Д. В. Лебедев

858 total citations
58 papers, 624 citations indexed

About

Д. В. Лебедев is a scholar working on Molecular Biology, Materials Chemistry and Control and Systems Engineering. According to data from OpenAlex, Д. В. Лебедев has authored 58 papers receiving a total of 624 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 16 papers in Materials Chemistry and 7 papers in Control and Systems Engineering. Recurrent topics in Д. В. Лебедев's work include Protein Structure and Dynamics (11 papers), Enzyme Structure and Function (10 papers) and RNA and protein synthesis mechanisms (7 papers). Д. В. Лебедев is often cited by papers focused on Protein Structure and Dynamics (11 papers), Enzyme Structure and Function (10 papers) and RNA and protein synthesis mechanisms (7 papers). Д. В. Лебедев collaborates with scholars based in Russia, Germany and France. Д. В. Лебедев's co-authors include Irina V. Ogneva, Б. С. Шенкман, Jochen J. Steil, Helge Ritter, A. I. Kuklin, Filatov Mv, А. Х. Исламов, А. В. Швецов, Anna A. Kulminskaya and Yury А. Skorik and has published in prestigious journals such as Journal of Applied Physics, The Journal of Physiology and Biochemistry.

In The Last Decade

Д. В. Лебедев

54 papers receiving 605 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Д. В. Лебедев Russia	13	277	74	69	60	57	58	624
Haitao Ding China	20	311 1.1×	220 3.0×	104 1.5×	53 0.9×	10 0.2×	65	957
Osamu Ichikawa Japan	24	93 0.3×	205 2.8×	143 2.1×	25 0.4×	10 0.2×	104	1.5k
Bian Li China	19	615 2.2×	116 1.6×	57 0.8×	6 0.1×	7 0.1×	82	1.2k
Bo-Rui Chen Taiwan	13	146 0.5×	35 0.5×	17 0.2×	29 0.5×	33 0.6×	36	563
Donghoon Kang South Korea	10	154 0.6×	69 0.9×	19 0.3×	5 0.1×	33 0.6×	24	555
Le Ye China	19	109 0.4×	430 5.8×	22 0.3×	21 0.3×	14 0.2×	143	1.3k
Ruifeng Gao China	15	96 0.3×	49 0.7×	181 2.6×	9 0.1×	21 0.4×	77	742
Weiyuan Chen China	19	106 0.4×	61 0.8×	61 0.9×	7 0.1×	53 0.9×	64	991
Chih‐Cheng Huang Taiwan	15	160 0.6×	207 2.8×	31 0.4×	64 1.1×	6 0.1×	40	614
Zhiyuan Li China	15	128 0.5×	65 0.9×	64 0.9×	5 0.1×	91 1.6×	45	906

Countries citing papers authored by Д. В. Лебедев

Since Specialization

Citations

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

Fields of papers citing papers by Д. В. Лебедев

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Д. В. Лебедев. 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 Д. В. Лебедев. The network helps show where Д. В. Лебедев may publish in the future.

Co-authorship network of co-authors of Д. В. Лебедев

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

All Works

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20 of 20 papers shown

Kwak, Myounghai, Koh Nakamura, Qiao‐Ping Xiang, et al.. (2024). Circular genetic structure of the Abies nephrolepis species complex shaped by the circular landform of Northeast Asia. Journal of Biogeography. 51(8). 1533–1548. 1 indexed citations

Shtam, Tatiana, Vladimir Burdakov, Luiza Garaeva, et al.. (2023). Experimental validation of proton boron capture therapy for glioma cells. Scientific Reports. 13(1). 1341–1341. 10 indexed citations

Gorshkova, Yu. E., A. D. Yapryntsev, А. Е. Баранчиков, et al.. (2023). Structure Evolution of CaCO3 Precipitates Formed during the Bacillus cereus Induced Biomineralization. Minerals. 13(6). 740–740. 2 indexed citations

