T. A. Trendeleva

556 total citations
20 papers, 344 citations indexed

About

T. A. Trendeleva is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Spectroscopy. According to data from OpenAlex, T. A. Trendeleva has authored 20 papers receiving a total of 344 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Spectroscopy. Recurrent topics in T. A. Trendeleva's work include Mitochondrial Function and Pathology (13 papers), Neuroscience and Neuropharmacology Research (4 papers) and Lipid Membrane Structure and Behavior (4 papers). T. A. Trendeleva is often cited by papers focused on Mitochondrial Function and Pathology (13 papers), Neuroscience and Neuropharmacology Research (4 papers) and Lipid Membrane Structure and Behavior (4 papers). T. A. Trendeleva collaborates with scholars based in Russia, Finland and Tajikistan. T. A. Trendeleva's co-authors include R. A. Zvyagilskaya, Anton G. Rogov, Inna I. Severina, Vladimir P. Skulachev, Boris V. Chernyak, Yuri N. Antonenko, Konstantin G. Lyamzaev, Tatyana I. Rokitskaya, Ruben A. Simonyan and Dmitry A. Cherepanov and has published in prestigious journals such as FEBS Letters, Biochimica et Biophysica Acta (BBA) - Bioenergetics and Oxidative Medicine and Cellular Longevity.

In The Last Decade

T. A. Trendeleva

20 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. A. Trendeleva Russia 12 242 48 32 27 27 20 344
Anton G. Rogov Russia 12 246 1.0× 36 0.8× 34 1.1× 29 1.1× 15 0.6× 25 373
Chunhuan Jin Japan 11 210 0.9× 18 0.4× 79 2.5× 14 0.5× 27 1.0× 22 459
Antonina V. Pustovidko Russia 9 353 1.5× 93 1.9× 7 0.2× 51 1.9× 39 1.4× 13 468
Serena Leoni Italy 6 251 1.0× 37 0.8× 14 0.4× 9 0.3× 28 1.0× 6 352
Sergio F. Martín Spain 14 414 1.7× 69 1.4× 6 0.2× 28 1.0× 12 0.4× 17 554
Masood‐ul‐Hassan Javed United Kingdom 7 255 1.1× 49 1.0× 5 0.2× 24 0.9× 31 1.1× 12 394
Dorothy M. Morré United States 9 226 0.9× 17 0.4× 12 0.4× 26 1.0× 16 0.6× 14 334
Egīls Bisenieks Latvia 11 153 0.6× 40 0.8× 8 0.3× 138 5.1× 23 0.9× 37 350
Ludovica Morera Italy 10 354 1.5× 34 0.7× 28 0.9× 49 1.8× 62 2.3× 10 584
Siwon Kim South Korea 11 216 0.9× 31 0.6× 18 0.6× 78 2.9× 33 1.2× 18 425

Countries citing papers authored by T. A. Trendeleva

Since Specialization
Citations

This map shows the geographic impact of T. A. Trendeleva'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 T. A. Trendeleva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. A. Trendeleva more than expected).

Fields of papers citing papers by T. A. Trendeleva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. A. Trendeleva. 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 T. A. Trendeleva. The network helps show where T. A. Trendeleva may publish in the future.

