Bapi Pahar

2.3k total citations
73 papers, 1.7k citations indexed

About

Bapi Pahar is a scholar working on Virology, Immunology and Infectious Diseases. According to data from OpenAlex, Bapi Pahar has authored 73 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Virology, 45 papers in Immunology and 25 papers in Infectious Diseases. Recurrent topics in Bapi Pahar's work include HIV Research and Treatment (45 papers), Immune Cell Function and Interaction (35 papers) and T-cell and B-cell Immunology (17 papers). Bapi Pahar is often cited by papers focused on HIV Research and Treatment (45 papers), Immune Cell Function and Interaction (35 papers) and T-cell and B-cell Immunology (17 papers). Bapi Pahar collaborates with scholars based in United States, India and Czechia. Bapi Pahar's co-authors include Ronald S. Veazey, Andrew A. Lackner, Arpita Das, Xavier Álvarez, Xiaolei Wang, Huanbin Xu, Mario T. Philipp, Marta L. Marthas, Koen K. A. Van Rompay and Giampiero Girolomoni and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The Journal of Immunology.

In The Last Decade

Bapi Pahar

71 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bapi Pahar United States 28 834 777 635 564 248 73 1.7k
Masashi Shingai Japan 23 799 1.0× 1.7k 2.2× 691 1.1× 776 1.4× 441 1.8× 56 2.6k
Michael B. Agy United States 20 992 1.2× 676 0.9× 428 0.7× 401 0.7× 409 1.6× 46 1.6k
George Lin United States 15 510 0.6× 601 0.8× 296 0.5× 347 0.6× 318 1.3× 24 1.4k
Alfred W. Legasse United States 21 1.2k 1.5× 1.4k 1.8× 529 0.8× 1.1k 1.9× 418 1.7× 31 2.4k
Stephen Norley Germany 26 983 1.2× 700 0.9× 458 0.7× 601 1.1× 304 1.2× 73 1.7k
Anita M. Trichel United States 23 926 1.1× 557 0.7× 478 0.8× 456 0.8× 229 0.9× 37 1.4k
Daniela Tudor France 17 566 0.7× 582 0.7× 250 0.4× 248 0.4× 252 1.0× 26 1.3k
David A. Garber United States 25 593 0.7× 530 0.7× 224 0.4× 747 1.3× 341 1.4× 48 1.6k
Ronald J. Messer United States 29 454 0.5× 1.5k 1.9× 315 0.5× 517 0.9× 256 1.0× 51 2.2k
Teri L. Kissner United States 14 630 0.8× 1.1k 1.4× 314 0.5× 295 0.5× 236 1.0× 19 1.6k

Countries citing papers authored by Bapi Pahar

Since Specialization
Citations

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

Fields of papers citing papers by Bapi Pahar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bapi Pahar. 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 Bapi Pahar. The network helps show where Bapi Pahar may publish in the future.

