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Valeriia Yu. Danilchenko

Observed names: Danilchenko, Valeriia, V. Yu. Danilchenko, V.Yu. Danilchenko, Valeria Yu. Danilchenko, Valeriia Danilchenko, В.Ю. Данильченко
ORCID: 0000-0001-5658-5974
Observed ORCIDs: 0000-0001-5658-5974, 0000-0003-0316-2948
OpenAlex ID: A5036099773
Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains
2023 · Olga L. Posukh, Ekaterina A. Maslova, et al. · Biomolecules · 27
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Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)
2021 · Valeriia Yu. Danilchenko, Marina V. Zytsar, et al. · Diagnostics · 24
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Gene Therapy for Angelman Syndrome: Contemporary Approaches and Future Endeavors
2020 · Christos Tsagkaris, Vasiliki Papakosta, et al. · Current Gene Therapy · 19
Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia
2018 · Marina V. Zytsar, Nikolay A. Barashkov, et al. · BMC Medical Genetics · 18
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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)
2019 · Olga L. Posukh, Marina V. Zytsar, et al. · Genes · 17
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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
2020 · Marina V. Zytsar, Marita S. Bady-Khoo, et al. · Genes · 15
Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss
2022 · Valeriia Yu. Danilchenko, Marina V. Zytsar, et al. · International Journal of Molecular Sciences · 11
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Insight into the Natural History of Pathogenic Variant c.919-2A>G in the SLC26A4 Gene Involved in Hearing Loss: The Evidence for Its Common Origin in Southern Siberia (Russia)
2023 · Valeriia Danilchenko, Marina Zytsar, et al. · Genes · 8
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Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay
2025 · Valeriia Yu. Danilchenko, Ekaterina A. Panina, et al. · International Journal of Molecular Sciences · 1
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Analysis by Minigene Assay of the Splicing Effect of a Novel Variant c.1545T>G in the SLC26A4 Gene Associated with Hearing Loss
2025 · E. A. Panina, V. Yu. Danilchenko, et al. · Russian Journal of Genetics · 1
Mithridatism for dementia? Hypoxic - Hyperoxic training in dementia
2020 · Christos Tsagkaris, Rehab Rayan, et al. · Mental Health Global Challenges Journal · 1
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Analysis of the mutational spectrum of the SLC26A4 gene and its contribution to the etiology of inherited hearing loss in the indigenous population of Southern Siberia
2020 · В.Ю. Данильченко, М.В. Зыцарь, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 1
A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss
2026 · M. V. Zytsar, V. Yu. Danilchenko, et al. · Vavilov Journal of Genetics and Breeding
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In vitro analysis of the effects of intronic variants c.940+3_940+6del, c.941-3C>G, and c.2389+5G>A in the LDLR gene on pre-mRNA splicing using a minigene assay
2026 · V. Yu. Danilchenko, D. E. Ivanoshchuk, et al. · Vavilov Journal of Genetics and Breeding
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Comparative analysis of haplotypes carrying pathogenic variants c.1545T>G, c.2027T>A and c.919-2A>G of the SLC26A4 gene in patients with hearing loss from the Tyva Republic (Southern Siberia)
2025 · V. Yu. Danilchenko, M. V. Zytsar, et al. · Vavilov Journal of Genetics and Breeding
Association of a Homozygous Gck Variant C.1019g>a With the Mody Phenotype
2025 · V.Yu. Danilchenko, D.E. Ivanoshchuk, et al. · Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов (OpenBio)
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Splicing Variants in the Etiology of Monogenic Diseases: Variants in the Slc26a4 Gene Associated With Hearing Loss
2024 · V.Yu. Danilchenko, E.A. Panina, et al. · Высшая школа: научные исследования
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Complex assessment of the pathogenetic significance of variant с.516G>C (p.Trp172Cys) in the GJB2 gene which is associated with hereditary hearing loss in indigenous population of Southern Siberia
2020 · Е.А. Маслова, М.В. Зыцарь, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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Works count: 20
Citation count: 143
H-index: 8
I10-index: 7
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