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Polina G. Tsygankova

Observed names: P G Tsygankova, P. G. Tsygankova, P. Tsygankova, P.G. Tsygankova, Polina Tsygankova, Tsygankova, Polina G, П Г Цыганкова, П.Г. Цыганкова
ORCID: 0000-0003-3998-3609
Observed ORCID: 0000-0003-3998-3609
OpenAlex ID: A5089485744
Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy
2021 · Sarah L. Stenton, Natalia L. Sheremet, et al. · Journal of Clinical Investigation · 161
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Plasma FGF‐21 and GDF‐15 are elevated in different inherited metabolic diseases and are not diagnostic for mitochondrial disorders
2019 · Polina G. Tsygankova, Yulia S. Itkis, et al. · Journal of Inherited Metabolic Disease · 49
Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy
2019 · Tatiana D. Krylova, Natalia L. Sheremet, et al. · Mitochondrion · 23
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia
2023 · Denis Kistol, Polina Tsygankova, et al. · International Journal of Molecular Sciences · 20
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Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes
2021 · I.O. Bychkov, Y.S. Itkis, et al. · Mitochondrion · 17
Diagnosing pediatric mitochondrial disease: lessons from 2,000 exomes
2021 · Sarah L. Stenton, Masaru Shimura, et al. · medRxiv · 14
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Characteristics of changes in retinal and optic nerve microvascularisature in Leber hereditary optic neuropathy patients seen with optical coherence tomography angiography
2020 · N.L. Sheremet, M.S. Shmelkova, et al. · Russian Annals of Ophthalmology · 13
New possibilities in diagnosis of hereditary optic neuropathies
2021 · N.L. Sheremet, T.D. Krylova, et al. · Russian Annals of Ophthalmology · 12
Previously unclassified mutation of mtDNA m.3472T>C: Evidence of pathogenicity in Leber’s hereditary optic neuropathy
2016 · N. L. Sheremet, T. A. Nevinitsyna, et al. · Biochemistry (Moscow) · 11
POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adults
2021 · Evgenii Nuzhnyi, Yury Seliverstov, et al. · Clinical Neurology and Neurosurgery · 10
Pleiotropic effects of MORC2 derive from its epigenetic signature
2025 · Fatemeh Peymani, Tomohiro Ebihara, et al. · Brain · 8
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Optic neuropathies as an interdisciplinary subject of research
2023 · N.L. Sheremet, D.D. Eliseeva, et al. · Russian Annals of Ophthalmology · 7
Leber’s hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation
2022 · N.A. Andreeva, Yu.K. Murakhovskaya, et al. · Russian Annals of Ophthalmology · 6
Autosomal recessive optic neuropathies: genetic variants, clinical manifestations
2022 · Yu.K. Murakhovskaya, N.L. Sheremet, et al. · Russian Annals of Ophthalmology · 5
Exploring the Phenotypic Heterogeneity and Bioenergetic Profile of the m.13513G>A mtDNA Substitution: A Heteroplasmy Perspective
2025 · Tatiana Krylova, Yulia Itkis, et al. · International Journal of Molecular Sciences · 4
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Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber’s hereditary optic neuropathy
2023 · N.A. Andreeva, Yu.K. Murakhovskaya, et al. · Russian Annals of Ophthalmology · 4
New Acylcarnitine Ratio as a Reliable Indicator of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
2023 · Galina V. Baydakova, Polina G. Tsygankova, et al. · International Journal of Neonatal Screening · 4
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Hereditary optic neuropathy associated with demyelinating diseases of the central nervous system
2023 · D.D. Eliseeva, A.K. Kalashnikova, et al. · S S Korsakov Journal of Neurology and Psychiatry · 4
Clinical features of vision improvement in patients with Leber hereditary optic neuropathy
2020 · N.L. Sheremet, N.A. Andreeva, et al. · POINT OF VIEW EAST – WEST · 4
Infantile and early childhood onset of mitochondrial myopathy due to mutations in the TK2 gene with a phenotype of spinal muscular atrophy 5q: the first cases in Russia
2019 · S. A. Kurbatov, P. G. Tsygankova, et al. · Neuromuscular Diseases · 4
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Molecular Genetics and Clinical Aspects of Monogenic Diabetes Mellitus
2012 · V. A. Peterkova, T. L. Kuraeva, et al. · Annals of the Russian academy of medical sciences · 4
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A New Case of Mitochondrial RNA Helicase SUPV3L1-Associated Neurodegenerative Disease: Ataxia, Spasticity, Optic Atrophy, and Skin Hypopigmentation (ASOASH)
2024 · Polina Tsygankova, Denis Chistol, et al. · Genes · 3
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New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants
2024 · Denis Kistol, Polina Tsygankova, et al. · International Journal of Molecular Sciences · 3
High-Resolution Respirometry in Diagnostics of Mitochondrial Diseases Caused by Mitochondrial Complex I Deficiency
2018 · T. D. Krylova, P. G. Tsygankova, et al. · Biochemistry (Moscow) Supplement Series B Biomedical Chemistry · 3
Differential diagnosis of mitochondrial neurogastrointestinal encephalomyopathy. First clinical description in Russia
2015 · S. A. Kurbatov, V. P. Fedotov, et al. · Neuromuscular Diseases · 3
Works count: 65
Citation count: 422
H-index: 10
I10-index: 10
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