MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia
Neuroscience Letters, ISSN: 0304-3940, Vol: 602, Page: 44-49
2015
- 21Citations
- 41Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations21
- Citation Indexes21
- 21
- CrossRef17
- Captures41
- Readers41
- 41
Article Description
Genome-wide association studies implicate the MIR137HG risk variant rs1625579 (MIR137HGrv) within the host gene for microRNA-137 as a potential regulator of schizophrenia susceptibility. We examined the influence of MIR137HGrv genotype on 17 subcortical and callosal volumes in a large sample of individuals with schizophrenia and healthy controls ( n = 841). Although the volumes were overall reduced relative to healthy controls, for individuals with schizophrenia the homozygous MIR137HGrv risk genotype was associated with attenuated reduction of mid-posterior corpus callosum volume ( p = 0.001), along with trend-level effects in the adjacent central and posterior corpus callosum. These findings are unique in the literature and remain robust after analysis in ethnically homogenous and single-scanner subsets of the larger sample. Thus, our study suggests that the mechanisms whereby MIR137HGrv works to increase schizophrenia risk are not those that generate the corpus callosum volume reductions commonly found in the disorder.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0304394015004826; http://dx.doi.org/10.1016/j.neulet.2015.06.039; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84936884659&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26123324; https://linkinghub.elsevier.com/retrieve/pii/S0304394015004826
Elsevier BV
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