|
| Entrez Id: |
9966 |
| Gene Symbol: |
TNFSF15 |
TNFSF15
|
0.200 |
GeneticVariation
|
disease |
GWASDB |
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
|
16221758 |
2005 |
|
| Entrez Id: |
944 |
| Gene Symbol: |
TNFSF8 |
TNFSF8
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
|
16221758 |
2005 |
|
| Entrez Id: |
50514 |
| Gene Symbol: |
DELEC1 |
DELEC1
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
|
16221758 |
2005 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
1.000 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
|
17068223 |
2006 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
|
17068223 |
2006 |
|
C1orf141
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
|
17068223 |
2006 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
1.000 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
1.000 |
GeneticVariation
|
disease |
GWASDB |
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
|
17447842 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
1.000 |
GeneticVariation
|
disease |
GWASDB |
A proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5.
|
17804789 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
1.000 |
GeneticVariation
|
disease |
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
1.000 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
55054 |
| Gene Symbol: |
ATG16L1 |
ATG16L1
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
345611 |
| Gene Symbol: |
IRGM |
IRGM
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
|
17447842 |
2007 |
|
| Entrez Id: |
55054 |
| Gene Symbol: |
ATG16L1 |
ATG16L1
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
|
| Entrez Id: |
55054 |
| Gene Symbol: |
ATG16L1 |
ATG16L1
|
0.700 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
|
| Entrez Id: |
6583 |
| Gene Symbol: |
SLC22A4 |
SLC22A4
|
0.500 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
1540 |
| Gene Symbol: |
CYLD |
CYLD
|
0.130 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
124460 |
| Gene Symbol: |
SNX20 |
SNX20
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
8927 |
| Gene Symbol: |
BSN |
BSN
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
8927 |
| Gene Symbol: |
BSN |
BSN
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |