Alexander V. Bocharov

2.6k total citations
41 papers, 2.1k citations indexed

About

Alexander V. Bocharov is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, Alexander V. Bocharov has authored 41 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Immunology and 14 papers in Surgery. Recurrent topics in Alexander V. Bocharov's work include Immune Response and Inflammation (11 papers), Cholesterol and Lipid Metabolism (7 papers) and Pancreatitis Pathology and Treatment (4 papers). Alexander V. Bocharov is often cited by papers focused on Immune Response and Inflammation (11 papers), Cholesterol and Lipid Metabolism (7 papers) and Pancreatitis Pathology and Treatment (4 papers). Alexander V. Bocharov collaborates with scholars based in United States, United Kingdom and Russia. Alexander V. Bocharov's co-authors include Tatyana G. Vishnyakova, Thomas L. Eggerman, Amy P. Patterson, Alan T. Remaley, Irina N. Baranova, György Csákó, John A. Stonik, Roger Kurlander, Edward B. Neufeld and Zhigang Chen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Alexander V. Bocharov

39 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexander V. Bocharov United States	22	954	848	503	352	318	41	2.1k
Thomas L. Eggerman United States	24	995 1.0×	957 1.1×	517 1.0×	297 0.8×	341 1.1×	60	2.4k
Tatyana G. Vishnyakova United States	19	787 0.8×	712 0.8×	464 0.9×	230 0.7×	279 0.9×	30	1.7k
Dominique Brees United States	20	1.0k 1.0×	662 0.8×	314 0.6×	363 1.0×	339 1.1×	42	2.1k
Jacques Schmitz France	27	625 0.7×	802 0.9×	631 1.3×	701 2.0×	167 0.5×	48	2.6k
Pin Mei Yao United States	13	948 1.0×	651 0.8×	584 1.2×	603 1.7×	183 0.6×	17	2.3k
Xinshou Ouyang United States	28	1.3k 1.4×	490 0.6×	1.3k 2.6×	645 1.8×	461 1.4×	50	3.3k
Gábor Járai United Kingdom	32	1.1k 1.2×	246 0.3×	525 1.0×	267 0.8×	347 1.1×	63	2.8k
Yu‐Li Chen Taiwan	29	996 1.0×	648 0.8×	565 1.1×	263 0.7×	889 2.8×	115	2.6k
Roberta Sferra Italy	27	840 0.9×	450 0.5×	281 0.6×	505 1.4×	325 1.0×	69	2.3k
Wendy Huang United States	17	1.3k 1.3×	500 0.6×	925 1.8×	333 0.9×	391 1.2×	28	2.3k

Countries citing papers authored by Alexander V. Bocharov

Since Specialization

Citations

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

Fields of papers citing papers by Alexander V. Bocharov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander V. Bocharov

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander V. Bocharov. A scholar is included among the top collaborators of Alexander V. Bocharov 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 Alexander V. Bocharov. Alexander V. Bocharov 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

Sorokin, Alexander V., Angel Aponte, Jingrong Tang, et al.. (2023). Association of oxidized ApoB and oxidized ApoA-I with high-risk coronary plaque features in cardiovascular disease. JCI Insight. 8(20). 6 indexed citations

Postnikova, Olga A., Rafael Villasmil, Igor B. Rogozin, et al.. (2023). Low-Density Lipoprotein Receptor (LDLR) Is Involved in Internalization of Lentiviral Particles Pseudotyped with SARS-CoV-2 Spike Protein in Ocular Cells. International Journal of Molecular Sciences. 24(14). 11860–11860. 9 indexed citations

Ke, Yunbo, Pratap Karki, Yue Li, et al.. (2023). Aging-Related Accumulation of Truncated Oxidized Phospholipids Augments Infectious Lung Injury and Endothelial Dysfunction via Cluster of Differentiation 36-Dependent Mechanism. Cells. 12(15). 1937–1937. 4 indexed citations

Chen, Zhigang, Thomas L. Eggerman, Alexander V. Bocharov, et al.. (2021). APOBEC3-induced mutation of the hepatitis virus B DNA genome occurs during its viral RNA reverse transcription into (−)-DNA. Journal of Biological Chemistry. 297(2). 100889–100889. 9 indexed citations

Vishnyakova, Tatyana G., Alexander V. Bocharov, Irina N. Baranova, et al.. (2020). SR-BI mediates neutral lipid sorting from LDL to lipid droplets and facilitates their formation. PLoS ONE. 15(10). e0240659–e0240659. 5 indexed citations

