Д. В. Зинченко

673 total citations
48 papers, 499 citations indexed

About

Д. В. Зинченко is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Immunology. According to data from OpenAlex, Д. В. Зинченко has authored 48 papers receiving a total of 499 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 10 papers in Immunology. Recurrent topics in Д. В. Зинченко's work include Neuroscience and Neuropharmacology Research (11 papers), Retinal Development and Disorders (9 papers) and Photoreceptor and optogenetics research (8 papers). Д. В. Зинченко is often cited by papers focused on Neuroscience and Neuropharmacology Research (11 papers), Retinal Development and Disorders (9 papers) and Photoreceptor and optogenetics research (8 papers). Д. В. Зинченко collaborates with scholars based in Russia, Finland and Germany. Д. В. Зинченко's co-authors include Pavel P. Philippov, Ivan I. Senin, Sergei E. Permyakov, Evgeni Yu. Zernii, Eugene A. Permyakov, А. И. Мирошников, T. A. Muranova, Valery M. Lipkin, Konstantin E. Komolov and Karl‐Wilhelm Koch and has published in prestigious journals such as Journal of Biological Chemistry, FEBS Letters and Free Radical Biology and Medicine.

In The Last Decade

Д. В. Зинченко

46 papers receiving 493 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Д. В. Зинченко Russia 12 348 156 90 76 58 48 499
Michael J. Francis United Kingdom 12 246 0.7× 49 0.3× 80 0.9× 32 0.4× 118 2.0× 14 495
Hye Won Choi South Korea 12 294 0.8× 95 0.6× 177 2.0× 42 0.6× 29 0.5× 17 683
Jens Carlsen Denmark 12 227 0.7× 155 1.0× 20 0.2× 45 0.6× 39 0.7× 22 431
Marie‐Jeanne Clément France 16 425 1.2× 25 0.2× 34 0.4× 125 1.6× 30 0.5× 31 614
Michael M. Crerar Canada 15 426 1.2× 63 0.4× 24 0.3× 69 0.9× 35 0.6× 24 698
Tat Cheung Cheng United States 9 301 0.9× 66 0.4× 59 0.7× 37 0.5× 63 1.1× 10 462
Jan Paul Bebelman Netherlands 10 285 0.8× 74 0.5× 49 0.5× 27 0.4× 28 0.5× 18 390
Joshua Holcomb United States 11 296 0.9× 56 0.4× 51 0.6× 29 0.4× 44 0.8× 22 481
Toshiaki Hosaka Japan 12 288 0.8× 88 0.6× 72 0.8× 28 0.4× 110 1.9× 29 523
D Amici Italy 13 342 1.0× 44 0.3× 33 0.4× 29 0.4× 17 0.3× 55 488

Countries citing papers authored by Д. В. Зинченко

Since Specialization
Citations

This map shows the geographic impact of Д. В. Зинченко'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. Зинченко 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. Зинченко more than expected).

