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Varvara A. Kadnikova

Observed names: V A Kadnikova, V. A. Kadnikova, V. Kadnikova, V.A. Kadnikova, Varvara Kadnikova, В. А. Кадникова, В.А. Кадникова, Кадникова В.А., Кадникова, В.А.
ORCID: 0000-0002-1245-4881
Observed ORCID: 0000-0002-1245-4881
OpenAlex ID: A5057299948
Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia
2019 · V. A. Kadnikova, G. E. Rudenskaya, et al. · Scientific Reports · 28
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A new case of infantile‐onset hereditary spastic paraplegia with complicated phenotype ( SPG 61) in a consanguineous Russian family
2019 · A. L. Chukhrova, I. A. Akimova, et al. · European Journal of Neurology · 15
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families
2020 · G. E. Rudenskaya, V. A. Kadnikova, et al. · BMC Neurology · 11
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Spastic ataxia of Charlevoix-Saguenay: the first Russian case report and literature review
2020 · G. E. Rudenskaya, V. A. Kadnikova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 6
Common forms of hereditary spastic paraplegias
2019 · G. E. Rudenskaya, V. A. Kadnikova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 5
Hereditary spastic paraplegia type 4 (SPG4) in Russian patients
2019 · G. E. Rudenskaya, V. A. Kadnikova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 5
Spectrum of pathogenic variants and high prevalence of pathogenic BBS7 variants in Russian patients with Bardet–Biedl syndrome
2024 · M. Orlova, P. Gundorova, et al. · Frontiers in Genetics · 4
Наследственные спастические параплегии в эпоху секвенирования нового поколения: генетическое разнообразие, эпидемиология, проблемы классификации
2018 · Г. Е. Руденская, В. А. Кадникова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 4
Two Years of Expanded Newborn Screening in Russia: High-Throughput Detection of Inherited Metabolic Disorders by Tandem Mass Spectrometry with Next-Generation Sequencing Confirmation
2026 · Ekaterina Y. Zakharova, Galina V. Baydakova, et al. · International Journal of Neonatal Screening · 3
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The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study
2024 · Artem Borovikov, Nailya Galeeva, et al. · Human Mutation · 3
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AP4-assocated hereditary spastic paraplegias
2021 · G.E. Rudenskaya, D.M. Guseva, et al. · S S Korsakov Journal of Neurology and Psychiatry · 3
Molecular Genetic Diversity and DNA Diagnostics of Hereditary Spastic Paraplegia
2019 · V. A. Kadnikova, O. P. Ryzhkova, et al. · Biology Bulletin Reviews · 3
Rare autosomal recessive spastic paraplegias
2019 · Г.Е. Руденская, В.А. Кадникова, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 2
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Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas
2024 · Artem Borovikov, Andrey Marakhonov, et al. · Frontiers in Genetics · 1
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Developmental and epileptic encephalopathy produced by the ATP1A2 mutation
2024 · G.E. Rudenskaya, D.M. Guseva, et al. · S S Korsakov Journal of Neurology and Psychiatry · 1
A case of spastic paraplegia with SPG4 and SPG3 associated mutations
2023 · G.E. Rudenskaya, A.S. Kuchina, et al. · S S Korsakov Journal of Neurology and Psychiatry · 1
Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia
2022 · I. M. Khidiyatova, E. V. Saifullina, et al. · Russian Journal of Genetics · 1
Atypical spastic paraplegia type 4 due to p.Arg499His mutation in SPAST gene
2022 · G.E. Rudenskaya, E.A. Shestopalova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 1
Autosomal recessive spastic paraplegias types 7 and 76
2021 · Galina E. Rudenskaya, Varvara A. Kadnikova, et al. · Annals of Clinical and Experimental Neurology · 1
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Autosomal dominant spastic paraplegias
2021 · G.E. Rudenskaya, V.A. Kadnikova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 1
Spastic paraplegias types 11 and 15
2020 · Galina E. Rudenskaya, Varvara A. Kadnikova, et al. · Annals of Clinical and Experimental Neurology · 1
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НАСЛЕДСТВЕННЫЕ СПАСТИЧЕСКИЕ ПАРАПЛЕГИИ: МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКОЕ РАЗНООБРАЗИЕ И ДНК-ДИАГНОСТИКА, "Успехи современной биологии"
2018 · В. А. Кадникова, О. П. Рыжкова, et al. · Успехи современной биологии · 1
[Rigid spine congenital muscular dystrophy produced by SEPN1 mutations (RSMD1)].
2014 · G E Rudenskaia, V A Kadnikova, et al. · PubMed · 1
Molecular Genetic and Biochemical Characterization of Hyperphenylalaninemia Based on Expanded Neonatal Screening Data from 2023 to 2024 in the Russian Federation
2026 · Ekaterina E. Lotnik, Alena L. Chukhrova, et al. · International Journal of Molecular Sciences
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Сейпинопатии: клинические варианты наследственной моторно-сенсорной нейропатии и спастической параплегии, обусловленные мутациями в гене BSCL2, у пациентов из Волго-Уральского региона
2025 · Irina M. Khidiyatova, Elena V. Saifullina, et al. · RESEARCH RESULTS IN BIOMEDICINE
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Works count: 34
Citation count: 103
H-index: 5
I10-index: 3
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