Candidate processes for autism spectrum disorders revealed by copy number variation analysis
https://doi.org/10.31363/2313-7053-2019-4-1-101-102
Abstract
About the Authors
M. A. ZelenovaRussian Federation
S. G. Vorsanova
Russian Federation
I. Y. Iourov
Russian Federation
References
1. Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Yurov YB. Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. Human Molecular Genetics. 2009:18:26562669. doi:10.1093/hmg/ddp207
2. Iourov IY, Vorsanova SG, Voinova VY, Yurov YB. 3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances. Molecular Cytogenetics. 2015:8:82. doi:10.1186/s13039-015-0185-9.
3. Iourov IY, Vorsanova SG, Zelenova MA, Korostelev SA, Yurov YB. Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism. International Journal of Genomics. 2015:2015:757680. doi: 10.1155/2015/757680.
4. Vorsanova SG, Yurov YB, Iourov IY. Neurogenomic pathway of autism spectrum disorders: linking germline and somatic mutations to geneticenvironmental interactions. Current Bioinformatics. 2017:12:19-26. doi:10.2174/1574893611666160606 164849
Review
For citations:
Zelenova M.A., Vorsanova S.G., Iourov I.Y. Candidate processes for autism spectrum disorders revealed by copy number variation analysis. V.M. BEKHTEREV REVIEW OF PSYCHIATRY AND MEDICAL PSYCHOLOGY. 2019;(4-1):101-102. (In Russ.) https://doi.org/10.31363/2313-7053-2019-4-1-101-102