Philip G. Stevenson

5.9k total citations
134 papers, 5.0k citations indexed

About

Philip G. Stevenson is a scholar working on Epidemiology, Oncology and Immunology. According to data from OpenAlex, Philip G. Stevenson has authored 134 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 127 papers in Epidemiology, 88 papers in Oncology and 46 papers in Immunology. Recurrent topics in Philip G. Stevenson's work include Cytomegalovirus and herpesvirus research (114 papers), Herpesvirus Infections and Treatments (96 papers) and Viral-associated cancers and disorders (88 papers). Philip G. Stevenson is often cited by papers focused on Cytomegalovirus and herpesvirus research (114 papers), Herpesvirus Infections and Treatments (96 papers) and Viral-associated cancers and disorders (88 papers). Philip G. Stevenson collaborates with scholars based in United Kingdom, Australia and United States. Philip G. Stevenson's co-authors include Peter C. Doherty, Janet S. May, Stacey Efstathiou, Laurent Gillet, Gabrielle T. Belz, Jessica M. Boname, Susanna Colaco, Brigitte D. de Lima, Rhonda D. Cardin and John D. Altman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and The EMBO Journal.

In The Last Decade

Philip G. Stevenson

134 papers receiving 5.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip G. Stevenson United Kingdom 42 3.7k 2.6k 1.9k 441 429 134 5.0k
Edward J. Usherwood United States 33 1.8k 0.5× 1.7k 0.7× 2.2k 1.2× 350 0.8× 324 0.8× 84 3.9k
Heiko Adler Germany 32 1.4k 0.4× 877 0.3× 1.3k 0.7× 595 1.3× 332 0.8× 75 3.1k
Stacey Efstathiou United Kingdom 44 5.4k 1.5× 2.9k 1.1× 1.5k 0.8× 1.0k 2.3× 707 1.6× 94 6.8k
Fumi Goshima Japan 33 1.8k 0.5× 990 0.4× 897 0.5× 804 1.8× 304 0.7× 114 3.1k
Anthony A. Scalzo Australia 38 2.4k 0.7× 603 0.2× 4.6k 2.4× 515 1.2× 269 0.6× 78 5.6k
Mark R. Wills United Kingdom 42 3.3k 0.9× 648 0.2× 2.9k 1.5× 1.0k 2.4× 666 1.6× 114 5.8k
Ana Angulo Spain 31 2.1k 0.6× 508 0.2× 2.8k 1.4× 729 1.7× 276 0.6× 84 4.2k
Mitsuharu Sato Japan 22 1.0k 0.3× 1.6k 0.6× 4.3k 2.2× 1.4k 3.1× 691 1.6× 32 5.5k
Andrew D. Yurochko United States 40 3.0k 0.8× 529 0.2× 2.1k 1.1× 1.1k 2.4× 366 0.9× 84 4.9k
Robert L. Hendricks United States 43 3.9k 1.1× 438 0.2× 3.0k 1.5× 681 1.5× 212 0.5× 120 6.4k

Countries citing papers authored by Philip G. Stevenson

Since Specialization
Citations

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

Fields of papers citing papers by Philip G. Stevenson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip G. Stevenson

