Jamal S. Lewis

1.5k total citations
42 papers, 1.2k citations indexed

About

Jamal S. Lewis is a scholar working on Immunology, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Jamal S. Lewis has authored 42 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Immunology, 18 papers in Molecular Biology and 6 papers in Biomedical Engineering. Recurrent topics in Jamal S. Lewis's work include Immunotherapy and Immune Responses (17 papers), RNA Interference and Gene Delivery (13 papers) and Immune Cell Function and Interaction (9 papers). Jamal S. Lewis is often cited by papers focused on Immunotherapy and Immune Responses (17 papers), RNA Interference and Gene Delivery (13 papers) and Immune Cell Function and Interaction (9 papers). Jamal S. Lewis collaborates with scholars based in United States, Thailand and France. Jamal S. Lewis's co-authors include Benjamin G. Keselowsky, Michael Clare‐Salzler, Natalia V. Dolgova, Toral Zaveri, Riley Allen, Noah Pacifici, Clive Wasserfall, Mark A. Atkinson, Ying Zhang and Abhinav P. Acharya and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Biomaterials.

In The Last Decade

Jamal S. Lewis

40 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jamal S. Lewis United States 19 578 396 290 182 175 42 1.2k
James I. Andorko United States 17 592 1.0× 455 1.1× 332 1.1× 138 0.8× 174 1.0× 28 1.1k
Woon Teck Yap United States 8 497 0.9× 282 0.7× 108 0.4× 129 0.7× 89 0.5× 10 852
Yu-Chieh Chiu United States 18 421 0.7× 363 0.9× 524 1.8× 195 1.1× 357 2.0× 20 1.2k
Corrine Ying Xuan Chua United States 20 180 0.3× 332 0.8× 357 1.2× 184 1.0× 157 0.9× 53 1.2k
Robert Nordon Australia 19 241 0.4× 630 1.6× 437 1.5× 176 1.0× 123 0.7× 57 1.5k
Ziad Julier Australia 10 369 0.6× 491 1.2× 339 1.2× 269 1.5× 241 1.4× 11 1.4k
David Zhang United States 17 417 0.7× 484 1.2× 449 1.5× 129 0.7× 156 0.9× 25 1.3k
Gijung Kwak South Korea 16 290 0.5× 683 1.7× 482 1.7× 97 0.5× 335 1.9× 27 1.4k
Ting‐Yu Shih United States 14 724 1.3× 473 1.2× 597 2.1× 95 0.5× 252 1.4× 28 1.4k
Libo Zhou China 17 728 1.3× 474 1.2× 374 1.3× 131 0.7× 108 0.6× 42 1.7k

Countries citing papers authored by Jamal S. Lewis

Since Specialization
Citations

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

Fields of papers citing papers by Jamal S. Lewis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jamal S. Lewis. 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 Jamal S. Lewis. The network helps show where Jamal S. Lewis may publish in the future.

