Oxana S. Kurinnaia
Moscow, MOW, Russian Federation
Last Updated: 09/26/2026
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Found 11 publications
Somatic mosaicism in the diseased brain.
Journal: Molecular cytogenetics
Published: September 20, 2022
The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging.
Journal: International journal of molecular sciences
Published: October 22, 2020
Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases
Journal: Molekuliarnaia biologiia
Published: June 29, 2020
Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: July 19, 2019
Structural variations of the genome in autistic spectrum disorders with intellectual disability
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: August 09, 2016
Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: December 05, 2013
An interstitial deletion at 10q26.2q26.3.
Journal: Case reports in genetics
Published: November 30, 2013
Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease.
Journal: Molecular cytogenetics
Published: November 15, 2013
Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: October 01, 2013
Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.
Journal: Molecular cytogenetics
Published: December 13, 2012
An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.
An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.
Journal: Case reports in genetics
Published: November 30, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026