Viktoriia E. Baksheeva

678 total citations
39 papers, 487 citations indexed

About

Viktoriia E. Baksheeva is a scholar working on Molecular Biology, Ophthalmology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Viktoriia E. Baksheeva has authored 39 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 11 papers in Ophthalmology and 11 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Viktoriia E. Baksheeva's work include Ocular Surface and Contact Lens (11 papers), Glaucoma and retinal disorders (7 papers) and Retinal Diseases and Treatments (5 papers). Viktoriia E. Baksheeva is often cited by papers focused on Ocular Surface and Contact Lens (11 papers), Glaucoma and retinal disorders (7 papers) and Retinal Diseases and Treatments (5 papers). Viktoriia E. Baksheeva collaborates with scholars based in Russia, France and United States. Viktoriia E. Baksheeva's co-authors include Evgeni Yu. Zernii, Pavel P. Philippov, Andrey A. Zamyatnin, Ivan I. Senin, Sergei E. Permyakov, Olga Gancharova, Е. Н. Иомдина, О. А. Аверина, Д. В. Зинченко and Marina V. Serebryakova and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Medicinal Chemistry and Biochimica et Biophysica Acta (BBA) - Biomembranes.

In The Last Decade

Viktoriia E. Baksheeva

38 papers receiving 484 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Viktoriia E. Baksheeva Russia	12	249	174	104	99	45	39	487
Yoshihiro Takamura Japan	14	343 1.4×	186 1.1×	19 0.2×	133 1.3×	22 0.5×	38	578
Yueping Ren China	15	250 1.0×	167 1.0×	329 3.2×	206 2.1×	16 0.4×	30	732
Jacques Tréton France	16	530 2.1×	127 0.7×	31 0.3×	47 0.5×	28 0.6×	29	741
Pierrette Dayhaw‐Barker United States	10	497 2.0×	415 2.4×	26 0.3×	145 1.5×	85 1.9×	19	781
Sonia Guha United States	11	215 0.9×	126 0.7×	18 0.2×	32 0.3×	29 0.6×	21	483
Lisa Brennan United States	16	719 2.9×	158 0.9×	30 0.3×	83 0.8×	17 0.4×	29	852
Harshini Chakravarthy United States	10	192 0.8×	121 0.7×	15 0.1×	33 0.3×	36 0.8×	17	383
M V Riley United States	17	288 1.2×	191 1.1×	140 1.3×	183 1.8×	45 1.0×	29	616
О. А. Аверина Russia	9	206 0.8×	57 0.3×	35 0.3×	45 0.5×	15 0.3×	35	379
Abbi L. Engel United States	13	693 2.8×	312 1.8×	15 0.1×	115 1.2×	117 2.6×	21	948

Countries citing papers authored by Viktoriia E. Baksheeva

Since Specialization

Citations

This map shows the geographic impact of Viktoriia E. Baksheeva's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Viktoriia E. Baksheeva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Viktoriia E. Baksheeva more than expected).

Fields of papers citing papers by Viktoriia E. Baksheeva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Viktoriia E. Baksheeva. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Viktoriia E. Baksheeva. The network helps show where Viktoriia E. Baksheeva may publish in the future.

Co-authorship network of co-authors of Viktoriia E. Baksheeva

This figure shows the co-authorship network connecting the top 25 collaborators of Viktoriia E. Baksheeva. A scholar is included among the top collaborators of Viktoriia E. Baksheeva based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Viktoriia E. Baksheeva. Viktoriia E. Baksheeva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Baksheeva, Viktoriia E., Diane Allegro, Carine Derviaux, et al.. (2025). NanoDSF Screening for Anti-tubulin Agents Uncovers New Structure–Activity Insights. Journal of Medicinal Chemistry. 68(16). 17485–17498.

Chistyakov, Dmitry V., Olga Gancharova, Viktoriia E. Baksheeva, et al.. (2024). Targeting Oxidative Stress and Inflammation in the Eye: Insights from a New Model of Experimental Autoimmune Uveitis. International Journal of Molecular Sciences. 25(23). 12910–12910. 3 indexed citations

Eyraud, Rémi, Stéphane Ayache, Philipp O. Tsvetkov, et al.. (2023). Plasma nanoDSF Denaturation Profile at Baseline Is Predictive of Glioblastoma EGFR Status. Cancers. 15(3). 760–760. 4 indexed citations

Baksheeva, Viktoriia E., Rémi Eyraud, François Devred, et al.. (2023). Tear nanoDSF Denaturation Profile Is Predictive of Glaucoma. International Journal of Molecular Sciences. 24(8). 7132–7132. 2 indexed citations

