Eugene V. Barsov

1.3k total citations
28 papers, 1.1k citations indexed

About

Eugene V. Barsov is a scholar working on Immunology, Virology and Oncology. According to data from OpenAlex, Eugene V. Barsov has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Immunology, 12 papers in Virology and 10 papers in Oncology. Recurrent topics in Eugene V. Barsov's work include HIV Research and Treatment (12 papers), Immune Cell Function and Interaction (10 papers) and Virus-based gene therapy research (8 papers). Eugene V. Barsov is often cited by papers focused on HIV Research and Treatment (12 papers), Immune Cell Function and Interaction (10 papers) and Virus-based gene therapy research (8 papers). Eugene V. Barsov collaborates with scholars based in United States, Russia and Spain. Eugene V. Barsov's co-authors include Stephen H. Hughes, David E. Ott, Jeffrey D. Lifson, Lori V. Coren, Charles M. Trubey, Elena Chertova, James D. Roser, Oleg Chertov, Raymond C. Sowder and Robert J. Fisher and has published in prestigious journals such as PLoS ONE, Journal of Virology and Gene.

In The Last Decade

Eugene V. Barsov

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eugene V. Barsov United States 15 485 417 357 212 204 28 1.1k
Farida Shaheen United States 16 516 1.1× 485 1.2× 364 1.0× 202 1.0× 211 1.0× 22 1.2k
Olga Latinovic United States 14 324 0.7× 531 1.3× 345 1.0× 120 0.6× 263 1.3× 40 1.1k
Christian L. Boutwell United States 13 507 1.0× 395 0.9× 281 0.8× 236 1.1× 133 0.7× 18 1.0k
Shilin Hu China 18 578 1.2× 573 1.4× 336 0.9× 367 1.7× 232 1.1× 42 1.3k
Harriet C. T. Groom United Kingdom 11 576 1.2× 611 1.5× 555 1.6× 133 0.6× 286 1.4× 13 1.3k
Michael D. Moore United States 17 427 0.9× 536 1.3× 453 1.3× 117 0.6× 288 1.4× 22 1.2k
Karen Tran United States 21 796 1.6× 622 1.5× 458 1.3× 255 1.2× 257 1.3× 33 1.4k
Jean-Marc Jacqué United States 11 884 1.8× 571 1.4× 431 1.2× 224 1.1× 183 0.9× 11 1.4k
Laurie Lamoreaux United States 13 441 0.9× 404 1.0× 637 1.8× 113 0.5× 350 1.7× 15 1.4k
Fabienne Rayne France 15 530 1.1× 338 0.8× 236 0.7× 200 0.9× 211 1.0× 20 961

Countries citing papers authored by Eugene V. Barsov

Since Specialization
Citations

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

Fields of papers citing papers by Eugene V. Barsov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eugene V. Barsov

