Jamie Rossjohn

48.0k total citations · 7 hit papers
480 papers, 32.0k citations indexed

About

Jamie Rossjohn is a scholar working on Immunology, Molecular Biology and Epidemiology. According to data from OpenAlex, Jamie Rossjohn has authored 480 papers receiving a total of 32.0k indexed citations (citations by other indexed papers that have themselves been cited), including 345 papers in Immunology, 115 papers in Molecular Biology and 93 papers in Epidemiology. Recurrent topics in Jamie Rossjohn's work include Immune Cell Function and Interaction (272 papers), T-cell and B-cell Immunology (248 papers) and Immunotherapy and Immune Responses (120 papers). Jamie Rossjohn is often cited by papers focused on Immune Cell Function and Interaction (272 papers), T-cell and B-cell Immunology (248 papers) and Immunotherapy and Immune Responses (120 papers). Jamie Rossjohn collaborates with scholars based in Australia, United Kingdom and United States. Jamie Rossjohn's co-authors include James McCluskey, Anthony W. Purcell, Dale I. Godfrey, Lars Kjer‐Nielsen, Stéphanie Gras, Travis Beddoe, Michael W. Parker, Onisha Patel, Andrëw G. Brööks and Zhenjun Chen and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Jamie Rossjohn

471 papers receiving 31.6k citations

Hit Papers

MR1 presents microbial vi... 2007 2026 2013 2019 2012 2007 2014 2014 2015 250 500 750

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Jamie Rossjohn 20.7k 8.5k 4.8k 4.6k 2.3k 480 32.0k
Martin F. Bachmann 18.0k 0.9× 8.3k 1.0× 3.6k 0.8× 5.1k 1.1× 4.1k 1.8× 371 31.3k
Ulrich H. von Andrian 26.1k 1.3× 9.8k 1.2× 7.6k 1.6× 3.2k 0.7× 1.6k 0.7× 256 42.9k
Michael B. Brenner 27.8k 1.3× 9.9k 1.2× 5.7k 1.2× 5.1k 1.1× 3.2k 1.4× 295 40.8k
Hans‐Georg Rammensee 19.6k 0.9× 11.3k 1.3× 6.0k 1.3× 3.7k 0.8× 1.4k 0.6× 361 28.0k
Takashi Saito 15.6k 0.8× 10.8k 1.3× 5.1k 1.1× 2.2k 0.5× 1.7k 0.7× 416 30.1k
Vincenzo Cerundolo 21.6k 1.0× 6.9k 0.8× 5.6k 1.2× 3.8k 0.8× 1.7k 0.7× 307 28.0k
Jay A. Berzofsky 17.8k 0.9× 9.3k 1.1× 5.0k 1.1× 4.8k 1.1× 2.6k 1.1× 435 29.3k
Edgar G. Engleman 15.5k 0.7× 6.0k 0.7× 5.8k 1.2× 3.7k 0.8× 1.5k 0.6× 277 24.9k
Tsuneyasu Kaisho 30.2k 1.5× 9.6k 1.1× 5.0k 1.1× 6.1k 1.3× 2.7k 1.2× 165 40.3k
Arthur Μ. Krieg 21.7k 1.0× 8.7k 1.0× 2.9k 0.6× 4.0k 0.9× 2.1k 0.9× 233 29.4k

Countries citing papers authored by Jamie Rossjohn

Since Specialization
Citations

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

Fields of papers citing papers by Jamie Rossjohn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jamie Rossjohn. 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 Jamie Rossjohn. The network helps show where Jamie Rossjohn may publish in the future.

