| Issue Date | Title | Author(s) |
| 2020 | 2q14 de novo interstitial deletion in a girl with intellectual disabilities and malformations | Alvarez, Y. B.; Garcia, A. G.; Rosales, L. M.; Méndez-Rosado, L. A. |
| 2026 | Clinical characterization of a child with de novo partial trisomy 9p24-9q12 | Garcia-Garcia, A.; Galarza, J. E.; Castelvi, A.; Barrios, A.; Morales-Peralta, E. |
| 2025 | Common CNVs modulate phenotypes in neurodevelopmental disorders (autism and intellectual disability): focus on SHANK3 and CHAMP1 | Iourov, I. Y.; Kurinnaia, O. S.; Iuditskaia, M. E.; Karpachev, E. S.; Vasin, K. S. |
| 2021 | Essentially pure partial trisomy 6(p21.31-p25) (case report and literature review) | Odalis Molina-Gamboa; Andurina Barrios-Martinez; Alina Garсia-Garсia; Luanda Maceira; Luis A. Mendez-Rosado |
| 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. |
| 2019 | The applicability of interphase chromosome-specific multicolor banding (ICS-MCB) for studying neurodevelopmental and neurodegenerative disorders | Iourov, I. Y.; Liehr, T.; Vorsanova, S. G.; Mendez-Rosado, L. A.; Yurov, Y. B. |
