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Shved Natalʹya Yurʹevna

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Articles - 6


Articles (6) More info

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 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 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 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 OpenAlex
6 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.