-
1
-
-
83755219473
-
Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review
-
Molodecky NA, Soon IS, Rabi DM, Ghali WA, Ferris M, et al. (2012) Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology 142: 46-54 e42.
-
(2012)
Gastroenterology
, vol.142
-
-
Molodecky, N.A.1
Soon, I.S.2
Rabi, D.M.3
Ghali, W.A.4
Ferris, M.5
-
2
-
-
84857074714
-
Optimal use and cost-effectiveness of biologic therapies in inflammatory bowel disease
-
Di Sabatino A, Liberato L, Marchetti M, Biancheri P, Corazza GR, (2011) Optimal use and cost-effectiveness of biologic therapies in inflammatory bowel disease. Intern Emerg Med 6 (Suppl 1): 17-27.
-
(2011)
Intern Emerg Med
, vol.6
, Issue.SUPPL. 1
, pp. 17-27
-
-
Di Sabatino, A.1
Liberato, L.2
Marchetti, M.3
Biancheri, P.4
Corazza, G.R.5
-
3
-
-
77954758654
-
The impact of the microbiota on the pathogenesis of IBD: lessons from mouse infection models
-
Nell S, Suerbaum S, Josenhans C, (2010) The impact of the microbiota on the pathogenesis of IBD: lessons from mouse infection models. Nat Rev Microbiol 8: 564-577.
-
(2010)
Nat Rev Microbiol
, vol.8
, pp. 564-577
-
-
Nell, S.1
Suerbaum, S.2
Josenhans, C.3
-
4
-
-
79952195585
-
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
-
Anderson CA, Boucher G, Lees CW, Franke A, D'Amato M, et al. (2011) Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nat Genet 43: 246-252.
-
(2011)
Nat Genet
, vol.43
, pp. 246-252
-
-
Anderson, C.A.1
Boucher, G.2
Lees, C.W.3
Franke, A.4
D'Amato, M.5
-
5
-
-
78649489009
-
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
-
Franke A, McGovern DP, Barrett JC, Wang K, Radford-Smith GL, et al. (2010) Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nat Genet 42: 1118-1125.
-
(2010)
Nat Genet
, vol.42
, pp. 1118-1125
-
-
Franke, A.1
McGovern, D.P.2
Barrett, J.C.3
Wang, K.4
Radford-Smith, G.L.5
-
6
-
-
80053551352
-
The quest for genetic risk factors for Crohn's disease in the post-GWAS era
-
Fransen K, Mitrovic M, van Diemen CC, Weersma RK, (2011) The quest for genetic risk factors for Crohn's disease in the post-GWAS era. Genome Med 3: 13.
-
(2011)
Genome Med
, vol.3
, pp. 13
-
-
Fransen, K.1
Mitrovic, M.2
van Diemen, C.C.3
Weersma, R.K.4
-
7
-
-
0030784426
-
Differences in risk of Crohn's disease in offspring of mothers and fathers with inflammatory bowel disease
-
Akolkar PN, Gulwani-Akolkar B, Heresbach D, Lin XY, Fisher S, et al. (1997) Differences in risk of Crohn's disease in offspring of mothers and fathers with inflammatory bowel disease. Am J Gastroenterol 92: 2241-2244.
-
(1997)
Am J Gastroenterol
, vol.92
, pp. 2241-2244
-
-
Akolkar, P.N.1
Gulwani-Akolkar, B.2
Heresbach, D.3
Lin, X.Y.4
Fisher, S.5
-
8
-
-
84863466421
-
Maternal imprinting and female predominance in familial Crohn's disease
-
Zelinkova Z, Stokkers PC, van der Linde K, Kuipers EJ, Peppelenbosch MP, et al. (2012) Maternal imprinting and female predominance in familial Crohn's disease. J Crohns Colitis.