Co-authorship network of co-authors of Jamal S. Lewis

This figure shows the co-authorship network connecting the top 25 collaborators of Jamal S. Lewis. A scholar is included among the top collaborators of Jamal S. Lewis 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 Jamal S. Lewis. Jamal S. Lewis 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.
Pacifici, Noah, et al.. (2025). Identification of signaling networks associated with lactate modulation of macrophages and dendritic cells. Heliyon. 11(3). e42098–e42098. 4 indexed citations
2.
Pacifici, Noah, et al.. (2023). Vomocytosis of Cryptococcus neoformans cells from murine, bone marrow-derived dendritic cells. PLoS ONE. 18(3). e0280692–e0280692. 5 indexed citations
3.
Yik, Jasper H. N., et al.. (2022). Intra-articular injection of flavopiridol-loaded microparticles for treatment of post-traumatic osteoarthritis. Acta Biomaterialia. 149. 347–358. 18 indexed citations
4.
Pacifici, Noah, et al.. (2022). Polymeric particle-based therapies for acute inflammatory diseases. Nature Reviews Materials. 7(10). 796–813. 73 indexed citations
5.
Tu, Allen B. & Jamal S. Lewis. (2021). Biomaterial-based immunotherapeutic strategies for rheumatoid arthritis. Drug Delivery and Translational Research. 11(6). 2371–2393. 13 indexed citations
6.
Lewis, Jamal S., et al.. (2021). Bioderived materials that disarm the gut mucosal immune system: Potential lessons from commensal microbiota. Acta Biomaterialia. 133. 187–207. 6 indexed citations
7.
Vapniarsky, Natalia, et al.. (2020). Biodistribution and toxicity of epitope‐functionalized dextran iron oxide nanoparticles in a pregnant murine model. Journal of Biomedical Materials Research Part A. 108(5). 1186–1202. 11 indexed citations
8.
Pacifici, Noah, et al.. (2020). Lactate Exposure Promotes Immunosuppressive Phenotypes in Innate Immune Cells. Cellular and Molecular Bioengineering. 13(5). 541–557. 53 indexed citations
9.
Pacifici, Noah, et al.. (2020). Stimuli‐Responsive Biomaterials for Vaccines and Immunotherapeutic Applications. Advanced Therapeutics. 3(11). 2000129–2000129. 36 indexed citations
10.
Kakwere, Hamilton, Elizabeth S. Ingham, Riley Allen, et al.. (2018). Unimicellar hyperstars as multi-antigen cancer nanovaccines displaying clustered epitopes of immunostimulating peptides. Biomaterials Science. 6(11). 2850–2858. 12 indexed citations
11.
Yik, Jasper H. N., et al.. (2018). Sustained intra-articular delivery of cyclin-dependent kinase 9 inhibitors protects against proteolytic activity in an ACL rupture rat model of PTOA. Osteoarthritis and Cartilage. 26. S303–S304. 2 indexed citations
12.
Allen, Riley, et al.. (2018). Correction to Latent, Immunosuppressive Nature of Poly(lactic-co-glycolic acid) Microparticles. ACS Biomaterials Science & Engineering. 4(6). 2224–2225. 2 indexed citations
13.
Allen, Riley, et al.. (2018). Latent, Immunosuppressive Nature of Poly(lactic-co-glycolic acid) Microparticles. ACS Biomaterials Science & Engineering. 4(3). 900–918. 91 indexed citations
14.
Keselowsky, Benjamin G. & Jamal S. Lewis. (2017). Dendritic cells in the host response to implanted materials. Seminars in Immunology. 29. 33–40. 32 indexed citations
15.
Acharya, Abhinav P., Jamal S. Lewis, Natalia V. Dolgova, et al.. (2015). A cell-based microarray to investigate combinatorial effects of microparticle-encapsulated adjuvants on dendritic cell activation. Journal of Materials Chemistry B. 4(9). 1672–1685. 26 indexed citations
16.
Lewis, Jamal S., et al.. (2015). A combination hydrogel microparticle-based vaccine prevents type 1 diabetes in non-obese diabetic mice. Scientific Reports. 5(1). 13155–13155. 67 indexed citations
17.
Zaveri, Toral, Jamal S. Lewis, Natalia V. Dolgova, Michael Clare‐Salzler, & Benjamin G. Keselowsky. (2014). Integrin-directed modulation of macrophage responses to biomaterials. Biomaterials. 35(11). 3504–3515. 137 indexed citations
18.
Lewis, Jamal S., Krishnendu Roy, & Benjamin G. Keselowsky. (2014). Materials that harness and modulate the immune system. MRS Bulletin. 39(1). 25–34. 38 indexed citations
19.
Acharya, Abhinav P., Jamal S. Lewis, & Benjamin G. Keselowsky. (2013). Combinatorial co-encapsulation of hydrophobic molecules in poly(lactide-co-glycolide) microparticles. Biomaterials. 34(13). 3422–3430. 23 indexed citations
20.
Lewis, Jamal S., et al.. (2012). Microparticle surface modifications targeting dendritic cells for non-activating applications. Biomaterials. 33(29). 7221–7232. 74 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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