This figure shows the co-authorship network connecting the top 25 collaborators of Eugene V. Barsov. A scholar is included among the top collaborators of Eugene V. Barsov 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 Eugene V. Barsov. Eugene V. Barsov 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.
Trivett, Matthew T., Claire Deléage, Lori V. Coren, et al.. (2019). Preferential Small Intestine Homing and Persistence of CD8 T Cells in Rhesus Macaques Achieved by Molecularly Engineered Expression of CCR9 and ReducedEx VivoManipulation. Journal of Virology. 93(21). 7 indexed citations
2.
Streltsova, Maria A., et al.. (2018). Current Approaches to Engineering of NK Cells for Cancer Immunotherapy. Current Pharmaceutical Design. 24(24). 2810–2824. 9 indexed citations
3.
Streltsova, Maria A., et al.. (2017). Retroviral gene transfer into primary human NK cells activated by IL-2 and K562 feeder cells expressing membrane-bound IL-21. Journal of Immunological Methods. 450. 90–94. 35 indexed citations
4.
Barsov, Eugene V., et al.. (2011). Transduction of SIV-Specific TCR Genes into Rhesus Macaque CD8+ T Cells Conveys the Ability to Suppress SIV Replication. PLoS ONE. 6(8). e23703–e23703. 15 indexed citations
5.
Barsov, Eugene V.. (2011). Immortalization of Human and Rhesus Macaque Primary Antigen‐Specific T Cells by Retrovirally Transduced Telomerase Reverse Transcriptase. Current Protocols in Immunology. 95(1). Unit 7.21B–Unit 7.21B. 5 indexed citations
6.
Minang, Jacob T., Matthew T. Trivett, Eugene V. Barsov, et al.. (2010). TCR triggering transcriptionally downregulates CCR5 expression on rhesus macaque CD4+ T-cells with no measurable effect on susceptibility to SIV infection. Virology. 409(1). 132–140. 4 indexed citations
7.
Pugacheva, Elena M., Teruhiko Suzuki, Svetlana Pack, et al.. (2010). The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer. PLoS ONE. 5(11). e13872–e13872. 52 indexed citations
8.
Minang, Jacob T., Matthew T. Trivett, Lori V. Coren, et al.. (2009). Nef-mediated MHC class I down-regulation unmasks clonal differences in virus suppression by SIV-specific CD8+ T cells independent of IFN-γ and CD107a responses. Virology. 391(1). 130–139. 17 indexed citations
9.
Barsov, Eugene V.. (2009). Selective Immortalization of Tumor-Specific T Cells to Establish Long-Term T-Cell Lines Maintaining Primary Cell Characteristics. Methods in molecular biology. 511. 143–158. 7 indexed citations
10.
Minang, Jacob T., Eugene V. Barsov, Fang Yuan, et al.. (2008). Efficient inhibition of SIV replication in rhesus CD4+ T-cell clones by autologous immortalized SIV-specific CD8+ T-cell clones. Virology. 372(2). 430–441. 17 indexed citations
11.
Minang, Jacob T., Matthew T. Trivett, Lori V. Coren, et al.. (2008). The Mamu B⁎17-restricted SIV Nef IW9 to TW9 mutation abrogates correct epitope processing and presentation without loss of replicative fitness. Virology. 375(1). 307–314. 11 indexed citations
12.
Andersen, Hanné, Eugene V. Barsov, Matthew T. Trivett, et al.. (2007). Transduction with Human Telomerase Reverse Transcriptase Immortalizes A Rhesus Macaque CD8 + T Cell Clone with Maintenance of Surface Marker Phenotype And Function. AIDS Research and Human Retroviruses. 23(3). 456–465. 18 indexed citations
13.
Chertova, Elena, Oleg Chertov, Lori V. Coren, et al.. (2006). Proteomic and Biochemical Analysis of Purified Human Immunodeficiency Virus Type 1 Produced from Infected Monocyte-Derived Macrophages. Journal of Virology. 80(18). 9039–9052. 372 indexed citations
14.
Barsov, Eugene V., Hanné Andersen, Vicky Coalter, et al.. (2005). Capture of antigen-specific T lymphocytes from human blood by selective immortalization to establish long-term T-cell lines maintaining primary cell characteristics☆. Immunology Letters. 105(1). 26–37. 13 indexed citations
15.
16.
Schaefer-Klein, Janet, I Givol, Eugene V. Barsov, et al.. (1998). The EV-O-Derived Cell Line DF-1 Supports the Efficient Replication of Avian Leukosis-Sarcoma Viruses and Vectors. Virology. 248(2). 305–311. 174 indexed citations
17.
18.
Morikawa, Yuko, Eugene V. Barsov, & Ian M. Jones. (1993). Legitimate and illegitimate cleavage of human immunodeficiency virus glycoproteins by furin. Journal of Virology. 67(6). 3601–3604. 55 indexed citations
19.
Bukrinsky, Michael, et al.. (1989). False‐positive sera do not react with human immunodeficiency virus (HIV) Gag‐encoded recombinant antigen. Journal of Medical Virology. 27(1). 72–75. 3 indexed citations
20.

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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