-
(2012)
J Crohns Colitis
-
-
Zelinkova, Z.1
Stokkers, P.C.2
van der Linde, K.3
Kuipers, E.J.4
Peppelenbosch, M.P.5
-
9
-
-
0035068575
-
Assessment of parent-of-origin effects in linkage analysis of quantitative traits
-
Hanson RL, Kobes S, Lindsay RS, Knowler WC, (2001) Assessment of parent-of-origin effects in linkage analysis of quantitative traits. Am J Hum Genet 68: 951-962.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 951-962
-
-
Hanson, R.L.1
Kobes, S.2
Lindsay, R.S.3
Knowler, W.C.4
-
10
-
-
72449122779
-
Parental origin of sequence variants associated with complex diseases
-
Kong A, Steinthorsdottir V, Masson G, Thorleifsson G, Sulem P, et al. (2009) Parental origin of sequence variants associated with complex diseases. Nature 462: 868-874.
-
(2009)
Nature
, vol.462
, pp. 868-874
-
-
Kong, A.1
Steinthorsdottir, V.2
Masson, G.3
Thorleifsson, G.4
Sulem, P.5
-
11
-
-
0033362236
-
Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
-
Weinberg CR, (1999) Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. Am J Hum Genet 65: 229-235.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 229-235
-
-
Weinberg, C.R.1
-
12
-
-
73349115848
-
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes
-
Wallace C, Smyth DJ, Maisuria-Armer M, Walker NM, Todd JA, et al. (2010) The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes. Nat Genet 42: 68-71.
-
(2010)
Nat Genet
, vol.42
, pp. 68-71
-
-
Wallace, C.1
Smyth, D.J.2
Maisuria-Armer, M.3
Walker, N.M.4
Todd, J.A.5
-
13
-
-
0037043658
-
Inflammatory bowel disease
-
Podolsky DK, (2002) Inflammatory bowel disease. N Engl J Med 347: 417-429.
-
(2002)
N Engl J Med
, vol.347
, pp. 417-429
-
-
Podolsky, D.K.1
-
14
-
-
35548958718
-
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci
-
Raelson JV, Little RD, Ruether A, Fournier H, Paquin B, et al. (2007) Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. Proc Natl Acad Sci U S A 104: 14747-14752.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 14747-14752
-
-
Raelson, J.V.1
Little, R.D.2
Ruether, A.3
Fournier, H.4
Paquin, B.5
-
15
-
-
79960279940
-
Promise and pitfalls of the Immunochip
-
Cortes A, Brown MA, (2011) Promise and pitfalls of the Immunochip. Arthritis Res Ther 13: 101.
-
(2011)
Arthritis Res Ther
, vol.13
, pp. 101
-
-
Cortes, A.1
Brown, M.A.2
-
16
-
-
82255192188
-
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
-
Trynka G, Hunt KA, Bockett NA, Romanos J, Mistry V, et al. (2011) Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet 43: 1193-1201.
-
(2011)
Nat Genet
, vol.43
, pp. 1193-1201
-
-
Trynka, G.1
Hunt, K.A.2
Bockett, N.A.3
Romanos, J.4
Mistry, V.5
-
17
-
-
57249114505
-
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
-
Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, et al. (2008) SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 24: 2938-2939.
-
(2008)
Bioinformatics
, vol.24
, pp. 2938-2939
-
-
Johnson, A.D.1
Handsaker, R.E.2
Pulit, S.L.3
Nizzari, M.M.4
O'Donnell, C.J.5
-
18
-
-
79551652513
-
An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians
-
Juyal G, Prasad P, Senapati S, Midha V, Sood A, et al. (2011) An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians. PLoS One 6: e16565.
-
(2011)
PLoS One
, vol.6
-
-
Juyal, G.1
Prasad, P.2
Senapati, S.3
Midha, V.4
Sood, A.5
-
19
-
-
37249059981
-
Computational and experimental identification of novel human imprinted genes
-
Luedi PP, Dietrich FS, Weidman JR, Bosko JM, Jirtle RL, et al. (2007) Computational and experimental identification of novel human imprinted genes. Genome Res 17: 1723-1730.
