Nicholas P. Restifo

96.1k total citations · 36 hit papers
347 papers, 65.0k citations indexed

About

Nicholas P. Restifo is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Nicholas P. Restifo has authored 347 papers receiving a total of 65.0k indexed citations (citations by other indexed papers that have themselves been cited), including 306 papers in Immunology, 192 papers in Oncology and 94 papers in Molecular Biology. Recurrent topics in Nicholas P. Restifo's work include Immunotherapy and Immune Responses (239 papers), CAR-T cell therapy research (156 papers) and Immune Cell Function and Interaction (140 papers). Nicholas P. Restifo is often cited by papers focused on Immunotherapy and Immune Responses (239 papers), CAR-T cell therapy research (156 papers) and Immune Cell Function and Interaction (140 papers). Nicholas P. Restifo collaborates with scholars based in United States, Australia and Malaysia. Nicholas P. Restifo's co-authors include Steven A. Rosenberg, Luca Gattinoni, Mark E. Dudley, James C. Yang, Zhiya Yu, Christopher A. Klebanoff, Douglas C. Palmer, Richard M. Sherry, Pawel Muranski and James Chih‐Hsin Yang and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Nicholas P. Restifo

344 papers receiving 63.8k citations

Hit Papers

Cancer immunotherapy: mov... 1993 2026 2004 2015 2004 2002 2006 2015 2011 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicholas P. Restifo United States 129 45.9k 39.1k 17.7k 9.7k 5.0k 347 65.0k
Carl H. June United States 139 40.7k 0.9× 52.4k 1.3× 24.4k 1.4× 16.4k 1.7× 14.0k 2.8× 657 85.8k
James P. Allison United States 125 50.0k 1.1× 39.1k 1.0× 13.1k 0.7× 5.1k 0.5× 2.4k 0.5× 487 72.3k
Mark J. Smyth Australia 143 52.9k 1.2× 37.6k 1.0× 20.2k 1.1× 3.7k 0.4× 3.3k 0.7× 595 81.6k
Drew M. Pardoll United States 132 46.7k 1.0× 45.0k 1.2× 23.5k 1.3× 6.0k 0.6× 3.7k 0.7× 403 83.2k
Suzanne L. Topalian United States 82 27.0k 0.6× 32.6k 0.8× 12.4k 0.7× 4.4k 0.4× 2.0k 0.4× 215 49.2k
Arlene H. Sharpe United States 130 47.7k 1.0× 28.8k 0.7× 16.3k 0.9× 5.8k 0.6× 1.1k 0.2× 408 75.8k
Laurence Zitvogel France 123 42.4k 0.9× 31.3k 0.8× 31.7k 1.8× 4.0k 0.4× 7.4k 1.5× 492 79.1k
Robert D. Schreiber United States 119 48.3k 1.1× 33.6k 0.9× 20.7k 1.2× 4.6k 0.5× 1.7k 0.3× 385 79.6k
Jedd D. Wolchok United States 119 29.7k 0.6× 45.3k 1.2× 16.2k 0.9× 2.8k 0.3× 3.7k 0.7× 568 65.0k
Gordon J. Freeman United States 141 54.1k 1.2× 38.6k 1.0× 14.7k 0.8× 4.1k 0.4× 1.9k 0.4× 419 82.7k

Countries citing papers authored by Nicholas P. Restifo

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas P. Restifo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas P. Restifo. 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 Nicholas P. Restifo. The network helps show where Nicholas P. Restifo may publish in the future.

