|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
Crohn Disease
|
1.000 |
GeneticVariation |
GWASCAT |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
Crohn Disease
|
1.000 |
GeneticVariation |
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
Crohn Disease
|
1.000 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
1.000 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
1.000 |
GeneticVariation |
GWASCAT |
A proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5.
|
17804789 |
2007 |
|
| Entrez Id: |
345611 |
| Gene Symbol: |
IRGM |
IRGM
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
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: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
|
| Entrez Id: |
8927 |
| Gene Symbol: |
BSN |
BSN
|
Crohn Disease
|
0.110 |
GeneticVariation |
GWASCAT |
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
|
Crohn Disease
|
0.110 |
GeneticVariation |
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
|
LINC01475
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASCAT |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
|
LINC01475
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
64127 |
| Gene Symbol: |
NOD2 |
NOD2
|
Crohn Disease
|
1.000 |
GeneticVariation |
GWASCAT |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
149233 |
| Gene Symbol: |
IL23R |
IL23R
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
345611 |
| Gene Symbol: |
IRGM |
IRGM
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
55054 |
| Gene Symbol: |
ATG16L1 |
ATG16L1
|
Crohn Disease
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
4485 |
| Gene Symbol: |
MST1 |
MST1
|
Crohn Disease
|
0.500 |
GeneticVariation |
GWASCAT |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
120892 |
| Gene Symbol: |
LRRK2 |
LRRK2
|
Crohn Disease
|
0.500 |
GeneticVariation |
GWASCAT |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |