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Основные публикации

  1. Striukova E.V., Maksimov V.N., RaginoYu.I, PolonskayaYa.V., Murashov I.S., Volkov A.M., Kurguzov A.V., Chernjavskii A.M., Kashtanova E.V. Polymorphisms in the CETP, APOC3 and APOE genes in men with unstable atherosclerotic plaques in the coronary arteries //Meta Gene, Volume 27, 2021,https://doi.org/10.1016/j.mgene.2020.100847.
  2. Voropaeva E.N/, Orlov Y.L., Pospelova T.I., Gurageva A.A., Voevoda M.I., Maksimov V.N., Seregina O.B., Churkina M.I. 2020. The rs78378222 prevalence and the copy loss of the protective allele A in the tumor tissue of diffuse large B-cell lymphoma. PeerJ 8:e10335https://doi.org/10.7717/peerj.10335
  3. Maximov V., Malyutina S., Orlov P., Ivanoschuk D., Mikhailova S.V., ShapkinaM.Yu., Hubacek J., Holmes M., BobakМ.,Voevoda M. Copy Number of the Mitochondrial DNA of Leucocytes as an Aging Marker and Risk Factors for the Development of Age-Related Diseases in Humans //Advances in Gerontology, 2020, Vol. 10, No. 1, pp. 1–8 DOI: 10.1134/S2079057020010129
  4. Leberfarb EY, Degtyareva AO, Brusentsov II, Maximov VN, Voevoda MI, Autenshlus AI, Morozov DV, Sokolov AV, Merkulova TI. Potential regulatory SNPs in the ATXN7L3B and KRT15 genes are associated with gender-specific colorectal cancer risk. //Per Med. 2020 Jan;17(1):43-54. doi: 10.2217/pme-2019-0059.
  5. NikulinaS.Yu., Artyukhov I.P., Shesternya P.A., Gavrilyuk O.A., Maksimov V.N., Voyevoda M.I., Brusentsov D.A. Clinical application of chromosome 9p21.3 genotyping in patients with coronary artery disease //Experimental and therapeutic medicine. - 2019. - V.18. - №4. - P.3100-3108https://doi.org/10.3892/etm.2019.7884
  6. Aftanas L.I., Anisimenko M.S., Berdyugina D.A., GaraninA.Yu., Maximov V.N., Voevoda M.I., Vyalova N.M., Bokhan N.A., Ivanova S.A., Danilenko K.V., Kovalenko S.P. SIRT1 allele frequencies in depressed patients of european descent in Russia //Frontiers in genetics. 2019. Т. 9. № JAN. С. 686.https://doi.org/10.3389/fgene.2018.00686
  7. Voropaeva EN, Pospelova TI, Voevoda MI, Maksimov VN, Orlov YL, Seregina OB. Clinical aspects of TP53 gene inactivation in diffuse large B-cell lymphoma. BMC Med Genomics. 2019 Mar 13;12(Suppl 2):35. doi: 10.1186/s12920-019-0484-9.
  8. Yudin N.S., Barkhash A.V., Maksimov V.N., Ignatieva E.V., Romaschenko A.G. Human Genetic Predisposition to Diseases Caused by Viruses from Flaviviridae Family //Molecular Biology, 2018, Vol. 52, No. 2, pp. 165–181.
  9. Shakhtshneider E.V., Mikhailova S.V., Ivanoshchuk D.E., Orlov P.S., Ovsyannikova A.K., Rymar O.D., RaginoYu.I.,Voevoda M.I.. Polymorphism of the GLIS3 gene in a caucasian population and among individuals with carbohydrate metabolism disorders in Russia. BMC Research Notes. 2018. Т. 11. № 1. С. 211.https://doi.org/10.1186/s13104-018-3338-1
  10. Stefler D., Malyutina S., Maximov V., Orlov P., Ivanoschuk D., Nikitin Y., Gafarov V., Ryabikov A., Voevoda M., Bobak M., Holmes M. Leukocyte telomere length and risk of coronary heart disease and stroke mortality: prospective evidence from a russian cohort //Scientific Reports. 2018. Т. 8. № 1. Р. 1-6. DOI: 10.1038/s41598-018-35122-y
  11. Cherepkova EV, Maksimov VN, Aftanas LI. Polymorphism of serotonin transporter gene in male subjects with antisocial behavior and MMA fighters. Transl Psychiatry. 2018 Nov 15;8(1):248. doi: 10.1038/s41398-018-0298-0.
  12. IvanovaAA, MaksimovVN, IvanoshchukDE, OrlovPS, NovoselovVP, SavchenkoSV, VoevodaMI. Association of Polymorphism in SCN5A, GJA5, and KCNN3 Gene with Sudden Cardiac Death. //Bull ExpBiol Med. 2017 May; 163 (1): 73-77.
