|
Waist-Hip Ratio
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
|
30239722 |
2019 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
GWASCAT |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
|
31249589 |
2019 |
|
Uterine Fibroids
|
0.130 |
Biomarker
|
group |
BEFREE |
BET1L and TNRC6B associate with uterine fibroid risk among European Americans.
|
23604678 |
2013 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
GWASCAT |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
BEFREE |
Two SNPs, rs2280543 from BET1L (χ<sup>2</sup> = 18.3, OR = 0.64, P = 1.87 × 10<sup>-5</sup>) and rs12484776 from TNRC6B (χ<sup>2</sup> = 19.7, OR = 1.40, P = 8.91 × 10<sup>-6</sup>), were identified as significantly associated with the disease status of UL.
|
29743541 |
2018 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
BEFREE |
Replication of GWAS loci revealed the moderate effect of TNRC6B locus on susceptibility of Saudi women to develop uterine leiomyomas.
|
27987337 |
2017 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
GWASDB |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
Uterine Fibroids
|
0.130 |
GeneticVariation
|
group |
GWASCAT |
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
|
30194396 |
2018 |
|
Systolic Pressure
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
|
Squamous cell carcinoma of esophagus
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Six miR-SNPs in miRNA processing machinery genes, including Dicer (rs3742330), RAN (rs14035), XPO5 (rs11077), TNRC6B (rs9623117), GEMIN3 (rs197412), and GEMIN4 (rs2740348), were evaluated for their association with esophageal squamous cell carcinoma (ESCC).
|
29226993 |
2018 |
|
Squamous cell carcinoma of esophagus
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Our results suggest that the trinucleotide repeat containing 6B mutation may be a candidate predisposing gene in esophageal squamous cell carcinoma.
|
28459198 |
2017 |
|
Sclerocystic Ovaries
|
0.300 |
Biomarker
|
disease |
CTD_human |
Progesterone resistance in PCOS endometrium: a microarray analysis in clomiphene citrate-treated and artificial menstrual cycles.
|
21411543 |
2011 |
|
Respiratory Failure
|
0.010 |
Biomarker
|
disease |
BEFREE |
However, the majority of TNRC6b and all TNRC6c mutants die within 24h after birth, the latter with respiratory failure.
|
28811219 |
2017 |
|
Red Blood Cell Count measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
|
Prostate carcinoma
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Sequence variants at 22q13 are associated with prostate cancer risk.
|
19117981 |
2009 |
|
Prostate carcinoma
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
|
29892016 |
2018 |
|
Prostate carcinoma
|
0.110 |
Biomarker
|
disease |
BEFREE |
Using a series of experiments in human prostate cancer cell lines, we validate the highest ranking prediction (TNRC6B) as a ceRNA of PTEN.
|
28798471 |
2017 |
|
Polycystic Ovary Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Progesterone resistance in PCOS endometrium: a microarray analysis in clomiphene citrate-treated and artificial menstrual cycles.
|
21411543 |
2011 |
|
Plexiform leiomyoma
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
|
31249589 |
2019 |
|
Plexiform leiomyoma
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
|
30194396 |
2018 |
|
Plexiform leiomyoma
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
Plexiform leiomyoma
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
Neurodevelopmental Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
|
28191889 |
2017 |
|
Nasopharyngeal carcinoma
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
|
20512145 |
2010 |