Léonid Volkov

426 total citations
19 papers, 353 citations indexed

About

Léonid Volkov is a scholar working on Molecular Biology, Nutrition and Dietetics and Organic Chemistry. According to data from OpenAlex, Léonid Volkov has authored 19 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 3 papers in Nutrition and Dietetics and 2 papers in Organic Chemistry. Recurrent topics in Léonid Volkov's work include Chemical Synthesis and Analysis (2 papers), Neurological diseases and metabolism (2 papers) and Prion Diseases and Protein Misfolding (2 papers). Léonid Volkov is often cited by papers focused on Chemical Synthesis and Analysis (2 papers), Neurological diseases and metabolism (2 papers) and Prion Diseases and Protein Misfolding (2 papers). Léonid Volkov collaborates with scholars based in Canada, France and Nigeria. Léonid Volkov's co-authors include Xavier Roucou, Cyntia Bissonnette, Éric Marsault, Vincent Praloran, Christine Lavoie, Marc‐André Bonin, Hassan Traboulsi, Jean‐Luc Parent, Jean‐Claude Aldigier and Christian Le Gouill and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neurochemistry and Experimental Cell Research.

In The Last Decade

Léonid Volkov

19 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Léonid Volkov Canada 12 242 48 45 41 38 19 353
Phyllis S. Frisa United States 11 260 1.1× 24 0.5× 62 1.4× 30 0.7× 21 0.6× 13 397
Juanita M. Phang Australia 5 249 1.0× 17 0.4× 55 1.2× 30 0.7× 50 1.3× 5 388
Michael Babich United States 12 208 0.9× 15 0.3× 54 1.2× 23 0.6× 24 0.6× 34 384
Shuichi Takagahara Japan 8 338 1.4× 76 1.6× 42 0.9× 18 0.4× 25 0.7× 10 488
Nathalie Desban France 13 410 1.7× 24 0.5× 69 1.5× 10 0.2× 39 1.0× 18 556
Torsten Exner Germany 7 334 1.4× 44 0.9× 30 0.7× 26 0.6× 9 0.2× 8 396
Yusuke Komi Japan 14 391 1.6× 10 0.2× 30 0.7× 21 0.5× 23 0.6× 16 512
R Klinger Germany 13 433 1.8× 76 1.6× 37 0.8× 25 0.6× 19 0.5× 32 565
Vasanti Natarajan Norway 9 298 1.2× 60 1.3× 36 0.8× 15 0.4× 10 0.3× 13 413
Simon J. Mountford Australia 10 208 0.9× 44 0.9× 52 1.2× 24 0.6× 5 0.1× 29 363

Countries citing papers authored by Léonid Volkov

Since Specialization
Citations

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

Fields of papers citing papers by Léonid Volkov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Léonid Volkov

