-
1
-
-
13344259990
-
Mapping of a susceptibility locus for Crohn's disease on chromosome 16
-
Hugot JP, Laurent-Puig P, Gower-Rousseau C, et al. 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
-
2
-
-
17144470134
-
Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16
-
Rioux JD, Daly MJ, Green T, et al. Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16. Gastroenterology. 1998;115:1062-1065.
-
(1998)
Gastroenterology
, vol.115
, pp. 1062-1065
-
-
Rioux, J.D.1
Daly, M.J.2
Green, T.3
-
3
-
-
16044373177
-
Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
-
Satsangi J, Parkes M, Louis E, et al. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Nat Genet. 1996;14:199-202.
-
(1996)
Nat. Genet.
, vol.14
, pp. 199-202
-
-
Satsangi, J.1
Parkes, M.2
Louis, E.3
-
4
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
-
IBD International Genetics Consortium
-
Cavanaugh J. IBD International Genetics Consortium. 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
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H, et al. 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
-
6
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura Y, Bonen DK, Inohara N, et al. 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
-
7
-
-
2442519456
-
Genetic variation in DLG5 is associated with inflammatory bowel disease
-
Stoll M, Corneliussen B, Costello CM, et al. 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
-
8
-
-
2442585704
-
Functional variants of OCTN cation transporter genes are associated with Crohn disease
-
Peltekova VD, Wintle RF, Rubin LA, et al. 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
-
9
-
-
0036202336
-
The molecular classification of the clinical manifestations of Crohn's disease
-
Ahmad T, Armuzzi A, Bunce M, et al. The molecular classification of the clinical manifestations of Crohn's disease. Gastroenterology. 2002;122: 854-866.
-
(2002)
Gastroenterology
, vol.122
, pp. 854-866
-
-
Ahmad, T.1
Armuzzi, A.2
Bunce, M.3
-
10
-
-
18444381172
-
CARD15 genetic variation in a Quebec population: Prevalence, genotype-phenotype relationship, and haplotype structure
-
Vermeire S, Wild G, Kocher K, et al. CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure. Am J Hum Genet. 2002;71:74-83.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 74-83
-
-
Vermeire, S.1
Wild, G.2
Kocher, K.3
-
11
-
-
10744221095
-
CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease
-
Newman B, Silverberg MS, Gu X, et al. CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease. Am J Gastroenterol. 2004;99:306-315.
-
(2004)
Am. J. Gastroenterol.
, vol.99
, pp. 306-315
-
-
Newman, B.1
Silverberg, M.S.2
Gu, X.3
-
12
-
-
0036725827
-
Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease
-
Abreu MT, Taylor KD, Lin YC, et al. Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease. Gastroenterology. 2002;123:679-688.
-
(2002)
Gastroenterology
, vol.123
, pp. 679-688
-
-
Abreu, M.T.1
Taylor, K.D.2
Lin, Y.C.3
-
13
-
-
0036080129
-
The c-insertion mutation of the NOD2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease
-
Radlmayr M, Torok HP, Martin K, et al. The c-insertion mutation of the NOD2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease. Gastroenterology. 2002;122:2091-2092.
-
(2002)
Gastroenterology
, vol.122
, pp. 2091-2092
-
-
Radlmayr, M.1
Torok, H.P.2
Martin, K.3
-
14
-
-
4344671141
-
NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: Evidence for genetic heterogeneity within Europe?
-
Arnott ID, Nimmo ER, Drummond HE, et al. NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe? Genes Immun. 2004;5:417-425.
-
(2004)
Genes Immun.
, vol.5
, pp. 417-425
-
-
Arnott, I.D.1
Nimmo, E.R.2
Drummond, H.E.3
-
15
-
-
0345688816
-
The contribution of human leucocyte antigen complex genes to disease phenotype in ulcerative colitis
-
Ahmad T, Armuzzi A, Neville M, et al. The contribution of human leucocyte antigen complex genes to disease phenotype in ulcerative colitis. Tissue Antigens. 2003;62:527-535.
-
(2003)
Tissue Antigens.
, vol.62
, pp. 527-535
-
-
Ahmad, T.1
Armuzzi, A.2
Neville, M.3
-
16
-
-
0030007093
-
Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease
-
Satsangi J, Welsh KI, Bunce M, et al. Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease. Lancet. 1996;347:1212-1217.
