Alexander V. Bogachev

2.1k total citations · 1 hit paper
70 papers, 1.6k citations indexed

About

Alexander V. Bogachev is a scholar working on Molecular Biology, Plant Science and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alexander V. Bogachev has authored 70 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 14 papers in Plant Science and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alexander V. Bogachev's work include Photosynthetic Processes and Mechanisms (31 papers), Photoreceptor and optogenetics research (12 papers) and ATP Synthase and ATPases Research (9 papers). Alexander V. Bogachev is often cited by papers focused on Photosynthetic Processes and Mechanisms (31 papers), Photoreceptor and optogenetics research (12 papers) and ATP Synthase and ATPases Research (9 papers). Alexander V. Bogachev collaborates with scholars based in Russia, Finland and Tajikistan. Alexander V. Bogachev's co-authors include Yulia V. Bertsova, Vladimir P. Skulachev, Michael I. Verkhovsky, Alexander A. Baykov, Dmitry A. Bloch, Marina Verkhovskaya, Alexander I. Shestopalov, Blanca Barquera, Marina V. Serebryakova and Mårten Wikström and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Applied and Environmental Microbiology.

In The Last Decade

Alexander V. Bogachev

66 papers receiving 1.6k citations

Hit Papers

OCTDL: Optical Coherence Tomography Dataset for Image-Bas... 2024 2026 2025 2024 10 20 30 40

Peers

Alexander V. Bogachev
Blanca Barquera United States
Richard Little United Kingdom
Arthur A. Guffanti United States
Gareth Butland United States
Christopher J. Law United Kingdom
A A Guffanti United States
Erik Vijgenboom Netherlands
Susan J. Rosser United Kingdom
Blanca Barquera United States
Alexander V. Bogachev
Citations per year, relative to Alexander V. Bogachev Alexander V. Bogachev (= 1×) peers Blanca Barquera

Countries citing papers authored by Alexander V. Bogachev

Since Specialization
Citations

This map shows the geographic impact of Alexander V. Bogachev'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 Alexander V. Bogachev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexander V. Bogachev more than expected).

Fields of papers citing papers by Alexander V. Bogachev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander V. Bogachev. 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 Alexander V. Bogachev. The network helps show where Alexander V. Bogachev may publish in the future.