-
(2007)
Genome Res
, vol.17
, pp. 1723-1730
-
-
Luedi, P.P.1
Dietrich, F.S.2
Weidman, J.R.3
Bosko, J.M.4
Jirtle, R.L.5
-
20
-
-
79960727512
-
High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients
-
Mitrovic M, Potocnik U, (2011) High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients. Dis Markers 30: 265-274.
-
(2011)
Dis Markers
, vol.30
, pp. 265-274
-
-
Mitrovic, M.1
Potocnik, U.2
-
21
-
-
0037080655
-
Sample size requirements for matched case-control studies of gene-environment interaction
-
Gauderman WJ, (2002) Sample size requirements for matched case-control studies of gene-environment interaction. Stat Med 21: 35-50.
-
(2002)
Stat Med
, vol.21
, pp. 35-50
-
-
Gauderman, W.J.1
-
22
-
-
84855674649
-
Dominant disease-causing effect of NOD2 mutations in a family with all family members affected by Crohn's disease
-
Schnitzler F, Seiderer J, Stallhofer J, Brand S, (2012) Dominant disease-causing effect of NOD2 mutations in a family with all family members affected by Crohn's disease. Inflamm Bowel Dis 18: 395-396.
-
(2012)
Inflamm Bowel Dis
, vol.18
, pp. 395-396
-
-
Schnitzler, F.1
Seiderer, J.2
Stallhofer, J.3
Brand, S.4
-
23
-
-
77955664679
-
The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotype
-
Jurgens M, Brand S, Laubender RP, Seiderer J, Glas J, et al. (2010) The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotype. J Gastroenterol 45: 721-731.
-
(2010)
J Gastroenterol
, vol.45
, pp. 721-731
-
-
Jurgens, M.1
Brand, S.2
Laubender, R.P.3
Seiderer, J.4
Glas, J.5
-
24
-
-
84855665333
-
Homozygosity for the NOD2 p.Leu1007fsX1008 variant is the main genetic predictor for fibrostenotic Crohn's disease
-
Brand S, (2012) Homozygosity for the NOD2 p.Leu1007fsX1008 variant is the main genetic predictor for fibrostenotic Crohn's disease. Inflamm Bowel Dis 18: 393-394.
-
(2012)
Inflamm Bowel Dis
, vol.18
, pp. 393-394
-
-
Brand, S.1
-
25
-
-
75749085686
-
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
-
Australo-Anglo-American Spondyloarthritis C, Reveille JD, Sims AM, Danoy P, Evans DM, et al. (2010) Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nat Genet 42: 123-127.
-
(2010)
Nat Genet
, vol.42
, pp. 123-127
-
-
Australo-Anglo-American Spondyloarthritis, C.1
Reveille, J.D.2
Sims, A.M.3
Danoy, P.4
Evans, D.M.5
-
26
-
-
67651209042
-
Evidence for association of an interleukin 23 receptor variant independent of the R381Q variant with rheumatoid arthritis
-
Hollis-Moffatt JE, Merriman ME, Rodger RA, Rowley KA, Chapman PT, et al. (2009) Evidence for association of an interleukin 23 receptor variant independent of the R381Q variant with rheumatoid arthritis. Ann Rheum Dis 68: 1340-1344.
-
(2009)
Ann Rheum Dis
, vol.68
, pp. 1340-1344
-
-
Hollis-Moffatt, J.E.1
Merriman, M.E.2
Rodger, R.A.3
Rowley, K.A.4
Chapman, P.T.5
-
27
-
-
59149106117
-
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways
-
Nair RP, Duffin KC, Helms C, Ding J, Stuart PE, et al. (2009) Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nat Genet 41: 199-204.
-
(2009)
Nat Genet
, vol.41
, pp. 199-204
-
-
Nair, R.P.1
Duffin, K.C.2
Helms, C.3
Ding, J.4
Stuart, P.E.5
-
28
-
-
70649086092
-
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk
-
Raychaudhuri S, Thomson BP, Remmers EF, Eyre S, Hinks A, et al. (2009) Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. Nat Genet 41: 1313-1318.
