M. Yu. Vyssokikh

3.4k total citations
51 papers, 1.7k citations indexed

About

M. Yu. Vyssokikh is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, M. Yu. Vyssokikh has authored 51 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 10 papers in Physiology and 7 papers in Clinical Biochemistry. Recurrent topics in M. Yu. Vyssokikh's work include Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (15 papers) and Metabolism and Genetic Disorders (7 papers). M. Yu. Vyssokikh is often cited by papers focused on Mitochondrial Function and Pathology (33 papers), ATP Synthase and ATPases Research (15 papers) and Metabolism and Genetic Disorders (7 papers). M. Yu. Vyssokikh collaborates with scholars based in Russia, Germany and Tajikistan. M. Yu. Vyssokikh's co-authors include Dieter Brdiczka, Vladimir P. Skulachev, Dmitry B. Zorov, Maxim V. Skulachev, Egor Y. Plotnikov, Н. К. Исаев, Fedor F. Severin, Konstantin G. Lyamzaev, Ljubava D. Zorova and Boris V. Chernyak and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Physiological Reviews.

In The Last Decade

M. Yu. Vyssokikh

47 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Yu. Vyssokikh Russia 20 1.1k 263 169 131 120 51 1.7k
Jaime Santo‐Domingo Switzerland 22 1.4k 1.2× 375 1.4× 142 0.8× 73 0.6× 321 2.7× 42 2.0k
Daniel J.M. Fernández‐Ayala Spain 22 1.3k 1.1× 272 1.0× 107 0.6× 45 0.3× 101 0.8× 32 1.8k
Filippo Scialò United Kingdom 15 665 0.6× 256 1.0× 76 0.4× 49 0.4× 86 0.7× 23 1.2k
Douglas Hinerfeld United States 14 785 0.7× 343 1.3× 103 0.6× 50 0.4× 107 0.9× 24 1.4k
Shona A. Mookerjee United States 19 1.5k 1.3× 578 2.2× 123 0.7× 77 0.6× 235 2.0× 24 2.3k
Anna Maria Sardanelli Italy 30 1.6k 1.4× 277 1.1× 319 1.9× 73 0.6× 192 1.6× 61 2.2k
Johan Palmfeldt Denmark 32 1.5k 1.3× 267 1.0× 304 1.8× 52 0.4× 139 1.2× 110 2.5k
Hikari Taka Japan 25 1.2k 1.0× 615 2.3× 65 0.4× 75 0.6× 155 1.3× 67 2.2k
Tina Wenz Germany 18 1.0k 0.9× 355 1.3× 196 1.2× 32 0.2× 68 0.6× 25 1.3k
Marta Artal‐Sanz Spain 21 1.6k 1.4× 255 1.0× 125 0.7× 38 0.3× 107 0.9× 37 2.2k

Countries citing papers authored by M. Yu. Vyssokikh

Since Specialization
Citations

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

Fields of papers citing papers by M. Yu. Vyssokikh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Yu. Vyssokikh. 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 M. Yu. Vyssokikh. The network helps show where M. Yu. Vyssokikh may publish in the future.

