Sciact
  • EN
  • RU
Profile

Osinovskaya Natalʹya Sergeevna

Employee

Science activity

Articles - 11


Articles (11) More info

1 Glotov A.S. , Nasykhova Y.A. , Lazareva T.E. , Dvoinova N.M. , Shabanova E. , Danilova M.M. , Osinovskaya N.S. , Barbitov Y.A. , Maretina M.A. , Gorodnicheva E. , Tonyan Z.N. , Kiselev A.V. , Basipova A.A. , Bespalova O.N. , Kogan I.Y.
Pilot Study of Preconception Carrier Screening in Russia: Initial Findings and Challenges
Genes. 2025. DOI: 10.3390/genes17010003 OpenAlex
2 Kiselev A. , Maretina M. , Shtykalova S. , Al-Hilal H. , Maslyanyuk N. , Plokhih M. , Serebryakova E. , Frolova M. , Shved N. , Krylova N. , Il’ina A. , Freund S. , Osinovskaya N. , Sultanov I. , Egorova A. , Lobenskaya A. , Koroteev A. , Sosnina I. , Gorelik Y. , Bespalova O. , Baranov V. , Kogan I. , Glotov A.
Establishment of a Pilot Newborn Screening Program for Spinal Muscular Atrophy in Saint Petersburg
International Journal of Neonatal Screening. 2024. V.10. N1. 9 . DOI: 10.3390/ijns10010009 WOS Scopus РИНЦ OpenAlex
3 Osinovskaya N. , Vashukova E. , Tarasenko O. , Danilova M. , Glavnova O. , Sultanov I. , Donnikov M. , Nasykhova Y. , Glotov A.
Analysis of the CYP21A2 gene pathogenic variants in CAH patients from Surgut using next-generation sequencing (NGS)
Egyptian Journal of Medical Human Genetics. 2024. V.25. N1. DOI: 10.1186/s43042-024-00502-9 WOS Scopus OpenAlex
4 Korf E.A. , Novozhilov A.V. , Mindukshev I.V. , Glotov A.S. , Kudryavtsev I.V. , Baidyuk E.V. , Dobrylko I.A. , Voitenko N.G. , Voronina P.A. , Habeeb S. , Ghanem A. , Osinovskaya N.S. , Serebryakova M.K. , Krivorotov D.V. , Jenkins R.O. , Goncharov N.V.
Testing Green Tea Extract and Ammonium Salts as Stimulants of Physical Performance in a Forced Swimming Rat Experimental Model
International Journal of Molecular Sciences. 2024. V.25. N19. 10438 . DOI: 10.3390/ijms251910438 WOS Scopus OpenAlex
5 Koltsova A.S. , Efimova O.A. , Pendina A.A. , Chiryaeva O.G. , Osinovskaya N.S. , Shved N.Y. , Yarmolinskaya M.I. , Polenov N.I. , Kunitsa V.V. , Sagurova Y.M. , Tral T.G. , Tolibova G.K. , Baranov V.S.
Uterine Leiomyomas with an Apparently Normal Karyotype Comprise Minor Heteroploid Subpopulations Differently Represented in vivo and in vitro
Cytogenetic and Genome Research. 2021. V.161. N1-2. P.43-51. DOI: 10.1159/000513173 WOS Scopus РИНЦ OpenAlex
6 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
7 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
8 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
9 Kol’tsova A.S. , Pendina A.A. , Efimova O.A. , Kaminskaya A.N. , Tikhonov A.V. , Osinovskaya N.S. , Sultanov I.Y. , Shved N.Y. , Kakhiani M.I. , Baranov V.S.
Differential DNA Hydroxymethylation in Human Uterine Leiomyoma Cells Depending on the Phase of Menstrual Cycle and Presence of MED12 Gene Mutations
Bulletin of Experimental Biology and Medicine. 2017. V.163. N5. P.646-649. DOI: 10.1007/s10517-017-3870-3 WOS Scopus РИНЦ
10 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
11 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

Identifiers

ORCID: 0000-0001-7831-9327
Scopus ID: 6507794800
ResearcherID: K-1168-2018
Elibrary ID: 95520
SciProfiles: 880216

Degrees

2007 - Ph.D.