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Articles (12) More info

1	Шалина М.А. , Малышева О.В. , Ярмолинская М.И. , Беганова А.К. , Шалина Я.А. Экспрессия гена стресс-индуцированного фосфопротеина 1 (STIP1) при аденомиозе: обсервационное исследование «случай — контроль» Кубанский научный медицинский вестник. 2024. V.31. N4. P.78-88. DOI: 10.25207/1608-6228-2024-31-4-78-88 Scopus РИНЦ OpenAlex
2	Tikhonov A.V. , Krapivin M.I. , Malysheva O.V. , Komarova E.M. , Golubeva A.V. , Efimova O.A. , Pendina A.A. Re-Examination of PGT-A Detected Genetic Pathology in Compartments of Human Blastocysts: A Series of 23 Cases Journal of Clinical Medicine. 2024. V.13. N11. 3289 . DOI: 10.3390/jcm13113289 WOS Scopus РИНЦ OpenAlex
3	Koltsova A.S. , Pendina A.A. , Malysheva O.V. , Trusova E.D. , Staroverov D.A. , Yarmolinskaya M.I. , Polenov N.I. , Glotov A.S. , Kogan I.Y. , Efimova O.A. In Vitro Effect of Estrogen and Progesterone on Cytogenetic Profile of Uterine Leiomyomas International Journal of Molecular Sciences. 2024. DOI: 10.3390/ijms26010096 WOS Scopus РИНЦ OpenAlex
4	Talantova O.E. , Koltsova A.S. , Tikhonov A.V. , Pendina A.A. , Malysheva O.V. , Tarasenko O.A. , Vashukova E.S. , Shabanova E.S. , Golubeva A.V. , Chiryaeva O.G. , Glotov A.S. , Bespalova O.N. , Efimova O.A. Prenatal Detection of Trisomy 2: Considerations for Genetic Counseling and Testing Genes. 2023. V.14. N4. 913 . DOI: 10.3390/genes14040913 WOS Scopus РИНЦ OpenAlex
5	Малышева О.В. , Ярмолинская М.И. Генетические детерминанты аденомиоза Акушерство и гинекология. 2023. N4. P.20-27. DOI: 10.18565/aig.2023.52 Scopus РИНЦ OpenAlex
6	Puppo I.L. , Tonyan Z.N. , Saifitdinova A.F. , Loginova J.A. , Kinunen A.A. , Panina A.N. , Pastuhova J.R. , Leonteva O.A. , Chiryaeva O.G. , Malysheva O.V. , Glotov O.S. , Poliakova I.V. , Tikhonov A.V. , Vavilova T.V. , Menshikova I.L. , Isakova E.V. , Glotov A.S. , Bichevaya N.K. Evaluating chromosomal segregation in a family where both spouses carry an autosomal translocation In compilation Reproductive and developmental medicine. – Wolters Kluwer Health., 2022. – C.189-192. DOI: 10.1097/rd9.0000000000000041 OpenAlex
7	Puppo I.L. , Tonyan Z.N. , Panina A.N. , Shunkina K.V. , Saifitdinova A.F. , Loginova Y.A. , Kinunen A.A. , Pastuhova J.R. , Leonteva O.A. , Chiryaeva O.G. , Маlysheva O.V. , Fedorova E.M. , Vavilova T.V. , Bichevaya N.K. Application of the FISH Method for Analyzing Chromosome Segregation Patterns in Preimplantation Embryos from Robertsonian Translocation Carriers OBM Genetics. 2022. V.6. N2. 1 . DOI: 10.21926/obm.genet.2202157 Scopus OpenAlex
8	Koltsova A.S. , Efimova O.A. , Malysheva O.V. , Osinovskaya N.S. , Liehr T. , Al-Rikabi A. , Shved N.Y. , Sultanov I.Y. , Chiryaeva O.G. , Yarmolinskaya M.I. , Polenov N.I. , Kunitsa V.V. , Kakhiani M.I. , Tral T.G. , Tolibova G.K. , Bespalova O.N. , Kogan I.Y. , Glotov A.S. , Baranov V.S. , Pendina A.A. Cytogenomic Profile of Uterine Leiomyoma: In Vivo vs. In Vitro Comparison Biomedicines. 2021. V.9. N12. 1777 . DOI: 10.3390/biomedicines9121777 WOS Scopus РИНЦ OpenAlex
9	Pendina A.A. , Shilenkova Y.V. , Talantova O.E. , Efimova O.A. , Chiryaeva O.G. , Malysheva O.V. , Dudkina V.S. , Petrova L.I. , Serebryakova E.A. , Shabanova E.S. , Mekina I.D. , Komarova E.M. , Koltsova A.S. , Tikhonov A.V. , Tral T.G. , Tolibova G.K. , Osinovskaya N.S. , Krapivin M.I. , Petrovskaia-Kaminskaia A.V. , Korchak T.S. , Ivashchenko T.E. , Glotov O.S. , Romanova O.V. , Shikov A.E. , Urazov S.P. , Tsay V.V. , Eismont Y.A. , Scherbak S.G. , Sagurova Y.M. , Vashukova E.S. , Kozyulina P.Y. , Dvoynova N.M. , Glotov A.S. , Baranov V.S. , Gzgzyan A.M. , Kogan I.Y. Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities Frontiers in Genetics. 2019. V.10. 1164 . DOI: 10.3389/fgene.2019.01164 WOS Scopus РИНЦ OpenAlex
10	Pendina A.A. , Koltsova A.S. , Efimova O.A. , Malysheva O.V. , Osinovskaya N.S. , Sultanov I.Y. , Tikhonov A.V. , Shved N.Y. , Chiryaeva O.G. , Simareva A.D. , Kakhiani M.I. , Baranov V.S. Case of chromothripsis in a large solitary non-recurrent uterine leiomyoma European Journal of Obstetrics & Gynecology and Reproductive Biology. 2017. V.219. P.134-136. DOI: 10.1016/j.ejogrb.2017.10.028 WOS Scopus РИНЦ OpenAlex
11	Dzhemlikhanova L.K. , Efimova O.A. , Osinovskaya N.S. , Parfenyev S.E. , Niauri D.A. , Sultanov I.Y. , Malysheva O.V. , Pendina A.A. , Shved N.Y. , Ivashchenko T.E. , Yarmolinskaya M.I. , Kakhiani M.I. , Gorovaya E.A. , Tkachenko A.N. , Baranov V.S. Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative forMED12exon 2 mutations Journal of Clinical Pathology. 2017. V.70. N3. P.233-236. DOI: 10.1136/jclinpath-2016-203976 WOS Scopus РИНЦ
12	Osinovskaya N.S. , Malysheva O.V. , Shved N.Y. , Ivashchenko T.E. , Sultanov I.Y. , Efimova O.A. , Yarmolinskaya M.I. , Bezhenar V.F. , Baranov V.S. Frequency and Spectrum of MED12 Exon 2 Mutations in Multiple Versus Solitary Uterine Leiomyomas From Russian Patients International Journal of Gynecological Pathology. 2016. V.35. N6. P.509-515. DOI: 10.1097/pgp.0000000000000255 WOS Scopus РИНЦ

Conference attendances (1) More info

1	Nasykhova Y.A. , Tonyan Z.N. , Lazareva T.E. , Dvoynova N.M. , Danilova M.M. , Malysheva O.V. , Mikhailova A.A. , Glotov A.S. Whole exome sequencing approaches to deciphering the genetic landscape of miscarriage European Human Genetics Conference 2025 24 May - 27 Jun 2025