Co-authorship network of co-authors of Alexander V. Bogachev

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander V. Bogachev. A scholar is included among the top collaborators of Alexander V. Bogachev 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 Alexander V. Bogachev. Alexander V. Bogachev is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Proskurina, Anastasia S., Genrikh S. Ritter, Yaroslav R. Efremov, et al.. (2025). A concept of natural genome reconstruction. Part 2. Effect of extracellular double-stranded DNA fragments on hematopoietic stem cells. Vavilov Journal of Genetics and Breeding. 28(8). 993–1007.
2.
Bertsova, Yulia V., et al.. (2024). Acrylate reductase of an anaerobic electron transport chain of the marine bacterium shewanella woodyi. 89(4). 666–676. 1 indexed citations
3.
Борисов, Василий, et al.. (2024). OCTDL: Optical Coherence Tomography Dataset for Image-Based Deep Learning Methods. Scientific Data. 11(1). 365–365. 41 indexed citations breakdown →
4.
Bertsova, Yulia V., Mahir D. Mamedov, & Alexander V. Bogachev. (2019). Na+-Translocating Ferredoxin:NAD+ Oxidoreductase Is a Component of Photosynthetic Electron Transport Chain in Green Sulfur Bacteria. Biochemistry (Moscow). 84(11). 1403–1410. 4 indexed citations
5.
Serebryakova, Marina V., Yulia V. Bertsova, С. С. Соколов, et al.. (2018). Catalytically important flavin linked through a phosphoester bond in a eukaryotic fumarate reductase. Biochimie. 149. 34–40. 11 indexed citations
6.
Kulik, Leonid V., Yulia V. Bertsova, & Alexander V. Bogachev. (2018). EPR evidence for a fast-relaxing iron center in Na+-translocating NADH:quinone-oxidoreductase. Journal of Inorganic Biochemistry. 184. 15–18. 1 indexed citations
7.
Bertsova, Yulia V., Alexander V. Bogachev, & Vladimir P. Skulachev. (2015). Proteorhodopsin from Dokdonia sp. PRO95 is a light-driven Na+-pump. Biochemistry (Moscow). 80(4). 449–454. 17 indexed citations
8.
Borshchevskiy, Valentin, Ekaterina Round, Yulia V. Bertsova, et al.. (2015). Structural and Functional Investigation of Flavin Binding Center of the NqrC Subunit of Sodium-Translocating NADH:Quinone Oxidoreductase from Vibrio harveyi. PLoS ONE. 10(3). e0118548–e0118548. 15 indexed citations
9.
Bertsova, Yulia V., et al.. (2013). Localization-controlled specificity of FAD:threonine flavin transferases in Klebsiella pneumoniae and its implications for the mechanism of Na+-translocating NADH:quinone oxidoreductase. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1837(7). 1122–1129. 19 indexed citations
10.
Verkhovsky, Michael I. & Alexander V. Bogachev. (2010). Sodium-translocating NADH:quinone oxidoreductase as a redox-driven ion pump. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797(6-7). 738–746. 77 indexed citations
11.
Bertsova, Yulia V., et al.. (2008). Site-directed mutagenesis of conserved cysteine residues in NqrD and NqrE subunits of Na+-translocating NADH:quinone oxidoreductase. Biochemistry (Moscow). 73(2). 123–129. 13 indexed citations
12.
Попов, В. Н., et al.. (2004). NADH Oxidation by Mitochondria from the Thermogenic Plant Arum orientale. Biochemistry (Moscow). 69(5). 580–584. 7 indexed citations
13.
Bogachev, Alexander V., et al.. (2002). Operation of the cbb3-Type Terminal Oxidase in Azotobacter vinelandii. Biochemistry (Moscow). 67(6). 622–626. 10 indexed citations
14.
Bogachev, Alexander V., Yulia V. Bertsova, E. K. Ruuge, Mårten Wikström, & Michael I. Verkhovsky. (2002). Kinetics of the spectral changes during reduction of the Na+-motive NADH:quinone oxidoreductase from Vibrio harveyi. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1556(2-3). 113–120. 34 indexed citations
15.
Bertsova, Yulia V., Alexander V. Bogachev, & Vladimir P. Skulachev. (1997). Generation of protonic potential by the bd‐type quinol oxidase of Azotobacter vinelandii. FEBS Letters. 414(2). 369–372. 40 indexed citations
16.
Bogachev, Alexander V., et al.. (1995). Induction of the Escherichia Coli Cytochrome d by Low ΔH+ and by Sodium Ions. European Journal of Biochemistry. 232(1). 304–308. 24 indexed citations
17.
Wikström, Mårten, Alexander V. Bogachev, Moshe Finel, et al.. (1994). Mechanism of proton translocation by the respiratory oxidases. The histidine cycle. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1187(2). 106–111. 94 indexed citations
18.
Bogachev, Alexander V., et al.. (1993). The role of protonic and sodium potentials in the motility of E. coli and Bacillus FTU. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1142(3). 321–326. 9 indexed citations
19.
Avetisyan, A. V., et al.. (1993). ATP‐driven Na+ transport and Na+‐dependent ATP synthesis in Escherichia coli grown at low \ΔgmH+. FEBS Letters. 317(3). 267–270. 23 indexed citations
20.
Avetisyan, A. V., et al.. (1992). Involvement of a d‐type oxidase in the Na+‐motive respiratory chain of Escherichia coli growing under low Δ\gmH+ conditions. FEBS Letters. 306(2-3). 199–202. 40 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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