-
1
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007; 447: 661-678.
-
(2007)
Nature.
, vol.447
, pp. 661-678
-
-
-
2
-
-
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: 955-962.
-
(2008)
Nat Genet.
, vol.40
, pp. 955-962
-
-
Barrett, J.C.1
Hansoul, S.2
Nicolae, D.L.3
-
3
-
-
78649489009
-
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
-
Franke A, McGovern D, Barrett JC, et al. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nat Genet. 2010; 42: 1118-1126.
-
(2010)
Nat Genet.
, vol.42
, pp. 1118-1126
-
-
Franke, A.1
McGovern, D.2
Barrett, J.C.3
-
4
-
-
70649113728
-
Common variants at five new loci associated with early-onset inflammatory bowel disease
-
Imielinski M, Baldassano RN, Griffiths A, et al. Common variants at five new loci associated with early-onset inflammatory bowel disease. Nat Genet. 2009; 41: 1335-1340.
-
(2009)
Nat Genet.
, vol.41
, pp. 1335-1340
-
-
Imielinski, M.1
Baldassano, R.N.2
Griffiths, A.3
-
5
-
-
34247554965
-
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
-
DOI 10.1038/ng2032, PII NG2032
-
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. (Pubitemid 46676115)
-
(2007)
Nature Genetics
, vol.39
, Issue.5
, pp. 596-604
-
-
Rioux, J.D.1
Xavier, R.J.2
Taylor, K.D.3
Silverberg, M.S.4
Goyette, P.5
Huett, A.6
Green, T.7
Kuballa, P.8
Barmada, M.M.9
Datta, L.W.10
Shugart, Y.Y.11
Griffiths, A.M.12
Targan, S.R.13
Ippoliti, A.F.14
Bernard, E.-J.15
Mei, L.16
Nicolae, D.L.17
Regueiro, M.18
Schumm, L.P.19
Steinhart, A.H.20
Rotter, J.I.21
Duerr, R.H.22
Cho, J.H.23
Daly, M.J.24
Brant, S.R.25
more..
-
6
-
-
51249103405
-
Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort
-
Roberts RL, Hollis-Moffatt JE, Gearry RB, et al. Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort. Genes Immunity. 2008; 6: 561-565.
-
(2008)
Genes Immunity.
, vol.6
, pp. 561-565
-
-
Roberts, R.L.1
Hollis-Moffatt, J.E.2
Gearry, R.B.3
-
7
-
-
61949327205
-
Rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4 and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population
-
Glas J, Seiderer J, Pasciuto G, et al. Rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4 and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population. Am J Gastroenterol. 2009; 104: 665-672.
-
(2009)
Am J Gastroenterol.
, vol.104
, pp. 665-672
-
-
Glas, J.1
Seiderer, J.2
Pasciuto, G.3
-
8
-
-
50249133280
-
Genetic variants in the autophagy pathway contribute to paediatric Crohn's disease
-
Peterson N, Guthery S, Denson L, et al. Genetic variants in the autophagy pathway contribute to paediatric Crohn's disease. Gut. 2008; 57: 1336-1337.
-
(2008)
Gut.
, vol.57
, pp. 1336-1337
-
-
Peterson, N.1
Guthery, S.2
Denson, L.3
-
9
-
-
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. 2007; 2: e691.
-
(2007)
PLoS.
, vol.2
-
-
Franke, A.1
Hampe, J.2
Rosenstiel, P.3
-
10
-
-
77955285576
-
Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children
-
Amre DK, Mack DR, Israel D, et al. Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children. Hum Genet. 2010; 128: 131-135.
-
(2010)
Hum Genet.
, vol.128
, pp. 131-135
-
-
Amre, D.K.1
MacK, D.R.2
Israel, D.3
-
11
-
-
77951782697
-
Susceptibility loci reported in genome-wide association studies are associated with Crohn's disease in children
-
Amre DK, Mack DR, Morgan K, et al. Susceptibility loci reported in genome-wide association studies are associated with Crohn's disease in children. Aliment Pharmacol Therap. 2010; 31: 1186-1191.
-
(2010)
Aliment Pharmacol Therap.
, vol.31
, pp. 1186-1191
-
-
Amre, D.K.1
MacK, D.R.2
Morgan, K.3
-
12
-
-
67349233285
-
Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children
-
Amre DK, Mack DR, Morgan K, et al. Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children. Inflamm Bowel Dis. 2009; 15: 501-507.
-
(2009)
Inflamm Bowel Dis.
, vol.15
, pp. 501-507
-
-
Amre, D.K.1
MacK, D.R.2
Morgan, K.3
-
13
-
-
72049130560
-
Investigation of reported associations between the 20a13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children
-
Amre DK, Mack DR, Morgan K, et al. Investigation of reported associations between the 20a13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children. Am J Gastroenterol. 2009; 104: 2824-2828.
-
(2009)
Am J Gastroenterol.
, vol.104
, pp. 2824-2828
-
-
Amre, D.K.1
MacK, D.R.2
Morgan, K.3
-
14
-
-
63849311502
-
Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease
-
Amre DK, Mack DR, Morgan K, et al. Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease. Aliment Pharmacol Therap. 2009; 29: 1025-1031.
-
(2009)
Aliment Pharmacol Therap.
