Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
|
28067908 |
2017 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
|
26192919 |
2015 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
BEFREE |
We identified genes that might be truly causative, but GWAS might have failed to identify for 148 out of the GWAS-identified SNPs; for example, TUFM (P = 3.3E-48) was identified for inflammatory bowel disease (early onset); ZFP90 (P = 4.4E-34) for ulcerative colitis; and IDUA (P = 2.2E-11) for Parkinson's disease.
|
24956270 |
2014 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
|
23128233 |
2012 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
|
23128233 |
2012 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
|
19915572 |
2009 |
Ulcerative Colitis
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
|
19915572 |
2009 |
Eosinophil count procedure
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Lupus Erythematosus, Systemic
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Transancestral mapping and genetic load in systemic lupus erythematosus.
|
28714469 |
2017 |
Lupus Erythematosus, Systemic
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus.
|
27399966 |
2016 |
Multiple Sclerosis
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
|
22190364 |
2011 |
Reasoning
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.
|
21107309 |
2011 |
Colorectal Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, these findings reveal a risk SNP-mediated long-range regulation on the NFATC2-ZFP90-BMP4 pathway underlying the initiation of CRC.
|
31641208 |
2020 |
Carcinogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Furthermore, ZFP90 affects several oncogenic pathways, including BMP4, and promotes carcinogenesis in patients and in animal models with ZFP90 specific genetic manipulation.
|
31641208 |
2020 |
Malignant neoplasm of colon and/or rectum
|
0.010 |
Biomarker
|
disease |
BEFREE |
A 16q22.1 variant confers susceptibility to colorectal cancer as a distal regulator of ZFP90.
|
31641208 |
2020 |
Non-alcoholic Fatty Liver Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We also identified novel loci for NAFLD disease severity, including one novel locus for NAS score near IL17RA (rs5748926, p = 3.80 × 10<sup>- 8</sup>), and another near ZFP90-CDH1 for fibrosis (rs698718, p = 2.74 × 10<sup>- 11</sup>).
|
31311600 |
2019 |
Inflammatory Bowel Diseases
|
0.010 |
GeneticVariation
|
group |
BEFREE |
We identified genes that might be truly causative, but GWAS might have failed to identify for 148 out of the GWAS-identified SNPs; for example, TUFM (P = 3.3E-48) was identified for inflammatory bowel disease (early onset); ZFP90 (P = 4.4E-34) for ulcerative colitis; and IDUA (P = 2.2E-11) for Parkinson's disease.
|
24956270 |
2014 |
Parkinson Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We identified genes that might be truly causative, but GWAS might have failed to identify for 148 out of the GWAS-identified SNPs; for example, TUFM (P = 3.3E-48) was identified for inflammatory bowel disease (early onset); ZFP90 (P = 4.4E-34) for ulcerative colitis; and IDUA (P = 2.2E-11) for Parkinson's disease.
|
24956270 |
2014 |
Congestive heart failure
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Notably, expression of Zfp90 mRNA was significantly upregulated in mouse and human hearts with chronic heart failure.
|
21284946 |
2011 |
Chronic heart failure
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Notably, expression of Zfp90 mRNA was significantly upregulated in mouse and human hearts with chronic heart failure.
|
21284946 |
2011 |