Christian Engwerda

13.4k total citations
153 papers, 8.3k citations indexed

About

Christian Engwerda is a scholar working on Public Health, Environmental and Occupational Health, Immunology and Epidemiology. According to data from OpenAlex, Christian Engwerda has authored 153 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Public Health, Environmental and Occupational Health, 99 papers in Immunology and 27 papers in Epidemiology. Recurrent topics in Christian Engwerda's work include Research on Leishmaniasis Studies (52 papers), Immune Cell Function and Interaction (52 papers) and Malaria Research and Control (49 papers). Christian Engwerda is often cited by papers focused on Research on Leishmaniasis Studies (52 papers), Immune Cell Function and Interaction (52 papers) and Malaria Research and Control (49 papers). Christian Engwerda collaborates with scholars based in Australia, United Kingdom and United States. Christian Engwerda's co-authors include Paul M. Kaye, Fiona H. Amante, Sara E. J. Cotterell, Amanda C. Stanley, Michael F. Good, Rajiv Kumar, Manabu Ato, Geoffrey R. Hill, Ashraful Haque and Sara C. Smelt and has published in prestigious journals such as Journal of Clinical Investigation, Nature Medicine and Nature Communications.

In The Last Decade

Christian Engwerda

149 papers receiving 8.1k citations

Peers

Christian Engwerda
Jean Langhorne United Kingdom
Paul M. Kaye United Kingdom
Geneviève Milon France
Marita Troye‐Blomberg Sweden
W. Robert McMaster Canada
Mary M. Stevenson Canada
Frederick P. Heinzel United States
Lynn Soong United States
Jacques Louis Switzerland
Bernhard Fleischer Germany
Jean Langhorne United Kingdom
Christian Engwerda
Citations per year, relative to Christian Engwerda Christian Engwerda (= 1×) peers Jean Langhorne

Countries citing papers authored by Christian Engwerda

Since Specialization
Citations

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

Fields of papers citing papers by Christian Engwerda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Engwerda

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Engwerda. A scholar is included among the top collaborators of Christian Engwerda 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 Christian Engwerda. Christian Engwerda 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.
Soon, Megan S. F., Zuleima Pava, Dean Andrew, et al.. (2025). Tfh2 and a subset of Tfh1 cells associate with antibody-mediated immunity to malaria. JCI Insight. 10(23).
2.
Loughland, Jessica R., Zuleima Pava, Dean Andrew, et al.. (2025). Age is an intrinsic driver of inflammatory responses to malaria. Nature Communications. 16(1). 8665–8665.
3.
Kumar, Shashi Bhushan, Shashi Bhushan Chauhan, Siddharth Singh, et al.. (2024). Altered IL-7 signaling in CD4+ T cells from patients with visceral leishmaniasis. PLoS neglected tropical diseases. 18(2). e0011960–e0011960. 1 indexed citations
4.
Boyle, Michelle J., Christian Engwerda, & Prasanna Jagannathan. (2024). The impact of Plasmodium-driven immunoregulatory networks on immunity to malaria. Nature reviews. Immunology. 24(9). 637–653. 9 indexed citations
5.
Edwards, Chelsea L., Jessica A. Engel, Fabian de Labastida Rivera, et al.. (2023). A molecular signature for IL-10–producing Th1 cells in protozoan parasitic diseases. JCI Insight. 8(24). 8 indexed citations
6.
Chabikwa, Tinashe, Zuleima Pava, Jessica R. Loughland, et al.. (2023). Single cell transcriptomics shows that malaria promotes unique regulatory responses across multiple immune cell subsets. Nature Communications. 14(1). 7387–7387. 16 indexed citations
7.
Li, Xian-Yang, Dillon Corvino, Bianca Nowlan, et al.. (2022). NKG7 Is Required for Optimal Antitumor T-cell Immunity. Cancer Immunology Research. 10(2). 154–161. 32 indexed citations
8.
Loughland, Jessica R., Tonia Woodberry, Matthew A. Field, et al.. (2020). Transcriptional profiling and immunophenotyping show sustained activation of blood monocytes in subpatent Plasmodium falciparum infection. Clinical & Translational Immunology. 9(6). e1144–e1144. 15 indexed citations
9.
de, Marcela Montes, Fabian de Labastida Rivera, Clay Winterford, et al.. (2020). IL-27 signalling regulates glycolysis in Th1 cells to limit immunopathology during infection. PLoS Pathogens. 16(10). e1008994–e1008994. 23 indexed citations
10.
Singh, Bhawana, Shashi Bhushan Chauhan, Rajiv Kumar, et al.. (2019). A molecular signature for CD8+ T cells from visceral leishmaniasis patients. Parasite Immunology. 41(11). e12669–e12669. 12 indexed citations
11.
Loughland, Jessica R., Dean Andrew, Fabian de Labastida Rivera, et al.. (2019). Loss of complement regulatory proteins on red blood cells in mild malarial anaemia and in Plasmodium falciparum induced blood-stage infection. Malaria Journal. 18(1). 312–312. 6 indexed citations
12.
Bunn, Patrick T., Marcela Montes de, Fabian de Labastida Rivera, et al.. (2018). Distinct Roles for CD4+ Foxp3+ Regulatory T Cells and IL-10–Mediated Immunoregulatory Mechanisms during Experimental Visceral Leishmaniasis Caused by Leishmania donovani. The Journal of Immunology. 201(11). 3362–3372. 34 indexed citations
13.
James, Kylie R., Megan S. F. Soon, Ismail Sebina, et al.. (2018). IFN Regulatory Factor 3 Balances Th1 and T Follicular Helper Immunity during Nonlethal Blood-Stage Plasmodium Infection. The Journal of Immunology. 200(4). 1443–1456. 22 indexed citations
14.
Kho, Steven, Jutta Marfurt, Irene Handayuni, et al.. (2016). Characterization of blood dendritic and regulatory T cells in asymptomatic adults with sub-microscopic Plasmodium falciparum or Plasmodium vivax infection. Malaria Journal. 15(1). 328–328. 12 indexed citations
15.
16.
de, Marcela Montes, Michael F. Good, James McCarthy, & Christian Engwerda. (2016). The Impact of Established Immunoregulatory Networks on Vaccine Efficacy and the Development of Immunity to Malaria. The Journal of Immunology. 197(12). 4518–4526. 17 indexed citations
17.
Sebina, Ismail, Kylie R. James, Megan S. F. Soon, et al.. (2016). IFNAR1-Signalling Obstructs ICOS-mediated Humoral Immunity during Non-lethal Blood-Stage Plasmodium Infection. PLoS Pathogens. 12(11). e1005999–e1005999. 52 indexed citations
18.
Pinzón‐Charry, Alberto, Tonia Woodberry, Vivian Kienzle, et al.. (2013). Apoptosis and dysfunction of blood dendritic cells in patients with falciparum and vivax malaria. The Journal of Experimental Medicine. 210(8). 1635–1646. 77 indexed citations
19.
Engwerda, Christian, et al.. (1998). Dendritic cells, but not macrophages, produce IL-12 immediately following Leishmania donovani infection. European Journal of Immunology. 28(2). 687–695. 12 indexed citations
20.
Engwerda, Christian, et al.. (1998). Dendritic cells, but not macrophages, produce IL-12 immediately followingLeishmania donovani infection. European Journal of Immunology. 28(2). 687–695. 229 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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