×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
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
Crohn Disease
1.000
GeneticVariation
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
Crohn Disease
1.000
GeneticVariation
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
Crohn Disease
1.000
GeneticVariation
GWASDB
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
GWASDB
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
17554300
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Diabetes Mellitus, Insulin-Dependent
0.900
GeneticVariation
GWASDB
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
17632545
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Diabetes Mellitus, Insulin-Dependent
0.900
GeneticVariation
GWASDB
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
17554260
2007
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASDB
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
17463246
2007
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASDB
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
17463249
2007
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASDB
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
17463248
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Rheumatoid Arthritis
0.700
GeneticVariation
GWASDB
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
17804836
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Rheumatoid Arthritis
0.700
GeneticVariation
GWASDB
Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis.
17159887
2007
×
Entrez Id:
7124
Gene Symbol:
TNF
TNF
Rheumatoid Arthritis
0.700
GeneticVariation
GWASDB
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
17804836
2007
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
Malignant neoplasm of breast
0.700
GeneticVariation
GWASDB
Genome-wide association study identifies novel breast cancer susceptibility loci.
17529967
2007
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
Malignant neoplasm of breast
0.700
GeneticVariation
GWASDB
We identified four SNPs in intron 2 of FGFR2 (which encodes a receptor tyrosine kinase and is amplified or overexpressed in some breast cancers ) that were highly associated with breast cancer and confirmed this association in 1,776 affected individuals and 2,072 controls from three additional studies.
17529973
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
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
Crohn Disease
0.700
GeneticVariation
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
Crohn Disease
0.700
GeneticVariation
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
Crohn Disease
0.700
GeneticVariation
GWASDB
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
17684544
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
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
Crohn Disease
0.700
GeneticVariation
GWASDB
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
17684544
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
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
Crohn Disease
0.700
GeneticVariation
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
Crohn Disease
0.700
GeneticVariation
GWASDB
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
17435756
2007
×
Entrez Id:
54901
Gene Symbol:
CDKAL1
CDKAL1
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASDB
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
17463249
2007