-
1
-
-
0037043658
-
Inflammatory bowel disease
-
Podolsky DK. Inflammatory bowel disease. New Engl J Med 2002;347:417-29.
-
(2002)
New Engl J Med
, vol.347
, pp. 417-429
-
-
Podolsky, D.K.1
-
2
-
-
0019990589
-
Incidence and prevalence of ulcerative colitis and Crohn's disease in the County of Copenhagen, 1962 to 1978
-
Binder V, Both H, Hansen PK, et al. Incidence and prevalence of ulcerative colitis and Crohn's disease in the County of Copenhagen, 1962 to 1978. Gastroenterology 1982;83:563-68.
-
(1982)
Gastroenterology
, vol.83
, pp. 563-568
-
-
Binder, V.1
Both, H.2
Hansen, P.K.3
-
3
-
-
0025966488
-
Familial occurrence of inflammatory bowel disease
-
Orholm M, Munkholm P, Langholz E, et al. Familial occurrence of inflammatory bowel disease. New Engl J Med 1991;324:84-8.
-
(1991)
New Engl J Med
, vol.324
, pp. 84-88
-
-
Orholm, M.1
Munkholm, P.2
Langholz, E.3
-
4
-
-
0038620498
-
Inflammatory bowel disease in a Swedish twin cohort: A long-term follow-up of concordance and clinical characteristics
-
Halfvarson J, Bodin L, Tysk C, et al. Inflammatory bowel disease in a Swedish twin cohort: a long-term follow-up of concordance and clinical characteristics. Gastroenterology 2003;124:1767-73.
-
(2003)
Gastroenterology
, vol.124
, pp. 1767-1773
-
-
Halfvarson, J.1
Bodin, L.2
Tysk, C.3
-
5
-
-
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;379:821-3.
-
(1996)
Nature
, vol.379
, pp. 821-823
-
-
Hugot, J.P.1
Laurent-Puig, P.2
Gower-Rousseau, C.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;411:603-6.
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
-
7
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux JD, Daly MJ, Silverberg MS, et al. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 2001;29:223-8.
-
(2001)
Nat Genet
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.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;36:471-5.
-
(2004)
Nat Genet
, vol.36
, pp. 471-475
-
-
Peltekova, V.D.1
Wintle, R.F.2
Rubin, L.A.3
-
9
-
-
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;36:476-80.
-
(2004)
Nat Genet
, vol.36
, pp. 476-480
-
-
Stoll, M.1
Corneliussen, B.2
Costello, C.M.3
-
10
-
-
38349113447
-
Gender-stratified analysis of DLG5 R30Q in 4707 Crohn's disease patients and 4973 controls from 12 Caucasian cohorts
-
Browning BL, Barclay ML, Bingham SA, et al. Gender-stratified analysis of DLG5 R30Q in 4707 Crohn's disease patients and 4973 controls from 12 Caucasian cohorts. J Med Genet 2008;45:36- 42.
-
(2008)
J Med Genet
, vol.45
, pp. 36-42
-
-
Browning, B.L.1
Barclay, M.L.2
Bingham, S.A.3
-
11
-
-
33846627302
-
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
-
Hampe J, Franke A, Rosenstiel P, et al. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet 2007;39:207-11.
-
(2007)
Nat Genet
, vol.39
, pp. 207-211
-
-
Hampe, J.1
Franke, A.2
Rosenstiel, P.3
-
12
-
-
34247554965
-
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
-
Rioux JD, Xavier RJ, Taylor KD, et al. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. Nat Genet 2007;39:596-604.
-
(2007)
Nat Genet
, vol.39
, pp. 596-604
-
-
Rioux, J.D.1
Xavier, R.J.2
Taylor, K.D.3
-
13
-
-
40949105649
-
ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands
-
Weersma RK, Zhernakova A, Nolte IM, et al. ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands. Am J Gastroenterol 2008;103:621-7.
-
(2008)
Am J Gastroenterol
, vol.103
, pp. 621-627
-
-
Weersma, R.K.1
Zhernakova, A.2
Nolte, I.M.3
-
14
-
-
33845340501
-
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
-
Duerr RH, Taylor KD, Brant SR, et al. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 2006;314:1461-3.
-
(2006)
Science
, vol.314
, pp. 1461-1463
-
-
Duerr, R.H.1
Taylor, K.D.2
Brant, S.R.3
-
15
-
-
34247560627
-
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease
-
Tremelling M, Cummings F, Fisher SA, et al. IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. Gastroenterology 2007;132:1657-64.
-
(2007)
Gastroenterology
, vol.132
, pp. 1657-1664
-
-
Tremelling, M.1
Cummings, F.2
Fisher, S.A.3
-
16
-
-
34247579326
-
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4
-
Libioulle C, Louis E, Hansoul S, et al. Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. PLoS Genet 2007;3:e58.
-
(2007)
PLoS Genet
, vol.3
-
-
Libioulle, C.1
Louis, E.2
Hansoul, S.3
-
17
-
-
37249034766
-
Systematic association mapping identifies NELL1 as a novel IBD disease gene
-
Franke A, Hampe J, Rosenstiel P, et al. Systematic association mapping identifies NELL1 as a novel IBD disease gene. PLoS ONE 2007;2:e691.
-
(2007)
PLoS ONE
, vol.2
-
-
Franke, A.1
Hampe, J.2
Rosenstiel, P.3
-
18
-
-
34347338690
-
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
-
Parkes M, Barrett JC, Prescott NJ, et al. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. Nat Genet 2007;39:830-2.
