Vladimir V. Shuvaev

5.2k total citations · 3 hit papers
74 papers, 3.6k citations indexed

About

Vladimir V. Shuvaev is a scholar working on Molecular Biology, Physiology and Immunology. According to data from OpenAlex, Vladimir V. Shuvaev has authored 74 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 19 papers in Physiology and 14 papers in Immunology. Recurrent topics in Vladimir V. Shuvaev's work include Nanoparticle-Based Drug Delivery (12 papers), Nitric Oxide and Endothelin Effects (11 papers) and Cell Adhesion Molecules Research (8 papers). Vladimir V. Shuvaev is often cited by papers focused on Nanoparticle-Based Drug Delivery (12 papers), Nitric Oxide and Endothelin Effects (11 papers) and Cell Adhesion Molecules Research (8 papers). Vladimir V. Shuvaev collaborates with scholars based in United States, France and Japan. Vladimir V. Shuvaev's co-authors include Vladimir R. Muzykantov, Blaine J. Zern, Gérard Siest, Melpo Christofidou‐Solomidou, Jingyan Han, Raisa Y. Kiseleva, Evguenia Arguiri, Silvia Muro, Hamideh Parhiz and Makan Khoshnejad and has published in prestigious journals such as Advanced Materials, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Vladimir V. Shuvaev

74 papers receiving 3.6k citations

Hit Papers

Targeting vascular (endothelial) dysfunction 2016 2026 2019 2022 2016 2021 2018 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vladimir V. Shuvaev United States 37 1.5k 781 523 519 457 74 3.6k
Yu Ishima Japan 34 2.0k 1.3× 612 0.8× 473 0.9× 602 1.2× 368 0.8× 143 4.0k
Farhad Rezaee Netherlands 27 1.3k 0.9× 850 1.1× 662 1.3× 705 1.4× 243 0.5× 57 3.3k
Florian Krötz Germany 26 1.4k 1.0× 379 0.5× 510 1.0× 354 0.7× 769 1.7× 64 3.9k
Michel Demeule Canada 35 2.2k 1.5× 878 1.1× 406 0.8× 284 0.5× 238 0.5× 87 4.7k
Heather Hatcher United States 18 1.5k 1.0× 324 0.4× 593 1.1× 362 0.7× 301 0.7× 23 3.9k
Thomas Simmet Germany 27 1.8k 1.2× 515 0.7× 382 0.7× 303 0.6× 1.3k 2.8× 46 4.2k
Uwe Michaelis Germany 33 1.7k 1.2× 570 0.7× 428 0.8× 616 1.2× 504 1.1× 62 4.1k
Jing Qin China 33 1.6k 1.1× 943 1.2× 853 1.6× 156 0.3× 895 2.0× 105 4.2k
Qin Lu China 32 1.2k 0.8× 732 0.9× 875 1.7× 113 0.2× 394 0.9× 106 3.0k

Countries citing papers authored by Vladimir V. Shuvaev

Since Specialization
Citations

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

Fields of papers citing papers by Vladimir V. Shuvaev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vladimir V. Shuvaev. 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 Vladimir V. Shuvaev. The network helps show where Vladimir V. Shuvaev may publish in the future.

