|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.
|
31374203 |
2019 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.
|
31268507 |
2019 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
|
30285260 |
2019 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
BEFREE |
Genome wide association studies demonstrate variants within miR-137 host gene are a risk factor for schizophrenia.
|
31361772 |
2019 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
BEFREE |
These findings shed further light on the risk architecture of the miR-137 region and provide a novel regulatory mechanism through VNTR length and alternative MIR137HG transcripts which contribute to risk for SZ.
|
31409837 |
2019 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
|
29483656 |
2018 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
|
28540026 |
2017 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
BEFREE |
We found that schizophrenia subjects homozygous for the MIR137HG risk allele show significant decreases in occipital, parietal and temporal lobe GMC with increasing miR-137-regulated GRS, whereas those carrying the protective minor allele show significant increases in GMC with GRS.
|
26836412 |
2016 |
|
MIR137HG
|
0.460 |
Biomarker
|
disease |
PSYGENET |
MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia.
|
26123324 |
2015 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study of schizophrenia in Ashkenazi Jews.
|
26198764 |
2015 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
BEFREE |
The most robust finding has been reported for rs1625579 located in MIR137HG, which was associated with schizophrenia on a genome-wide level.
|
25395183 |
2015 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
BEFREE |
MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia.
|
26123324 |
2015 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Biological insights from 108 schizophrenia-associated genetic loci.
|
25056061 |
2014 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
|
23453885 |
2013 |
|
MIR137HG
|
0.460 |
Biomarker
|
disease |
PSYGENET |
A recent meta-analysis of genome-wide association studies indicated a significant association between schizophrenia and a common intronic variation in MIR137HG (microRNA 137 host gene) encoding the primary microRNA-137.
|
23683160 |
2013 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
BEFREE |
A recent meta-analysis of genome-wide association studies indicated a significant association between schizophrenia and a common intronic variation in MIR137HG (microRNA 137 host gene) encoding the primary microRNA-137.
|
23683160 |
2013 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies five new schizophrenia loci.
|
21926974 |
2011 |
|
MIR137HG
|
0.460 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies five new schizophrenia loci.
|
21926974 |
2011 |