Christopher E. Rudd

16.4k total citations · 2 hit papers
205 papers, 12.9k citations indexed

About

Christopher E. Rudd is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Christopher E. Rudd has authored 205 papers receiving a total of 12.9k indexed citations (citations by other indexed papers that have themselves been cited), including 162 papers in Immunology, 66 papers in Molecular Biology and 61 papers in Oncology. Recurrent topics in Christopher E. Rudd's work include T-cell and B-cell Immunology (111 papers), Immune Cell Function and Interaction (104 papers) and Cell Adhesion Molecules Research (43 papers). Christopher E. Rudd is often cited by papers focused on T-cell and B-cell Immunology (111 papers), Immune Cell Function and Interaction (104 papers) and Cell Adhesion Molecules Research (43 papers). Christopher E. Rudd collaborates with scholars based in United States, United Kingdom and Canada. Christopher E. Rudd's co-authors include Helga Schneider, Stuart F. Schlossman, Alison Taylor, Monika Raab, Kartik Prasad, James M. Trevillyan, J D Dasgupta, Antonio J. da Silva, Linda L. Wong and Monika Raab and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Christopher E. Rudd

203 papers receiving 12.7k citations

Hit Papers

CD28 and CTLA‐4 coreceptor expression ... 1988 2026 2000 2013 2009 1988 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher E. Rudd United States 64 9.1k 3.8k 3.7k 1.8k 1.4k 205 12.9k
André Veillette Canada 67 9.9k 1.1× 5.7k 1.5× 3.5k 0.9× 1.3k 0.7× 1.8k 1.3× 182 14.7k
Roger M. Perlmutter United States 62 7.5k 0.8× 5.9k 1.6× 3.4k 0.9× 1.0k 0.6× 2.3k 1.7× 125 13.2k
J A Ledbetter United States 52 9.4k 1.0× 3.2k 0.9× 2.0k 0.5× 1.5k 0.8× 2.1k 1.5× 99 12.7k
Joseph B. Bolen United States 71 7.8k 0.9× 6.8k 1.8× 4.1k 1.1× 2.0k 1.1× 2.7k 2.0× 171 16.0k
Dennis Y. Loh United States 46 8.1k 0.9× 4.2k 1.1× 2.8k 0.7× 457 0.3× 1.1k 0.8× 77 12.2k
Hamid Band United States 60 4.0k 0.4× 6.1k 1.6× 3.0k 0.8× 616 0.3× 932 0.7× 199 11.4k
Raymond J. Paxton United States 29 3.2k 0.4× 2.8k 0.7× 2.3k 0.6× 1.5k 0.9× 1.1k 0.8× 50 8.4k
Charles T. Rauch United States 24 5.3k 0.6× 8.2k 2.2× 3.2k 0.9× 1.4k 0.8× 598 0.4× 33 14.1k
Ivan D. Horak United States 62 5.7k 0.6× 4.8k 1.3× 3.9k 1.0× 399 0.2× 1.8k 1.3× 205 14.0k
Michael Reth Germany 73 10.9k 1.2× 7.5k 2.0× 1.8k 0.5× 1.0k 0.6× 4.1k 2.9× 219 18.1k

Countries citing papers authored by Christopher E. Rudd

Since Specialization
Citations

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

Fields of papers citing papers by Christopher E. Rudd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher E. Rudd. 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 Christopher E. Rudd. The network helps show where Christopher E. Rudd may publish in the future.