This figure shows the co-authorship network connecting the top 25 collaborators of Philip G. Stevenson. A scholar is included among the top collaborators of Philip G. Stevenson 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 Philip G. Stevenson. Philip G. Stevenson 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.
Stevenson, Philip G.. (2019). Immune Control of γ -Herpesviruses. Viral Immunology. 33(3). 225–232. 5 indexed citations
2.
Yunis, Joseph, Helen E. Farrell, Kimberley Bruce, et al.. (2018). Murine cytomegalovirus degrades MHC class II to colonize the salivary glands. PLoS Pathogens. 14(2). e1006905–e1006905. 27 indexed citations
3.
Farrell, Helen E., Kimberley Bruce, Clara Lawler, et al.. (2017). Murine Cytomegalovirus Spreads by Dendritic Cell Recirculation. mBio. 8(5). 58 indexed citations
4.
Shivkumar, Maitreyi, et al.. (2016). Herpes Simplex Virus 1 Interaction with Myeloid CellsIn Vivo. Journal of Virology. 90(19). 8661–8672. 8 indexed citations
5.
Gill, Michael B., et al.. (2014). KSHV ‐ TK is a tyrosine kinase that disrupts focal adhesions and induces Rho‐mediated cell contraction. The EMBO Journal. 34(4). 448–465. 14 indexed citations
6.
Frederico, Bruno, et al.. (2014). A Murid Gamma-Herpesviruses Exploits Normal Splenic Immune Communication Routes for Systemic Spread. Cell Host & Microbe. 15(4). 457–470. 50 indexed citations
7.
Tan, Cindy S. E., Bruno Frederico, & Philip G. Stevenson. (2014). Herpesvirus delivery to the murine respiratory tract. Journal of Virological Methods. 206. 105–114. 21 indexed citations
8.
9.
Gaspar, Miguel, Janet S. May, Soumi Sukla, et al.. (2011). Murid Herpesvirus-4 Exploits Dendritic Cells to Infect B Cells. PLoS Pathogens. 7(11). e1002346–e1002346. 50 indexed citations
10.
Kupresanin, Fiona, Jonathan Chow, Adele M. Mount, et al.. (2007). Dendritic Cells Present Lytic Antigens and Maintain Function throughout Persistent γ-Herpesvirus Infection. The Journal of Immunology. 179(11). 7506–7513. 10 indexed citations
11.
Gillet, Laurent & Philip G. Stevenson. (2007). Antibody evasion by the N terminus of murid herpesvirus-4 glycoprotein B. The EMBO Journal. 26(24). 5131–5142. 24 indexed citations
12.
Gillet, Laurent, Janet S. May, Susanna Colaco, & Philip G. Stevenson. (2007). The Murine Gammaherpesvirus-68 gp150 Acts as an Immunogenic Decoy to Limit Virion Neutralization. PLoS ONE. 2(8). e705–e705. 41 indexed citations
13.
Stevenson, Philip G. & Stacey Efstathiou. (2005). Immune Mechanisms in Murine Gammaherpesvirus-68 Infection. Viral Immunology. 18(3). 445–456. 56 indexed citations
14.
Coleman, Heather M., Brigitte D. de Lima, Victoria L. Morton, & Philip G. Stevenson. (2003). Murine Gammaherpesvirus 68 Lacking Thymidine Kinase Shows Severe Attenuation of Lytic Cycle Replication In Vivo but Still Establishes Latency. Journal of Virology. 77(4). 2410–2417. 54 indexed citations
15.
Stevenson, Philip G., Jena May, Xin Smith, et al.. (2002). K3-mediated evasion of CD8+ T cells aids amplification of a latent γ-herpesvirus. Nature Immunology. 3(8). 733–740. 141 indexed citations
16.
Boname, Jessica M. & Philip G. Stevenson. (2001). MHC Class I Ubiquitination by a Viral PHD/LAP Finger Protein. Immunity. 15(4). 627–636. 168 indexed citations
17.
Belz, Gabrielle T., Philip G. Stevenson, & Peter C. Doherty. (2000). Contemporary Analysis of MHC-Related Immunodominance Hierarchies in the CD8+ T Cell Response to Influenza A Viruses. The Journal of Immunology. 165(5). 2404–2409. 93 indexed citations
18.
Stevenson, Philip G., Gabrielle T. Belz, Maria Rita Castrucci, John D. Altman, & Peter C. Doherty. (1999). A γ-herpesvirus sneaks through a CD8+T cell response primed to a lytic-phase epitope. Proceedings of the National Academy of Sciences. 96(16). 9281–9286. 97 indexed citations
19.
Stevenson, Philip G., S Hawke, & Charles R. M. Bangham. (1997). Protection against Influenza Virus Encephalitis by Adoptive Lymphocyte Transfer. Virology. 232(1). 158–166. 12 indexed citations
20.
Stevenson, Philip G., Charles R. M. Bangham, & Simon Hawke. (1997). Recruitment, activation and proliferation of CD8+ memory T cells in an immunoprivileged site. European Journal of Immunology. 27(12). 3259–3268. 23 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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