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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. |