Co-authorship network of co-authors of Bapi Pahar

This figure shows the co-authorship network connecting the top 25 collaborators of Bapi Pahar. A scholar is included among the top collaborators of Bapi Pahar 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 Bapi Pahar. Bapi Pahar 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.
Platt, Andrew P., B. C. Barr, Vincent J. Munster, et al.. (2025). Cellular immunophenotyping in human and primate tissues during healthy conditions and Ebola and Nipah infections. JCI Insight. 10(11).
2.
Carey, Brian D., Shuǐqìng Yú, Chengjin Ye, et al.. (2024). A Lassa virus live attenuated vaccine candidate that is safe and efficacious in guinea pigs. npj Vaccines. 9(1). 220–220. 4 indexed citations
3.
Spear, Mark, Jia Guo, Yajing Fu, et al.. (2024). Suppression of viral rebound by a Rev-dependent lentiviral particle in SIV-infected rhesus macaques. Gene Therapy. 32(1). 16–24.
4.
Liu, David X., Bapi Pahar, Donna L. Perry, et al.. (2023). Depletion of Bone Marrow Hematopoietic Cells in Ebolavirus-Infected Rhesus Macaques. American Journal Of Pathology. 193(12). 2031–2046. 2 indexed citations
5.
Das, Arpita, et al.. (2023). Toll-like Receptor 2 Mediated Immune Regulation in Simian Immunodeficiency Virus-Infected Rhesus Macaques. Vaccines. 11(12). 1861–1861. 2 indexed citations
6.
7.
8.
Das, Arpita, et al.. (2021). Enhanced Intestinal TGF-β/SMAD-Dependent Signaling in Simian Immunodeficiency Virus Infected Rhesus Macaques. Cells. 10(4). 806–806. 11 indexed citations
9.
Pahar, Bapi, Stefania Madonna, Arpita Das, Cristina Albanesi, & Giampiero Girolomoni. (2020). Immunomodulatory Role of the Antimicrobial LL-37 Peptide in Autoimmune Diseases and Viral Infections. Vaccines. 8(3). 517–517. 88 indexed citations
10.
Embers, Monica E., Bapi Pahar, Hannah K. Wilder, et al.. (2019). Immunological Responses to the Relapsing Fever Spirochete Borrelia turicatae in Infected Rhesus Macaques: Implications for Pathogenesis and Diagnosis. Infection and Immunity. 87(4). 3 indexed citations
11.
Lackner, Andrew A., et al.. (2017). The Role of Defensins in HIV Pathogenesis. Mediators of Inflammation. 2017. 1–12. 32 indexed citations
12.
Pahar, Bapi, Preston A. Marx, Sudesh Srivastav, et al.. (2016). Breadth and magnitude of antigen-specific antibody responses in the control of plasma viremia in simian immunodeficiency virus infected macaques. Virology Journal. 13(1). 200–200. 7 indexed citations
13.
Stanfield, Brent, Bapi Pahar, Vladimir N. Chouljenko, Ronald S. Veazey, & Konstantin G. Kousoulas. (2016). Vaccination of rhesus macaques with the live-attenuated HSV-1 vaccine VC2 stimulates the proliferation of mucosal T cells and germinal center responses resulting in sustained production of highly neutralizing antibodies. Vaccine. 35(4). 536–543. 33 indexed citations
14.
Breed, Matthew W., Andrea P. O. Jordan, Pyone P. Aye, et al.. (2012). Loss of a Tyrosine-Dependent Trafficking Motif in the Simian Immunodeficiency Virus Envelope Cytoplasmic Tail Spares Mucosal CD4 Cells but Does Not Prevent Disease Progression. Journal of Virology. 87(3). 1528–1543. 27 indexed citations
15.
Sestak, Karol, Jason Dufour, Xavier Álvarez, et al.. (2012). Experimental Inoculation of Juvenile Rhesus Macaques with Primate Enteric Caliciviruses. PLoS ONE. 7(5). e37973–e37973. 37 indexed citations
16.
Wang, Xiaolei, Huanbin Xu, Xavier Álvarez, et al.. (2011). Distinct Expression Patterns of CD69 in Mucosal and Systemic Lymphoid Tissues in Primary SIV Infection of Rhesus Macaques. PLoS ONE. 6(11). e27207–e27207. 21 indexed citations
17.
Traina‐Dorge, Vicki, Bapi Pahar, Preston A. Marx, et al.. (2010). Recombinant varicella vaccines induce neutralizing antibodies and cellular immune responses to SIV and reduce viral loads in immunized rhesus macaques. Vaccine. 28(39). 6483–6490. 12 indexed citations
18.
Wang, Xishan, Haifeng C. Xu, Bapi Pahar, et al.. (2009). Monitoring α4β7 integrin expression on circulating CD4+ T cells as a surrogate marker for tracking intestinal CD4+ T-cell loss in SIV infection. Mucosal Immunology. 2(6). 518–526. 62 indexed citations
19.
Wang, Xiaolei, Bapi Pahar, Terri Rasmussen, et al.. (2008). Differential cross-reactivity of monoclonal antibody OPD4 (anti-CD45RO) in macaques. Developmental & Comparative Immunology. 32(7). 859–868. 2 indexed citations
20.
Pahar, Bapi, Jun Li, & Michael B. McChesney. (2005). Detection of T cell memory to measles virus in experimentally infected rhesus macaques by cytokine flow cytometry. Journal of Immunological Methods. 304(1-2). 174–183. 8 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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