-
(1996)
Lancet
, vol.347
, pp. 1212-1217
-
-
Satsangi, J.1
Welsh, K.I.2
Bunce, M.3
-
17
-
-
0034464732
-
Susceptibility to severe ulcerative colitis is associated with polymorphism in the central MHC gene IKBL
-
de la Concha EG, Fernandez-Arquero M, Lopez-Nava G, et al. Susceptibility to severe ulcerative colitis is associated with polymorphism in the central MHC gene IKBL. Gastroenterology. 2000;119:1491-1495.
-
(2000)
Gastroenterology
, vol.119
, pp. 1491-1495
-
-
de la Concha, E.G.1
Fernandez-Arquero, M.2
Lopez-Nava, G.3
-
18
-
-
0035083730
-
Association of the interleukin 1 receptor antagonist gene with ulcerative colitis in Northern European Caucasians
-
Carter MJ, di Giovine FS, Jones S, et al. Association of the interleukin 1 receptor antagonist gene with ulcerative colitis in Northern European Caucasians. Gut. 2001;48:461-467.
-
(2001)
Gut
, vol.48
, pp. 461-467
-
-
Carter, M.J.1
di Giovine, F.S.2
Jones, S.3
-
19
-
-
0037404387
-
Colon carcinogenesis in inflammatory bowel disease: Applying molecular genetics to clinical practice
-
Itzkowitz S. Colon carcinogenesis in inflammatory bowel disease: applying molecular genetics to clinical practice. J Clin Gastroenterol. 2003;36(Suppl 5):S70-S74.
-
(2003)
J. Clin. Gastroenterol.
, vol.36
, Issue.SUPPL. 5
-
-
Itzkowitz, S.1
-
20
-
-
0034913340
-
Association of the tumour necrosis factor alpha-308 but not the interleukin 10-627 promoter polymorphism with genetic susceptibility to primary sclerosing cholangitis
-
European Study Group of Primary Sclerosing Cholangitis
-
Mitchell SA, Grove J, Spurkland A, et al. European Study Group of Primary Sclerosing Cholangitis. Association of the tumour necrosis factor alpha-308 but not the interleukin 10-627 promoter polymorphism with genetic susceptibility to primary sclerosing cholangitis. Gut. 2001;49:288-294.
-
(2001)
Gut
, vol.49
, pp. 288-294
-
-
Mitchell, S.A.1
Grove, J.2
Spurkland, A.3
-
21
-
-
0034067784
-
Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease
-
Dubinsky MC, Lamothe S, Yang HY, et al. Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease. Gastroenterology. 2000;118:705-713.
-
(2000)
Gastroenterology
, vol.118
, pp. 705-713
-
-
Dubinsky, M.C.1
Lamothe, S.2
Yang, H.Y.3
-
22
-
-
1542619842
-
Pharmacogenetics and inflammatory bowel disease: Progress and prospects
-
Ho GT, Lees C, Satsangi J. Pharmacogenetics and inflammatory bowel disease: progress and prospects. Inflamm Bowel Dis. 2004;10:148-158.
-
(2004)
Inflamm. Bowel Dis.
, vol.10
, pp. 148-158
-
-
Ho, G.T.1
Lees, C.2
Satsangi, J.3
-
23
-
-
14844308021
-
A genetic panel strongly predicts the need for colectomy in ulcerative colitis
-
McGovern DP, Ahmad T, van Heel D, et al. A genetic panel strongly predicts the need for colectomy in ulcerative colitis. Gastroenterology. 2004;126:A68.
-
(2004)
Gastroenterology
, vol.126
-
-
McGovern, D.P.1
Ahmad, T.2
van Heel, D.3
-
24
-
-
0038823632
-
Gene transfer approaches for the treatment of inflammatory bowel disease
-
Wirtz S, Neurath MF. Gene transfer approaches for the treatment of inflammatory bowel disease. Gene Ther. 2003;10(Suppl 2):854-860.
-
(2003)
Gene Ther.
, vol.10
, Issue.SUPPL. 2
, pp. 854-860
-
-
Wirtz, S.1
Neurath, M.F.2
-
25
-
-
18944395602
-
Demand for genetic testing for inflammatory bowel disease
-
Appelton JI, Mascarenhas J, Esplen MJ, et al. Demand for genetic testing for inflammatory bowel disease. Gastroenterology. 2004;126(Suppl 2): A352-A353.
-
(2004)
Gastroenterology
, vol.126
, Issue.SUPPL. 2
-
-
Appelton, J.I.1
Mascarenhas, J.2
Esplen, M.J.3
|