| Issue Date | Title | Author(s) |
| 2020 | Bioinformatic analysis of microduplications at 5p15.33: identification of TPPP as a candidate gene for autism and intellectual disability | Vasin, K. S.; Vorsanova, S. G.; Kurinnaia, O. S.; Shmitova, N. S.; Voinova, V. Y. |
| 2022 | Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesis | Vorsanova, S. G.; Demidova, I. A.; Kolotii, A. D.; Kurinnaia, O. S.; Iourov, I. Y. |
| 2022 | Molecular cytogenetic and cytopostgenomic analysis of the human genome | Iourov, I. Y.; Vorsanova, S. G.; Kurinnaia, O. S.; Zelenova, M. A.; Vasin, K. S. |
| 2023 | Outcomes 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 disorders | Kurinnaia, O. S.; Vasin, K. S.; Zelenova, M. A.; Yurov, Yu. B.; Voinova, V. Y. |
| 2022 | Somatic mosaicism in the diseased brain | Iourov, I. Y.; Vorsanova, S. G.; Kurinnaia, O. S.; Kutsev, S. I.; Yurov, Yu. B. |
| 2020 | The Cytogenomic "Theory of Everything": Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging | Iourov, I. Y.; Vorsanova, S. G.; Yurov, Yu. B.; Zelenova, M. A.; Kurinnaia, O. S. |
| 2021 | Turner’s syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesis | Vorsanova, S. G.; Kolotii, A. D.; Kurinnaia, O. S.; Kravets, V. S.; Iourov, I. Y |