Baksheeva, Viktoriia E., Philipp O. Tsvetkov, Arthur O. Zalevsky, et al.. (2022). Zinc Modulation of Neuronal Calcium Sensor Proteins: Three Modes of Interaction with Different Structural Outcomes. Biomolecules. 12(7). 956–956. 6 indexed citations

Baksheeva, Viktoriia E., Claude Villard, François Devred, et al.. (2021). Mechanism of Zn2+ and Ca2+ Binding to Human S100A1. Biomolecules. 11(12). 1823–1823. 4 indexed citations

Chistyakov, Dmitry V., Viktoriia E. Baksheeva, Sergei V. Goriainov, et al.. (2020). Mechanisms and Treatment of Light-Induced Retinal Degeneration-Associated Inflammation: Insights from Biochemical Profiling of the Aqueous Humor. International Journal of Molecular Sciences. 21(3). 704–704. 26 indexed citations

Chistyakov, Dmitry V., Olga Gancharova, Viktoriia E. Baksheeva, et al.. (2020). Inflammation in Dry Eye Syndrome: Identification and Targeting of Oxylipin-Mediated Mechanisms. Biomedicines. 8(9). 344–344. 11 indexed citations

Chistyakov, Dmitry V., Nadezhda V. Azbukina, Alina A. Astakhova, et al.. (2020). Comparative lipidomic analysis of inflammatory mediators in the aqueous humor and tear fluid of humans and rabbits. Metabolomics. 16(2). 27–27. 10 indexed citations

10.

Makarov, Vladimir, Lyudmila V. Savvateeva, Marina V. Serebryakova, et al.. (2019). Novel applications of modification of thiol enzymes and redox-regulated proteins using S-methyl methanethiosulfonate (MMTS). Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1867(11). 140259–140259. 12 indexed citations

11.

Zernii, Evgeni Yu., Viktoriia E. Baksheeva, Alexei S. Kazakov, et al.. (2018). Photoreceptor calcium sensor proteins in detergent-resistant membrane rafts are regulated via binding to caveolin-1. Cell Calcium. 73. 55–69. 11 indexed citations

12.

Baksheeva, Viktoriia E., Olga Gancharova, Pavel P. Philippov, et al.. (2018). Suppression of Light-Induced Oxidative Stress in the Retina by Mitochondria-Targeted Antioxidant. Antioxidants. 8(1). 3–3. 38 indexed citations

13.

Baksheeva, Viktoriia E., Olga Gancharova, Е. Н. Иомдина, et al.. (2018). Iatrogenic Damage of Eye Tissues: Current Problems and Possible Solutions. Biochemistry (Moscow). 83(12-13). 1563–1574. 6 indexed citations

14.

Zernii, Evgeni Yu., Olga Gancharova, Andrey A. Zamyatnin, et al.. (2018). Mitochondria-targeted antioxidant SKQ1 protects cornea from oxidative damage induced by ultraviolet irradiation and mechanical injury. BMC Ophthalmology. 18(1). 336–336. 21 indexed citations

15.

Zernii, Evgeni Yu., Viktoriia E. Baksheeva, Olga Gancharova, et al.. (2018). Mitochondria-targeted antioxidant SkQ1 improves corneal healing after UV-induced damage in rabbits. 8(1). 215–215. 4 indexed citations

16.

Zernii, Evgeni Yu., Olga Gancharova, Viktoriia E. Baksheeva, et al.. (2017). Mitochondria‐Targeted Antioxidant SkQ1 Prevents Anesthesia‐Induced Dry Eye Syndrome. Oxidative Medicine and Cellular Longevity. 2017(1). 9281519–9281519. 44 indexed citations

17.

Zernii, Evgeni Yu., Viktoriia E. Baksheeva, Е. Н. Иомдина, et al.. (2016). Rabbit Models of Ocular Diseases: New Relevance for Classical Approaches. CNS & Neurological Disorders - Drug Targets. 15(3). 267–291. 94 indexed citations

18.

Baksheeva, Viktoriia E., Д. В. Зинченко, Marina V. Serebryakova, et al.. (2015). Ca<sup>2+</sup>-Myristoyl Switch in Neuronal Calcium Sensor-1: A Role of C-Terminal Segment. CNS & Neurological Disorders - Drug Targets. 14(4). 437–451. 14 indexed citations

19.

Antonenko, Yuri N., Viktoriia E. Baksheeva, Tatyana I. Rokitskaya, et al.. (2015). Intramitochondrial accumulation of cationic Atto520-biotin proceeds via voltage-dependent slow permeation through lipid membrane. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1848(6). 1277–1284. 3 indexed citations

20.

Zernii, Evgeni Yu., Ilya I. Grigoriev, Konstantin E. Komolov, et al.. (2013). New mechanisms of regulatory activity of photoreceptor calcium sensors. FEBS Journal. 280. 438–439. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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