Baranova, Irina N., Ana C. P. Souza, Alexander V. Bocharov, et al.. (2017). Human SR-BII mediates SAA uptake and contributes to SAA pro-inflammatory signaling in vitro and in vivo. PLoS ONE. 12(4). e0175824–e0175824. 17 indexed citations

Souza, Ana C. P., Alexander V. Bocharov, Irina N. Baranova, et al.. (2016). Antagonism of scavenger receptor CD36 by 5A peptide prevents chronic kidney disease progression in mice independent of blood pressure regulation. Kidney International. 89(4). 809–822. 62 indexed citations

Baranova, Irina N., Ana C. P. Souza, Alexander V. Bocharov, et al.. (2016). Human SR-BI and SR-BII Potentiate Lipopolysaccharide-Induced Inflammation and Acute Liver and Kidney Injury in Mice. The Journal of Immunology. 196(7). 3135–3147. 52 indexed citations

Souza, Ana C. P., Takayuki Tsuji, Irina N. Baranova, et al.. (2015). TLR4 mutant mice are protected from renal fibrosis and chronic kidney disease progression. Physiological Reports. 3(9). e12558–e12558. 84 indexed citations

10.

Baranova, Irina N., Alexander V. Bocharov, Tatyana G. Vishnyakova, et al.. (2010). CD36 Is a Novel Serum Amyloid A (SAA) Receptor Mediating SAA Binding and SAA-induced Signaling in Human and Rodent Cells. Journal of Biological Chemistry. 285(11). 8492–8506. 86 indexed citations

11.

Chen, Zhigang, Thomas L. Eggerman, Alexander V. Bocharov, et al.. (2010). Hypermutation induced by APOBEC-1 overexpression can be eliminated. RNA. 16(5). 1040–1052. 19 indexed citations

12.

Baranova, Irina N., Tatyana G. Vishnyakova, Alexander V. Bocharov, et al.. (2004). Serum Amyloid A Binding to CLA-1 (CD36 and LIMPII Analogous-1) Mediates Serum Amyloid A Protein-induced Activation of ERK1/2 and p38 Mitogen-activated Protein Kinases. Journal of Biological Chemistry. 280(9). 8031–8040. 152 indexed citations

13.

Bocharov, Alexander V., Irina N. Baranova, Tatyana G. Vishnyakova, et al.. (2004). Targeting of Scavenger Receptor Class B Type I by Synthetic Amphipathic α-Helical-containing Peptides Blocks Lipopolysaccharide (LPS) Uptake and LPS-induced Pro-inflammatory Cytokine Responses in THP-1 Monocyte Cells. Journal of Biological Chemistry. 279(34). 36072–36082. 58 indexed citations

14.

Stonik, John A., Alan T. Remaley, Steve J. Demosky, et al.. (2004). Serum Amyloid a promotes ABCA1-dependent and ABCA1-independent lipid efflux from cells. Biochemical and Biophysical Research Communications. 321(4). 936–941. 65 indexed citations

15.

Remaley, Alan T., Thomas Fairwell, John A. Stonik, et al.. (2003). Synthetic amphipathic helical peptides promote lipid efflux from cells by an ABCA1-dependent and an ABCA1-independent pathway. Journal of Lipid Research. 44(4). 828–836. 166 indexed citations

16.

Vishnyakova, Tatyana G., Alexander V. Bocharov, Irina N. Baranova, et al.. (2003). Binding and Internalization of Lipopolysaccharide by Cla-1, a Human Orthologue of Rodent Scavenger Receptor B1. Journal of Biological Chemistry. 278(25). 22771–22780. 124 indexed citations

17.

Remaley, Alan T., John A. Stonik, Edward B. Neufeld, et al.. (2001). Apolipoprotein Specificity for Lipid Efflux by the Human ABCAI Transporter. Biochemical and Biophysical Research Communications. 280(3). 818–823. 267 indexed citations

18.

Bocharov, Alexander V., Tatyana G. Vishnyakova, Irina N. Baranova, et al.. (2000). Heat Shock Protein 60 Is a High-Affinity High-Density Lipoprotein Binding Protein. Biochemical and Biophysical Research Communications. 277(1). 228–235. 20 indexed citations

19.

Huang, Wei, et al.. (1994). Characteristics of high-density lipoprotein binding sites in cultured parenchymal, endothelial, and Kupffer's cells from rat liver. Bulletin of Experimental Biology and Medicine. 117(3). 270–272. 1 indexed citations

20.

Smirnova, О. V., et al.. (1992). Evidence for direct action of testosterone on rat liver cells: In vivo and in vitro induction of unusual estrogen-binding protein. The Journal of Steroid Biochemistry and Molecular Biology. 42(2). 243–249. 7 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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