  13. Voropaeva E.N., Voevoda M.I., Maksimov V.N., Pospelova T.I. Frequency, spectrum, and functional significance of TP53 mutations in patients with diffuse large B-cell lymphoma //Molecular Biology. 2017. Т. 51. № 1. Р. 53-60.
  14. Maximov V.N., Malyutina S.K., Orlov P.S., Ivanoschuk D.E., Voropaeva E.N., Bobak M., Voevoda M.I. Leukocyte Telomere Length as an Aging Marker and Risk Factor for Human Age-Related Diseases //Advances in Gerontology, 2017, Vol. 7, No. 2, pp. 101–106.
  15. Belyavskaya V.A., Prudnikova T.Y., Domanitskaya N.V., Litviakov N.V., Maksimov V.N., Cherdyntseva N.V., Grigorieva E.V. GLCE rs3865014 (Val597Ile) polymorphism is associated with breast cancer susceptibility and triple-negative breast cancer in Siberian population //Gene. 2017 Sep 10;628:224-229. doi:10.1016/j.gene.2017.07.054.
  16. Cherepkova E, Maksimov V, Kushnarev A, Shakhmatov I, Aftanas LI. The polymorphism of dopamine receptor D4 (DRD4) and dopamine transporter (DAT) genes in the men with antisocial behavior and mixed martial arts fighters. //World J Biol Psychiatry. 2017 Aug 11:1-26. doi: 10.1080/15622975.2017.1366056. [Epub ahead of print] PubMed PMID: 28797200.
  17. Cherdyntseva N., Gervas P., Denisov E., Pisareva L., Malinovskaya E., Choynzonov E., Voropaeva E., Maksimov V., Voevoda M., Cherdyntsev E., Perinov D., Panferova Y. New variants in the BRCA1 gene in buryatmongol breast cancer patients: report from two families //Cancer Biomarkers. 2017. Т. 18. № 3. С. 291-296. DOI: 10.3233/CBM-161649
  18. Gubina MA, Babenko VN, Ivanoshchuk DE, Shuryaeva AK, Latieva OO, Solov'eva IG, Ponomareva MN, Konovalova NA, Maksimov VN, Voevoda MI. Polymorphism of the c-fms, ITGB3, CCR2, and DBH genes in the populations of old believers of the Tyumen oblast and Russian residents of Novosibirsk //MolBiol (Mosk). 2016 Mar-Apr;50(2):246-54.
  19. Mikhailova SV, Babenko VN, Ivanoshchuk DE, Gubina MA, Maksimov VN, Solovjova IG, Voevoda MI. Haplotype analysis of the HFE gene among populations of Northern Eurasia, in patients with metabolic disorders or stomach cancer, and in long-lived people. BMC Genet. 2016 Jun 17;17(1):83.
  20. Ivanova A.A., Maksimov V.N., Orlov P.S., Ivanoshchuk D.E., Savchenko S.V., Voevoda M.I. Association of the genetic markers for myocardial infarction with sudden cardiac death //Indian Heart J. (2016),http://dx.doi.org/10.1016/j.ihj.2016.07.016
  21. Apsalikov B, Manambaeva Z, Ospanov E, Massabayeva M, Zhabagin K, Zhagiparova Z, Maximov V, Voropaeva E, Apsalikov K, Belikhina T, Abdrahmanov R, Cherepkova E, Tanatarov S, Massadykov A, Urazalina N. BRCA1 and TP53 Gene-Mutations: Family Predisposition and Radioecological Risk of Developing Breast Cancer. //Asian Pac J Cancer Prev. 2016;17(8):4059-62.
