|
Malignant neoplasm of prostate
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Sequence variants at 22q13 are associated with prostate cancer risk.
|
19117981 |
2009 |
|
Prostate carcinoma
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Sequence variants at 22q13 are associated with prostate cancer risk.
|
19117981 |
2009 |
|
Body Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
|
19570815 |
2009 |
|
Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
|
19570815 |
2009 |
|
Nasopharyngeal carcinoma
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
|
20512145 |
2010 |
|
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 |
|
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 |
|
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 |
GWASDB |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
Plexiform leiomyoma
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
Uterine Fibroids
|
0.130 |
Biomarker
|
group |
BEFREE |
BET1L and TNRC6B associate with uterine fibroid risk among European Americans.
|
23604678 |
2013 |
|
Fibroid Tumor
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans.
|
23892540 |
2013 |
|
Autism Spectrum Disorders
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We did not identify a significant association of TNRC6B mutations with ASD.
|
25228304 |
2014 |
|
Chronic Lymphocytic Leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We found nine statistically significant associations with CLL risk after FDR correction, seven in miRNA processing genes (rs3805500 and rs6877842 in DROSHA, rs1057035 in DICER1, rs17676986 in SND1, rs9611280 in TNRC6B, rs784567 in TRBP and rs11866002 in CNOT1) and two in pre-miRNAs (rs11614913 in miR196a2 and rs2114358 in miR1206).
|
25793711 |
2015 |
|
Body mass index
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
|
26426971 |
2015 |
|
Circadian Rhythms
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank.
|
26955885 |
2016 |
|
Circadian Rhythms
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.
|
27494321 |
2016 |
|
Mean Corpuscular Volume (result)
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
Finding of Mean Corpuscular Hemoglobin
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
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 |
|
Neurodevelopmental Disorders
|
0.300 |
Biomarker
|
group |
CTD_human |
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
|
28191889 |
2017 |
|
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 |
|
Circadian Rhythms
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
|
28604731 |
2017 |
|
Malignant neoplasm of prostate
|
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 |
|
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 |