Prida Malasit

11.2k total citations · 3 hit papers
117 papers, 7.5k citations indexed

About

Prida Malasit is a scholar working on Public Health, Environmental and Occupational Health, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Prida Malasit has authored 117 papers receiving a total of 7.5k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Public Health, Environmental and Occupational Health, 63 papers in Infectious Diseases and 23 papers in Molecular Biology. Recurrent topics in Prida Malasit's work include Mosquito-borne diseases and control (79 papers), Viral Infections and Vectors (60 papers) and Viral Infections and Outbreaks Research (19 papers). Prida Malasit is often cited by papers focused on Mosquito-borne diseases and control (79 papers), Viral Infections and Vectors (60 papers) and Viral Infections and Outbreaks Research (19 papers). Prida Malasit collaborates with scholars based in Thailand, United Kingdom and United States. Prida Malasit's co-authors include Juthathip Mongkolsapaya, Gavin Screaton, Thaneeya Duangchinda, Wanwisa Dejnirattisai, Chunya Puttikhunt, Panisadee Avirutnan, Sirijitt Vasanawathana, Watchara Kasinrerk, Pa‐thai Yenchitsomanus and Visith Thongboonkerd and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Prida Malasit

113 papers receiving 7.3k citations

Hit Papers

Cross-Reacting Antibodies Enhance Dengue Virus Infection ... 2003 2026 2010 2018 2010 2016 2003 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Prida Malasit Thailand 41 5.0k 4.3k 1.4k 678 669 117 7.5k
Trai‐Ming Yeh Taiwan 47 4.4k 0.9× 4.0k 0.9× 1.0k 0.8× 957 1.4× 816 1.2× 143 6.9k
Mark T. Heise United States 49 2.5k 0.5× 5.6k 1.3× 1.8k 1.3× 2.4k 3.5× 1.3k 2.0× 145 8.8k
Thomas E. Morrison United States 39 2.3k 0.5× 3.1k 0.7× 917 0.7× 1.6k 2.4× 873 1.3× 116 5.5k
Andreas Suhrbier Australia 55 3.9k 0.8× 3.8k 0.9× 2.1k 1.6× 2.9k 4.3× 1.9k 2.8× 218 9.4k
Laurence Briant France 36 2.1k 0.4× 1.9k 0.4× 983 0.7× 1.2k 1.8× 854 1.3× 83 4.8k
Kovit Pattanapanyasat Thailand 31 1.9k 0.4× 1.8k 0.4× 1.0k 0.8× 1.4k 2.0× 724 1.1× 209 5.1k
Lionel Gresh United States 36 2.4k 0.5× 2.4k 0.6× 1.3k 0.9× 293 0.4× 817 1.2× 74 5.0k
Hui Zhao China 28 817 0.2× 1.3k 0.3× 641 0.5× 264 0.4× 431 0.6× 112 2.6k
Anavaj Sakuntabhai France 36 2.6k 0.5× 2.3k 0.5× 1.2k 0.9× 448 0.7× 653 1.0× 119 5.3k
Lynn Soong United States 48 3.7k 0.7× 989 0.2× 811 0.6× 2.1k 3.2× 2.3k 3.4× 156 6.2k

Countries citing papers authored by Prida Malasit

Since Specialization
Citations

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

Fields of papers citing papers by Prida Malasit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Prida Malasit

