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Galina E. Rudenskaya

Observed names: G E Rudenskaya, G. E. Rudenskaya, G.E. Rudenskaya, G.Rudenskaya, GE Rudenskaya, Galina Rudenskaya
ORCID: 0000-0002-8244-9367
Observed ORCID: 0000-0002-8244-9367
OpenAlex ID: A5019593630
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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Ataxia with Oculomotor Apraxia Type 4 with PNKP Common “Portuguese” and Novel Mutations in Two Belarusian Families
2019 · Galina Rudenskaya, Andrey Marakhonov, et al. · Journal of Pediatric Genetics · 21
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Emery‐Dreifuss syndrome: Genetic and clinical varieties
1994 · G. E. Rudenskaya, E. K. Ginter, et al. · American Journal of Medical Genetics · 16
Genetic and Clinical Spectrum of GNE Myopathy in Russia
2022 · Aysylu Murtazina, Sergey Nikitin, et al. · Genes · 14
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MLPA-based evidence for sequence gain: Pitfalls in confirmation and necessity for exclusion of false positives
2011 · Rita-Eva Varga, Rizwan Mumtaz, et al. · Analytical Biochemistry · 14
Complex Diagnostics of Non-Specific Intellectual Developmental Disorder
2022 · Olga Levchenko, Elena Dadali, et al. · International Journal of Molecular Sciences · 11
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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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SMN1 gene point mutations in type I–IV proximal spinal muscular atrophy patients with a single copy of SMN1
2015 · V. V. Zabnenkova, E. L. Dadali, et al. · Russian Journal of Genetics · 11
Laminopathies in Russian families
2008 · GE Rudenskaya, AV Polyakov, et al. · Clinical Genetics · 9
Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of “8p Inverted Duplication/Deletion Syndrome”
2022 · Darya A. Yurchenko, Marina E. Minzhenkova, et al. · Biomedicines · 6
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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
Rare Cause 5q SMA : Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN Locus
2025 · Kristina Mikhalchuk, Viktoria Zabnenkova, et al. · Clinical Genetics · 4
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Gerstmann—Sträussler disease: a familial case with common PRNP mutation and atypical features
2023 · G.E. Rudenskaya, F.A. Konovalov, et al. · S S Korsakov Journal of Neurology and Psychiatry · 4
Ataxia with oculomotor apraxia type 4 detected by next-generation sequencing
2018 · G. E. Rudenskaya, E. I. Surkova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 4
A case of rare hereditary Siddiqi syndrome with novel neuropsychiatric signs
2024 · G.E. Rudenskaya, F.M. Bostanova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 3
AP4-assocated hereditary spastic paraplegias
2021 · G.E. Rudenskaya, D.M. Guseva, et al. · S S Korsakov Journal of Neurology and Psychiatry · 3
Clinical, molecular, and genetic characteristics of the hereditary spastic paraplegia type 3
2020 · G.E. Rudenskaya, V.A. Kadnikova, et al. · Annals of Clinical and Experimental Neurology · 3
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Molecular Genetic Diversity and DNA Diagnostics of Hereditary Spastic Paraplegia
2019 · V. A. Kadnikova, O. P. Ryzhkova, et al. · Biology Bulletin Reviews · 3
Ataxia-telangiectasia with rare phenotype and unusual pedigree
2019 · G. E. Rudenskaya, O. A. Shchagina, et al. · S S Korsakov Journal of Neurology and Psychiatry · 3
A Spectrum of Pathogenic Variants in the LAMA2 Gene in the Russian Federation
2025 · Polina Chausova, Tatiana Cherevatova, et al. · International Journal of Molecular Sciences · 2
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Autosomal dominant intellectual disability associated with the MED13L gene
2022 · O. A. Levchenko, G. E. Rudenskaya, et al. · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) · 2
Structural organization of medical information as exemplified in pediatric neurological diagnosis
1995 · I. P. Lukashevich, R. I. Machinskaya, et al. · Biomedical Engineering · 2
The Russian FSHD registry: a first look at the cohort
2026 · Anna Kuchina, Darya Sherstyukova, et al. · Human Genetics · 1
Works count: 61
Citation count: 203
H-index: 9
I10-index: 8
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