Fields of papers citing papers by Д. В. Зинченко

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Д. В. Зинченко. A scholar is included among the top collaborators of Д. В. Зинченко 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. Зинченко. Д. В. Зинченко 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.
Navolotskaya, E. V., et al.. (2023). The Anti-Inflammatory Effect of Peptide LKEKK. Russian Journal of Bioorganic Chemistry. 49(1). 35–40. 1 indexed citations
2.
Navolotskaya, E. V., et al.. (2023). Anti-Inflammatory Effect of Peptide LKEKK. Биоорганическая химия. 49(1). 41–47.
3.
Navolotskaya, E. V., et al.. (2023). Effect of the Synthetic Peptide LKEKK on Psoriasis. Russian Journal of Bioorganic Chemistry. 49(6). 1346–1352. 1 indexed citations
4.
Potoldykova, Natalia V., et al.. (2022). Non-Invasive Diagnostics of Renal Cell Carcinoma Using Ultrasensitive Immunodetection of Cancer-Retina Antigens. Biochemistry (Moscow). 87(7). 658–666. 2 indexed citations
5.
Zernii, Evgeni Yu., Viktoriia E. Baksheeva, Alexei S. Kazakov, et al.. (2018). Photoreceptor calcium sensor proteins in detergent-resistant membrane rafts are regulated via binding to caveolin-1. Cell Calcium. 73. 55–69. 11 indexed citations
6.
Baldin, Alexey V., D. O. Korolev, Ekaterina Kuznetsova, et al.. (2018). Autoantibody against arrestin-1 as a potential biomarker of renal cell carcinoma. Biochimie. 157. 26–37. 10 indexed citations
7.
Navolotskaya, E. V., et al.. (2018). Interaction of Cholera Toxin B Subunit with Rat Intestinal Epithelial Cells. Russian Journal of Bioorganic Chemistry. 44(4). 403–407. 3 indexed citations
8.
Muranova, T. A., et al.. (2018). Hydrolysis of Soybean Proteins with Kamchatka Crab Hepatopancreas Enzyme Complex. Applied Biochemistry and Microbiology. 54(1). 76–82. 5 indexed citations
9.
Navolotskaya, E. V., В. Б. Садовников, Д. В. Зинченко, et al.. (2017). Interaction of cholera toxin B-subunit with human T-lymphocytes. Biochemistry (Moscow). 82(9). 1036–1041. 2 indexed citations
10.
Navolotskaya, E. V., В. Б. Садовников, Д. В. Зинченко, Valery M. Lipkin, & V.P. Zav′yalov. (2017). Interaction of cholera toxin B subunit with T and B lymphocytes. International Immunopharmacology. 50. 279–282. 4 indexed citations
11.
Navolotskaya, E. V., et al.. (2016). Binding of synthetic LKEKK peptide to human T-lymphocytes. Biochemistry (Moscow). 81(8). 871–875. 10 indexed citations
12.
Zernii, Evgeni Yu., Ilya I. Grigoriev, Alexander Scholten, et al.. (2015). Regulatory function of the C-terminal segment of guanylate cyclase-activating protein 2. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1854(10). 1325–1337. 9 indexed citations
13.
Baksheeva, Viktoriia E., Д. В. Зинченко, Marina V. Serebryakova, et al.. (2015). Ca<sup>2+</sup>-Myristoyl Switch in Neuronal Calcium Sensor-1: A Role of C-Terminal Segment. CNS & Neurological Disorders - Drug Targets. 14(4). 437–451. 14 indexed citations
14.
Permyakov, Sergei E., Evgeni Yu. Zernii, Ekaterina L. Knyazeva, et al.. (2011). Oxidation mimicking substitution of conservative cysteine in recoverin suppresses its membrane association. Amino Acids. 42(4). 1435–1442. 29 indexed citations
15.
16.
Komolov, Konstantin E., Д. В. Зинченко, Oliver H. Weiergräber, et al.. (2005). One of the Ca2+ binding sites of recoverin exclusively controls interaction with rhodopsin kinase. Biological Chemistry. 386(3). 285–9. 6 indexed citations
17.
Senin, Ivan I., Torsten Fischer, Konstantin E. Komolov, et al.. (2002). Ca2+-Myristoyl Switch in the Neuronal Calcium Sensor Recoverin Requires Different Functions of Ca2+-binding Sites. Journal of Biological Chemistry. 277(52). 50365–50372. 59 indexed citations
18.
Permyakov, Sergei E., L. A. Wasserman, Ivan I. Senin, et al.. (2002). Recoverin Is a Zinc-Binding Protein. Journal of Proteome Research. 2(1). 51–57. 27 indexed citations
19.
Permyakov, Sergei E., Ivan I. Senin, A.A. Zargarov, et al.. (2000). Effects of mutations in the calcium-binding sites of recoverin on its calcium affinity: evidence for successive filling of the calcium binding sites. Protein Engineering Design and Selection. 13(11). 783–790. 40 indexed citations
20.
Зинченко, Д. В., Svetlana Shulga‐Morskaya, Ivan I. Senin, et al.. (1998). Obtaining and characterization of EF‐hand mutants of recoverin. FEBS Letters. 440(1-2). 116–118. 18 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026