Tyler G. Searles

543 total citations
7 papers, 235 citations indexed

About

Tyler G. Searles is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Tyler G. Searles has authored 7 papers receiving a total of 235 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Immunology, 6 papers in Oncology and 1 paper in Molecular Biology. Recurrent topics in Tyler G. Searles's work include Immunotherapy and Immune Responses (4 papers), Cancer Immunotherapy and Biomarkers (4 papers) and CAR-T cell therapy research (3 papers). Tyler G. Searles is often cited by papers focused on Immunotherapy and Immune Responses (4 papers), Cancer Immunotherapy and Biomarkers (4 papers) and CAR-T cell therapy research (3 papers). Tyler G. Searles collaborates with scholars based in United States and South Africa. Tyler G. Searles's co-authors include Mary Jo Turk, Jichang Han, Christina V. Angeles, Nikhil Khatwani, Keisuke Shirai, Yanding Zhao, Aleksey Molodtsov, Jiang Gui, Chao Cheng and Shaofeng Yan and has published in prestigious journals such as The Journal of Immunology, Cancer Research and Seminars in Immunology.

In The Last Decade

Tyler G. Searles

6 papers receiving 231 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tyler G. Searles United States	5	169	148	53	31	22	7	235
Gena G. Foster United States	3	193 1.1×	209 1.4×	83 1.6×	40 1.3×	36 1.6×	5	304
Jolien Ceusters Belgium	7	109 0.6×	161 1.1×	67 1.3×	17 0.5×	21 1.0×	19	248
Brittany Fitzgerald United States	3	201 1.2×	216 1.5×	89 1.7×	45 1.5×	39 1.8×	6	321
Andrew Baessler United States	5	147 0.9×	151 1.0×	67 1.3×	23 0.7×	21 1.0×	6	267
Caleb Lampenfeld United States	4	176 1.0×	170 1.1×	61 1.2×	40 1.3×	39 1.8×	4	268
Jessica Mariel Sierra Argentina	7	125 0.7×	192 1.3×	35 0.7×	24 0.8×	22 1.0×	10	276
Mark Schmidt United States	4	125 0.7×	93 0.6×	43 0.8×	29 0.9×	31 1.4×	8	186
Lieke L. van der Woude Netherlands	6	212 1.3×	187 1.3×	77 1.5×	42 1.4×	27 1.2×	10	306
Annie Tasker Australia	4	286 1.7×	267 1.8×	50 0.9×	36 1.2×	14 0.6×	6	362
Rachael M. Zemek Australia	8	160 0.9×	152 1.0×	49 0.9×	29 0.9×	21 1.0×	15	240

Countries citing papers authored by Tyler G. Searles

Since Specialization

Citations

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

Fields of papers citing papers by Tyler G. Searles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tyler G. Searles. 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 Tyler G. Searles. The network helps show where Tyler G. Searles may publish in the future.

Co-authorship network of co-authors of Tyler G. Searles

This figure shows the co-authorship network connecting the top 25 collaborators of Tyler G. Searles. A scholar is included among the top collaborators of Tyler G. Searles 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 Tyler G. Searles. Tyler G. Searles is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

Travers, Meghan, Tyler G. Searles, Gustavo Martínez, et al.. (2025). Abstract 2196: Characterizing the impact of SOCS1 and Regnase-1 inactivation on tumor reactive T cells present in CRISPR/Cas9-engineered TIL (eTIL®) therapies derived from melanoma and NSCLC tumors through functional and single cell analyses. Cancer Research. 85(8_Supplement_1). 2196–2196.

Searles, Tyler G., Chun‐Chieh Lin, Keisuke Shirai, et al.. (2024). CD39 Is Expressed on Functional Effector and Tissue-resident Memory CD8+ T Cells. The Journal of Immunology. 213(5). 588–599. 4 indexed citations

Searles, Tyler G., Tiffany Chen, J. Louise Lines, et al.. (2024). Depletion of conventional CD4⁺ T cells is required for robust priming and dissemination of tumor antigen-specific CD8⁺ T cells in the setting of anti-CD4 therapy. Journal for ImmunoTherapy of Cancer. 12(11). e010170–e010170. 4 indexed citations

Searles, Tyler G., et al.. (2023). Validation of Ligand Tetramers for the Detection of Antigen-Specific Lymphocytes. The Journal of Immunology. 210(8). 1156–1165. 5 indexed citations

Phillips, Joseph D., Peisheng Zhang, Daniel W. Mielcarz, et al.. (2023). The Effect of Lung Resection for NSCLC on Circulating Immune Cells: A Pilot Study. Current Oncology. 30(5). 5116–5134. 2 indexed citations

Han, Jichang, Yanding Zhao, Keisuke Shirai, et al.. (2021). Resident and circulating memory T cells persist for years in melanoma patients with durable responses to immunotherapy. Nature Cancer. 2(3). 300–311. 91 indexed citations

Han, Jichang, Nikhil Khatwani, Tyler G. Searles, Mary Jo Turk, & Christina V. Angeles. (2020). Memory CD8+ T cell responses to cancer. Seminars in Immunology. 49. 101435–101435. 129 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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