  22. Striukova EV, Maksimov VN, Ragino YI, Polonskaya YV, Murashov IS, Volkov AM, Kurguzov AV, Chernjavskii AM, Kashtanova EV Polymorphisms in CCL2 and IL6 genes in men with unstable atherosclerotic plaques in the coronary arteries. //Journal of Cardiovascular Disease Research, 2021; 12(1): 68-74. doi:10.31838/jcdr.2021.12.01.16
  23. Malyutina, S.; Chervova, O.; Tillmann, T.; Maximov, V.; Ryabikov, A.; Gafarov, V.; Hubacek, J.A.; Pikhart, H.; Beck, S.; Bobak, M. The Relationship between Epigenetic Age and Myocardial Infarction/Acute Coronary Syndrome in a Population-Based Nested Case-Control Study. J. Pers. Med. 2022, 12, 110. https://doi.org/10.3390/jpm12010110
  24. Voropaeva, E.N.; Pospelova, T.I.; Orlov, Y.L.; Churkina, M.I.; Berezina, O.V.; Gurazheva, A.A.; Ageeva, T.A.; Seregina, O.B.; Maksimov, V.N. The Methylation of the p53 Targets the Genes MIR-203, MIR-129-2, MIR-34A and MIR-34B/C in the Tumor Tissue of Diffuse Large B-Cell Lymphoma. Genes 2022, 13, 1401. https://doi.org/10.3390/genes13081401
  25. Chervova O, Chernysheva E, Panteleeva K, Widayati TA, Hrbkova N, Schneider J, Maximov V, Ryabikov A, Tillmann T, Pikhart H, Bobak M, Voloshin V, Malyutina S, Beck S. Evaluation of Epigenetic Age Acceleration Scores and Their Associations with CVD-Related Phenotypes in a Population Cohort. Biology. 2023; 12(1):68. https://doi.org/10.3390/biology12010068
  26. Malyutina S.K., Maximov V.N., Chervova O. Orlov P.S., Voloshin V., Ryabikov A.N., Voevoda M.I., Nikitenko T.M. Leukocyte telomere length and mitochondrial DNA copy number association with colorectal cancer risk in an aging population //Global Translational Medicine. – 2023. – Vol. 2, No. 1. – P. 184. – DOI 10.36922/gtm.v2i1.184.
  27. Malyutina S, Maximov V, Chervova O, Orlov P, Ivanova A, Mazdorova E, Ryabikov A, Simonova G, Voevoda M. The Relationship between All-Cause Natural Mortality and Copy Number of Mitochondrial DNA in a 15-Year Follow-Up Study. Int J Mol Sci. 2023 Jun 21;24(13):10469. doi: 10.3390/ijms241310469. PMID: 37445647; PMCID: PMC10341474.
  28. Gafarov V.V., Gromova E.A., Tripelgorn A.N. Gagulin I.V., Maksimov V.N., Gafarova A.V. Circadian Rhythm Genes and Sleep Disorders in an Open Population of Men Aged 25–64 Years (an Epidemiological Study under the WHO MONICA-Psychosocial Program). Neuroscience and Behavioral Physiology. – 2024. – Vol. 54, No. 1. – P. 10-15. – DOI 10.1007/s11055-024-01561-6. – EDN PDPWAP.
  29. Malyutina S, Chervova O, Maximov V, Nikitenko T, Ryabikov A, Voevoda M. Blood-Based Epigenetic Age Acceleration and Incident Colorectal Cancer Risk: Findings from a Population-Based Case-Control Study. Int J Mol Sci. 2024 Apr 29;25(9):4850. doi: 10.3390/ijms25094850. PMID: 38732069; PMCID: PMC11084311.
  30. Maksimov V.N., Minnikh S.V., Ivanova A.A. Modern approaches to the assessment of individual risk of CHD development: status, problems, prospects. Ateroscleroz. 2024;20(2):154-161. (In Russ.) https://doi.org/10.52727/2078-256X-2024-20-2-154-1...
  31. Ivanova A.A., Apartseva N.E., Kashirina A.P., Nemcova E.G., Ivanova J.V., Kruchinina M.V., Kurilovich S.A., Maksimov V.N. Results of UGT1A1 gene sequencing in individuals with the Gilbert syndrome phenotype. Bulletin of Siberian Medicine. 2024;23(2):65-73. https://doi.org/10.20538/1682-0363-2024-2-65-73
  32. Ivanova А.А., Apartseva N.E., Kashirina A.P., Nemtsova E.G., Ivanova Y.V., Kruchinina M.V., Kurilovich S.A., Maksimov V.N. Detection of major mutations in CFTR, SERPINA1, HFE genes in benign unconjugated hyperbilirubinemia phenotype. Sovremennye tehnologii v medicine 2024; 16(4): 38, https://doi.org/10.17691/stm2024.16.4.04
  33. Gafarov V.V., Gromova E.A., Gubina M.A, Gagulin I.V., Maksimov V.N., Gafarova A.V. Association of Polymorphisms of the Serotonin Transporter Gene SLC6A4 with Depression //Neuroscience and Behavioral Physiology. – 2024. – Vol. 54, No. 5. – P. 655-659. – DOI 10.1007/s11055-024-01645-3. – EDN YAIDXC.
  34. Voropaeva EN, Orlov YL, Loginova AB, Seregina OB, Maksimov VN, Pospelova TI. 2025. Deregulation mechanisms and therapeutic opportunities of p53-responsive microRNAs in diffuse large B-cell lymphoma. PeerJ 13:e18661 https://doi.org/10.7717/peerj.18661