Vladimir Chekulayev

1.1k total citations
44 papers, 890 citations indexed

About

Vladimir Chekulayev is a scholar working on Molecular Biology, Cancer Research and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Vladimir Chekulayev has authored 44 papers receiving a total of 890 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 13 papers in Cancer Research and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Vladimir Chekulayev's work include Mitochondrial Function and Pathology (23 papers), ATP Synthase and ATPases Research (14 papers) and Cancer, Hypoxia, and Metabolism (13 papers). Vladimir Chekulayev is often cited by papers focused on Mitochondrial Function and Pathology (23 papers), ATP Synthase and ATPases Research (14 papers) and Cancer, Hypoxia, and Metabolism (13 papers). Vladimir Chekulayev collaborates with scholars based in Estonia, France and Austria. Vladimir Chekulayev's co-authors include Igor Shevchuk, Tuuli Käämbre, Kersti Tepp, Natalja Timohhina, Valdur Saks, Aleksandr Klepinin, Rita Guzun, Marju Puurand, Vahur Valvere and Minna Varikmaa and has published in prestigious journals such as PLoS ONE, International Journal of Cancer and American Journal of Physiology-Cell Physiology.

In The Last Decade

Vladimir Chekulayev

43 papers receiving 877 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vladimir Chekulayev Estonia 20 621 273 202 117 106 44 890
Igor Shevchuk Estonia 20 632 1.0× 271 1.0× 201 1.0× 103 0.9× 110 1.0× 44 892
Brian Cunniff United States 14 582 0.9× 134 0.5× 95 0.5× 101 0.9× 122 1.2× 28 915
Jiaze An China 18 685 1.1× 442 1.6× 100 0.5× 112 1.0× 47 0.4× 37 1.1k
Ya‐Ju Hsieh Taiwan 14 509 0.8× 237 0.9× 52 0.3× 184 1.6× 103 1.0× 29 876
Xiaojian Zhao United States 19 672 1.1× 358 1.3× 145 0.7× 59 0.5× 90 0.8× 27 1.1k
Ahmad A. Cluntun United States 12 964 1.6× 690 2.5× 163 0.8× 64 0.5× 50 0.5× 20 1.5k
Hailin Zhang China 15 562 0.9× 253 0.9× 81 0.4× 169 1.4× 49 0.5× 56 1.1k
Michal Koc Czechia 17 327 0.5× 93 0.3× 177 0.9× 78 0.7× 63 0.6× 37 746
Clemens Röhrl Austria 20 461 0.7× 229 0.8× 45 0.2× 55 0.5× 123 1.2× 45 930
Hiroyuki Kawagishi Japan 14 391 0.6× 121 0.4× 162 0.8× 86 0.7× 31 0.3× 23 893

Countries citing papers authored by Vladimir Chekulayev

Since Specialization
Citations

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

Fields of papers citing papers by Vladimir Chekulayev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vladimir Chekulayev. 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 Vladimir Chekulayev. The network helps show where Vladimir Chekulayev may publish in the future.

