Arthritis, Gouty
0.100
GeneticVariation
disease
GWASCAT
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
31578528
2019
Glomerular Filtration Rate
0.100
GeneticVariation
phenotype
GWASCAT
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
31152163
2019
×
CUI:
C0018099
Disease:
Gout
Gout
0.100
GeneticVariation
disease
GWASCAT
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
31578528
2019
Intelligence
0.100
GeneticVariation
phenotype
GWASCAT
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
29326435
2019
Uric acid measurement (procedure)
0.100
GeneticVariation
phenotype
GWASCAT
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
31578528
2019
Circadian Rhythms
0.100
GeneticVariation
phenotype
GWASCAT
Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability.
30120083
2018
Glomerular Filtration Rate
0.100
GeneticVariation
phenotype
GWASCAT
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
29124443
2018
Intelligence
0.100
GeneticVariation
phenotype
GWASCAT
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
29844566
2018
Intelligence
0.100
GeneticVariation
phenotype
GWASCAT
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
29942086
2018
Kidney Failure, Chronic
0.100
GeneticVariation
disease
GWASCAT
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
29124443
2018
Creatinine measurement, serum (procedure)
0.100
GeneticVariation
phenotype
GWASCAT
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
29124443
2018
Uric acid measurement (procedure)
0.100
GeneticVariation
phenotype
GWASCAT
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
29124443
2018
Hyperuricemia
0.100
GeneticVariation
disease
GWASCAT
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
29124443
2018
Hip circumference
0.100
GeneticVariation
phenotype
GWASCAT
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
28552196
2017
Ulcerative Colitis
0.100
GeneticVariation
disease
GWASCAT
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
26192919
2015
Schizophrenia
0.100
GeneticVariation
disease
GWASCAT
Genome-wide association study of schizophrenia in Ashkenazi Jews.
26198764
2015
Arthritis, Gouty
0.100
GeneticVariation
disease
GWASDB
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
23263486
2013
×
CUI:
C0018099
Disease:
Gout
Gout
0.100
GeneticVariation
disease
GWASDB
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
23263486
2013
Ulcerative Colitis
0.100
GeneticVariation
disease
GWASDB
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
23128233
2012
Ulcerative Colitis
0.100
GeneticVariation
disease
GWASCAT
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
23128233
2012
Malignant tumor of cervix
0.010
Biomarker
disease
BEFREE
MicroRNA-218 inhibits EMT, migration and invasion by targeting SFMBT1 and DCUN1D1 in cervical cancer .
27285984
2016
Cervix carcinoma
0.010
Biomarker
disease
BEFREE
MicroRNA-218 inhibits EMT, migration and invasion by targeting SFMBT1 and DCUN1D1 in cervical cancer .
27285984
2016
Tumor Cell Invasion
0.010
Biomarker
phenotype
BEFREE
Taken together, our results revealed that HPV16 E6 promoted EMT and invasion in cervical cancer via the repression of miR-218, while miR-218 inhibited EMT and invasion in cervical cancer by targeting SFMBT1 and DCUN1D1.
27285984
2016
Idiopathic normal pressure hydrocephalus (INPH)
0.010
GeneticVariation
disease
BEFREE
The present study demonstrates that a copy number loss within intron 2 of the SFMBT1 gene may be a genetic risk factor for shunt-responsive definite iNPH .
27861535
2016
cervical cancer
0.010
Biomarker
disease
BEFREE
MicroRNA-218 inhibits EMT, migration and invasion by targeting SFMBT1 and DCUN1D1 in cervical cancer .
27285984
2016