Co-authorship network of co-authors of Christopher E. Rudd

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher E. Rudd. A scholar is included among the top collaborators of Christopher E. Rudd 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 Christopher E. Rudd. Christopher E. Rudd 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.
Tu, Thai Hien, et al.. (2025). The identification of a SARs-CoV2 S2 protein derived peptide with super-antigen-like stimulatory properties on T-cells. Communications Biology. 8(1). 14–14. 2 indexed citations
2.
Adnani, Lata, Brian Meehan, Minjun Kim, et al.. (2025). Immune cell infiltration into brain tumor microenvironment is mediated by Rab27-regulated vascular wall integrity. Science Advances. 11(21). eadr6940–eadr6940. 1 indexed citations
3.
Rudd, Christopher E., et al.. (2025). CD4/CD8–p56lck Induced T-Cell Receptor Signaling and Its Implications for Immunotherapy. Biomolecules. 15(8). 1096–1096.
4.
Tu, Thai Hien, et al.. (2024). Decreased progenitor TCF1 + T-cells correlate with COVID-19 disease severity. Communications Biology. 7(1). 526–526. 2 indexed citations
5.
Rudd, Christopher E., et al.. (2022). Mechanisms orchestrating the enzymatic activity and cellular functions of deubiquitinases. Journal of Biological Chemistry. 298(8). 102198–102198. 25 indexed citations
6.
Steele, Lynette P., et al.. (2021). Non-redundant activity of GSK-3α and GSK-3β in T cell-mediated tumor rejection. iScience. 24(6). 102555–102555. 9 indexed citations
7.
Raab, Monika, Klaus Strebhardt, & Christopher E. Rudd. (2019). Immune adaptor SKAP1 acts a scaffold for Polo-like kinase 1 (PLK1) for the optimal cell cycling of T-cells. Scientific Reports. 9(1). 10462–10462. 20 indexed citations
8.
Taylor, Alison, David M. Rothstein, & Christopher E. Rudd. (2017). Small-Molecule Inhibition of PD-1 Transcription Is an Effective Alternative to Antibody Blockade in Cancer Therapy. Cancer Research. 78(3). 706–717. 85 indexed citations
9.
Dai, Hehua, Karim Yatim, Khodor I. Abou‐Daya, et al.. (2016). CD8+ Effector T Cell Migration to Pancreatic Islet Grafts Is Dependent on Cognate Antigen Presentation by Donor Graft Cells. The Journal of Immunology. 197(4). 1471–1476. 9 indexed citations
10.
Gibbons, Deena L., Lucie Abeler‐Dörner, Tim Raine, et al.. (2011). Cutting Edge: Regulator of G Protein Signaling-1 Selectively Regulates Gut T Cell Trafficking and Colitic Potential. The Journal of Immunology. 187(5). 2067–2071. 62 indexed citations
11.
Rudd, Christopher E., James M. Trevillyan, J D Dasgupta, Linda L. Wong, & Stuart F. Schlossman. (2010). Pillars Article: The CD4 Receptor Is Complexed in Detergent Lysates to a Protein-Tyrosine Kinase (Pp58) from Human T Lymphocytes. Proc. Natl. Acad. Sci. USA 1988. 85: 5190–5194. The Journal of Immunology. 185(5). 2645–2649. 2 indexed citations
12.
Schneider, Helga, Elke Valk, Rufina Leung, & Christopher E. Rudd. (2008). CTLA-4 Activation of Phosphatidylinositol 3-Kinase (PI 3-K) and Protein Kinase B (PKB/AKT) Sustains T-Cell Anergy without Cell Death. PLoS ONE. 3(12). e3842–e3842. 70 indexed citations
13.
Valk, Elke, Rufina Leung, Hyun Kang, et al.. (2006). T Cell Receptor-Interacting Molecule Acts as a Chaperone to Modulate Surface Expression of the CTLA-4 Coreceptor. Immunity. 25(5). 807–821. 63 indexed citations
14.
Schneider, Helga, Elke Valk, Silvy da Rocha Dias, Bin Wei, & Christopher E. Rudd. (2005). CTLA-4 up-regulation of lymphocyte function-associated antigen 1 adhesion and clustering as an alternate basis for coreceptor function. Proceedings of the National Academy of Sciences. 102(36). 12861–12866. 99 indexed citations
15.
Chen, Daohong, Hideki Iijima, Takashi Nagaishi, et al.. (2004). Carcinoembryonic Antigen-Related Cellular Adhesion Molecule 1 Isoforms Alternatively Inhibit and Costimulate Human T Cell Function. The Journal of Immunology. 172(6). 3535–3543. 78 indexed citations
16.
Schneider, Helga, Didier A. Mandelbrot, Rebecca J. Greenwald, et al.. (2002). Cutting Edge: CTLA-4 (CD152) Differentially Regulates Mitogen-Activated Protein Kinases (Extracellular Signal-Regulated Kinase and c-Jun N-Terminal Kinase) in CD4+ T Cells from Receptor/Ligand-Deficient Mice. The Journal of Immunology. 169(7). 3475–3479. 60 indexed citations
17.
Rudd, Christopher E.. (1999). Adaptors and Molecular Scaffolds in Immune Cell Signaling. Cell. 96(1). 5–8. 201 indexed citations
18.
Schneider, Hal E., Kartik Prasad, Steven E. Shoelson, & Christopher E. Rudd. (1995). CTLA-4 binding to the lipid kinase phosphatidylinositol 3-kinase in T cells.. The Journal of Experimental Medicine. 181(1). 351–355. 143 indexed citations
19.
Raab, Monika, et al.. (1994). The T-Cell Antigen CD5 Acts as a Receptor and Substrate for the Protein-Tyrosine Kinase p56 lck . Molecular and Cellular Biology. 14(5). 2862–2870. 65 indexed citations
20.
Rudd, Christopher E., J. G. Bodmer, Walter F. Bodmer, & Michaël J. Crumpton. (1984). Glycosylation and biosynthesis of human HLA-D region antigen-associated invariant polypeptides. Disease Markers. 2. 153–160. 1 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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