Co-authorship network of co-authors of Vladimir Chekulayev

This figure shows the co-authorship network connecting the top 25 collaborators of Vladimir Chekulayev. A scholar is included among the top collaborators of Vladimir Chekulayev 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 Vladimir Chekulayev. Vladimir Chekulayev 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.
Klepinin, Aleksandr, Vladimir Chekulayev, Heiki Vija, et al.. (2021). Colon cancer cell differentiation by sodium butyrate modulates metabolic plasticity of Caco-2 cells via alteration of phosphotransfer network. PLoS ONE. 16(1). e0245348–e0245348. 23 indexed citations
2.
Timohhina, Natalja, et al.. (2020). Metabolic and OXPHOS Activities Quantified by Temporal ex vivo Analysis Display Patient-Specific Metabolic Vulnerabilities in Human Breast Cancers. Frontiers in Oncology. 10. 1053–1053. 6 indexed citations
3.
Tepp, Kersti, Marju Puurand, Natalja Timohhina, et al.. (2020). Adaptation of striated muscles to Wolframin deficiency in mice: Alterations in cellular bioenergetics. Biochimica et Biophysica Acta (BBA) - General Subjects. 1864(4). 129523–129523. 3 indexed citations
4.
Chekulayev, Vladimir, et al.. (2019). On the role of tubulin, plectin, desmin, and vimentin in the regulation of mitochondrial energy fluxes in muscle cells. American Journal of Physiology-Cell Physiology. 316(5). C657–C667. 32 indexed citations
5.
Puurand, Marju, Kersti Tepp, Natalja Timohhina, et al.. (2019). Tubulin βII and βIII Isoforms as the Regulators of VDAC Channel Permeability in Health and Disease. Cells. 8(3). 239–239. 33 indexed citations
6.
Shevchuk, Igor, Aleksandr Klepinin, Vladimir Chekulayev, et al.. (2017). Mitochondrial Respiration in Human Colorectal and Breast Cancer Clinical Material Is Regulated Differently. Oxidative Medicine and Cellular Longevity. 2017(1). 1372640–1372640. 32 indexed citations
7.
Klepinin, Aleksandr, Rita Guzun, Vladimir Chekulayev, et al.. (2016). Simple oxygraphic analysis for the presence of adenylate kinase 1 and 2 in normal and tumor cells. Journal of Bioenergetics and Biomembranes. 48(5). 531–548. 23 indexed citations
8.
Chekulayev, Vladimir, Igor Shevchuk, Aleksandr Klepinin, et al.. (2015). Metabolic remodeling in human colorectal cancer and surrounding tissues: alterations in regulation of mitochondrial respiration and metabolic fluxes. Biochemistry and Biophysics Reports. 4. 111–125. 62 indexed citations
9.
Varikmaa, Minna, Natalja Timohhina, Kersti Tepp, et al.. (2014). Formation of highly organized intracellular structure and energy metabolism in cardiac muscle cells during postnatal development of rat heart. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1837(8). 1350–1361. 35 indexed citations
10.
Klepinin, Aleksandr, Vladimir Chekulayev, Igor Shevchuk, et al.. (2014). An in situ study of bioenergetic properties of human colorectal cancer: The regulation of mitochondrial respiration and distribution of flux control among the components of ATP synthasome. The International Journal of Biochemistry & Cell Biology. 55. 171–186. 62 indexed citations
11.
Käämbre, Tuuli, Vladimir Chekulayev, Igor Shevchuk, et al.. (2013). Metabolic control analysis of respiration in human cancer tissue. Frontiers in Physiology. 4. 151–151. 19 indexed citations
12.
Käämbre, Tuuli, Vladimir Chekulayev, Igor Shevchuk, et al.. (2012). Metabolic control analysis of cellular respiration in situ in intraoperational samples of human breast cancer. Journal of Bioenergetics and Biomembranes. 44(5). 539–558. 42 indexed citations
13.
Tepp, Kersti, Igor Shevchuk, Vladimir Chekulayev, et al.. (2011). High efficiency of energy flux controls within mitochondrial interactosome in cardiac intracellular energetic units. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1807(12). 1549–1561. 33 indexed citations
14.
González‐Granillo, Marcela, Alexeï Grichine, Rita Guzun, et al.. (2011). Studies of the role of tubulin beta II isotype in regulation of mitochondrial respiration in intracellular energetic units in cardiac cells. Journal of Molecular and Cellular Cardiology. 52(2). 437–447. 29 indexed citations
15.
Tepp, Kersti, Natalja Timohhina, Vladimir Chekulayev, et al.. (2010). Metabolic control analysis of integrated energy metabolism in permeabilized cardiomyocytes. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797. 138–139. 1 indexed citations
16.
Chekulayev, Vladimir, et al.. (2008). Active oxygen intermediates in the degradation of hematoporphyrin derivative in tumor cells subjected to photodynamic therapy. Journal of Photochemistry and Photobiology B Biology. 93(2). 94–107. 18 indexed citations
17.
Shevchuk, Igor, et al.. (2006). Hydrogen Peroxide, Superoxide, and Hydroxyl Radicals are Involved in the Phototoxic Action of Hematoporphyrin Derivative against Tumor Cells. Journal of Environmental Pathology Toxicology and Oncology. 25(1-2). 51–70. 33 indexed citations
18.
Chekulayev, Vladimir, et al.. (2000). L-BUTHIONINE-[S,R]-SULFOXIMINE MAY ENHANCE THE RATE OF HAEMATOPORPHYRIN DERIVATIVE PHOTOSENSITIZED INACTIVATION OF TUMOUR CELLS WITHOUT LOWERING THE INTRACELLULAR CONTENT OF GLUTATHIONE. Proceedings of the Estonian Academy of Sciences Chemistry. 49(2). 109–120. 1 indexed citations
19.
Chekulayev, Vladimir, et al.. (1998). EFFECTS OF LIGHT EXPOSURE ON THE UPTAKE AND DESTRUCTION OF HEMATOPORPHYRIN DERIVATIVE IN EHRLICH CARCINOMA CELL SUSPENSION. Proceedings of the Estonian Academy of Sciences Chemistry. 47(2). 73–91. 4 indexed citations
20.
Chekulayev, Vladimir, et al.. (1992). <title>Influence of metronidazole and some electron acceptors on the chlorin e<formula><inf><roman>6</roman></inf></formula> photosensitized killing of Ehrlich carcinoma cells</title>. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 1645. 131–140. 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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