CommentaryMicroRNAs in Copy Number Variants in Schizophrenia: Misregulation of Genome-wide Gene Expression Programs
Section snippets
Acknowledgments and Disclosures
EMM reports no biomedical financial interests or potential conflicts of interest.
References (10)
- et al.
Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets
Biol Psychiatry
(2015) Genomic copy number variation in disorders of cognitive development
J Am Acad Child Adolesc Psychiatry
(2010)Genome-wide association study identifies five new schizophrenia loci
Nat Genet
(2011)- Xu B, Hsu PK, Karayiorgou M, Gogos J (2012): MicroRNA dysregulation in neuropsychiatric disorders and cognitive...
- et al.
22q11 deletion syndrome in adults with schizophrenia
Am J Med Genet
(1998)
There are more references available in the full text version of this article.
Cited by (4)
Classification of heterogeneous genetic variations of microRNA regulome in cancer
2018, Cancer LettersCitation Excerpt :Various miRNAs are located in human cancer associated genomic regions (98 miRNAs), frequently (80 miRNAs) in minimal regions of amplification and minimal regions of loss of heterozygosis [28]. Additionally, miRNA genes have been reported to be enriched within CNV regions [29]. A 30 kb deletion in 13q in chronic lymphocytic leukaemia contains a miRNA cluster MIR15A/MIR16-1 (miR-15/16), whose miRNAs function as tumour suppressors [30].
Differentiation value of miR-26b for major depressive disorder, schizophrenia, generalized anxiety disorder
2023, Indian Journal of PsychiatryClassification of miRNA-related sequence variations
2018, EpigenomicsWhole-genome sequencing suggests schizophrenia risk mechanisms in humans with 22q11.2 deletion syndrome
2015, G3: Genes, Genomes, Genetics
Copyright © 2015 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.