Co-authorship network of co-authors of Nicholas P. Restifo

This figure shows the co-authorship network connecting the top 25 collaborators of Nicholas P. Restifo. A scholar is included among the top collaborators of Nicholas P. Restifo 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 Nicholas P. Restifo. Nicholas P. Restifo 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.
Wang, Qiong J., et al.. (2016). Identification of T-cell Receptors Targeting KRAS-Mutated Human Tumors. Cancer Immunology Research. 4(3). 204–214. 175 indexed citations
2.
Slaney, Clare Y., Bianca von Scheidt, Alexander J. Davenport, et al.. (2016). Dual-specific Chimeric Antigen Receptor T Cells and an Indirect Vaccine Eradicate a Variety of Large Solid Tumors in an Immunocompetent, Self-antigen Setting. Clinical Cancer Research. 23(10). 2478–2490. 89 indexed citations
3.
Shi, Zhong, Zhiya Yu, Ivan Liadi, et al.. (2016). Constitutive Lck Activity Drives Sensitivity Differences between CD8+ Memory T Cell Subsets. The Journal of Immunology. 197(2). 644–654. 16 indexed citations
4.
Zhang, Ling, Richard A. Morgan, Joal D. Beane, et al.. (2015). Tumor-Infiltrating Lymphocytes Genetically Engineered with an Inducible Gene Encoding Interleukin-12 for the Immunotherapy of Metastatic Melanoma. Clinical Cancer Research. 21(10). 2278–2288. 332 indexed citations
5.
Stevanović, Sanja, Lindsey M. Draper, Michelle M. Langhan, et al.. (2015). Complete Regression of Metastatic Cervical Cancer After Treatment With Human Papillomavirus–Targeted Tumor-Infiltrating T Cells. Journal of Clinical Oncology. 33(14). 1543–1550. 506 indexed citations breakdown →
6.
Robbins, Paul F., Sadik H. Kassim, Thai L.N. Tran, et al.. (2014). A Pilot Trial Using Lymphocytes Genetically Engineered with an NY-ESO-1–Reactive T-cell Receptor: Long-term Follow-up and Correlates with Response. Clinical Cancer Research. 21(5). 1019–1027. 585 indexed citations breakdown →
7.
Chinnasamy, Dhanalakshmi, Eric Tran, Zhiya Yu, et al.. (2013). Simultaneous Targeting of Tumor Antigens and the Tumor Vasculature Using T Lymphocyte Transfer Synergize to Induce Regression of Established Tumors in Mice. Cancer Research. 73(11). 3371–3380. 90 indexed citations
8.
Tran, Eric, Dhanalakshmi Chinnasamy, Zhiya Yu, et al.. (2013). Immune targeting of fibroblast activation protein triggers recognition of multipotent bone marrow stromal cells and cachexia. The Journal of Experimental Medicine. 210(6). 1125–1135. 349 indexed citations
9.
Chinnasamy, Dhanalakshmi, Zhiya Yu, Sid P. Kerkar, et al.. (2012). Local Delivery of lnterleukin-12 Using T Cells Targeting VEGF Receptor-2 Eradicates Multiple Vascularized Tumors in Mice. Clinical Cancer Research. 18(6). 1672–1683. 234 indexed citations
10.
Klebanoff, Christopher A., Luca Gattinoni, Douglas C. Palmer, et al.. (2011). Determinants of Successful CD8+ T-Cell Adoptive Immunotherapy for Large Established Tumors in Mice. Clinical Cancer Research. 17(16). 5343–5352. 225 indexed citations
11.
Quezada, Sergio A., Tyler R. Simpson, Karl S. Peggs, et al.. (2010). Tumor-reactive CD4+ T cells develop cytotoxic activity and eradicate large established melanoma after transfer into lymphopenic hosts. The Journal of Experimental Medicine. 207(3). 637–650. 635 indexed citations breakdown →
12.
Gattinoni, Luca, Yun Ji, & Nicholas P. Restifo. (2010). Wnt/β-Catenin Signaling in T-Cell Immunity and Cancer Immunotherapy. Clinical Cancer Research. 16(19). 4695–4701. 142 indexed citations
13.
Muranski, Pawel, Andrea Boni, Paul A. Antony, et al.. (2008). Tumor-specific Th17-polarized cells eradicate large established melanoma. Blood. 112(2). 362–373. 638 indexed citations breakdown →
14.
Dudley, Mark E., James Chih‐Hsin Yang, Richard M. Sherry, et al.. (2008). Adoptive Cell Therapy for Patients With Metastatic Melanoma: Evaluation of Intensive Myeloablative Chemoradiation Preparative Regimens. Journal of Clinical Oncology. 26(32). 5233–5239. 1017 indexed citations breakdown →
15.
Hinrichs, Christian S., Rosanne Spolski, Chrystal M. Paulos, et al.. (2008). IL-2 and IL-21 confer opposing differentiation programs to CD8+ T cells for adoptive immunotherapy. Blood. 111(11). 5326–5333. 358 indexed citations
16.
Morgan, Richard A., Mark E. Dudley, John R. Wunderlich, et al.. (2006). Cancer Regression in Patients After Transfer of Genetically Engineered Lymphocytes. Science. 314(5796). 126–129. 1961 indexed citations breakdown →
17.
Zeng, Rong, Rosanne Spolski, Steven E. Finkelstein, et al.. (2005). Synergy of IL-21 and IL-15 in regulating CD8+ T cell expansion and function. The Journal of Experimental Medicine. 201(1). 139–148. 592 indexed citations breakdown →
18.
Gattinoni, Luca, Steven E. Finkelstein, Christopher A. Klebanoff, et al.. (2005). Removal of homeostatic cytokine sinks by lymphodepletion enhances the efficacy of adoptively transferred tumor-specific CD8 + T cells. The Journal of Experimental Medicine. 202(7). 907–912. 812 indexed citations breakdown →
19.
Klebanoff, Christopher A., Steven E. Finkelstein, Deborah R. Surman, et al.. (2004). IL-15 enhances the in vivo antitumor activity of tumor-reactive CD8 + T Cells. Proceedings of the National Academy of Sciences. 101(7). 1969–1974. 481 indexed citations
20.
Phan, Giao Q., James Chih‐Hsin Yang, Richard M. Sherry, et al.. (2003). Cancer regression and autoimmunity induced by cytotoxic T lymphocyte-associated antigen 4 blockade in patients with metastatic melanoma. Proceedings of the National Academy of Sciences. 100(14). 8372–8377. 1234 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.

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