioux JD. IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis. Am J Hum Genet 2003; 73: 205-211
-
(2003)
Am J Hum Genet
, vol.73
, pp. 205-211
-
-
Giallourakis, C.1
Stoll, M.2
Miller, K.3
Hampe, J.4
Lander, E.S.5
Daly, M.J.6
Schreiber, S.7
Rioux, J.D.8
-
20
-
-
0347362514
-
Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis
-
McGovern DP, Van Heel DA, Negoro K, Ahmad T, Jewell DP. Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis. Am J Hum Genet 2003; 73: 1465-1466
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1465-1466
-
-
McGovern, D.P.1
Van Heel, D.A.2
Negoro, K.3
Ahmad, T.4
Jewell, D.P.5
-
21
-
-
12744274602
-
Association analysis of SL-C22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
-
Yamazaki K, Takazoe M, Tanaka T, Ichimori T, Saito S, Iida A, Onouchi Y, Hata A, Nakamura Y. Association analysis of SL-C22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease. J Hum Genet 2004; 49: 664-668
-
(2004)
J Hum Genet
, vol.49
, pp. 664-668
-
-
Yamazaki, K.1
Takazoe, M.2
Tanaka, T.3
Ichimori, T.4
Saito, S.5
Iida, A.6
Onouchi, Y.7
Hata, A.8
Nakamura, Y.9
-
22
-
-
0037474487
-
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5)
-
Lamhonwah A, Skaug J, Scherer SW, Tein L. A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5). Biochem Biophys Res Commun 2003; 301: 98-101
-
(2003)
Biochem Biophys Res Commun
, vol.301
, pp. 98-101
-
-
Lamhonwah, A.1
Skaug, J.2
Scherer, S.W.3
Tein, L.4
-
23
-
-
0037383554
-
Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease
-
Mirza MM, Fisher SA, King K, Cuthbert AP, Hampe J, Sanderson J, Mansfield J, Donaldson P, Macpherson AJ, Forbes A, Schreiber S, Lewis CM, Mathew CG. Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease. Am J Hum Genet 2003; 72: 1018-1022
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1018-1022
-
-
Mirza, M.M.1
Fisher, S.A.2
King, K.3
Cuthbert, A.P.4
Hampe, J.5
Sanderson, J.6
Mansfield, J.7
Donaldson, P.8
Macpherson, A.J.9
Forbes, A.10
Schreiber, S.11
Lewis, C.M.12
Mathew, C.G.13
-
24
-
-
21344449654
-
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease
-
Torok HP, Glas J, Tonenchi L, Lohse P, Muller-Myhsok B, Limbersky O, Neugebauer C, Schnitzler F, Seidere J, Tillack C, Brand S, Brunnler G, Jagiello P, Epplen JT, Griga T, Klein W, Schiemann U, Folwaczny M, Ochsenkuhn T, Folwaczny C. Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. Gut 2005; 54: 1421-1427
-
(2005)
Gut
, vol.54
, pp. 1421-1427
-
-
Torok, H.P.1
Glas, J.2
Tonenchi, L.3
Lohse, P.4
Muller-Myhsok, B.5
Limbersky, O.6
Neugebauer, C.7
Schnitzler, F.8
Seidere, J.9
Tillack, C.10
Brand, S.11
Brunnler, G.12
Jagiello, P.13
Epplen, J.T.14
Griga, T.15
Klein, W.16
Schiemann, U.17
Folwaczny, M.18
Ochsenkuhn, T.19
Folwaczny, C.20
more..
-
25
-
-
0037622913
-
Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31
-
Armuzzi A, Ahmad T, Ling KL, de Silva A, Cullen S, van Heel D, Orchard TR, Welsh KI, Marshall SE, Jewell DP. Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31. Gut 2003; 52: 1133-1139
-
(2003)
Gut
, vol.52
, pp. 1133-1139
-
-
Armuzzi, A.1
Ahmad, T.2
Ling, K.L.3
de Silva, A.4
Cullen, S.5
van Heel, D.6
Orchard, T.R.7
Welsh, K.I.8
Marshall, S.E.9
Jewell, D.P.10
-
26
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, Delmonte T, Kocher K, Miller K, Guschwan S, Kulbokas EJ, O'Leary S, Winchester E, Dewar K, Green T, Stone V, Chow C, Cohen A, Langelier D, Lapointe G, Gaudet D, Faith J, Branco N, Bull SB, McLeod RS, Griffiths AM, Bitton A, Greenberg GR, Lander ES, Siminovitch KA, Hudson TJ. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 2001; 29: 223-228
-
(2001)
Nat Genet
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
Lindblad, K.4
Steinhart, H.5
Cohen, Z.6
Delmonte, T.7
Kocher, K.8
Miller, K.9
Guschwan, S.10
Kulbokas, E.J.11
O'Leary, S.12
Winchester, E.13
Dewar, K.14
Green, T.15
Stone, V.16
Chow, C.17
Cohen, A.18
Langelier, D.19
Lapointe, G.20
Gaudet, D.21
Faith, J.22
Branco, N.23
Bull, S.B.24
McLeod, R.S.25
Griffiths, A.M.26
Bitton, A.27
Greenberg, G.R.28
Lander, E.S.29
Siminovitch, K.A.30
Hudson, T.J.31
more..
-
27
-
-
13444279863
-
Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers
-
Crawford NP, Colliver DW, Funke AA, Young MN, Kelley S, Cobbs GA, Petras RE, Galandiuk S. Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers. Hum Mutat 2005; 25: 156-166
-
(2005)
Hum Mutat
, vol.25
, pp. 156-166
-
-
Crawford, N.P.1
Colliver, D.W.2
Funke, A.A.3
Young, M.N.4
Kelley, S.5
Cobbs, G.A.6
Petras, R.E.7
Galandiuk, S.8
-
28
-
-
14944356373
-
A risk haplotype in the solute carrier family 22A4/22A5 gene cluster influences phenotypic expression on the Crohn's disease
-
Newman B, Gu X, Winlte R, Cescon D, Yazdanpanah M, Liu X, Peltekova V, Van Oene M, Amos CI, Siminovitch KA. A risk haplotype in the solute carrier family 22A4/22A5 gene cluster influences phenotypic expression on the Crohn's disease. Gastroenterology 2005; 128: 260-269
-
(2005)
Gastroenterology
, vol.128
, pp. 260-269
-
-
Newman, B.1
Gu, X.2
Winlte, R.3
Cescon, D.4
Yazdanpanah, M.5
Liu, X.6
Peltekova, V.7
Van Oene, M.8
Amos, C.I.9
Siminovitch, K.A.10
-
29
-
-
21344435414
-
DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population
-
Noble CL, Nimmo ER, Drummond H, Smith L, Arnott ID, Satsangi J. DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population. Gut 2005; 54: 1416-1420
-
(2005)
Gut
, vol.54
, pp. 1416-1420
-
-
Noble, C.L.1
Nimmo, E.R.2
Drummond, H.3
Smith, L.4
Arnott, I.D.5
Satsangi, J.6
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