Dawn Shepherd

4.6k total citations
55 papers, 3.7k citations indexed

About

Dawn Shepherd is a scholar working on Immunology, Molecular Biology and Physiology. According to data from OpenAlex, Dawn Shepherd has authored 55 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Immunology, 9 papers in Molecular Biology and 7 papers in Physiology. Recurrent topics in Dawn Shepherd's work include Immune Cell Function and Interaction (29 papers), T-cell and B-cell Immunology (24 papers) and Immunotherapy and Immune Responses (13 papers). Dawn Shepherd is often cited by papers focused on Immune Cell Function and Interaction (29 papers), T-cell and B-cell Immunology (24 papers) and Immunotherapy and Immune Responses (13 papers). Dawn Shepherd collaborates with scholars based in United Kingdom, United States and Germany. Dawn Shepherd's co-authors include Vincenzo Cerundolo, Mariolina Salio, Gang Tong, Craig E. Jahr, Gurdyal S. Besra, E. Yvonne Jones, Richard R. Schmidt, Stephan D. Gadola, Gerd Ritter and Michael Koch and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Dawn Shepherd

54 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dawn Shepherd United Kingdom 30 2.5k 863 480 400 378 55 3.7k
Éva Rajnavölgyi Hungary 37 2.0k 0.8× 1.8k 2.0× 471 1.0× 226 0.6× 432 1.1× 153 4.6k
Einar Martin Aandahl Norway 30 1.8k 0.7× 1.1k 1.3× 666 1.4× 165 0.4× 312 0.8× 65 3.5k
Anna Erdei Hungary 36 2.5k 1.0× 1.3k 1.6× 230 0.5× 703 1.8× 310 0.8× 176 4.8k
Thomas Leist United States 39 2.1k 0.9× 790 0.9× 860 1.8× 221 0.6× 656 1.7× 124 4.9k
Jean Kanellopoulos France 36 3.2k 1.3× 1.5k 1.7× 798 1.7× 130 0.3× 435 1.2× 83 5.3k
Barbara A. Torres United States 27 1.2k 0.5× 661 0.8× 491 1.0× 273 0.7× 242 0.6× 53 2.5k
Richard H. Weisbart United States 27 1.6k 0.7× 1.2k 1.3× 521 1.1× 255 0.6× 274 0.7× 81 3.5k
Evelina Gatti France 35 1.9k 0.8× 2.1k 2.4× 351 0.7× 270 0.7× 966 2.6× 60 4.8k
Juraj Kabát United States 32 2.0k 0.8× 1.8k 2.1× 495 1.0× 222 0.6× 1.2k 3.2× 73 4.7k
Tamás Oravecz United States 28 1.0k 0.4× 1.5k 1.8× 665 1.4× 163 0.4× 359 0.9× 47 3.0k

Countries citing papers authored by Dawn Shepherd

Since Specialization
Citations

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

Fields of papers citing papers by Dawn Shepherd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dawn Shepherd