-
(2009)
Nat Genet
, vol.41
, pp. 1313-1318
-
-
Raychaudhuri, S.1
Thomson, B.P.2
Remmers, E.F.3
Eyre, S.4
Hinks, A.5
-
29
-
-
70350650472
-
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
-
Gateva V, Sandling JK, Hom G, Taylor KE, Chung SA, et al. (2009) A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus. Nat Genet 41: 1228-1233.
-
(2009)
Nat Genet
, vol.41
, pp. 1228-1233
-
-
Gateva, V.1
Sandling, J.K.2
Hom, G.3
Taylor, K.E.4
Chung, S.A.5
-
30
-
-
80053092312
-
Fox and Blimp in NK-cell lymphoma
-
Sokol L, (2011) Fox and Blimp in NK-cell lymphoma. Blood 118: 3192-3193.
-
(2011)
Blood
, vol.118
, pp. 3192-3193
-
-
Sokol, L.1
-
31
-
-
79961155567
-
Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma
-
Best T, Li D, Skol AD, Kirchhoff T, Jackson SA, et al. (2011) Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma. Nat Med 17: 941-943.
-
(2011)
Nat Med
, vol.17
, pp. 941-943
-
-
Best, T.1
Li, D.2
Skol, A.D.3
Kirchhoff, T.4
Jackson, S.A.5
-
32
-
-
77952161419
-
The serotonin1A receptor gene as a genetic and prenatal maternal environmental factor in anxiety
-
Gleason G, Liu B, Bruening S, Zupan B, Auerbach A, et al. (2010) The serotonin1A receptor gene as a genetic and prenatal maternal environmental factor in anxiety. Proc Natl Acad Sci U S A 107: 7592-7597.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 7592-7597
-
-
Gleason, G.1
Liu, B.2
Bruening, S.3
Zupan, B.4
Auerbach, A.5
-
33
-
-
0034924997
-
Positive and negative selection on the human genome
-
Fay JC, Wyckoff GJ, Wu CI, (2001) Positive and negative selection on the human genome. Genetics 158: 1227-1234.
-
(2001)
Genetics
, vol.158
, pp. 1227-1234
-
-
Fay, J.C.1
Wyckoff, G.J.2
Wu, C.I.3
-
35
-
-
77957887124
-
Ancestral paternal genotype controls body weight and food intake for multiple generations
-
Yazbek SN, Spiezio SH, Nadeau JH, Buchner DA, (2010) Ancestral paternal genotype controls body weight and food intake for multiple generations. Hum Mol Genet 19: 4134-4144.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4134-4144
-
-
Yazbek, S.N.1
Spiezio, S.H.2
Nadeau, J.H.3
Buchner, D.A.4
-
36
-
-
0035977895
-
Environmental effects on genomic imprinting in mammals
-
Thompson SL, Konfortova G, Gregory RI, Reik W, Dean W, et al. (2001) Environmental effects on genomic imprinting in mammals. Toxicol Lett 120: 143-150.
-
(2001)
Toxicol Lett
, vol.120
, pp. 143-150
-
-
Thompson, S.L.1
Konfortova, G.2
Gregory, R.I.3
Reik, W.4
Dean, W.5
-
37
-
-
79960832974
-
Methods for detecting interactions between imprinted genes and environmental exposures using birth cohort designs with mother-offspring pairs
-
Wang S, Yu Z, Miller RL, Tang D, Perera FP, (2011) Methods for detecting interactions between imprinted genes and environmental exposures using birth cohort designs with mother-offspring pairs. Hum Hered 71: 196-208.
-
(2011)
Hum Hered
, vol.71
, pp. 196-208
-
-
Wang, S.1
Yu, Z.2
Miller, R.L.3
Tang, D.4
Perera, F.P.5
|