-
(2007)
Nat Genet
, vol.39
, pp. 830-832
-
-
Parkes, M.1
Barrett, J.C.2
Prescott, N.J.3
-
19
-
-
33749465291
-
TUCAN (CARD8) genetic variants and inflammatory bowel disease
-
McGovern DP, Butler H, Ahmad T, et al. TUCAN (CARD8) genetic variants and inflammatory bowel disease. Gastroenterology 2006;131:1190-6.
-
(2006)
Gastroenterology
, vol.131
, pp. 1190-1196
-
-
McGovern, D.P.1
Butler, H.2
Ahmad, T.3
-
20
-
-
0037370188
-
Improving the prediction of complex diseases by testing for multiple disease-susceptibility genes
-
Yang Q, Khoury MJ, Botto L, et al. Improving the prediction of complex diseases by testing for multiple disease-susceptibility genes. Am J Hum Genet 2003;72:636-49.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 636-649
-
-
Yang, Q.1
Khoury, M.J.2
Botto, L.3
-
21
-
-
33750876203
-
Combining information from common type 2 diabetes risk polymorphisms improves disease prediction
-
Weedon MN, McCarthy MI, Hitman G, et al. Combining information from common type 2 diabetes risk polymorphisms improves disease prediction. PLoS Med 2006;3:1877-82.
-
(2006)
PLoS Med
, vol.3
, pp. 1877-1882
-
-
Weedon, M.N.1
McCarthy, M.I.2
Hitman, G.3
-
22
-
-
0034181513
-
Analysis of a positional candidate gene for inflammatory bowel disease: NRAMP2
-
Stokkers PC, Huibregtse K Jr, Leegwater AC, et al. Analysis of a positional candidate gene for inflammatory bowel disease: NRAMP2. Inflamm Bowel Dis 2000;6:92-8.
-
(2000)
Inflamm Bowel Dis
, vol.6
, pp. 92-98
-
-
Stokkers, P.C.1
Huibregtse Jr, K.2
Leegwater, A.C.3
-
23
-
-
33845622964
-
Genetic variation in myosin IXB is associated with ulcerative colitis
-
van Bodegraven AA, Curley CR, Hunt KA, et al. Genetic variation in myosin IXB is associated with ulcerative colitis. Gastroenterology 2006;131:1768-74.
-
(2006)
Gastroenterology
, vol.131
, pp. 1768-1774
-
-
van Bodegraven, A.A.1
Curley, C.R.2
Hunt, K.A.3
-
24
-
-
42749096082
-
Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP
-
Zhernakova A, Festen EM, Franke L, et al. Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP. Am J Hum Genet 2008;82:1202-10.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 1202-1210
-
-
Zhernakova, A.1
Festen, E.M.2
Franke, L.3
-
25
-
-
0035005481
-
Gender-related differences in the clinical course of Crohn's disease
-
Wagtmans MJ, Verspaget HW, Lamers CB, et al. Gender-related differences in the clinical course of Crohn's disease. Am J Gastroenterol 2001;96:1541-6.
-
(2001)
Am J Gastroenterol
, vol.96
, pp. 1541-1546
-
-
Wagtmans, M.J.1
Verspaget, H.W.2
Lamers, C.B.3
-
26
-
-
0037378891
-
Genetic polymorphisms in biotransformation enzymes in Crohn's disease: Association with microsomal epoxide hydrolase
-
de Jong DJ, van der Logt EM, van Schaik A, et al. Genetic polymorphisms in biotransformation enzymes in Crohn's disease: association with microsomal epoxide hydrolase. Gut 2003;52:547-51.
-
(2003)
Gut
, vol.52
, pp. 547-551
-
-
de Jong, D.J.1
van der Logt, E.M.2
van Schaik, A.3
-
27
-
-
0002063230
-
A simple classification of Crohn's disease: Report of the Working Party for the World Congresses of Gastroenterology, Vienna 1998
-
Gasche C, Scholmerich J, Brynskov J, et al. A simple classification of Crohn's disease: report of the Working Party for the World Congresses of Gastroenterology, Vienna 1998. Inflamm Bowel Dis 2000;6:8-15.
-
(2000)
Inflamm Bowel Dis
, vol.6
, pp. 8-15
-
-
Gasche, C.1
Scholmerich, J.2
Brynskov, J.3
-
28
-
-
34548651642
-
Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease
-
de Ridder L, Weersma RK, Dijkstra G, et al. Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease. Inflamm Bowel Dis 2007;13:1083- 92.
-
(2007)
Inflamm Bowel Dis
, vol.13
, pp. 1083-1092
-
-
de Ridder, L.1
Weersma, R.K.2
Dijkstra, G.3
-
29
-
-
33847640214
-
Most published research findings are false - but a little replication goes a long way
-
Moonesinghe R, Khoury MJ, Janssens AC. Most published research findings are false - but a little replication goes a long way. PLoS Med 2007;4:e28.
-
(2007)
PLoS Med
, vol.4
-
-
Moonesinghe, R.1
Khoury, M.J.2
Janssens, A.C.3
-
30
-
-
34247566585
-
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5
-
Prescott NJ, Fisher SA, Franke A, et al. A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5. Gastroenterology 2007;132:1665-71.
-
(2007)
Gastroenterology
, vol.132
, pp. 1665-1671
-
-
Prescott, N.J.1
Fisher, S.A.2
Franke, A.3
-
31
-
-
48349136889
-
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
-
Barrett JC, Hansoul S, Nicolae DL, et al. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet 2008;40:955-62.
-
(2008)
Nat Genet
, vol.40
, pp. 955-962
-
-
Barrett, J.C.1
Hansoul, S.2
Nicolae, D.L.3
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