Juthathip Mongkolsapaya

22.8k total citations · 4 hit papers
63 papers, 6.2k citations indexed

About

Juthathip Mongkolsapaya is a scholar working on Infectious Diseases, Public Health, Environmental and Occupational Health and Immunology. According to data from OpenAlex, Juthathip Mongkolsapaya has authored 63 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Infectious Diseases, 46 papers in Public Health, Environmental and Occupational Health and 9 papers in Immunology. Recurrent topics in Juthathip Mongkolsapaya's work include Mosquito-borne diseases and control (46 papers), Viral Infections and Vectors (37 papers) and Malaria Research and Control (17 papers). Juthathip Mongkolsapaya is often cited by papers focused on Mosquito-borne diseases and control (46 papers), Viral Infections and Vectors (37 papers) and Malaria Research and Control (17 papers). Juthathip Mongkolsapaya collaborates with scholars based in United Kingdom, Thailand and United States. Juthathip Mongkolsapaya's co-authors include Gavin Screaton, Wanwisa Dejnirattisai, Prida Malasit, Thaneeya Duangchinda, Sirijitt Vasanawathana, F.A. Rey, Nattaya Tangthawornchaikul, Alexander Rouvinski, Giovanna Barba–Spaeth and Wiyada Wongwiwat and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Juthathip Mongkolsapaya

62 papers receiving 6.1k citations

Hit Papers

Cross-Reacting Antibodies Enhance Dengue Virus Infection ... 2003 2026 2010 2018 2010 2016 2003 2016 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Cross-Reacting Antibodies Enhance Dengue Virus Infection in Humans
    2010 698 citations Wanwisa Dejnirattisai, Amonrat Jumnainsong et al. profile →
  2. Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with zika virus
    2016 663 citations Wanwisa Dejnirattisai, Piyada Supasa et al. Nature Immunology profile →
  3. Original antigenic sin and apoptosis in the pathogenesis of dengue hemorrhagic fever
    2003 633 citations Juthathip Mongkolsapaya, Wanwisa Dejnirattisai et al. Nature Medicine profile →
  4. Structural basis of potent Zika–dengue virus antibody cross-neutralization
    2016 392 citations Giovanna Barba–Spaeth, Wanwisa Dejnirattisai et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Juthathip Mongkolsapaya United Kingdom 34 4.6k 4.5k 968 732 614 63 6.2k
Anna P. Durbin United States 48 4.8k 1.1× 4.2k 0.9× 1.3k 1.4× 538 0.7× 483 0.8× 126 6.4k
Philippe Desprès France 40 4.2k 0.9× 3.8k 0.8× 1.1k 1.1× 1.0k 1.4× 848 1.4× 67 5.9k
Jorge L. Muñoz‐Jordán United States 38 4.2k 0.9× 3.5k 0.8× 837 0.9× 468 0.6× 482 0.8× 117 5.3k
Sharone Green United States 45 7.2k 1.6× 6.1k 1.4× 656 0.7× 823 1.1× 548 0.9× 79 8.3k
Stephen S. Whitehead United States 52 5.6k 1.2× 5.7k 1.3× 2.5k 2.6× 499 0.7× 489 0.8× 140 8.4k
Jorge E. Osorio United States 42 2.9k 0.6× 2.7k 0.6× 1.3k 1.3× 440 0.6× 979 1.6× 150 5.2k
Kristen A. Bernard United States 36 3.2k 0.7× 3.0k 0.7× 440 0.5× 369 0.5× 367 0.6× 59 4.2k
Wellington Sun United States 34 3.4k 0.8× 3.0k 0.7× 577 0.6× 496 0.7× 297 0.5× 55 4.3k
Sutee Yoksan Thailand 41 6.4k 1.4× 5.1k 1.1× 575 0.6× 320 0.4× 506 0.8× 152 7.2k
Sonja M. Best United States 36 1.9k 0.4× 2.7k 0.6× 926 1.0× 890 1.2× 586 1.0× 84 4.1k

Countries citing papers authored by Juthathip Mongkolsapaya

Since Specialization
Citations

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

Fields of papers citing papers by Juthathip Mongkolsapaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juthathip Mongkolsapaya

