Todd D. Armstrong

6.4k total citations · 1 hit paper
54 papers, 3.3k citations indexed

About

Todd D. Armstrong is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Todd D. Armstrong has authored 54 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Immunology, 39 papers in Oncology and 13 papers in Molecular Biology. Recurrent topics in Todd D. Armstrong's work include Immunotherapy and Immune Responses (35 papers), Cancer Immunotherapy and Biomarkers (19 papers) and CAR-T cell therapy research (17 papers). Todd D. Armstrong is often cited by papers focused on Immunotherapy and Immune Responses (35 papers), Cancer Immunotherapy and Biomarkers (19 papers) and CAR-T cell therapy research (17 papers). Todd D. Armstrong collaborates with scholars based in United States, Croatia and Germany. Todd D. Armstrong's co-authors include Elizabeth M. Jaffee, Leisha A. Emens, Virginia K. Clements, Suzanne Ostrand‐Rosenberg, Theodore Kouo, Lanqing Huang, Alexandra B. Pucsek, Sara Solt, Lukas W. Pfannenstiel and Elizabeth A. Manning and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Experimental Medicine.

In The Last Decade

Todd D. Armstrong

53 papers receiving 3.2k citations

Hit Papers

Galectin-3 Shapes Antitumor Immune Responses by Suppressi... 2015 2026 2018 2022 2015 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Todd D. Armstrong United States 29 2.3k 2.0k 843 232 230 54 3.3k
Eric R. Lutz United States 15 2.3k 1.0× 2.6k 1.3× 673 0.8× 307 1.3× 298 1.3× 37 3.5k
Susana Inogés Spain 28 1.8k 0.8× 1.2k 0.6× 912 1.1× 163 0.7× 238 1.0× 65 3.0k
Hung T. Khong United States 25 1.7k 0.8× 1.9k 1.0× 980 1.2× 330 1.4× 211 0.9× 71 3.0k
Ainhoa Arina United States 28 2.7k 1.2× 2.3k 1.2× 1.1k 1.3× 363 1.6× 486 2.1× 50 4.2k
Andrei I. Chapoval United States 25 3.4k 1.5× 2.0k 1.0× 645 0.8× 183 0.8× 190 0.8× 60 4.4k
Dana R. Leach United States 7 2.4k 1.1× 2.5k 1.2× 631 0.7× 180 0.8× 294 1.3× 8 3.5k
Natalia Aptsiauri Spain 31 1.9k 0.9× 1.6k 0.8× 726 0.9× 175 0.8× 200 0.9× 55 2.9k
Arantza Azpilikueta Spain 26 1.8k 0.8× 1.6k 0.8× 438 0.5× 144 0.6× 125 0.5× 47 2.4k
William L. Redmond United States 28 2.3k 1.0× 1.9k 1.0× 593 0.7× 217 0.9× 508 2.2× 79 3.3k
Todd T. Moore United States 12 1.4k 0.6× 1.8k 0.9× 686 0.8× 373 1.6× 257 1.1× 17 2.8k

Countries citing papers authored by Todd D. Armstrong

Since Specialization
Citations

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

Fields of papers citing papers by Todd D. Armstrong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Todd D. Armstrong. 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 Todd D. Armstrong. The network helps show where Todd D. Armstrong may publish in the future.

