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  1. Gene expression changes in the ventral tegmental area of male mice with alternative social behavior experience in chronic agonistic interactions

    Redina, O., Babenko, V., Smagin, D., Kovalenko, I., Galyamina, A., Efimov, V. & Kudryavtseva, N., 2 Sept 2020, In: International Journal of Molecular Sciences. 21, 18, p. 1-32 32 p., 6599.

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

  2. Gene-based association tests using GWAS summary statistics

    Svishcheva, G. R., Belonogova, N. M., Zorkoltseva, I. V., Kirichenko, A. V. & Axenovich, T. I., 1 Oct 2019, In: Bioinformatics (Oxford, England). 35, 19, p. 3701-3708 8 p.

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

  3. Gene-based association analysis identifies 190 genes affecting neuroticism

    Belonogova, N. M., Zorkoltseva, I. V., Tsepilov, Y. A. & Axenovich, T. I., 28 Jan 2021, In: Scientific Reports. 11, 1, 2484.

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

  4. Gender differences in Russian adolescent mental health from 1999 to 2021

    Privodnova, E. Y., Semenova, N. B., Kornienko, O. S., Varshal, A. V. & Slobodskaya, H. R., Mar 2024, In: Journal of Research on Adolescence. 34, 1, p. 222-234 13 p.

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

  5. Function and Evolution of the Loop Extrusion Machinery in Animals

    Kabirova, E., Nurislamov, A., Shadskiy, A., Smirnov, A., Popov, A., Salnikov, P., Battulin, N. & Fishman, V., 6 Mar 2023, In: International Journal of Molecular Sciences. 24, 5, 5017.

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

  6. 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

  7. 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

  8. From Alzheimer's disease to chronical kidney disease: Reticulons in human diseases

    Morozova, K. N. & Kiseleva, E. V., 1 Jan 2017, In: Цитология. 59, 6, p. 394-404 11 p.

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

  9. Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia

    Barashkov, N. A., Vychuzhina, L. S., Solovyev, A. V., Teryutin, F. M., Pshennikova, V. G., Burtseva, T. E., Tomsky, M. I., Platonov, F. A., Romanov, G. P., Gotovtsev, N. N., Khusnutdinova, E. K., Posukh, O. L. & Fedororva, S. A., Oct 2019, In: European journal of human genetics. 27, p. 1220-1221 2 p.

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

  10. Fold-change-specific enrichment analysis (FSEA): Quantification of transcriptional response magnitude for functional gene groups

    Wiebe, D. S., Omelyanchuk, N. A., Mukhin, A. M., Grosse, I., Lashin, S. A., Zemlyanskaya, E. V. & Mironova, V. V., 17 Apr 2020, In: Genes. 11, 4, 14 p., 434.

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

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