Crohn Disease
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Inflammatory Bowel Disease 10
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
Crohn Disease
|
0.700 |
Biomarker
|
disease |
BEFREE |
Twenty one patients with IBD (10 with ulcerative colitis (UC), 11 with Crohn's disease (CD)), seven disease specificity controls (DSC), and seven healthy controls were studied.
|
11171821 |
2001 |
Ulcerative Colitis
|
0.200 |
Biomarker
|
disease |
BEFREE |
Twenty one patients with IBD (10 with ulcerative colitis (UC), 11 with Crohn's disease (CD)), seven disease specificity controls (DSC), and seven healthy controls were studied.
|
11171821 |
2001 |
Ulcerative Colitis
|
0.200 |
Biomarker
|
disease |
BEFREE |
Seventeen steroid-dependent consecutive patients with IBD (10 UC mean age 36 +/- 12, and 7 Crohn's disease mean age 31 +/- 5) were consecutively recruited.
|
16494108 |
2006 |
Crohn Disease
|
0.700 |
Biomarker
|
disease |
CTD_human |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
|
17200669 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
LHGDN |
Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease.
|
17625155 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
|
17484864 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
Recently, positive association of CD with the variants in interleukin 23 receptor (IL23R), autophagy-related 16-like 1 (ATG16L1) genes and chromosome 5p13.1 locus was reported through genome-wide association studies which are now recognised as a robust tool for the identification of susceptibility genes for complex diseases.
|
17534574 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
BEFREE |
We replicated the previously reported associations between CD and rs11209026 and rs2241880, confirming that IL23R and ATG16L1 are susceptibility loci for CD in the New Zealand population.
|
17894849 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
Crohn Disease
|
0.700 |
Biomarker
|
disease |
LHGDN |
We replicated the previously reported associations between CD and rs11209026 and rs2241880, confirming that IL23R and ATG16L1 are susceptibility loci for CD in the New Zealand population.
|
17894849 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
LHGDN |
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
|
17200669 |
2007 |
Crohn Disease
|
0.700 |
Biomarker
|
disease |
BEFREE |
We confirmed the findings that ATG16L1 is a CD susceptibility gene and found no evidence of interaction with CARD15, IL23R, or IBD5.
|
17455206 |
2007 |
Crohn Disease
|
0.700 |
Biomarker
|
disease |
LHGDN |
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
|
17484864 |
2007 |
Crohn Disease
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
Inflammatory Bowel Disease 10
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
Inflammatory Bowel Disease 10
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
|
17200669 |
2007 |
Inflammatory Bowel Disease 10
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
|
17484864 |
2007 |
Inflammatory Bowel Diseases
|
0.500 |
Biomarker
|
group |
LHGDN |
No significant association was observed between IL23R genotype or ATG16L1 genotype and IBD subphenotypes.
|
17894849 |
2007 |
Inflammatory Bowel Diseases
|
0.500 |
Biomarker
|
group |
BEFREE |
The association of ATG16L1 with Crohn's disease and possibly with ulcerative colitis supports a role for autophagy in the pathogenesis of inflammatory bowel disease.
|
17484864 |
2007 |