Co-authorship network of co-authors of M. Yu. Vyssokikh

This figure shows the co-authorship network connecting the top 25 collaborators of M. Yu. Vyssokikh. A scholar is included among the top collaborators of M. Yu. Vyssokikh 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 M. Yu. Vyssokikh. M. Yu. Vyssokikh 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
2.
Orekhov, Alexander N., Vasily V. Sinyov, M. Yu. Vyssokikh, et al.. (2024). Relationship between Cellular Oxygen Consumption and Atherosclerosis-associated Mitochondrial Mutations (Variants of the Mitochondrial Genome). Current Medicinal Chemistry. 33(8). 1538–1550. 1 indexed citations
3.
Rubtsova, Maria P., et al.. (2024). Telomere Reprogramming and Cellular Metabolism: Is There a Link?. International Journal of Molecular Sciences. 25(19). 10500–10500. 2 indexed citations
4.
Vyssokikh, M. Yu., et al.. (2024). Age-Dependent Changes in the Production of Mitochondrial Reactive Oxygen Species in Human Skeletal Muscle. Biochemistry (Moscow). 89(2). 299–312.
5.
Shabalina, Irina G., Daniel Edgar, Anastasia Kalinovich, et al.. (2024). Enhanced ROS Production in Mitochondria from Prematurely Aging mtDNA Mutator Mice. Biochemistry (Moscow). 89(2). 279–298. 5 indexed citations
6.
Аверина, О. А., Vadim Kumeiko, Maria V. Marey, et al.. (2023). Kidney-Related Function of Mitochondrial Protein Mitoregulin. International Journal of Molecular Sciences. 24(10). 9106–9106. 7 indexed citations
7.
Skulachev, Vladimir P., M. Yu. Vyssokikh, Boris V. Chernyak, et al.. (2023). Mitochondrion-targeted antioxidant SkQ1 prevents rapid animal death caused by highly diverse shocks. Scientific Reports. 13(1). 4326–4326. 16 indexed citations
8.
Ашапкин, В. В., et al.. (2019). Biological Diversity and Remodeling of Cardiolipin in Oxidative Stress and Age-Related Pathologies. Biochemistry (Moscow). 84(12-13). 1469–1483. 13 indexed citations
9.
Донников, А. Е., et al.. (2017). The role of adipokines and gene regulators adipokines in the effectiveness of assisted reproductive technology programs in overweight patients. Akusherstvo i ginekologiia. 2_2017. 71–78. 1 indexed citations
10.
Vyssokikh, M. Yu., et al.. (2015). Methodology for Use of Mitochondria-Targeted Cations in the Field of Oxidative Stress-Related Research. Methods in molecular biology. 1265. 149–159. 10 indexed citations
11.
Vyssokikh, M. Yu., Olga Kolesnikova, Nina Entelis, et al.. (2012). Isoform porin 2 is involved in tRNALys transport from cytosol to mitochondria in yeast. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1817. S124–S125. 4 indexed citations
12.
Mufazalov, Ilgiz A., Boris V. Chernyak, Olga Yu. Pletjushkina, et al.. (2009). Preparation and characterization of mouse embryonic fibroblasts with K72W mutation in somatic cytochrome C gene. Molecular Biology. 43(4). 596–603. 7 indexed citations
13.
Tashlitsky, Vadim N., Vitaliy Yu. Markov, Galina A. Korshunova, et al.. (2009). Molecular mechanisms of transformation of SkQ mitotropic quinones and the search for new approaches to creation of selective free radical traps. Biochemistry (Moscow). 74(10). 1114–1124. 2 indexed citations
14.
Vyssokikh, M. Yu., et al.. (2008). Interaction of positively charged ubiquinone analog (MitoQ10) with DT-diaphorase from liver mitochondria. Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology. 2(1). 33–39. 3 indexed citations
15.
Severina, Inna I., M. Yu. Vyssokikh, Antonina V. Pustovidko, et al.. (2007). Effects of lipophilic dications on planar bilayer phospholipid membrane and mitochondria. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1767(9). 1164–1168. 10 indexed citations
16.
Plotnikov, Egor Y., A.V. Kazachenko, M. Yu. Vyssokikh, et al.. (2007). The role of mitochondria in oxidative and nitrosative stress during ischemia/reperfusion in the rat kidney. Kidney International. 72(12). 1493–1502. 173 indexed citations
17.
Knorre, Dmitry A., V.I. Dedukhova, M. Yu. Vyssokikh, & E. N. Mokhova. (2003). Cyclosporin A-Sensitive Cytochrome c Release and Activation of External Pathway of NADH Oxidation in Liver Mitochondria Due to Pore Opening by Acidification of Phosphate-Containing Incubation Medium. Bioscience Reports. 23(2-3). 67–75. 8 indexed citations
18.
Vyssokikh, M. Yu., Ljubava D. Zorova, Dmitry B. Zorov, et al.. (2003). The intra-mitochondrial cytochrome c distribution varies correlated to the formation of a complex between VDAC and the adenine nucleotide translocase: this affects Bax-dependent cytochrome c release. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1644(1). 27–36. 45 indexed citations
19.
Pletjushkina, Olga Yu., A. V. Avetisyan, L. E. Bakeeva, et al.. (2002). Oligomycin, inhibitor of the F0 part of H+-ATP-synthase, suppresses the TNF-induced apoptosis. Oncogene. 21(53). 8149–8157. 136 indexed citations
20.
Манухов, И. В., et al.. (1999). Folding and refolding of thermolabile and thermostable bacterial luciferases: the role of DnaKJ heat‐shock proteins. FEBS Letters. 448(2-3). 265–268. 34 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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