ICG  

Accounting System of Scientific Activity (ASSA)

      

Marina Zytsar`

Department: Sector of Monogenic Forms of Common Diseases
Pluralist: Sector of Monogenic Forms of Common Diseases
Position: Junior Researcher
Room: 3413
Email: zytzar@bionet.nsc.ru
Work phone: +7 (383) 363-49-63*3413


Publications

2020 High rates of three common GJB2 mutations c.516G>C, c.-23+1G>A, c.235delC in deaf patients from Southern Siberia are due to the founder effect.
Zytsar M.V., Bady-Khoo M.S., Danilchenko V.Y., Maslova E.A., Barashkov N.A., Morozov I.V., Bondar A.A., Posukh O.L.
[Genes]
2019 Unique mutational spectrum of the GJB2 gene and its pathogenic contribution to deafness in Tuvinians (Southern Siberia, Russia): a high prevalence of rare variant c.516G>C (p.Trp172Cys).
Posukh O.L., Zytsar M.V., Bady-Khoo M.S., Danilchenko V.Yu., Maslova E.A., Barashkov N.A., Bondar A.A., Morozov I.V., Maximov V.N., Voevoda M.I.
[Genes]
2018 Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
Zytsar M.V., Barashkov N.A., Bady-Khoo M.S., Shubina-Olejnik O.A., Danilenko N.G., Bondar A.A., Morozov I.V., Solovyev A.V., Danilchenko V.Yu., Maximov V.N., Posukh O.L.
[BMC MED GENET]
2017 Reconstruction of SNP haplotypes with mutation c.-23+1G>A in human gene GJB2 (Chromosome 13) in some populations of Eurasia.
Solovyev A.V., Barashkov N.A., Bady-Khoo M.S., Zytsar M.V., Posukh O.L., Romanov G.P., Rafailov A.M., Sazonov N.N., Alexeev A.N., Dzhemileva L.U., Khusnutdinova E.K., Fedorova S.A.
[RUSS J GENET+]
2016 Impact of socio-demographic structure of the deaf people communities in prevalence of hereditary hearing loss.
Posukh O.L., Bady-Khoo M.S., Zytsar M.V., Mikhalskaia V.Yu., Lashin S.A., Barashkov N.A., Romanov G.P.
[Russian Journal of Genetics: Applied Research]
Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)
Сhurbanov AY, Karafet TM, Morozov IV, Mikhalskaia VY, Zytsar MV, Bondar AA, Posukh OL.
[PloS One]
2014 Изучение наследственных форм тугоухости / глухоты в Республике Тыва. Cообщение I. Эпидемиология нарушений слуха в Республике Тыва.
Бады-Хоо М.С., Посух О.Л., Зоркольцева И.В., Скиданова О.В., Барашков Н.А., Омзар О.С., Монгуш Р.Ш., Бамба О.М., Тукар В.М., Зыцарь М.В., Михальская В.Ю.
[Медицинская генетика]
Изучение наследственных форм тугоухости / глухоты в Республике Тыва. Cообщение II. Оценка спектра мутаций гена GJB2 (Cx26) и их вклада в этиологию потери слуха.
Бады-Хоо М.С., Бондарь А.А., Морозов И.В., Зыцарь М.В., Михальская В.Ю., Скиданова О.В., Барашков Н.А., Монгуш Р.Ш., Омзар О.С., Тукар В.М., Посух О.Л.
[Медицинская генетика]
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