Mark A. Travis

5.6k total citations · 3 hit papers
55 papers, 4.2k citations indexed

About

Mark A. Travis is a scholar working on Immunology, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Mark A. Travis has authored 55 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Immunology, 17 papers in Molecular Biology and 16 papers in Immunology and Allergy. Recurrent topics in Mark A. Travis's work include Cell Adhesion Molecules Research (16 papers), Immune Response and Inflammation (9 papers) and Immunotherapy and Immune Responses (8 papers). Mark A. Travis is often cited by papers focused on Cell Adhesion Molecules Research (16 papers), Immune Response and Inflammation (9 papers) and Immunotherapy and Immune Responses (8 papers). Mark A. Travis collaborates with scholars based in United Kingdom, United States and Germany. Mark A. Travis's co-authors include Dean Sheppard, John J. Worthington, Joanna E. Klementowicz, Edward D. Hall, Andrew C. Melton, Aoife Kelly, Martin J. Humphries, B. Czajkowska, Jeffrey A. Bluestone and Thomas M. Fenton and has published in prestigious journals such as Nature, Science and Journal of Biological Chemistry.

In The Last Decade

Mark A. Travis

54 papers receiving 4.1k citations

Hit Papers

TGF-β Activation and Function in Immunity 2013 2026 2017 2021 2013 2021 2021 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
Mark A. Travis United Kingdom 32 1.8k 1.3k 689 608 377 55 4.2k
Rami Hershkoviz Israel 35 1.4k 0.8× 1.2k 0.9× 548 0.8× 819 1.3× 238 0.6× 98 3.9k
Sunil K. Shaw United States 30 2.2k 1.2× 1.4k 1.1× 563 0.8× 1.2k 2.0× 190 0.5× 64 4.9k
Toshiyuki Tanaka Japan 42 2.5k 1.4× 2.0k 1.6× 1.2k 1.7× 511 0.8× 359 1.0× 229 6.1k
Elisabetta Ferrero Italy 37 1.9k 1.1× 1.2k 0.9× 721 1.0× 517 0.9× 207 0.5× 114 4.5k
Per Anderson Spain 31 1.3k 0.7× 1.4k 1.1× 658 1.0× 268 0.4× 250 0.7× 69 4.0k
Ryuji Suzuki Japan 35 2.1k 1.2× 929 0.7× 984 1.4× 417 0.7× 360 1.0× 160 4.9k
Martin Stacey United Kingdom 39 2.1k 1.2× 2.4k 1.9× 478 0.7× 750 1.2× 628 1.7× 68 5.7k
Bryan Heit Canada 29 1.8k 1.0× 1.2k 1.0× 276 0.4× 789 1.3× 176 0.5× 66 3.6k
Alexei Gratchev Germany 39 2.0k 1.1× 2.7k 2.1× 1.0k 1.5× 264 0.4× 374 1.0× 123 5.4k
Keiko Sakai Japan 31 1.1k 0.6× 1.8k 1.4× 549 0.8× 534 0.9× 155 0.4× 111 4.4k

Countries citing papers authored by Mark A. Travis

Since Specialization
Citations

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

Fields of papers citing papers by Mark A. Travis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark A. Travis. 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 Mark A. Travis. The network helps show where Mark A. Travis may publish in the future.