Co-authorship network of co-authors of Vladimir V. Shuvaev

This figure shows the co-authorship network connecting the top 25 collaborators of Vladimir V. Shuvaev. A scholar is included among the top collaborators of Vladimir V. Shuvaev 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 Vladimir V. Shuvaev. Vladimir V. Shuvaev 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.
Shuvaev, Vladimir V., et al.. (2024). Engineered Dual Antioxidant Enzyme Complexes Targeting ICAM-1 on Brain Endothelium Reduce Brain Injury-Associated Neuroinflammation. Bioengineering. 11(3). 200–200. 3 indexed citations
2.
Parhiz, Hamideh, Vladimir V. Shuvaev, Qin Li, et al.. (2024). Physiologically based modeling of LNP-mediated delivery of mRNA in the vascular system. Molecular Therapy — Nucleic Acids. 35(2). 102175–102175. 11 indexed citations
3.
Ferguson, Laura T., Jacob W. Myerson, Jichuan Wu, et al.. (2023). Mechanisms by Which Liposomes Improve Inhaled Drug Delivery for Alveolar Diseases. SHILAP Revista de lepidopterología. 3(3). 2200106–2200106. 19 indexed citations
4.
Ferguson, Laura T., Jacob W. Myerson, Jichuan Wu, et al.. (2023). Mechanisms by Which Liposomes Improve Inhaled Drug Delivery for Alveolar Diseases. Advanced NanoBiomed Research. 3(3). 10 indexed citations
5.
Tombácz, István, Dorottya Laczkó, Hamna Shahnawaz, et al.. (2021). Highly efficient CD4+ T cell targeting and genetic recombination using engineered CD4+ cell-homing mRNA-LNPs. Molecular Therapy. 29(11). 3293–3304. 183 indexed citations breakdown →
6.
Lutton, Evan M., S. Katie Farney, Allison M. Andrews, et al.. (2019). Endothelial Targeted Strategies to Combat Oxidative Stress: Improving Outcomes in Traumatic Brain Injury. Frontiers in Neurology. 10. 582–582. 31 indexed citations
7.
Khoshnejad, Makan, Hamideh Parhiz, Vladimir V. Shuvaev, Ivan J. Dmochowski, & Vladimir R. Muzykantov. (2018). Ferritin-based drug delivery systems: Hybrid nanocarriers for vascular immunotargeting. Journal of Controlled Release. 282. 13–24. 114 indexed citations
8.
Parhiz, Hamideh, Vladimir V. Shuvaev, Norbert Pardi, et al.. (2018). PECAM-1 directed re-targeting of exogenous mRNA providing two orders of magnitude enhancement of vascular delivery and expression in lungs independent of apolipoprotein E-mediated uptake. Journal of Controlled Release. 291. 106–115. 154 indexed citations breakdown →
9.
Goitre, Luca, Peter V. DiStefano, Andrea Moglia, et al.. (2017). Up-regulation of NADPH oxidase-mediated redox signaling contributes to the loss of barrier function in KRIT1 deficient endothelium. Scientific Reports. 7(1). 8296–8296. 48 indexed citations
10.
Kiseleva, Raisa Y., Colin F. Greineder, Carlos H. Villa, et al.. (2017). Mechanism of Collaborative Enhancement of Binding of Paired Antibodies to Distinct Epitopes of Platelet Endothelial Cell Adhesion Molecule-1. PLoS ONE. 12(1). e0169537–e0169537. 11 indexed citations
11.
Myerson, Jacob W., et al.. (2017). Fluorescence Microscopy Imaging Calibration for Quantifying Nanocarrier Binding to Cells During Shear Flow Exposure. Journal of Biomedical Nanotechnology. 13(6). 737–745. 6 indexed citations
12.
Lutton, Evan M., Roshanak Razmpour, Allison M. Andrews, et al.. (2017). Acute administration of catalase targeted to ICAM-1 attenuates neuropathology in experimental traumatic brain injury. Scientific Reports. 7(1). 3846–3846. 61 indexed citations
13.
Shuvaev, Vladimir V., et al.. (2015). Targeted endothelial nanomedicine for common acute pathological conditions. Journal of Controlled Release. 219. 576–595. 42 indexed citations
14.
Ferrer, M. Carme Coll, Vladimir V. Shuvaev, Blaine J. Zern, et al.. (2014). ICAM-1 Targeted Nanogels Loaded with Dexamethasone Alleviate Pulmonary Inflammation. PLoS ONE. 9(7). e102329–e102329. 73 indexed citations
15.
Hood, Elizabeth D., Colin F. Greineder, Chandra Dodia, et al.. (2012). Antioxidant protection by PECAM-targeted delivery of a novel NADPH-oxidase inhibitor to the endothelium in vitro and in vivo. Journal of Controlled Release. 163(2). 161–169. 64 indexed citations
16.
Shuvaev, Vladimir V., Melpo Christofidou‐Solomidou, Faiz Y. Bhora, et al.. (2009). Targeted Detoxification of Selected Reactive Oxygen Species in the Vascular Endothelium. Journal of Pharmacology and Experimental Therapeutics. 331(2). 404–411. 64 indexed citations
17.
Laffont, Isabelle, Vladimir V. Shuvaev, Olivier Briand, et al.. (2002). Early-glycation of apolipoprotein E: effect on its binding to LDL receptor, scavenger receptor A and heparan sulfates. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1583(1). 99–107. 19 indexed citations
18.
Shuvaev, Vladimir V., Junichi Fujii, Yoshimi Kawasaki, et al.. (1999). Glycation of apolipoprotein E impairs its binding to heparin: identification of the major glycation site. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1454(3). 296–308. 29 indexed citations
19.
Schiele, F, et al.. (1999). Capillary electrophoretic analysis of recombinant human apolipoprotein E. Journal of Chromatography A. 853(1-2). 237–241. 5 indexed citations
20.
Dergunov, Alexander D., Vladimir V. Shuvaev, & Perova Nv. (1990). [Dynamic behavior of apoproteins of human plasma very low density lipoproteins and lipolysis regulation].. PubMed. 55(1). 134–46. 11 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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