This figure shows the co-authorship network connecting the top 25 collaborators of Prida Malasit. A scholar is included among the top collaborators of Prida Malasit 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 Prida Malasit. Prida Malasit 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.
Haddawy, Peter, Wannee Limpitikul, Nasikarn Angkasekwinai, et al.. (2025). Prognostic prediction of dengue hemorrhagic fever in pediatric patients with suspected dengue infection: A multi-site study. PLoS ONE. 20(8). e0327360–e0327360.
2.
Srisawat, Chatchawan, Wannee Limpitikul, Prida Malasit, et al.. (2022). Smartphone multiplex microcapillary diagnostics using Cygnus: Development and evaluation of rapid serotype-specific NS1 detection with dengue patient samples. PLoS neglected tropical diseases. 16(4). e0010266–e0010266. 6 indexed citations
3.
Sangsrakru, Duangjai, et al.. (2021). Genetic diversity of the dengue virus population in dengue fever and dengue hemorrhagic fever patients. Asian Pacific Journal of Allergy and Immunology. 41(4). 361–371. 3 indexed citations
4.
Roytrakul, Sittiruk, Yodying Yingchutrakul, Bunpote Siridechadilok, et al.. (2021). Potential Phosphorylation of Viral Nonstructural Protein 1 in Dengue Virus Infection. Viruses. 13(7). 1393–1393. 8 indexed citations
5.
Puttikhunt, Chunya, et al.. (2021). Increased capsid oligomerization is deleterious to dengue virus particle production. Journal of General Virology. 102(8).
6.
Tangthawornchaikul, Nattaya, Adisak Songjaeng, Panisadee Avirutnan, et al.. (2021). High performance dengue virus antigen-based serotyping-NS1-ELISA (plus): A simple alternative approach to identify dengue virus serotypes in acute dengue specimens. PLoS neglected tropical diseases. 15(2). e0009065–e0009065. 13 indexed citations
7.
Songjaeng, Adisak, Panisadee Avirutnan, Chunya Puttikhunt, et al.. (2019). Enhanced production of infectious particles by adaptive modulation of C–prM processing and C–C interaction during propagation of dengue pseudoinfectious virus in stable CprME-expressing cells. Journal of General Virology. 101(1). 59–72. 5 indexed citations
8.
Lert-itthiporn, Worachart, Bruno Cavadas, Verónica Fernandes, et al.. (2018). Joint ancestry and association test indicate two distinct pathogenic pathways involved in classical dengue fever and dengue shock syndrome. PLoS neglected tropical diseases. 12(2). e0006202–e0006202. 15 indexed citations
9.
Dejnirattisai, Wanwisa, Piyada Supasa, Wiyada Wongwiwat, et al.. (2016). Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with zika virus. Nature Immunology. 17(9). 1102–1108. 663 indexed citations breakdown →
10.
Keelapang, Poonsook, Rungtawan Sriburi, Rojjanaporn Pulmanausahakul, et al.. (2015). Generation and preclinical immunogenicity study of dengue type 2 virus-like particles derived from stably transfected mosquito cells. Vaccine. 33(42). 5613–5622. 23 indexed citations
11.
King, Jennifer C., Janjuree Netsawang, Pa‐thai Yenchitsomanus, et al.. (2012). Adaptor protein 1 complexes regulate intracellular trafficking of the kidney anion exchanger 1 in epithelial cells. American Journal of Physiology-Cell Physiology. 303(5). C554–C566. 16 indexed citations
12.
Netsawang, Janjuree, Sansanee Noisakran, Wiyada Wongwiwat, et al.. (2011). Cell death gene expression profile: Role of RIPK2 in dengue virus-mediated apoptosis. Virus Research. 156(1-2). 25–34. 33 indexed citations
13.
Sritippayawan, Suchai, Atchara Paemanee, Wattanachai Susaengrat, et al.. (2009). Evidence suggesting a genetic contribution to kidney stone in northeastern Thai population. Urological Research. 37(3). 141–146. 15 indexed citations
14.
Netsawang, Janjuree, Sansanee Noisakran, Chunya Puttikhunt, et al.. (2009). Nuclear localization of dengue virus capsid protein is required for DAXX interaction and apoptosis. Virus Research. 147(2). 275–283. 74 indexed citations
15.
Puttikhunt, Chunya, et al.. (2007). Novel anti‐dengue monoclonal antibody recognizing conformational structure of the prM‐E heterodimeric complex of dengue virus. Journal of Medical Virology. 80(1). 125–133. 16 indexed citations
16.
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
17.
Puttikhunt, Chunya, et al.. (2006). Enhancement of recombinant soluble dengue virus 2 envelope domain III protein production in Escherichia coli trxB and gor double mutant. Journal of Bioscience and Bioengineering. 102(4). 333–339. 13 indexed citations
18.
Kaitwatcharachai, Charoen, Somkiat Vasuvattakul, Pa‐thai Yenchitsomanus, et al.. (1999). Distal renal tubular acidosis and high urine carbon dioxide tension in a patient with southeast asian ovalocytosis. American Journal of Kidney Diseases. 33(6). 1147–1152. 18 indexed citations
19.
Ong-Ajyooth, Leena, P Parichatikanond, Prida Malasit, et al.. (1995). Glomerulonephritis in beta-thalassemia Hb-E disease: clinical manifestations, histopathologic studies and outcome.. PubMed. 78(3). 119–26. 1 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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