Rachel E. Hewitt

1.4k total citations
28 papers, 1.0k citations indexed

About

Rachel E. Hewitt is a scholar working on Immunology, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Rachel E. Hewitt has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Immunology, 7 papers in Molecular Biology and 5 papers in Biomedical Engineering. Recurrent topics in Rachel E. Hewitt's work include Immunotherapy and Immune Responses (6 papers), T-cell and B-cell Immunology (6 papers) and Immune Cell Function and Interaction (5 papers). Rachel E. Hewitt is often cited by papers focused on Immunotherapy and Immune Responses (6 papers), T-cell and B-cell Immunology (6 papers) and Immune Cell Function and Interaction (5 papers). Rachel E. Hewitt collaborates with scholars based in United Kingdom, United States and Canada. Rachel E. Hewitt's co-authors include David A. Price, Jonathan J. Powell, Andrew K. Sewell, Anya Lissina, Laetitia Pele, John W. Wills, Ravin Jugdaohsingh, Helen F. Chappell, Riyaz Mehta and Michael P. Crawford and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nature Communications.

In The Last Decade

Rachel E. Hewitt

26 papers receiving 992 citations

Peers

Rachel E. Hewitt
Pedro Paulo Chaves de Souza Brazil
Masanori Sasaki Japan
Weibin Zhang China
Manuela Rizzi Italy
Wenhao Wang China
Geetanjali B. Tomar India
Feiqiu Wen China
Jacopo Uggeri Italy
Mei Zhang China
Jialu Xu China
Pedro Paulo Chaves de Souza Brazil
Rachel E. Hewitt
Citations per year, relative to Rachel E. Hewitt Rachel E. Hewitt (= 1×) peers Pedro Paulo Chaves de Souza

Countries citing papers authored by Rachel E. Hewitt

Since Specialization
Citations

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

Fields of papers citing papers by Rachel E. Hewitt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel E. Hewitt

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel E. Hewitt. A scholar is included among the top collaborators of Rachel E. Hewitt 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 Rachel E. Hewitt. Rachel E. Hewitt 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.
Wills, John W., Jack Robertson, Huw D. Summers, et al.. (2025). Immunocompetent cell targeting by food-additive titanium dioxide. Nature Communications. 16(1). 6067–6067.
2.
Wills, John W., Jack Robertson, Claire M. Barnes, et al.. (2023). Label-free cell segmentation of diverse lymphoid tissues in 2D and 3D. Cell Reports Methods. 3(2). 100398–100398. 4 indexed citations
3.
Bistrović, Andrea, et al.. (2023). A catch-and-release nano-based gene delivery system. Nanoscale Horizons. 8(11). 1588–1594. 5 indexed citations
4.
Hewitt, Rachel E., et al.. (2022). Modification of avian pathogenic Escherichia coli χ7122 lipopolysaccharide increases accessibility to glycoconjugate antigens. Microbial Cell Factories. 21(1). 181–181. 2 indexed citations
5.
Chen, Xu, Nakul Rampal, Rachel E. Hewitt, et al.. (2021). Formulation of Metal–Organic Framework-Based Drug Carriers by Controlled Coordination of Methoxy PEG Phosphate: Boosting Colloidal Stability and Redispersibility. Journal of the American Chemical Society. 143(34). 13557–13572. 131 indexed citations
6.
Wills, John W., Claire M. Barnes, Matthew A. Rodrigues, et al.. (2021). Inter-laboratory automation of the in vitro micronucleus assay using imaging flow cytometry and deep learning. Archives of Toxicology. 95(9). 3101–3115. 20 indexed citations
7.
Powell, Jonathan J., et al.. (2020). Imaging flow cytometry methods for quantitative analysis of label-free crystalline silica particle interactions with immune cells. AIMS Biophysics. 7(3). 144–166. 3 indexed citations
8.
Hewitt, Rachel E., Helen F. Chappell, & Jonathan J. Powell. (2020). Small and dangerous? Potential toxicity mechanisms of common exposure particles and nanoparticles. Current Opinion in Toxicology. 19. 93–98. 34 indexed citations
9.
Hewitt, Rachel E., et al.. (2020). Gastrointestinal absorption and toxicity of nanoparticles and microparticles: Myth, reality and pitfalls explored through titanium dioxide. Current Opinion in Toxicology. 19. 112–120. 30 indexed citations
10.
Cortés, Alba, John W. Wills, Rachel E. Hewitt, et al.. (2020). Infection with the sheep gastrointestinal nematode Teladorsagia circumcincta increases luminal pathobionts. Microbiome. 8(1). 60–60. 34 indexed citations
11.
Hewitt, Rachel E., et al.. (2019). Ultrasmall silica nanoparticles directly ligate the T cell receptor complex. Proceedings of the National Academy of Sciences. 117(1). 285–291. 19 indexed citations
12.
Pele, Laetitia, Don Otter, Rachel E. Hewitt, et al.. (2017). Pro-inflammatory adjuvant properties of pigment-grade titanium dioxide particles are augmented by a genotype that potentiates interleukin 1β processing. Particle and Fibre Toxicology. 14(1). 51–51. 24 indexed citations
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15.
Pele, Laetitia, Rachel E. Hewitt, Jack Robertson, et al.. (2016). Synthetic mimetics of the endogenous gastrointestinal nanomineral: Silent constructs that trap macromolecules for intracellular delivery. Nanomedicine Nanotechnology Biology and Medicine. 13(2). 619–630. 17 indexed citations
16.
Robertson, Jack, Laetitia Pele, Tom P. Monie, et al.. (2016). Intestinal APCs of the endogenous nanomineral pathway fail to express PD-L1 in Crohn’s disease. Scientific Reports. 6(1). 26747–26747. 32 indexed citations
17.
Pele, Laetitia, et al.. (2014). Artefactual Nanoparticle Activation of the Inflammasome Platform: in Vitro Evidence with a Nano-Formed Calcium Phosphate. Nanomedicine. 10(9). 1379–1390. 9 indexed citations
18.
Hewitt, Rachel E., Laetitia Pele, Mark Tremelling, et al.. (2012). Immuno-inhibitory PD-L1 can be induced by a Peptidoglycan/NOD2 mediated pathway in primary monocytic cells and is deficient in Crohn's patients with homozygous NOD2 mutations.. Clinical Immunology. 143(2). 162–169. 27 indexed citations
19.
Wooldridge, Linda, Mathew Clement, Anna Lissina, et al.. (2010). MHC Class I Molecules with Superenhanced CD8 Binding Properties Bypass the Requirement for Cognate TCR Recognition and Nonspecifically Activate CTLs. The Journal of Immunology. 184(7). 3357–3366. 29 indexed citations
20.
Ellmerich, Stéphan, Marcin P. Mycko, Katalin Takács, et al.. (2005). High Incidence of Spontaneous Disease in an HLA-DR15 and TCR Transgenic Multiple Sclerosis Model. The Journal of Immunology. 174(4). 1938–1946. 57 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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