L. E. Bakeeva

2.5k total citations
53 papers, 1.5k citations indexed

About

L. E. Bakeeva is a scholar working on Molecular Biology, Physiology and Plant Science. According to data from OpenAlex, L. E. Bakeeva has authored 53 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 12 papers in Physiology and 11 papers in Plant Science. Recurrent topics in L. E. Bakeeva's work include Mitochondrial Function and Pathology (24 papers), Plant Stress Responses and Tolerance (6 papers) and Adipose Tissue and Metabolism (6 papers). L. E. Bakeeva is often cited by papers focused on Mitochondrial Function and Pathology (24 papers), Plant Stress Responses and Tolerance (6 papers) and Adipose Tissue and Metabolism (6 papers). L. E. Bakeeva collaborates with scholars based in Russia, Tajikistan and United States. L. E. Bakeeva's co-authors include Vladimir P. Skulachev, Yu. S. Chentsov, Dmitry B. Zorov, V. B. Saprunova, Т. Й. Кару, A. Jasaitis, L. Grinius, Dmitri O. Levitsky, Inna I. Severina and E.A. Liberman and has published in prestigious journals such as The Journal of Cell Biology, Oncogene and FEBS Letters.

In The Last Decade

L. E. Bakeeva

51 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L. E. Bakeeva Russia 19 1.1k 248 221 203 178 53 1.5k
William A. Taylor Canada 23 979 0.9× 308 1.2× 117 0.5× 296 1.5× 100 0.6× 63 1.7k
Herman G.P. Swarts Netherlands 31 1.9k 1.8× 140 0.6× 229 1.0× 190 0.9× 97 0.5× 96 2.5k
Jonathan J. Ruprecht United Kingdom 22 1.7k 1.6× 223 0.9× 474 2.1× 328 1.6× 100 0.6× 30 2.0k
Eric Turk United States 19 1.4k 1.3× 209 0.8× 61 0.3× 147 0.7× 107 0.6× 25 2.2k
Kathy Ragheb United States 10 943 0.9× 156 0.6× 78 0.4× 138 0.7× 84 0.5× 15 1.8k
Véronique Trézéguet France 22 2.1k 2.0× 275 1.1× 532 2.4× 118 0.6× 83 0.5× 52 2.5k
Harvey R. Knull United States 22 1.2k 1.1× 270 1.1× 145 0.7× 211 1.0× 97 0.5× 49 1.7k
Jörg Reinders Germany 27 2.2k 2.1× 112 0.5× 154 0.7× 92 0.5× 190 1.1× 74 3.2k
Sepehr Eskandari United States 26 1.5k 1.4× 183 0.7× 46 0.2× 510 2.5× 238 1.3× 41 2.6k
Jacques Doussière France 23 1.0k 1.0× 557 2.2× 115 0.5× 106 0.5× 126 0.7× 40 2.0k

Countries citing papers authored by L. E. Bakeeva

Since Specialization
Citations

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

Fields of papers citing papers by L. E. Bakeeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L. E. Bakeeva. 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 L. E. Bakeeva. The network helps show where L. E. Bakeeva may publish in the future.

Co-authorship network of co-authors of L. E. Bakeeva

This figure shows the co-authorship network connecting the top 25 collaborators of L. E. Bakeeva. A scholar is included among the top collaborators of L. E. Bakeeva 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 L. E. Bakeeva. L. E. Bakeeva 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.
Аверина, О. А., et al.. (2020). Ultrastructure of Hepatocytes from Laboratory Mice Fed a Standard Dry Laboratory Animal Diet. Biochemistry (Moscow). 85(9). 1082–1092. 1 indexed citations
2.
3.
Holtze, Susanne, et al.. (2016). Study of age-dependent structural and functional changes of mitochondria in skeletal muscles and heart of naked mole rats (Heterocephalus glaber). Biochemistry (Moscow). 81(12). 1429–1437. 16 indexed citations
4.
Bakeeva, L. E.. (2015). Age-related changes in ultrastructure of mitochondria. Effect of SkQ1. Biochemistry (Moscow). 80(12). 1582–1588. 6 indexed citations
5.
Bakeeva, L. E., et al.. (2014). Ultrastructural Changes in Ageing Lacrimal Gland in Wistar Rats. Bulletin of Experimental Biology and Medicine. 157(2). 268–272. 5 indexed citations
6.
Saprunova, V. B., et al.. (2012). SkQ1 slows development of age-dependent destructive processes in retina and vascular layer of eyes of wistar and OXYS rats. Biochemistry (Moscow). 77(6). 648–658. 28 indexed citations
7.
Saprunova, V. B., et al.. (2008). Cytochrome c oxidase activity in mitochondria of cardiomyocytes from isolated cardiac tissue incubated under long-term hypoxic conditions. Cell and Tissue Biology. 2(2). 153–157. 3 indexed citations
8.
Saprunova, V. B., et al.. (2007). Mitochondrial ultrastructure – the biological marker of the aging. Успехи геронтологии. 20(3). 68–69. 1 indexed citations
9.
Bakeeva, L. E., et al.. (2006). Programmed cell death in plants: Effect of protein synthesis inhibitors and structural changes in pea guard cells. Biochemistry (Moscow). 71(4). 395–405. 12 indexed citations
10.
Bakeeva, L. E., et al.. (2005). Effect of “External” Superoxide Anion on Apoptosis in Coleoptiles of Wheat Seedlings. Biochemistry (Moscow). 70(10). 1095–1103.
11.
Vanyushin, B. F., et al.. (2004). Apoptosis in Plants: Specific Features of Plant Apoptotic Cells and Effect of Various Factors and Agents. International review of cytology. 233. 135–179. 41 indexed citations
12.
Aleksandrushkina, N. I., et al.. (2004). Apoptosis in Wheat Seedlings Grown under Normal Daylight. Biochemistry (Moscow). 69(3). 285–294. 4 indexed citations
13.
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
14.
Bakeeva, L. E., et al.. (2002). Apoptosis in the Initial Leaf of Etiolated Wheat Seedlings: Influence of the Antioxidant Ionol (BHT) and Peroxides. Biochemistry (Moscow). 67(2). 212–221. 10 indexed citations
15.
Saprunova, V. B., et al.. (2002). Induction of Apoptosis in Rat Myocardium under Anoxic Conditions. Biochemistry (Moscow). 67(2). 246–253. 9 indexed citations
16.
17.
Bakeeva, L. E., et al.. (1999). Subcellular reorganization of mitochondria producing heavy DNA in aging wheat coleoptiles. FEBS Letters. 457(1). 122–125. 38 indexed citations
18.
Bakeeva, L. E., et al.. (1997). Ultrastructural changes in chondriome of human lymphocytes after irradiation with HeNe laser: Appearance of giant mitochondria. Journal of Photochemistry and Photobiology B Biology. 38(1). 25–30. 72 indexed citations
19.
Brustovetsky, N.N., et al.. (1993). Relationship between structure and function of liver mitochondria from hibernating and active ground squirrels, Citellus undulatus. Comparative Biochemistry and Physiology Part B Comparative Biochemistry. 106(1). 125–130. 18 indexed citations
20.
Bakeeva, L. E., et al.. (1986). MEMBRANOUS ELECTRIC CABLES .1. FILAMENTOUS MITOCHONDRIA IN FIBROPLASTS. Биологические мембраны Журнал мембранной и клеточной биологии. 3(11). 1130–1136. 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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