Co-authorship network of co-authors of Jamie Rossjohn

This figure shows the co-authorship network connecting the top 25 collaborators of Jamie Rossjohn. A scholar is included among the top collaborators of Jamie Rossjohn 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 Jamie Rossjohn. Jamie Rossjohn 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.
2.
Ito, E., Anthony W. Purcell, Sho Yamasaki, et al.. (2025). The antigen-presenting molecule MR1 binds host-generated riboflavin catabolites. The Journal of Experimental Medicine. 223(2).
3.
Loh, Tiing Jen, Jia Jia Lim, Claerwen M. Jones, et al.. (2024). The molecular basis underlying T cell specificity towards citrullinated epitopes presented by HLA-DR4. Nature Communications. 15(1). 6201–6201. 10 indexed citations
4.
Pymm, Phillip, Philippa M. Saunders, Sushma Anand, et al.. (2024). The Structural Basis for Recognition of Human Leukocyte Antigen Class I Molecules by the Pan-HLA Antibody W6/32. The Journal of Immunology. 213(6). 876–885.
5.
MacLachlan, Bruce J., Lucy C. Sullivan, Andrëw G. Brööks, Jamie Rossjohn, & J.P. Vivian. (2023). Structure of the murine CD94NKG2A receptor in complex with Qa‐1b presenting an MHC‐I leader peptide. FEBS Journal. 291(7). 1530–1544. 1 indexed citations
6.
Borstel, Anouk von, Thi H. O. Nguyen, Louise C. Rowntree, et al.. (2023). Circulating effector γδ T cell populations are associated with acute coronavirus disease 19 in unvaccinated individuals. Immunology and Cell Biology. 101(4). 321–332. 6 indexed citations
7.
Suliman, Sara, Lars Kjer‐Nielsen, Liyen Loh, et al.. (2022). Dual TCR-α Expression on Mucosal-Associated Invariant T Cells as a Potential Confounder of TCR Interpretation. The Journal of Immunology. 208(6). 1389–1395. 6 indexed citations
8.
Wegrecki, Marcin, T. Praveena, Lijing Bu, et al.. (2021). The molecular assembly of the marsupial γμ T cell receptor defines a third T cell lineage. Science. 371(6536). 1383–1388. 16 indexed citations
9.
Frick, Rahel, Lene S. Høydahl, Jan Petersen, et al.. (2021). A high-affinity human TCR-like antibody detects celiac disease gluten peptide–MHC complexes and inhibits T cell activation. Science Immunology. 6(62). 18 indexed citations
10.
Reinink, Peter, Adam Shahine, Stéphanie Gras, et al.. (2019). A TCR β-Chain Motif Biases toward Recognition of Human CD1 Proteins. The Journal of Immunology. 203(12). 3395–3406. 11 indexed citations
11.
Sandt, Carolien E. van de, E. Bridie Clemens, Emma J. Grant, et al.. (2019). Challenging immunodominance of influenza-specific CD8+ T cell responses restricted by the risk-associated HLA-A*68:01 allomorph. Nature Communications. 10(1). 5579–5579. 19 indexed citations
12.
Rowntree, Louise C., Thi H. O. Nguyen, Hanim Halim, et al.. (2018). Inability To Detect Cross-Reactive Memory T Cells Challenges the Frequency of Heterologous Immunity among Common Viruses. The Journal of Immunology. 200(12). 3993–4003. 12 indexed citations
13.
Rouxel, Ophélie, Jennifer Da Silva, Lucie Beaudoin, et al.. (2017). Cytotoxic and regulatory roles of mucosal-associated invariant T cells in type 1 diabetes. Nature Immunology. 18(12). 1321–1331. 184 indexed citations
14.
Du, Victor Y., Anju Bansal, Jonathan M. Carlson, et al.. (2016). HIV-1–Specific CD8 T Cells Exhibit Limited Cross-Reactivity during Acute Infection. The Journal of Immunology. 196(8). 3276–3286. 19 indexed citations
15.
Fung, Ka Yee, Niamh E. Mangan, Helen Cumming, et al.. (2013). Interferon-ε Protects the Female Reproductive Tract from Viral and Bacterial Infection. Science. 339(6123). 1088–1092. 170 indexed citations
16.
Scally, S.W., Jan Petersen, Soi Cheng Law, et al.. (2013). A molecular basis for the association of the HLA-DRB1 locus, citrullination, and rheumatoid arthritis. The Journal of Experimental Medicine. 210(12). 2569–2582. 308 indexed citations
17.
Berry, Richard, Lars Kjer‐Nielsen, Matthew A. Perugini, et al.. (2012). The structural basis for autonomous dimerization of the pre-T-cell antigen receptor. Queensland's institutional digital repository (The University of Queensland). 9 indexed citations
18.
Kedzierska, Katherine, Carole Guillonneau, Stéphanie Gras, et al.. (2008). Complete modification of TCR specificity and repertoire selection does not perturb a CD8 + T cell immunodominance hierarchy. Proceedings of the National Academy of Sciences. 105(49). 19408–19413. 34 indexed citations
19.
Ely, Lauren K., Travis Beddoe, Craig S. Clements, et al.. (2006). Disparate thermodynamics governing T cell receptor–MHC-I interactions implicate extrinsic factors in guiding MHC restriction. Proceedings of the National Academy of Sciences. 103(17). 6641–6646. 46 indexed citations
20.
Macdonald, W.A., Anthony W. Purcell, Nicole A. Mifsud, et al.. (2003). A Naturally Selected Dimorphism within the HLA-B44 Supertype Alters Class I Structure, Peptide Repertoire, and T Cell Recognition. The Journal of Experimental Medicine. 198(5). 679–691. 167 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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