Gordon J. Freeman

130.1k total citations · 51 hit papers
419 papers, 82.7k citations indexed

About

Gordon J. Freeman is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Gordon J. Freeman has authored 419 papers receiving a total of 82.7k indexed citations (citations by other indexed papers that have themselves been cited), including 301 papers in Immunology, 194 papers in Oncology and 60 papers in Molecular Biology. Recurrent topics in Gordon J. Freeman's work include Immune Cell Function and Interaction (195 papers), Cancer Immunotherapy and Biomarkers (141 papers) and T-cell and B-cell Immunology (132 papers). Gordon J. Freeman is often cited by papers focused on Immune Cell Function and Interaction (195 papers), Cancer Immunotherapy and Biomarkers (141 papers) and T-cell and B-cell Immunology (132 papers). Gordon J. Freeman collaborates with scholars based in United States, United Kingdom and China. Gordon J. Freeman's co-authors include Arlene H. Sharpe, Mary Keir, Manish J. Butte, Rafi Ahmed, E. John Wherry, Lee M. Nadler, Vijay K. Kuchroo, Kathleen M. Mahoney, Rebecca J. Greenwald and Baogong Zhu and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Gordon J. Freeman

414 papers receiving 81.6k citations

Hit Papers

PD-1 and Its Ligands in Tolerance and Immunity 1991 2026 2002 2014 2008 2018 2005 2014 2005 1000 2.0k 3.0k 4.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gordon J. Freeman United States 141 54.1k 38.6k 14.7k 8.3k 6.8k 419 82.7k
Drew M. Pardoll United States 132 46.7k 0.9× 45.0k 1.2× 23.5k 1.6× 8.8k 1.1× 5.7k 0.8× 403 83.2k
Mark J. Smyth Australia 143 52.9k 1.0× 37.6k 1.0× 20.2k 1.4× 5.1k 0.6× 5.5k 0.8× 595 81.6k
Arlene H. Sharpe United States 130 47.7k 0.9× 28.8k 0.7× 16.3k 1.1× 4.6k 0.6× 5.9k 0.9× 408 75.8k
Robert D. Schreiber United States 119 48.3k 0.9× 33.6k 0.9× 20.7k 1.4× 4.4k 0.5× 8.7k 1.3× 385 79.6k
Jedd D. Wolchok United States 119 29.7k 0.5× 45.3k 1.2× 16.2k 1.1× 11.0k 1.3× 3.3k 0.5× 568 65.0k
Lieping Chen United States 112 36.0k 0.7× 34.3k 0.9× 9.2k 0.6× 6.6k 0.8× 3.4k 0.5× 368 55.6k
Wolf H. Fridman France 100 31.2k 0.6× 27.6k 0.7× 16.6k 1.1× 8.5k 1.0× 2.6k 0.4× 529 57.4k
Hideo Yagita∥ Japan 128 43.5k 0.8× 21.7k 0.6× 18.2k 1.2× 3.3k 0.4× 5.2k 0.8× 912 67.3k
Paola Allavena Italy 93 33.3k 0.6× 22.0k 0.6× 14.6k 1.0× 4.9k 0.6× 4.1k 0.6× 295 56.8k
Vijay K. Kuchroo United States 133 59.0k 1.1× 20.6k 0.5× 13.2k 0.9× 2.7k 0.3× 5.2k 0.8× 426 79.1k

Countries citing papers authored by Gordon J. Freeman

Since Specialization
Citations

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

Fields of papers citing papers by Gordon J. Freeman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gordon J. Freeman. 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 Gordon J. Freeman. The network helps show where Gordon J. Freeman may publish in the future.

