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Browsing by Author Kurinnaia, O. S.

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Showing results 2 to 7 of 7 < previous 
Issue DateTitleAuthor(s)
2022Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesisVorsanova, S. G.; Demidova, I. A.; Kolotii, A. D.; Kurinnaia, O. S.; Iourov, I. Y.
2022Molecular cytogenetic and cytopostgenomic analysis of the human genomeIourov, I. Y.; Vorsanova, S. G.; Kurinnaia, O. S.; Zelenova, M. A.; Vasin, K. S.
2023Outcomes of ROHs (runs of homozygosity)/ LCSHs (long contiguous stretches of homozygosity) spanning the imprinted loci of chromosomes 7, 11 and 15 among children with neurodevelopmental disordersKurinnaia, O. S.; Vasin, K. S.; Zelenova, M. A.; Yurov, Yu. B.; Voinova, V. Y.
2022Somatic mosaicism in the diseased brainIourov, I. Y.; Vorsanova, S. G.; Kurinnaia, O. S.; Kutsev, S. I.; Yurov, Yu. B.
2020The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and AgingIourov, I. Y.; Vorsanova, S. G.; Yurov, Yu. B.; Zelenova, M. A.; Kurinnaia, O. S.
2021Turner’s syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesisVorsanova, S. G.; Kolotii, A. D.; Kurinnaia, O. S.; Kravets, V. S.; Iourov, I. Y