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  1. 2025

  2. Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay

    Danilchenko, V. Y., Panina, E. A., Zytzar, M. V., Orishchenko, K. E. & Posukh, O. L., 4 Nov 2025, In: International Journal of Molecular Sciences. 26, 21, 16 p., 10732.

    Research output: Contribution to journal › Article › peer-review

  3. Analysis by Minigene Assay of the Splicing Effect of a Novel Variant c.1545T>G in the SLC26A4 Gene Associated with Hearing Loss

    Panina, E. A., Danilchenko, V. Y., Zytsar, M. V., Orishchenko, K. E. & Posukh, O. L., 10 Jun 2025, In: Russian Journal of Genetics. 61, 5, p. 602-607 6 p.

    Research output: Contribution to journal › Article › peer-review

  4. Сравнительный анализ гаплотипов, несущих патогенные варианты C.1545T>G, C.2027T>A и C.919-2A>G гена SLC26A4, у пациентов с потерей слуха из Республики Тыва (Южная Сибирь)

    Danilchenko, V. Y., Zytsar, M. V., Panina, E. A., Orishchenko, K. E. & Posukh, O. L., Feb 2025, In: Vavilovskii Zhurnal Genetiki i Selektsii. 29, 1, p. 144-152 9 p.

    Research output: Contribution to journal › Article › peer-review

  5. 2024

  6. Способ разделения водной и органической фаз при очистке раствора ДНК фенол-хлороформным методом

    Орищенко, К. Е. & Баттулин, Н. Р., 21 Oct 2024, Patent No. 2828850, 12 Dec 2023, Priority date 12 Dec 2023, Priority No. 2023132841

    Research output: Patent › Patent for invention

  7. Crosstalk between BER and NHEJ in XRCC4-Deficient Cells Depending on hTERT Overexpression

    Sergeeva, S. V., Loshchenova, P. S., Oshchepkov, D. Y. & Orishchenko, K. E., 27 Sept 2024, In: International Journal of Molecular Sciences. 25, 19, 10405.

    Research output: Contribution to journal › Article › peer-review

  8. A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

    Karamysheva, T. V., Lebedev, I. N., Minaycheva, L. I., Nazarenko, L. P., Kashevarova, A. A., Fedotov, D. A., Skryabin, N. A., Lopatkina, M. E., Cheremnykh, A. D., Fonova, E. A., Nikitina, T. V., Sazhenova, E. A., Skleimova, M. M., Kolesnikov, N. A., Drozdov, G. V., Yakovleva, Y. S., Seitova, G. N., Orishchenko, K. E. & Rubtsov, N. B., Mar 2024, In: Frontiers in Genetics. 15, 1331066.

    Research output: Contribution to journal › Article › peer-review

  9. 2023

  10. Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains

    Posukh, O. L., Maslova, E. A., Danilchenko, V. Y., Zytsar, M. V. & Orishchenko, K. E., 13 Oct 2023, In: Biomolecules. 13, 10, 1521.

    Research output: Contribution to journal › Review article › peer-review

  11. Генетическая конструкция для экспрессии рекомбинантных дезаминаз на основе АРОВЕС1 для направленной модификации цитозиновых оснований митохондриальной ДНК

    Музыка, В. В., Орищенко, К. Е. & Закирова, Э. Г., 20 Jul 2023, Роспатент - Федеральная служба по интеллектуальной собственности, Patent No. 2800362, 1 Dec 2022, Priority date 1 Dec 2022, Priority No. 2022131360

    Research output: Patent › Patent for invention

  12. Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia)

    Danilchenko, V. Y., Zytsar, M. V., Maslova, E. A., Orishchenko, K. E. & Posukh, O. L., 17 Apr 2023, In: Genes. 14, 4, 928.

    Research output: Contribution to journal › Article › peer-review

  13. 2022

  14. The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing

    Карамышева, Т. В., Татьяна, Г., Елисафенко, Е. А., Трифонов, В. А., Закирова, Э. Г., Орищенко, К. Е., Мария, П. А., Лопаткина, М. Е., Скрябин, Н. А., Лебедев, И. Н. & Рубцов, Н. Б., 14 Dec 2022, In: Biomedicines. 10, 12, 3255.

