1. A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

    Koksharova, G., Kokh, N., Gridina, M., Khapaev, R., Nimaev, V. & Fishman, V., May 2024, In: International Journal of Molecular Sciences. 25, 10, 5464.

    Research output: Contribution to journalArticlepeer-review

  2. Benefits of NGS for Genetic Testing of Primary Lymphedema

    Kokh, N. V., Sergeevna, K. G., Gridina, M., Ivanoshchuk, D., Fishman, V. & Nimaev, V., 2023, 2023 IEEE Ural-Siberian Conference on Computational Technologies in Cognitive Science, Genomics and Biomedicine, CSGB 2023 - Proceedings. Institute of Electrical and Electronics Engineers Inc., p. 133-136 4 p. (2023 IEEE Ural-Siberian Conference on Computational Technologies in Cognitive Science, Genomics and Biomedicine, CSGB 2023 - Proceedings).

    Research output: Chapter in Book/Report/Conference proceedingConference contributionResearchpeer-review

  3. Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants

    Gridina, M., Lagunov, T., Belokopytova, P., Torgunakov, N., Nuriddinov, M., Nurislamov, A., Nazarenko, L. P., Kashevarova, A. A., Lopatkina, M. E., Vasilyev, S., Zuev, A., Belyaeva, E. O., Salyukova, O. A., Cheremnykh, A. D., Sukhanova, N. N., Minzhenkova, M. E., Markova, Z. G., Demina, N. A., Stepanchuk, Y., Khabarova, A., & 22 othersYan, A., Valeev, E., Koksharova, G., Grigor’eva, E. V., Kokh, N., Lukjanova, T., Maximova, Y., Musatova, E., Shabanova, E., Kechin, A., Khrapov, E., Boyarskih, U., Ryzhkova, O., Suntsova, M., Matrosova, A., Karoli, M., Manakhov, A., Filipenko, M., Rogaev, E., Shilova, N. V., Lebedev, I. N. & Fishman, V., 7 May 2025, In: Genome Medicine. 17, 1, p. 47 47.

    Research output: Contribution to journalArticlepeer-review

  4. Genetic risk factors of cytolysis syndrome in the treatment of recrudescence of chronic cardiovascular diseases

    Koch, N. V., Voronina, E. N., Efremova, T. B., Soldatova, G. S. & Lifshitz, G. I., 1 Jan 2018, In: Russian Journal of Cardiology. 23, 10, p. 76-82 7 p.

    Research output: Contribution to journalArticlepeer-review

  5. Ассоциация генетических предпосылок дефицита витамина D с тяжестью перенесенной COVID-19 инфекцией

    Shrayner, E. V., Petukhova, S. K., Khavkin, A. I., Kokh, N. V. & Lifshits, G. I., 2022, In: Eksperimental'naya i Klinicheskaya Gastroenterologiya. 202, 6, p. 50-55 6 p., 7.

    Research output: Contribution to journalArticlepeer-review

  6. Ассоциация средовых факторов с избыточной массой тела и ожирением у детей дошкольного и младшего школьного возраста

    Shrayner, E. V., Kokh, N. V. & Lifshits, G. I., 2021, In: Sibirskij Zurnal Kliniceskoj i Eksperimental'noj Mediciny. 36, 3, p. 148-153 6 p., 18.

    Research output: Contribution to journalArticlepeer-review

  7. Варианты нуклеотидной последовательности в генах IL4 и TNFa у пациентов с дерматозами и ксерозом

    Makeenko, O. A., Eremina, A. A., Kovalevskaya-Kucheryavenko, T. V., Kokh, N. V., Voronina, E. N., Yurina, N. V. & Sergeeva, I. G., 2025, In: Klinicheskaya Dermatologiya i Venerologiya. 24, 2, p. 178-184 7 p.

    Research output: Contribution to journalArticlepeer-review

  8. Взаимосвязь желчнокаменной болезни и метаболического синдрома: роль генетических факторов

    Novikova, M. S., Shrayner, E. V., Lifshits, G. I., Kokh, N. V. & Khavkin, A. I., 2022, In: Eksperimental'naya i Klinicheskaya Gastroenterologiya. 203, 7, p. 204-210 7 p., 25.

    Research output: Contribution to journalReview articlepeer-review

  9. Исследование ассоциации гена FUT2 с инфицированностью и клиническими проявлениями инфекции Helicobacter pylori

    Klimova, A. S., Shrayner, E. V., Khavkin, A. I., Kokh, N. V., Lifshits, G. I. & Zamaytina, Y. E., 2021, In: Eksperimental'naya i Klinicheskaya Gastroenterologiya. 9 (193), p. 27-32 6 p., 3.

    Research output: Contribution to journalArticlepeer-review

Previous 1 2 Next

ID: 3438534