Co-authorship network of co-authors of Gordon J. Freeman

This figure shows the co-authorship network connecting the top 25 collaborators of Gordon J. Freeman. A scholar is included among the top collaborators of Gordon J. Freeman 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 Gordon J. Freeman. Gordon J. Freeman 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.
Park, Joon Seok, Francesca S. Gazzaniga, Meng–Huang Wu, et al.. (2023). Targeting PD-L2–RGMb overcomes microbiome-related immunotherapy resistance. Nature. 617(7960). 377–385. 120 indexed citations breakdown →
2.
Bu, Xia, Vikram R. Juneja, Carol Reynolds, et al.. (2021). Monitoring PD-1 Phosphorylation to Evaluate PD-1 Signaling during Antitumor Immune Responses. Cancer Immunology Research. 9(12). 1465–1475. 11 indexed citations
3.
Derks, Sarah, Leonie K. de Klerk, Xiaoshu Xu, et al.. (2020). Characterizing diversity in the tumor-immune microenvironment of distinct subclasses of gastroesophageal adenocarcinomas. Annals of Oncology. 31(8). 1011–1020. 107 indexed citations
4.
Chaudhri, Apoorvi, et al.. (2018). PD-L1 Binds to B7-1 Only In Cis on the Same Cell Surface. Cancer Immunology Research. 6(8). 921–929. 136 indexed citations
5.
Kansy, Benjamin, Fernando Concha‐Benavente, Raghvendra M. Srivastava, et al.. (2017). PD-1 Status in CD8+ T Cells Associates with Survival and Anti-PD-1 Therapeutic Outcomes in Head and Neck Cancer. Cancer Research. 77(22). 6353–6364. 174 indexed citations
6.
Kamphorst, Alice O., Andreas Wieland, Tahseen H. Nasti, et al.. (2017). Rescue of exhausted CD8 T cells by PD-1–targeted therapies is CD28-dependent. Science. 355(6332). 1423–1427. 724 indexed citations breakdown →
7.
Zhou, Jun, Kathleen M. Mahoney, Anita Giobbie‐Hurder, et al.. (2017). Soluble PD-L1 as a Biomarker in Malignant Melanoma Treated with Checkpoint Blockade. Cancer Immunology Research. 5(6). 480–492. 284 indexed citations
8.
Sridharan, Vishwajith, Evisa Gjini, Xiaoyun Liao, et al.. (2016). Immune Profiling of Adenoid Cystic Carcinoma: PD-L2 Expression and Associations with Tumor-Infiltrating Lymphocytes. Cancer Immunology Research. 4(8). 679–687. 77 indexed citations
9.
Callea, Marcella, Laurence Albigès, Mamta Gupta, et al.. (2015). Differential Expression of PD-L1 between Primary and Metastatic Sites in Clear-Cell Renal Cell Carcinoma. Cancer Immunology Research. 3(10). 1158–1164. 266 indexed citations
10.
Paterson, Alison M., Scott B. Lovitch, Peter T. Sage, et al.. (2015). Deletion of CTLA-4 on regulatory T cells during adulthood leads to resistance to autoimmunity. The Journal of Experimental Medicine. 212(10). 1603–1621. 172 indexed citations
11.
Giraldo, Nicolás A., Étienne Becht, Franck Pagès, et al.. (2015). Orchestration and Prognostic Significance of Immune Checkpoints in the Microenvironment of Primary and Metastatic Renal Cell Cancer. Clinical Cancer Research. 21(13). 3031–3040. 356 indexed citations breakdown →
12.
Mahoney, Kathleen M., Heather H. Sun, Xiaoyun Liao, et al.. (2015). PD-L1 Antibodies to Its Cytoplasmic Domain Most Clearly Delineate Cell Membranes in Immunohistochemical Staining of Tumor Cells. Cancer Immunology Research. 3(12). 1308–1315. 103 indexed citations
13.
Reardon, David A., Prafulla C. Gokhale, Sarah R. Klein, et al.. (2015). Glioblastoma Eradication Following Immune Checkpoint Blockade in an Orthotopic, Immunocompetent Model. Cancer Immunology Research. 4(2). 124–135. 302 indexed citations
14.
Concha‐Benavente, Fernando, Raghvendra M. Srivastava, Sumita Trivedi, et al.. (2015). Identification of the Cell-Intrinsic and -Extrinsic Pathways Downstream of EGFR and IFNγ That Induce PD-L1 Expression in Head and Neck Cancer. Cancer Research. 76(5). 1031–1043. 253 indexed citations
15.
Du, Ziming, Malak Abedalthagafi, Ayal A. Aizer, et al.. (2014). Increased expression of the immune modulatory molecule PD-L1 (CD274) in anaplastic meningioma. Oncotarget. 6(7). 4704–4716. 126 indexed citations
16.
Chen, Benjamin J., Bjoern Chapuy, Jing Ouyang, et al.. (2013). PD-L1 Expression Is Characteristic of a Subset of Aggressive B-cell Lymphomas and Virus-Associated Malignancies. Clinical Cancer Research. 19(13). 3462–3473. 657 indexed citations breakdown →
17.
Fuller, Michael J., Benoît Callendret, Baogong Zhu, et al.. (2013). Immunotherapy of chronic hepatitis C virus infection with antibodies against programmed cell death-1 (PD-1). Proceedings of the National Academy of Sciences. 110(37). 15001–15006. 140 indexed citations
18.
Lichterfeld, Mathias, Danlei Mou, Thai Cung, et al.. (2008). Telomerase activity of HIV-1–specific CD8+ T cells: constitutive up-regulation in controllers and selective increase by blockade of PD ligand 1 in progressors. Blood. 112(9). 3679–3687. 59 indexed citations
19.
Radziewicz, Henry, Chris Ibegbu, Marina L. Fernandez, et al.. (2006). Liver-Infiltrating Lymphocytes in Chronic Human Hepatitis C Virus Infection Display an Exhausted Phenotype with High Levels of PD-1 and Low Levels of CD127 Expression. Journal of Virology. 81(6). 2545–2553. 387 indexed citations
20.
Latchman, Yvette, Spencer C. Liang, Yin Wu, et al.. (2004). PD-L1-deficient mice show that PD-L1 on T cells, antigen-presenting cells, and host tissues negatively regulates T cells. Proceedings of the National Academy of Sciences. 101(29). 10691–10696. 521 indexed citations breakdown →

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