Galina Baydakova - Concepedia

Author

Galina Baydakova

Research Centre for Medical Genetics ORCID

Also Known As

G. Baydakova, G. V. Baydakova, G.V. Baydakova, G.V. Baydakova Baydakova, Galina Baydakova, Galina V. Baydakova, Galina Viktorovna Baydakova, N.S. Nikolaeva

Publications

763

Citations

H-Index

Concepts

All Affiliations

Research Centre for Medical Genetics First Pavlov State Medical University of St. Petersburg Petersburg Nuclear Physics Institute Institute of the Human Brain National Medical Research Center for Obstetrics, Gynecology and Perinatology named after Academician V.I.Kulakov of the Ministry of Healthcare of the Russian Federation

About

Galina Baydakova is an author at Research Centre for Medical Genetics specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	307
2	Biochemistry	3	3	112
3	Public Health	1	1	16
4	Biology	1	1	30
5	Cell Biology	1	1	30

Galina Baydakova

Publications

645

Citations

H-Index

Page 1

	Year	Citations
Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson’s disease Alexander Emelyanov, Galina Baydakova, Pavel A. Andoskin, Neuroscience Letters Neurodegenerative DiseasesBiochemistryOligomeric α-SynucleinDegenerative PathologyNeurochemical Biomarkers	2016	75
Ambroxol increases glucocerebrosidase (GCase) activity and restores GCase translocation in primary patient-derived macrophages in Gaucher disease and Parkinsonism Alena E. Kopytova, Georgy N. Rychkov, Galina Baydakova, Parkinsonism & Related Disorders Neurodegenerative DiseasesGaucher DiseaseMedicineExperimental NeuropathologyPrimary Patient-derived Macrophages	2021	59
Microbiome-Metabolome Signature of Acute Kidney Injury Nadezda V. Andrianova, Vasily A. Popkov, Natalia Klimenko, Metabolites	2020	49
Effects of Traumatic Brain Injury on the Gut Microbiota Composition and Serum Amino Acid Profile in Rats Anastasiia Taraskina, Olga Ignatyeva, Darya Lisovaya, Cells	2022	49
Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations Sofya Pchelina, Galina Baydakova, Konstantin Senkevich, Movement Disorders	2018	43
Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up Patryk Lipiński, Ladislav Kuchař, Ekaterina Zakharova, Orphanet Journal of Rare Diseases	2019	35
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features Marcello Scala, Geok Lin Chua, Cheen Fei Chin, European Journal of Human Genetics Biallelic Mfsd2a VariantsDevelopmental AnomalyDevelopmental BiologyBrain DevelopmentGenetic Disorder	2020	33
Oxidized DNA induces an adaptive response in human fibroblasts Svetlana V. Kostyuk, V. J. Tabakov, Valerij V. Chestkov, Mutation research. Fundamental and molecular mechanisms of mutagenesis ChromatinGenome InstabilityDna DamageMolecular BiologyRedox Biology	2013	30
α-Galactosidase A/lysoGb3 ratio as a potential marker for Fabry disease in females Galina Baydakova, Alexandra Ilyushkina, Sergey Moiseev, Clinica Chimica Acta BiologyFabry DiseaseMendelian DisorderGeneticsPathogenesis	2019	30
Molecular and biochemical study of glutaric aciduria type 1 in 49 Russian families: nine novel mutations in the GCDH gene Marina V. Kurkina, Svetlana Mikhaylova, Galina Baydakova, Metabolic Brain Disease Glutaric AciduriaGenetic DisorderGeneticsInherited Metabolic DiseaseGlycobiology	2020	27

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