This figure shows the co-authorship network connecting the top 25 collaborators of Juthathip Mongkolsapaya. A scholar is included among the top collaborators of Juthathip Mongkolsapaya 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 Juthathip Mongkolsapaya. Juthathip Mongkolsapaya 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.
Liu, Chang, Xianglin Ji, Yun Wang, et al.. (2025). Engineering Genome‐Free Bacterial Cells for Effective SARS ‐ COV ‐2 Neutralisation. Microbial Biotechnology. 18(3). e70109–e70109.
2.
Liu, Chang, Raksha Das, Aiste Dijokaite-Guraliuc, et al.. (2024). Emerging variants develop total escape from potent monoclonal antibodies induced by BA.4/5 infection. Nature Communications. 15(1). 3284–3284. 11 indexed citations
3.
Zhou, Daming, Piyada Supasa, Chang Liu, et al.. (2024). The SARS-CoV-2 neutralizing antibody response to SD1 and its evasion by BA.2.86. Nature Communications. 15(1). 2734–2734. 6 indexed citations
4.
Assawakosri, Suvichada, Sitthichai Kanokudom, Nungruthai Suntronwong, et al.. (2023). Immunogenicity and durability against Omicron BA.1, BA.2 and BA.4/5 variants at 3–4 months after a heterologous COVID-19 booster vaccine in healthy adults with a two-doses CoronaVac vaccination. Heliyon. 10(1). e23892–e23892. 5 indexed citations
5.
Assawakosri, Suvichada, Sitthichai Kanokudom, Nungruthai Suntronwong, et al.. (2022). Neutralizing Activities Against the Omicron Variant After a Heterologous Booster in Healthy Adults Receiving Two Doses of CoronaVac Vaccination. The Journal of Infectious Diseases. 226(8). 1372–1381. 41 indexed citations
6.
Assawakosri, Suvichada, Sitthichai Kanokudom, Jira Chansaenroj, et al.. (2022). Persistence of immunity against Omicron BA.1 and BA.2 variants following homologous and heterologous COVID-19 booster vaccines in healthy adults after a two-dose AZD1222 vaccination. International Journal of Infectious Diseases. 122. 793–801. 13 indexed citations
7.
Suntronwong, Nungruthai, Suvichada Assawakosri, Sitthichai Kanokudom, et al.. (2022). Strong Correlations between the Binding Antibodies against Wild-Type and Neutralizing Antibodies against Omicron BA.1 and BA.2 Variants of SARS-CoV-2 in Individuals Following Booster (Third-Dose) Vaccination. Diagnostics. 12(8). 1781–1781. 13 indexed citations
8.
Kanokudom, Sitthichai, Suvichada Assawakosri, Nungruthai Suntronwong, et al.. (2022). Comparison of the reactogenicity and immunogenicity of a reduced and standard booster dose of the mRNA COVID-19 vaccine in healthy adults after two doses of inactivated vaccine. Vaccine. 40(39). 5657–5663. 7 indexed citations
9.
Sharma, Arvind, Xiaokang Zhang, Wanwisa Dejnirattisai, et al.. (2021). The epitope arrangement on flavivirus particles contributes to Mab C10’s extraordinary neutralization breadth across Zika and dengue viruses. Cell. 184(25). 6052–6066.e18. 50 indexed citations
10.
Abbink, Peter, Rafael A. Larocca, Wanwisa Dejnirattisai, et al.. (2018). Therapeutic and protective efficacy of a dengue antibody against Zika infection in rhesus monkeys. Nature Medicine. 24(6). 721–723. 32 indexed citations
11.
Mongkolsapaya, Juthathip, et al.. (2018). Which Dengue Vaccine Approach Is the Most Promising, and Should We Be Concerned about Enhanced Disease after Vaccination?. Cold Spring Harbor Perspectives in Biology. 10. 3 indexed citations
12.
Fernández, Estefanı́a, Wanwisa Dejnirattisai, Bin Cao, et al.. (2017). Human antibodies to the dengue virus E-dimer epitope have therapeutic activity against Zika virus infection. Nature Immunology. 18(11). 1261–1269. 87 indexed citations
13.
Barba–Spaeth, Giovanna, Wanwisa Dejnirattisai, Alexander Rouvinski, et al.. (2016). Structural basis of potent Zika–dengue virus antibody cross-neutralization. Nature. 536(7614). 48–53. 392 indexed citations breakdown →
14.
Décembre, Élodie, Sonia Assil, Marine L. B. Hillaire, et al.. (2014). Sensing of Immature Particles Produced by Dengue Virus Infected Cells Induces an Antiviral Response by Plasmacytoid Dendritic Cells. PLoS Pathogens. 10(10). e1004434–e1004434. 56 indexed citations
15.
Roberts, Catherine, Juthathip Mongkolsapaya, & Gavin Screaton. (2012). Dengue fever: a practical guide. British Journal of Hospital Medicine. 73(4). C60–C64. 1 indexed citations
16.
Midgley, Claire M., Aleksandra Flanagan, Hai B. Tran, et al.. (2012). Structural Analysis of a Dengue Cross-Reactive Antibody Complexed with Envelope Domain III Reveals the Molecular Basis of Cross-Reactivity. The Journal of Immunology. 188(10). 4971–4979. 73 indexed citations
17.
Watson, Aleksandra A., Andrey A. Lebedev, Benjamin A. Hall, et al.. (2011). Structural Flexibility of the Macrophage Dengue Virus Receptor CLEC5A. Journal of Biological Chemistry. 286(27). 24208–24218. 42 indexed citations
18.
Wu, Hao, Huiping Yan, Shiwu Ma, et al.. (2008). T Cell Responses to Whole SARS Coronavirus in Humans. The Journal of Immunology. 181(8). 5490–5500. 365 indexed citations
19.
Mongkolsapaya, Juthathip, Thaneeya Duangchinda, Wanwisa Dejnirattisai, et al.. (2006). T Cell Responses in Dengue Hemorrhagic Fever: Are Cross-Reactive T Cells Suboptimal?. The Journal of Immunology. 176(6). 3821–3829. 207 indexed citations
20.
Malasit, Prida, David A. Warrell, Pornthep Chanthavanich, et al.. (1986). Prediction, prevention, and mechanism of early (anaphylactic) antivenom reactions in victims of snake bites.. BMJ. 292(6512). 17–20. 166 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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