Co-authorship network of co-authors of Mark A. Travis

This figure shows the co-authorship network connecting the top 25 collaborators of Mark A. Travis. A scholar is included among the top collaborators of Mark A. Travis 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 Mark A. Travis. Mark A. Travis 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.
Barendrecht, Arjan D., Harald Peeters, Diana Torres‐García, et al.. (2025). trans-Cyclooctene-caged-IL-1β immunocytokine-constructs ligated to unmodified nanobodies allow click-2-release-based control of cytokine activity. RSC Chemical Biology. 6(7). 1068–1078. 1 indexed citations
2.
Hall, Jamie, Daniel Hind, Stephen J. Walters, et al.. (2025). Mesenteric excision and Kono‐S anastomosis trial (MEErKAT): A study protocol for a multicentre, 2 × 2 factorial, randomised controlled, open‐label superiority trial. Colorectal Disease. 27(9). e70212–e70212. 1 indexed citations
3.
Cytlak, Urszula, Peter Barry, Edward Emmott, et al.. (2025). Effect of elexacaftor/tezacaftor/ivacaftor on systemic inflammation in cystic fibrosis. Thorax. 80(9). 604–615.
4.
Cytlak, Urszula, Craig P. McEntee, Catherine Smedley, et al.. (2023). Group 2 Innate Lymphoid Cells Are Detrimental to the Control of Infection with Francisella tularensis. The Journal of Immunology. 210(5). 618–627. 3 indexed citations
5.
Cytlak, Urszula, Douglas P. Dyer, Jamie Honeychurch, et al.. (2021). Immunomodulation by radiotherapy in tumour control and normal tissue toxicity. Nature reviews. Immunology. 22(2). 124–138. 167 indexed citations breakdown →
6.
Mani, V., Shannon K. Bromley, Tarmo Äijö, et al.. (2019). Migratory DCs activate TGF-β to precondition naïve CD8 + T cells for tissue-resident memory fate. Science. 366(6462). 146 indexed citations
7.
Cohen, Taylor S., Virginia Takahashi, Jessica Bonnell, et al.. (2019). Staphylococcus aureus drives expansion of low-density neutrophils in diabetic mice. Journal of Clinical Investigation. 129(5). 2133–2144. 31 indexed citations
8.
Houston, Stephanie, Suélen Andreia Rossi, E. Diane Williamson, et al.. (2019). CD200R deletion promotes a neutrophil niche for Francisella tularensis and increases infectious burden and mortality. Nature Communications. 10(1). 2121–2121. 23 indexed citations
9.
Melo-González, Felipe, Thomas M. Fenton, Catherine Smedley, et al.. (2018). Intestinal mucin activates human dendritic cells and IL-8 production in a glycan-specific manner. Journal of Biological Chemistry. 293(22). 8543–8553. 26 indexed citations
10.
Brignall, Ruth, Pierre Cauchy, Sarah L. Bevington, et al.. (2017). Integration of Kinase and Calcium Signaling at the Level of Chromatin Underlies Inducible Gene Activation in T Cells. The Journal of Immunology. 199(8). 2652–2667. 53 indexed citations
11.
Luda, Katarzyna M., Thorsten Joeris, Emma K. Persson, et al.. (2016). IRF8 dependent classical dendritic cells are essential for intestinal T cell homeostasis. Technical University of Denmark, DTU Orbit (Technical University of Denmark, DTU). 1 indexed citations
12.
Worthington, John J., Joanna E. Klementowicz, B. Czajkowska, et al.. (2013). Loss of the TGFβ-Activating Integrin αvβ8 on Dendritic Cells Protects Mice from Chronic Intestinal Parasitic Infection via Control of Type 2 Immunity. PLoS Pathogens. 9(10). e1003675–e1003675. 32 indexed citations
13.
Kimber, Ian, Mark A. Travis, Stefan F. Martin, & Rebecca J. Dearman. (2012). Immunoregulation of skin sensitization and regulatory T cells. Contact Dermatitis. 67(4). 179–183. 25 indexed citations
14.
Klementowicz, Joanna E., Mark A. Travis, & Richard K. Grencis. (2012). Trichuris muris: a model of gastrointestinal parasite infection. Seminars in Immunopathology. 34(6). 815–828. 109 indexed citations
15.
Giacomini, Marilyn M., Mark A. Travis, Makoto Kudo, & Dean Sheppard. (2012). Epithelial cells utilize cortical actin/myosin to activate latent TGF-β through integrin αvβ6-dependent physical force. Experimental Cell Research. 318(6). 716–722. 79 indexed citations
16.
Ilić, Nataša, John J. Worthington, Alisa Gruden‐Movsesijan, et al.. (2011). Trichinella spiralis antigens prime mixed Th1/Th2 response but do not induce de novo generation of Foxp3+ T cells in vitro. Parasite Immunology. 33(10). 572–582. 52 indexed citations
17.
Worthington, John J., B. Czajkowska, Andrew C. Melton, & Mark A. Travis. (2011). Intestinal Dendritic Cells Specialize to Activate Transforming Growth Factor-β and Induce Foxp3+ Regulatory T Cells via Integrin αvβ8. Gastroenterology. 141(5). 1802–1812. 135 indexed citations
18.
Worthington, John J., B. Czajkowska, & Mark A. Travis. (2010). Enhanced induction of Foxp3+regulatory T-cells by specialised gut dendritic cells is dependent on TGF-beta activation by the integrin alphaVbeta8. Research Explorer (The University of Manchester). 1 indexed citations
19.
Travis, Mark A., Jonathan D. Humphries, & Martin J. Humphries. (2003). An unraveling tale of how integrins are activated from within. Trends in Pharmacological Sciences. 24(4). 192–197. 49 indexed citations
20.
Travis, Mark A., et al.. (1978). Management of a patient with hereditary angioneurotic edema.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 36(11). 890–2. 5 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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