This figure shows the co-authorship network connecting the top 25 collaborators of Dawn Shepherd. A scholar is included among the top collaborators of Dawn Shepherd 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 Dawn Shepherd. Dawn Shepherd 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.
Yates, Abi G., Dawn Shepherd, Elisabete Pires, et al.. (2025). Role of B vitamins in modulating homocysteine and metabolic pathways linked to brain atrophy: Metabolomics insights from the VITACOG trial. Alzheimer s & Dementia. 21(7). e70521–e70521.
2.
González‐Ortiz, Fernando, Thomas K. Karikari, Daniëlle te Vruchte, et al.. (2024). Plasma phosphorylated-tau217 is increased in Niemann–Pick disease type C. Brain Communications. 6(6). fcae375–fcae375. 7 indexed citations
3.
Puglisi, Antonino, Graziella Vecchio, Ece Bayır, et al.. (2023). Grafting of Cyclodextrin to Theranostic Nanoparticles Improves Blood-Brain Barrier Model Crossing. Biomolecules. 13(3). 573–573. 6 indexed citations
4.
Howson, Lauren J., Giorgio Napolitani, Dawn Shepherd, et al.. (2018). MAIT cell clonal expansion and TCR repertoire shaping in human volunteers challenged with Salmonella Paratyphi A. Nature Communications. 9(1). 253–253. 77 indexed citations
5.
Kurioka, Ayako, Bonnie van Wilgenburg, Andries J. van Tonder, et al.. (2017). Diverse Streptococcus pneumoniae Strains Drive a Mucosal-Associated Invariant T-Cell Response Through Major Histocompatibility Complex class I–Related Molecule–Dependent and Cytokine-Driven Pathways. The Journal of Infectious Diseases. 217(6). 988–999. 43 indexed citations
6.
Timosenko, Elina, Hemza Ghadbane, Jonathan D. Silk, et al.. (2016). Nutritional Stress Induced by Tryptophan-Degrading Enzymes Results in ATF4-Dependent Reprogramming of the Amino Acid Transporter Profile in Tumor Cells. Cancer Research. 76(21). 6193–6204. 47 indexed citations
7.
Torreño-Pina, Juan A., Carlo Manzo, Mariolina Salio, et al.. (2016). The actin cytoskeleton modulates the activation of iNKT cells by segregating CD1d nanoclusters on antigen-presenting cells. Proceedings of the National Academy of Sciences. 113(6). E772–81. 27 indexed citations
8.
Polzella, Paolo, Christian Rankl, Rong Zhu, et al.. (2011). Binding Strength and Dynamics of Invariant Natural Killer Cell T Cell Receptor/CD1d-Glycosphingolipid Interaction on Living Cells by Single Molecule Force Spectroscopy. Journal of Biological Chemistry. 286(18). 15973–15979. 17 indexed citations
9.
Duman, Memed, Rong Zhu, Christian Rankl, et al.. (2010). Improved localization of cellular membrane receptors using combined fluorescence microscopy and simultaneous topography and recognition imaging. Nanotechnology. 21(11). 115504–115504. 31 indexed citations
10.
Stewart-Jones, Guillaume B. E., Sarah Sainsbury, Dawn Shepherd, et al.. (2009). Some lessons from the systematic production and structural analysis of soluble αβ T-cell receptors. Journal of Immunological Methods. 350(1-2). 14–21. 10 indexed citations
11.
Silk, Jonathan D., Mariolina Salio, Bharat Reddy, et al.. (2008). Cutting Edge: Nonglycosidic CD1d Lipid Ligands Activate Human and Murine Invariant NKT Cells. The Journal of Immunology. 180(10). 6452–6456. 62 indexed citations
12.
Hermans, Ian F., Jonathan D. Silk, Uzi Gileadi, et al.. (2007). Dendritic Cell Function Can Be Modulated through Cooperative Actions of TLR Ligands and Invariant NKT Cells. The Journal of Immunology. 178(5). 2721–2729. 68 indexed citations
13.
McCarthy, Corinna, Dawn Shepherd, Sebastian J. Fleire, et al.. (2007). The length of lipids bound to human CD1d molecules modulates the affinity of NKT cell TCR and the threshold of NKT cell activation. The Journal of Experimental Medicine. 204(5). 1131–1144. 184 indexed citations
14.
Gadola, Stephan D., Michael Koch, Jon Marles‐Wright, et al.. (2006). Structure and binding kinetics of three different human CD1d–α-galactosylceramide–specific T cell receptors. The Journal of Experimental Medicine. 203(3). 699–710. 74 indexed citations
15.
Koch, Michael, Dawn Shepherd, Stephan D. Gadola, et al.. (2005). The crystal structure of human CD1d with and without α-galactosylceramide. Nature Immunology. 6(8). 819–826. 324 indexed citations
16.
Silk, Jonathan D., Ian F. Hermans, Uzi Gileadi, et al.. (2004). Utilizing the adjuvant properties of CD1d-dependent NK T cells in T cell–mediated immunotherapy. Journal of Clinical Investigation. 114(12). 1800–1811. 14 indexed citations
17.
Batuwangala, Thil, Dawn Shepherd, Stephan D. Gadola, et al.. (2004). The Crystal Structure of Human CD1b with a Bound Bacterial Glycolipid. The Journal of Immunology. 172(4). 2382–2388. 127 indexed citations
18.
Smith, C., P. Rod Dunbar, Fareed Mirza, et al.. (2004). Recombinant modified vaccinia Ankara primes functionally activated CTL specific for a melanoma tumor antigen epitope in melanoma patients with a high risk of disease recurrence. International Journal of Cancer. 113(2). 259–266. 72 indexed citations
19.
Salio, Mariolina, Dawn Shepherd, P. Rod Dunbar, et al.. (2001). Mature Dendritic Cells Prime Functionally Superior Melan-A-Specific CD8+ Lymphocytes as Compared with Nonprofessional APC. The Journal of Immunology. 167(3). 1188–1197. 59 indexed citations
20.
Dunbar, P. Rod, C. Smith, David Chao, et al.. (2000). A Shift in the Phenotype of Melan-A-Specific CTL Identifies Melanoma Patients with an Active Tumor-Specific Immune Response. The Journal of Immunology. 165(11). 6644–6652. 122 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026