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

All Works

19 of 19 papers shown
1.
Volkov, Léonid, et al.. (2022). Debate: The War in Ukraine, Sanctions against Russia, and the Russian Opposition, June 26, 2022 Moderator: Alexander Plushchev. Ab imperio. 2022(2). 267–287. 1 indexed citations
2.
Volkov, Léonid, et al.. (2017). Modular sub-monomeric cell-penetrating guanidine-rich peptoids – synthesis, assembly and biological evaluation. RSC Advances. 7(10). 6059–6063. 13 indexed citations
3.
Volkov, Léonid, et al.. (2017). Bioresource Sector of the Russian Far East. Spatial Economics. 2(50). 110–137. 1 indexed citations
4.
Strokotov, Dmitry I., et al.. (2016). Influence of magnesium sulfate on HCO 3 /Cl transmembrane exchange rate in human erythrocytes. Journal of Theoretical Biology. 393. 194–202. 12 indexed citations
5.
Traboulsi, Hassan, et al.. (2015). Macrocyclic Cell Penetrating Peptides: A Study of Structure-Penetration Properties. Bioconjugate Chemistry. 26(3). 405–411. 60 indexed citations
6.
Lucien, Fabrice, et al.. (2014). Simultaneous pH Measurement in Endocytic and Cytosolic Compartments in Living Cells using Confocal Microscopy. Journal of Visualized Experiments. 16 indexed citations
7.
Siqueira, Jarbas Mota, Mareni Rocha Farías, Léonid Volkov, et al.. (2009). Evaluation of the antitumoral effect of dihydrocucurbitacin-B in both in vitro and in vivo models. Cancer Chemotherapy and Pharmacology. 64(3). 529–538. 17 indexed citations
8.
Bissonnette, Cyntia, et al.. (2007). Aggregation of cellular prion protein is initiated by proximity‐induced dimerization. Journal of Neurochemistry. 102(4). 1195–1205. 11 indexed citations
9.
Bissonnette, Cyntia, et al.. (2006). Molecular morphology and toxicity of cytoplasmic prion protein aggregates in neuronal and non‐neuronal cells. Journal of Neurochemistry. 97(5). 1456–1466. 54 indexed citations
10.
Bkaily, Ghassan, et al.. (2003). Des-Arg9-bradykinin increases intracellular Ca2+ in bronchoalveolar eosinophils from ovalbumin-sensitized and -challenged mice. European Journal of Pharmacology. 475(1-3). 129–137. 9 indexed citations
11.
Gouill, Christian Le, et al.. (1999). Selective Modulation of Wild Type Receptor Functions by Mutants of G-Protein-coupled Receptors. Journal of Biological Chemistry. 274(18). 12548–12554. 49 indexed citations
12.
Volkov, Léonid, et al.. (1997). Effects of the angiotensin‐converting enzyme inhibitor enalapril on blood haematopoietic progenitors and Acetyl‐N‐Ser‐Asp‐Lys‐Pro concentrations. European Journal of Clinical Investigation. 27(9). 788–790. 42 indexed citations
13.
Volkov, Léonid, et al.. (1997). AcSDKP plasma concentrations in patients with solid tumours: comparison of two chemotherapeutic regimens. Cancer Letters. 112(1). 1–4. 4 indexed citations
14.
J, Li, et al.. (1997). Production and consumption of the tetrapeptide AcSDKP, a negative regulator of hematopoietic stem cells, by hematopoietic microenvironmental cells.. PubMed. 25(2). 140–6. 28 indexed citations
15.
Volkov, Léonid, et al.. (1996). The Tetrapeptide AcSDKP, a Physiological Inhibitor of Normal Cell Proliferation, Reduces the S Phase Entry of Continuous Cell Lines. Experimental Cell Research. 223(1). 112–116. 12 indexed citations
16.
Volkov, Léonid, et al.. (1996). The Tetrapeptide AcSDKP, a Negative Regulator of Cell Cycle Entry, Inhibits the Proliferation of Human and Chicken Lymphocytes. Cellular Immunology. 168(2). 302–306. 12 indexed citations
17.
Frindel, E, Aline Massé, P. Pradelles, Léonid Volkov, & Michel Rigaud. (1992). Correlation of endogenous acetyl-ser-asp-lys-pro plasma levels in mice and the kinetics of pluripotent hemopoietic stem cells entry into the cycle after cytosine arabinoside treatment: fundamental and clinical aspects.. PubMed. 6(6). 599–601. 8 indexed citations
18.
Frindel, E, Aline Massé, Léonid Volkov, C Lavignac, & Michel Rigaud. (1992). Inhibitory effects of AcSDKP on the mixed lymphocyte reaction (MLR). Part I. MLR with mouse spleen cells.. PubMed. 6(10). 1043–4. 2 indexed citations
19.
Lavignac, C, Léonid Volkov, Aline Massé, Michel Rigaud, & E Frindel. (1992). Inhibitory effects of AcSDKP on the mixed lymphocyte reaction (MLR). Part II. Human whole blood cells.. PubMed. 6(10). 1045–7. 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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