Vv, Egorov, Yana Zabrodskaya, А. Е. Баранчиков, et al.. (2023). Matrix is everywhere: extracellular DNA is a link between biofilm and mineralization in Bacillus cereus planktonic lifestyle. npj Biofilms and Microbiomes. 9(1). 9–9. 15 indexed citations

Obluchinskaya, Ekaterina D., et al.. (2021). Antibacterial Properties of Fucoidans from the Brown Algae Fucus vesiculosus L. of the Barents Sea. Biology. 10(1). 67–67. 64 indexed citations

Лебедев, Д. В., et al.. (2021). Neutron Scattering Techniques and Complementary Methods for Structural and Functional Studies of Biological Macromolecules and Large Macromolecular Complexes. Crystallography Reports. 66(2). 242–253. 1 indexed citations

Лебедев, Д. В., Luiza Garaeva, Vladimir Burdakov, et al.. (2020). RADIOSENSITIZING EFFECT OF BORON ENHANCES THE EFFECTIVENESS OF PROTON THERAPY IN VITRO. 4 indexed citations

Лебедев, Д. В., et al.. (2020). FRAGMENTED ALGORITHM FOR ADAPTED GRID CONSTRUCTION. 71(3). 37–44.

Лебедев, Д. В., Yana Zabrodskaya, Vitaliy Pipich, et al.. (2019). Effect of alpha-lactalbumin and lactoferrin oleic acid complexes on chromatin structural organization. Biochemical and Biophysical Research Communications. 520(1). 136–139. 11 indexed citations

10.

Zabrodskaya, Yana, Д. В. Лебедев, А. В. Швецов, et al.. (2018). The amyloidogenicity of the influenza virus PB1-derived peptide sheds light on its antiviral activity. Biophysical Chemistry. 234. 16–23. 12 indexed citations

11.

Ilatovskiy, Andrey V., Igor Nazarov, А. В. Швецов, et al.. (2016). Partially Assembled Nucleosome Structures at Atomic Detail. Biophysical Journal. 112(3). 460–472. 44 indexed citations

12.

Швецов, А. В., et al.. (2014). Structure of RecX protein complex with the presynaptic RecA filament: Molecular dynamics simulations and small angle neutron scattering. FEBS Letters. 588(6). 948–955. 15 indexed citations

13.

Vv, Egorov, et al.. (2014). A conservative mutant of a proteolytic fragment produced during fibril formation enhances fibrillogenesis. Prion. 8(5). 369–373. 5 indexed citations

14.

Vv, Egorov, et al.. (2013). Amyloidogenic peptide homologous to fragment 129–148 of human myocilin. Prion. 7(3). 248–253. 2 indexed citations

15.

Ogneva, Irina V., Д. В. Лебедев, & Б. С. Шенкман. (2010). Transversal Stiffness and Young's Modulus of Single Fibers from Rat Soleus Muscle Probed by Atomic Force Microscopy. Biophysical Journal. 98(3). 418–424. 85 indexed citations

16.

Petukhov, Michael, et al.. (2006). Conformational flexibility of RecA protein filament: Transitions between compressed and stretched states. Proteins Structure Function and Bioinformatics. 65(2). 296–304. 7 indexed citations

17.

Лебедев, Д. В., Jochen J. Steil, & Helge Ritter. (2005). The dynamic wave expansion neural network model for robot motion planning in time-varying environments. Neural Networks. 18(3). 267–285. 42 indexed citations

18.

Лебедев, Д. В., Filatov Mv, A. I. Kuklin, et al.. (2005). Fractal nature of chromatin organization in interphase chicken erythrocyte nuclei: DNA structure exhibits biphasic fractal properties. FEBS Letters. 579(6). 1465–1468. 63 indexed citations

19.

Лебедев, Д. В., et al.. (2003). Analytical model for determination of parameters of helical structures in solution by small angle scattering: comparison of RecA structures by SANS. FEBS Letters. 537(1-3). 182–186. 19 indexed citations

20.

Basavappa, Srisaila, et al.. (1995). SWELLING-ACTIVATED CL- CHANNELS IN THE HUMAN NEUROBLASTOMA CELL-LINE CHP-100. The Journal of Physiology. 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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