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1	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
2	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
3	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
4	Glotov O. , Serebryakova E. , Turkunova M. , Efimova O. , Glotov A. , Barbitoff Y. , Nasykhova Y. , Predeus A. , Polev D. , Fedyakov M. , Polyakova I. , Ivashchenko T. , Shved N. , Shabanova E. , Tiselko A. , Romanova O. , Sarana A. , Pendina A. , Scherbak S. , Musina E. , Petrovskaia‑Kaminskaia A. , Lonishin L. , Ditkovskaya L. , Zhelenina L. , Tyrtova L. , Berseneva O. , Skitchenko R. , Suspitsin E. , Bashnina E. , Baranov V. Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes Molecular Medicine Reports. 2019. V.20. P.4905-4914. DOI: 10.3892/mmr.2019.10751 WOS Scopus РИНЦ OpenAlex
5	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
6	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
7	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
8	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
9	Baranov V.S. , Ivashchenko T.E. , Shved N.Y. , Aseev M.V. , Yarmolinskaya M.I. , Selkov S.A. Feasible predictive genetic test for the treatment efficiency response in endometriosis patients Balkan Journal of medical genetics. 1999. V.2. N2. P.29-34.