    Research output: Contribution to journal › Article › peer-review

  15. 2021

  16. A Method for Assessing the Efficiency of the Nucleotide Excision Repair System Ex Vivo

    Popov, A. A., Orishchenko, K. E., Naumenko, K. N., Evdokimov, A. N., Petruseva, I. O. & Lavrik, O. I., Sept 2021, In: Acta Naturae. 13, 3, p. 122-125 4 p., 13.

    Research output: Contribution to journal › Article › peer-review

  17. New Data on Organization and Spatial Localization of B-Chromosomes in Cell Nuclei of the Yellow-Necked Mouse Apodemus flavicollis

    Karamysheva, T., Romanenko, S., Makunin, A., Rajičić, M., Bogdanov, A., Trifonov, V., Blagojević, J., Vujošević, M., Orishchenko, K. & Rubtsov, N., 19 Jul 2021, In: Cells. 10, 7, 1819.

    Research output: Contribution to journal › Article › peer-review

  18. Adaptation of CRISPR/Cas9 system for directed elimination of mitochondrial DNA copies with mutations

    Zakirova, E., Mazunin, I. & Orishchenko, K., Jul 2021, In: FEBS Open Bio. 11, p. 118-118 1 p.

    Research output: Contribution to journal › Meeting Abstract › peer-review

  19. Natural and artificial mechanisms of mitochondrial genome elimination

    Zakirova, E. G., Muzyka, V. V., Mazunin, I. O. & Orishchenko, K. E., Feb 2021, In: Life. 11, 2, p. 1-22 22 p., 76.

    Research output: Contribution to journal › Review article › peer-review

  20. Recent Advances in the Development of Exogenous dsRNA for the Induction of RNA Interference in Cancer Therapy

    Golubeva, T. S., Cherenko, V. A. & Orishchenko, K. E., 29 Jan 2021, In: Molecules (Basel, Switzerland). 26, 3, 701.

    Research output: Contribution to journal › Review article › peer-review

  21. Functional evaluation of a rare variant c.516g>c (p.trp172cys) in the GJB2 (connexin 26) gene associated with nonsyndromic hearing loss

    Maslova, E. A., Orishchenko, K. E. & Posukh, O. L., Jan 2021, In: Biomolecules. 11, 1, p. 1-15 15 p., 61.

    Research output: Contribution to journal › Article › peer-review

  22. 2020

  23. Complex assessment of pathogenicity of novel variant c.516G > C (p.Trp172Cys) in the GJB2 gene associated with hearing loss in indigenous peoples of Southern Siberia (Russia)

    Maslova, E. A., Zytsar, M. V., Danilchenko, V. Y., Orishchenko, K. E. & Posukh, O. L., 1 Dec 2020, In: European journal of human genetics. 28, Suppl 1, p. 191-192 2 p., P02.27.B.

    Research output: Contribution to journal › Meeting Abstract › peer-review

  24. Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function

    Karamysheva, T. V., Gayner, T. A., Muzyka, V. V., Orishchenko, K. E. & Rubtsov, N. B., Dec 2020, In: Genes. 11, 12, p. 1-19 19 p., 1511.

    Research output: Contribution to journal › Article › peer-review

  25. Using Computer Vision and Deep Learning for Cells Recognition

    Kudinov, V. Y., Mashukov, M. Y., Maslova, E. A., Orishchenko, K. E., Okunev, A. G. & Matveev, A. V., 14 Nov 2020, Proceedings - 2020 Science and Artificial Intelligence Conference, S.A.I.ence 2020. Institute of Electrical and Electronics Engineers Inc., p. 17-20 4 p. 9303201. (Proceedings - 2020 Science and Artificial Intelligence Conference, S.A.I.ence 2020).

    Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › Research › peer-review

  26. Изучение влияния детерминант митохондриального импорта в структуре нРНК на активность комплекса нРНК/SpCas9 in vitro

    Zakirova, E. G., Vyatkin, Y. V., Verechshagina, N. A., Muzyka, V. V., Mazunin, I. O. & Orishchenko, K. E., Aug 2020, In: Вавиловский журнал генетики и селекции. 24, 5, p. 512-518 7 p.

    Research output: Contribution to journal › Article › peer-review

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