Co-authorship network of co-authors of Todd D. Armstrong

This figure shows the co-authorship network connecting the top 25 collaborators of Todd D. Armstrong. A scholar is included among the top collaborators of Todd D. Armstrong 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 Todd D. Armstrong. Todd D. Armstrong 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.
Zabransky, Daniel J., Yash Chhabra, Mitchell E. Fane, et al.. (2024). Fibroblasts in the Aged Pancreas Drive Pancreatic Cancer Progression. Cancer Research. 84(8). 1221–1236. 13 indexed citations
2.
Huff, Amanda L., Jacob T. Mitchell, Emily F. Davis-Marcisak, et al.. (2023). CD4 T cell–activating neoantigens enhance personalized cancer vaccine efficacy. JCI Insight. 8(23). 14 indexed citations
3.
Korangath, Preethi, James D. Barnett, Anirudh Sharma, et al.. (2020). Nanoparticle interactions with immune cells dominate tumor retention and induce T cell–mediated tumor suppression in models of breast cancer. Science Advances. 6(13). eaay1601–eaay1601. 131 indexed citations
4.
Anders, Robert A., Elana J. Fertig, Alexander C. Hopkins, et al.. (2020). Inhibition of miR-21 Regulates Mutant KRAS Effector Pathways and Intercepts Pancreatic Ductal Adenocarcinoma Development. Cancer Prevention Research. 13(7). 569–582. 15 indexed citations
5.
Hayley, S., Evanthia T. Roussos Torres, John-William Sidhom, et al.. (2019). A CD40 Agonist and PD-1 Antagonist Antibody Reprogram the Microenvironment of Nonimmunogenic Tumors to Allow T-cell–Mediated Anticancer Activity. Cancer Immunology Research. 7(3). 428–442. 94 indexed citations
6.
Blair, Alex B., Victoria M. Kim, Stephen Muth, et al.. (2019). Dissecting the Stromal Signaling and Regulation of Myeloid Cells and Memory Effector T Cells in Pancreatic Cancer. Clinical Cancer Research. 25(17). 5351–5363. 64 indexed citations
7.
Hopkins, Alexander C., Eric R. Lutz, Annie A. Wu, et al.. (2018). Combining STING-based neoantigen-targeted vaccine with checkpoint modulators enhances antitumor immunity in murine pancreatic cancer. JCI Insight. 3(20). 132 indexed citations
8.
Foote, Jeremy B., Marleen Kok, James M. Leatherman, et al.. (2017). A STING Agonist Given with OX40 Receptor and PD-L1 Modulators Primes Immunity and Reduces Tumor Growth in Tolerized Mice. Cancer Immunology Research. 5(6). 468–479. 117 indexed citations
9.
Kouo, Theodore, Lanqing Huang, Alexandra B. Pucsek, et al.. (2015). Galectin-3 Shapes Antitumor Immune Responses by Suppressing CD8+ T Cells via LAG-3 and Inhibiting Expansion of Plasmacytoid Dendritic Cells. Cancer Immunology Research. 3(4). 412–423. 415 indexed citations breakdown →
10.
Armstrong, Todd D., et al.. (2015). Nonviral Oncogenic Antigens and the Inflammatory Signals Driving Early Cancer Development as Targets for Cancer Immunoprevention. Clinical Cancer Research. 21(7). 1549–1557. 37 indexed citations
11.
Weiß, Vivian, Hong Song, Theodore Kouo, et al.. (2012). Trafficking of High Avidity HER-2/neu-Specific T Cells into HER-2/neu-Expressing Tumors after Depletion of Effector/Memory-Like Regulatory T Cells. PLoS ONE. 7(2). e31962–e31962. 34 indexed citations
12.
Pfannenstiel, Lukas W., Samuel S.K. Lam, Leisha A. Emens, Elizabeth M. Jaffee, & Todd D. Armstrong. (2010). Paclitaxel enhances early dendritic cell maturation and function through TLR4 signaling in mice. Cellular Immunology. 263(1). 79–87. 124 indexed citations
13.
Le, Dung T., Brian H. Ladle, Timothy Lee, et al.. (2010). CD8+Foxp3+ tumor infiltrating lymphocytes accumulate in the context of an effective anti‐tumor response. International Journal of Cancer. 129(3). 636–647. 18 indexed citations
14.
Kim, Peter, Todd D. Armstrong, Hong Song, et al.. (2008). Antibody association with HER-2/neu–targeted vaccine enhances CD8+ T cell responses in mice through Fc-mediated activation of DCs. Journal of Clinical Investigation. 118(5). 1700–1711. 66 indexed citations
16.
Murata, Satoshi, Brian H. Ladle, Peter Kim, et al.. (2006). OX40 Costimulation Synergizes with GM-CSF Whole-Cell Vaccination to Overcome Established CD8+ T Cell Tolerance to an Endogenous Tumor Antigen. The Journal of Immunology. 176(2). 974–983. 79 indexed citations
17.
Armstrong, Todd D., Virginia K. Clements, & Suzanne Ostrand‐Rosenberg. (1998). Class II-Transfected Tumor Cells Directly Present Endogenous Antigen to CD4+ T Cells In Vitro and Are APCs for Tumor-Encoded Antigens In Vivo. Journal of Immunotherapy. 21(3). 218–224. 31 indexed citations
18.
Ostrand‐Rosenberg, Suzanne, Beth A. Pulaski, Todd D. Armstrong, & Virginia K. Clements. (1998). Immunotherapy of Established Tumor with MHC Class II and B7.1 Cell-Based Tumor Vaccines. Advances in experimental medicine and biology. 451. 259–264. 9 indexed citations
19.
Armstrong, Todd D., et al.. (1998). Tumor antigen presentation: changing the rules. Cancer Immunology Immunotherapy. 46(2). 70–74. 38 indexed citations
20.
Clements, Virginia K., Sivasubramanian Baskar, Todd D. Armstrong, & Suzanne Ostrand‐Rosenberg. (1992). Invariant chain alters the malignant phenotype of MHC class II+ tumor cells. The Journal of Immunology. 149(7). 2391–2396. 56 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026