Pavel P. Philippov

3.3k total citations · 1 hit paper
96 papers, 2.4k citations indexed

About

Pavel P. Philippov is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Pavel P. Philippov has authored 96 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 34 papers in Cellular and Molecular Neuroscience and 14 papers in Ophthalmology. Recurrent topics in Pavel P. Philippov's work include Retinal Development and Disorders (37 papers), Photoreceptor and optogenetics research (26 papers) and Receptor Mechanisms and Signaling (26 papers). Pavel P. Philippov is often cited by papers focused on Retinal Development and Disorders (37 papers), Photoreceptor and optogenetics research (26 papers) and Receptor Mechanisms and Signaling (26 papers). Pavel P. Philippov collaborates with scholars based in Russia, Germany and Tajikistan. Pavel P. Philippov's co-authors include Ivan I. Senin, Alexandr V. Bazhin, Svetlana Karakhanova, Jens Werner, Yuhui Yang, Jan DʼHaese, Werner Hartwig, Evgeni Yu. Zernii, Karl‐Wilhelm Koch and Andrey A. Zamyatnin and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Molecular Biology and Analytical Chemistry.

In The Last Decade

Pavel P. Philippov

96 papers receiving 2.3k citations

Hit Papers

Mitochondria and Mitochondrial ROS in Cancer: Novel Targe... 2016 2026 2019 2022 2016 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pavel P. Philippov Russia 27 1.6k 666 304 255 194 96 2.4k
Austin J. Yang United States 29 1.8k 1.1× 349 0.5× 87 0.3× 489 1.9× 210 1.1× 59 3.2k
Philip V. LoGrasso United States 38 2.7k 1.6× 332 0.5× 112 0.4× 332 1.3× 239 1.2× 79 4.0k
Arthur S. Polans United States 28 2.3k 1.4× 1.1k 1.7× 430 1.4× 318 1.2× 242 1.2× 48 3.1k
Koji Igarashi Japan 33 3.5k 2.1× 520 0.8× 176 0.6× 906 3.6× 130 0.7× 116 4.8k
Neena Singh United States 33 2.0k 1.2× 133 0.2× 105 0.3× 241 0.9× 321 1.7× 77 2.9k
Ming Zou China 21 848 0.5× 233 0.3× 82 0.3× 406 1.6× 90 0.5× 65 1.8k
Masatoshi Tomi Japan 29 771 0.5× 258 0.4× 234 0.8× 314 1.2× 54 0.3× 87 2.2k
Yangbo Feng United States 31 1.7k 1.0× 194 0.3× 102 0.3× 155 0.6× 83 0.4× 65 2.6k
Yoshito Kinoshita United States 25 1.8k 1.1× 714 1.1× 39 0.1× 260 1.0× 195 1.0× 43 2.6k
Konstantin Petrukhin United States 28 2.4k 1.5× 431 0.6× 1.1k 3.8× 292 1.1× 41 0.2× 58 3.5k

Countries citing papers authored by Pavel P. Philippov

Since Specialization
Citations

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

Fields of papers citing papers by Pavel P. Philippov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pavel P. Philippov. 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 Pavel P. Philippov. The network helps show where Pavel P. Philippov may publish in the future.

Co-authorship network of co-authors of Pavel P. Philippov

This figure shows the co-authorship network connecting the top 25 collaborators of Pavel P. Philippov. A scholar is included among the top collaborators of Pavel P. Philippov 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 Pavel P. Philippov. Pavel P. Philippov 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.
Chistyakov, Dmitry V., Olga Gancharova, Viktoriia E. Baksheeva, et al.. (2024). Targeting Oxidative Stress and Inflammation in the Eye: Insights from a New Model of Experimental Autoimmune Uveitis. International Journal of Molecular Sciences. 25(23). 12910–12910. 3 indexed citations
2.
Adam, Thomas C., et al.. (2019). In Vivo Immunological Effects of CD73 Deficiency. Cellular Physiology and Biochemistry. 52(5). 1193–1202. 1 indexed citations
3.
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
4.
Baksheeva, Viktoriia E., Olga Gancharova, Pavel P. Philippov, et al.. (2018). Suppression of Light-Induced Oxidative Stress in the Retina by Mitochondria-Targeted Antioxidant. Antioxidants. 8(1). 3–3. 38 indexed citations
5.
Zernii, Evgeni Yu., Olga Gancharova, Viktoriia E. Baksheeva, et al.. (2017). Mitochondria‐Targeted Antioxidant SkQ1 Prevents Anesthesia‐Induced Dry Eye Syndrome. Oxidative Medicine and Cellular Longevity. 2017(1). 9281519–9281519. 44 indexed citations
6.
Yang, Yuhui, Svetlana Karakhanova, Werner Hartwig, et al.. (2016). Mitochondria and Mitochondrial ROS in Cancer: Novel Targets for Anticancer Therapy. Journal of Cellular Physiology. 231(12). 2570–2581. 516 indexed citations breakdown →
7.
Korolev, D. O., Olga Gancharova, Ekaterina A. Alekseeva, et al.. (2016). The cancer-retina antigen recoverin as a potential biomarker for renal tumors. Tumor Biology. 37(7). 9899–9907. 23 indexed citations
8.
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
9.
Soltek, Sabine, Svetlana Karakhanova, Jan DʼHaese, et al.. (2015). Anti-tumor properties of the cGMP/protein kinase G inhibitor DT3 in pancreatic adenocarcinoma. Naunyn-Schmiedeberg s Archives of Pharmacology. 388(11). 1121–1128. 3 indexed citations
10.
Bazhin, Alexandr V., et al.. (2014). Cancer-retina antigens — A new group of tumor antigens. Biochemistry (Moscow). 79(8). 733–739. 9 indexed citations
11.
Zernii, Evgeni Yu., Ilya I. Grigoriev, Konstantin E. Komolov, et al.. (2013). New mechanisms of regulatory activity of photoreceptor calcium sensors. FEBS Journal. 280. 438–439. 2 indexed citations
12.
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
13.
Bazhin, Alexandr V., Dirk Schadendorf, Robert W. Owen, et al.. (2008). Visible Light Modulates the Expression of Cancer-Retina Antigens. Molecular Cancer Research. 6(1). 110–118. 13 indexed citations
14.
Grigoryan, E. N., et al.. (2007). New method of in vitro culturing of pigment retinal epithelium in the structure of the posterior eye sector of adult rat. Bulletin of Experimental Biology and Medicine. 144(4). 618–625. 6 indexed citations
15.
Weiergräber, Oliver H., Ivan I. Senin, Pavel P. Philippov, Joachim Granzin, & Karl‐Wilhelm Koch. (2003). Impact of N-terminal Myristoylation on the Ca2+-dependent Conformational Transition in Recoverin. Journal of Biological Chemistry. 278(25). 22972–22979. 37 indexed citations
16.
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
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.
Bazhin, Alexandr V., et al.. (2001). Low titre autoantibodies against recoverin in sera of patients with small cell lung cancer but without a loss of vision. Lung Cancer. 34(1). 99–104. 29 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.
Philippov, Pavel P., et al.. (1993). The presence of a calcium‐sensitive p26‐containing complex in bovine retina rod cells. FEBS Letters. 335(2). 277–279. 47 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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