Co-authorship network of co-authors of T. A. Trendeleva

This figure shows the co-authorship network connecting the top 25 collaborators of T. A. Trendeleva. A scholar is included among the top collaborators of T. A. Trendeleva 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 T. A. Trendeleva. T. A. Trendeleva 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.
Rogov, Anton G., et al.. (2020). Mitochondrial Dysfunctions May Be One of the Major Causative Factors Underlying Detrimental Effects of Benzalkonium Chloride. Oxidative Medicine and Cellular Longevity. 2020. 1–14. 27 indexed citations
2.
Rogov, Anton G., et al.. (2019). SkQThy, a novel and promising mitochondria-targeted antioxidant. Mitochondrion. 49. 206–216. 15 indexed citations
3.
Trendeleva, T. A. & R. A. Zvyagilskaya. (2018). Retrograde Signaling as a Mechanism of Yeast Adaptation to Unfavorable Factors. Biochemistry (Moscow). 83(2). 98–106. 8 indexed citations
4.
Rogov, Anton G., et al.. (2018). New Data on Effects of SkQ1 and SkQT1 on Rat Liver Mitochondria and Yeast Cells. Biochemistry (Moscow). 83(5). 552–561. 9 indexed citations
5.
Rogov, Anton G., et al.. (2016). More about interactions of rhodamine 19 butyl ester with rat liver mitochondria. Biochemistry (Moscow). 81(4). 432–438. 8 indexed citations
6.
Trendeleva, T. A., et al.. (2014). Mechanisms of sensing and adaptive responses to low oxygen conditions in mammals and yeasts. Biochemistry (Moscow). 79(8). 750–760. 9 indexed citations
7.
Khailova, Ljudmila S., Д. Н. Силачев, Tatyana I. Rokitskaya, et al.. (2014). A short-chain alkyl derivative of Rhodamine 19 acts as a mild uncoupler of mitochondria and a neuroprotector. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1837(10). 1739–1747. 46 indexed citations
8.
Chernyak, Boris V., Yuri N. Antonenko, L. V. Domnina, et al.. (2013). Novel Penetrating Cations for Targeting Mitochondria. Current Pharmaceutical Design. 19(15). 2795–2806. 15 indexed citations
9.
Severina, Inna I., Fedor F. Severin, Galina A. Korshunova, et al.. (2013). In search of novel highly active mitochondria‐targeted antioxidants: Thymoquinone and its cationic derivatives. FEBS Letters. 587(13). 2018–2024. 57 indexed citations
10.
Trendeleva, T. A., et al.. (2012). Interaction of tetraphenylphosphonium and dodecyltriphenylphosphonium with lipid membranes and mitochondria. Biochemistry (Moscow). 77(9). 1021–1028. 19 indexed citations
11.
Trendeleva, T. A., et al.. (2012). Role of charge screening and delocalization for lipophilic cation permeability of model and mitochondrial membranes. Mitochondrion. 13(5). 500–506. 24 indexed citations
12.
Pustovidko, Antonina V., Tatyana I. Rokitskaya, Inna I. Severina, et al.. (2012). Derivatives of the cationic plant alkaloids berberine and palmatine amplify protonophorous activity of fatty acids in model membranes and mitochondria. Mitochondrion. 13(5). 520–525. 16 indexed citations
13.
Chernyak, Boris V., Yuri N. Antonenko, Evgeniy R. Galimov, et al.. (2012). Novel mitochondria-targeted compounds composed of natural constituents: Conjugates of plant alkaloids berberine and palmatine with plastoquinone. Biochemistry (Moscow). 77(9). 983–995. 16 indexed citations
14.
Леонова, О.Г., et al.. (2012). Effect of nucleocapsid on multimerization of gypsy structural protein GAG. Molecular Biology. 46(2). 270–278. 1 indexed citations
15.
Trendeleva, T. A., et al.. (2011). Effect of prooxidants on yeast mitochondria. Journal of Bioenergetics and Biomembranes. 43(6). 633–644. 10 indexed citations
16.
Trendeleva, T. A., et al.. (2011). Mitochondria from Dipodascus (Endomyces) magnusii and Yarrowia lipolytica yeasts did not undergo a Ca2+-dependent permeability transition even under anaerobic conditions. Journal of Bioenergetics and Biomembranes. 43(6). 623–631. 9 indexed citations
17.
Trendeleva, T. A., et al.. (2010). Induction of permeability of the inner membrane of yeast mitochondria. Biochemistry (Moscow). 75(3). 297–303. 11 indexed citations
18.
Trendeleva, T. A., et al.. (2010). Interaction of yeast mitochondria with fatty acids and mitochondria-targeted lipophilic cations. Biochemistry (Moscow). 75(2). 139–144. 16 indexed citations
19.
Trendeleva, T. A., et al.. (2009). Induction of a non-specific permeability transition in mitochondria from Yarrowia lipolytica and Dipodascus (Endomyces) magnusii yeasts. Journal of Bioenergetics and Biomembranes. 41(3). 239–249. 27 indexed citations
20.
Zvyagilskaya, R. A., et al.. (2008). S3.34 Mitochondrial permeability transition pore (mPTP) in different yeast species is dissimilarly regulated. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1777. S32–S32. 1 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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