, vol.29
, pp. 1025-1031
-
-
Amre, D.K.1
MacK, D.R.2
Morgan, K.3
-
15
-
-
40949096976
-
Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: Results from a case-control and family-based study among Canadian children
-
DOI 10.1111/j.1572-0241.2007.01661.x
-
Amre DK, Mack D, Israel D, et al. Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children. Am J Gastroenterol. 2008; 103: 615-620. (Pubitemid 351405996)
-
(2008)
American Journal of Gastroenterology
, vol.103
, Issue.3
, pp. 615-620
-
-
Amre, D.K.1
Mack, D.2
Israel, D.3
Morgan, K.4
Lambrette, P.5
Law, L.6
Grimard, G.7
Deslandres, C.8
Krupoves, A.9
Bucionis, V.10
Costea, I.11
Bissonauth, V.12
Feguery, H.13
D'Souza, S.14
Levy, E.15
Seidman, E.G.16
-
16
-
-
33646778482
-
The Montreal classification of inflammatory bowel disease: Controversies, consensus, and implications
-
DOI 10.1136/gut.2005.082909
-
Satsangi J, Silverberg MS, Vermiere S, et al. The Montreal classification of inflammatory bowel disease: controversies, consensus, and implications. Gut. 2006; 55: 749-753. (Pubitemid 43764536)
-
(2006)
Gut
, vol.55
, Issue.6
, pp. 749-753
-
-
Satsangi, J.1
Silverberg, M.S.2
Vermeire, S.3
Colombel, J.-F.4
-
17
-
-
0346373654
-
Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium
-
DOI 10.1086/381000
-
Carlson CS, Eberle MA, Rieder MJ, et al. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. Am J Hum Genet. 2004; 74: 106-120. (Pubitemid 38085242)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.1
, pp. 106-120
-
-
Carlson, C.S.1
Eberle, M.A.2
Rieder, M.J.3
Yi, Q.4
Kruglyak, L.5
Nickerson, D.A.6
-
18
-
-
0029842074
-
Genomic structure, chromosomal localization, start of transcription, and tissue expression of the human p40-phox, a new component of the nicotinamide adenine dinucleotide phosphate-oxidase complex
-
Zhan S, Vazquez N, Zhan S, et al. Genomic structure, chromosomal localization, start of transcription, and tissue expression of the human p40-phox, a new component of the nicotinamide adenine dinucleotide phosphate-oxidase complex. Blood. 1996; 88: 2714-2721. (Pubitemid 26327525)
-
(1996)
Blood
, vol.88
, Issue.7
, pp. 2714-2721
-
-
Zhan, S.1
Vazquez, N.2
Zhan, S.3
Wientjes, F.B.4
Budarf, M.L.5
Schrock, E.6
Ried, T.7
Green, E.D.8
Chanock, S.J.9
-
19
-
-
0024453201
-
Genetic variants of chronic granulomatous disease: Prevalence of deficiencies of two cytosolic components of the NADPH oxidase system
-
Clark RA, Malech HL, Gallin JI, et al. Genetic variants of chronic granulomatous disease: prevalence of deficiencies of two cytosolic components of the NADPH oxidase system. N Engl J Med. 1989; 321: 647-652. (Pubitemid 19221309)
-
(1989)
New England Journal of Medicine
, vol.321
, Issue.10
, pp. 647-652
-
-
Clark, R.A.1
Malech, H.L.2
Gallin, J.I.3
Nunoi, H.4
Volpp, B.D.5
Pearson, D.W.6
Nauseef, W.M.7
Curnutte, J.T.8
-
21
-
-
77956014955
-
The role of NELL-1, a growth factor associated with craniosynostosis, in promoting bone regeneration
-
Zhang X, Zara J, Siu RK, et al. The role of NELL-1, a growth factor associated with craniosynostosis, in promoting bone regeneration. J Dent Res. 2010; 89: 865-878.
-
(2010)
J Dent Res.
, vol.89
, pp. 865-878
-
-
Zhang, X.1
Zara, J.2
Siu, R.K.3
-
22
-
-
0033614426
-
The neuronal EGF-related genes NELL1 and NELL2 are expressed in hemopoietic cells and developmentally regulated in the B lineage
-
DOI 10.1016/S0378-1119(99)00093-1, PII S0378111999000931
-
Luce MJ, Burrows PD,. The neuronal EGF-related genes NELL1 and NELL2 are expressed in hemopoetic cells and developmentally regulated in the B lineage. Gene. 1999; 231: 121-126. (Pubitemid 29307780)
-
(1999)
Gene
, vol.231
, Issue.1-2
, pp. 121-126
-
-
Luce, M.J.1
Burrows, P.D.2
-
23
-
-
78650155713
-
SNPexp - A web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels
-
Holm K, Melum E, Franke A, et al. SNPexp - a web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels. BMC Bioinformatics. 2010; 11: 600-604.
-
(2010)
BMC Bioinformatics.
, vol.11
, pp. 600-604
-
-
Holm, K.1
Melum, E.2
Franke, A.3
-
24
-
-
65949107547
-
Common genetic variation and human traits
-
Goldstein DB,. Common genetic variation and human traits. N Engl J Med. 2009; 360: 1696-1698.
-
(2009)
N Engl J Med.
, vol.360
, pp. 1696-1698
-
-
Goldstein, D.B.1
-
25
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson SP, Wang K, Krantz I, et al. Rare variants create synthetic genome-wide associations. PLoS Biol. 2010; 8: e1000294.
-
(2010)
PLoS Biol.
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
|