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Galina Baydakova

Observed names: G Baidakova, G V Baydakova, G. Baydakova, G. V. Baidakova, G. V. Baydakova, G.     V. Baidakova, G.V. Baydakova, G.V. Baydakova Baydakova, Galina V. Baydakova, Galina V. Baydakova, Galina Viktorovna Baydakova
ORCID: 0000-0001-8806-5287
Observed ORCID: 0000-0001-8806-5287
OpenAlex ID: A5078283527
Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson’s disease
2016 · S. Pchelina, A. Emelyanov, et al. · Neuroscience Letters · 82
Ambroxol increases glucocerebrosidase (GCase) activity and restores GCase translocation in primary patient-derived macrophages in Gaucher disease and Parkinsonism
2021 · A.E. Kopytova, G.N. Rychkov, et al. · Parkinsonism & Related Disorders · 70
Effects of Traumatic Brain Injury on the Gut Microbiota Composition and Serum Amino Acid Profile in Rats
2022 · Anastasiia Taraskina, Olga Ignatyeva, et al. · Cells · 66
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Microbiome-Metabolome Signature of Acute Kidney Injury
2020 · Nadezda V. Andrianova, Vasily A. Popkov, et al. · Metabolites · 51
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Extracellular DNA oxidation stimulates activation of NRF2 and reduces the production of ROS in human mesenchymal stem cells
2012 · Polina Loseva, S Kostyuk, et al. · Expert Opinion on Biological Therapy · 50
Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations
2018 · Sofya Pchelina, Galina Baydakova, et al. · Movement Disorders · 48
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features
2020 · Marcello Scala, Geok Lin Chua, et al. · European Journal of Human Genetics · 41
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Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up
2019 · Patryk Lipiński, Ladislav Kuchar, et al. · Orphanet Journal of Rare Diseases · 37
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α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females
2019 · G.V. Baydakova, A.A. Ilyushkina, et al. · Clinica Chimica Acta · 35
Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl
2019 · A. N. Semyachkina, E. Y. Voskoboeva, et al. · BMC Medical Genetics · 31
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Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson’s Disease
2023 · Elena V. Grigor’eva, Alena E. Kopytova, et al. · International Journal of Molecular Sciences · 30
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Oxidized DNA induces an adaptive response in human fibroblasts
2013 · Svetlana V. Kostyuk, Viacheslav J. Tabakov, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 29
Advanced neonatal screening for hereditary diseases in Russia: first results and future prospects
2024 · S.V. Voronin, E.Yu. Zakharova, et al. · PEDIATRIA Journal named after G N SPERANSKY · 28
Molecular and biochemical study of glutaric aciduria type 1 in 49 Russian families: nine novel mutations in the GCDH gene
2020 · Marina V. Kurkina, Svetlana V. Mihaylova, et al. · Metabolic Brain Disease · 26
Impaired Sphingolipid Hydrolase Activities in Dementia with Lewy Bodies and Multiple System Atrophy
2022 · T. S. Usenko, K. A. Senkevich, et al. · Molecular Neurobiology · 23
Mitochondrial peptide Mtln contributes to oxidative metabolism in mice
2022 · Olga A. Averina, Oleg A. Permyakov, et al. · Biochimie · 22
Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson’s Disease
2023 · Alena E. Kopytova, George N. Rychkov, et al. · International Journal of Molecular Sciences · 19
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Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?
2022 · Alena E. Kopytova, Tatiana S. Usenko, et al. · Movement Disorders · 18
Oxysterol/chitotriosidase based selective screening for Niemann-Pick type C in infantile cholestasis syndrome patients
2019 · Anna V. Degtyareva, Tatiana Y. Proshlyakova, et al. · BMC Medical Genetics · 18
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Complex Transposon Insertion as a Novel Cause of Pompe Disease
2021 · Igor Bychkov, Galina Baydakova, et al. · International Journal of Molecular Sciences · 17
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Human Peripheral Blood Macrophages As a Model for Studying Glucocerebrosidase Dysfunction
2019 · M. A. Nikolaev, A. E. Kopytova, et al. · Cell and Tissue Biology · 16
Altered Sphingolipid Hydrolase Activities and Alpha-Synuclein Level in Late-Onset Schizophrenia
2023 · Tatiana Usenko, Anastasia Bezrukova, et al. · Metabolites · 15
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BH4-deficient hyperphenylalaninemia in Russia
2021 · Polina Gundorova, Irina A. Kuznetcova, et al. · PLoS ONE · 15
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Elevated LysoGb3 Concentration in the Neuronopathic Forms of Mucopolysaccharidoses
2020 · Galina Baydakova, Alex Ilyushkina, et al. · Diagnostics · 15
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The role of tandem mass spectrometry in the diagnosis of inherited metabolic diseases
2018 · G. V. Baydakova, T. A. Ivanova, et al. · Russian Journal of Pediatric Hematology and Oncology · 15
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Works count: 85
Citation count: 985
H-index: 18
I10-index: 29
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