Natapong Jupatanakul

1.8k total citations
26 papers, 1.1k citations indexed

About

Natapong Jupatanakul is a scholar working on Public Health, Environmental and Occupational Health, Insect Science and Molecular Biology. According to data from OpenAlex, Natapong Jupatanakul has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Public Health, Environmental and Occupational Health, 16 papers in Insect Science and 8 papers in Molecular Biology. Recurrent topics in Natapong Jupatanakul's work include Mosquito-borne diseases and control (22 papers), Insect symbiosis and bacterial influences (16 papers) and Malaria Research and Control (9 papers). Natapong Jupatanakul is often cited by papers focused on Mosquito-borne diseases and control (22 papers), Insect symbiosis and bacterial influences (16 papers) and Malaria Research and Control (9 papers). Natapong Jupatanakul collaborates with scholars based in Thailand, United States and France. Natapong Jupatanakul's co-authors include George Dimopoulos, Shuzhen Sim, Nathan Dennison, Seokyoung Kang, Yesseinia Angleró-Rodríguez, Jenny Carlson, Hamish Mohammed, José L. Ramírez, Claudia M. Romero-Vivas and Hannah J. MacLeod and has published in prestigious journals such as Nature Communications, PLoS ONE and Antimicrobial Agents and Chemotherapy.

In The Last Decade

Natapong Jupatanakul

23 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natapong Jupatanakul Thailand 13 876 795 348 239 148 26 1.1k
Seokyoung Kang United States 14 678 0.8× 603 0.8× 264 0.8× 194 0.8× 133 0.9× 22 871
Luc Abate France 16 929 1.1× 688 0.9× 152 0.4× 288 1.2× 159 1.1× 27 1.2k
Eric P. Caragata United States 18 1.1k 1.3× 1.3k 1.6× 217 0.6× 125 0.5× 109 0.7× 43 1.5k
Majoline T. Tchioffo France 13 725 0.8× 618 0.8× 139 0.4× 198 0.8× 113 0.8× 17 930
Sandrine E. Nsango Cameroon 17 1.0k 1.2× 723 0.9× 149 0.4× 375 1.6× 191 1.3× 34 1.3k
Margus Varjak United Kingdom 18 805 0.9× 390 0.5× 540 1.6× 221 0.9× 347 2.3× 32 1.2k
Claire L. Donald United Kingdom 15 628 0.7× 429 0.5× 361 1.0× 174 0.7× 288 1.9× 24 940
Kerri L. Coon United States 12 824 0.9× 1.2k 1.5× 139 0.4× 166 0.7× 109 0.7× 30 1.3k
Jaclyn C. Scott United States 5 804 0.9× 509 0.6× 454 1.3× 189 0.8× 281 1.9× 6 1.0k
Charles B. Pumpuni United States 14 982 1.1× 591 0.7× 245 0.7× 259 1.1× 115 0.8× 17 1.2k

Countries citing papers authored by Natapong Jupatanakul

Since Specialization
Citations

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

Fields of papers citing papers by Natapong Jupatanakul

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natapong Jupatanakul

This figure shows the co-authorship network connecting the top 25 collaborators of Natapong Jupatanakul. A scholar is included among the top collaborators of Natapong Jupatanakul 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 Natapong Jupatanakul. Natapong Jupatanakul 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.
Jupatanakul, Natapong, et al.. (2025). Insights into spatio-temporal dynamics of Anopheles vectors while approaching malaria elimination along the Thailand-Cambodia border. Acta Tropica. 263. 107545–107545. 1 indexed citations
2.
Samung, Yudthana, et al.. (2025). Comprehensive intra-host infection kinetics reveals high arbo-orthoflavivirus transmission potential by neglected vector species, Aedes scutellaris. PLoS neglected tropical diseases. 19(5). e0012530–e0012530.
3.
Merkling, Sarah H., Stéphanie Dabo, Josquin Daron, et al.. (2025). Dengue virus susceptibility in Aedes aegypti linked to natural cytochrome P450 promoter variants. Nature Communications. 16(1). 7468–7468.
4.
5.
Saeung, Atiporn, et al.. (2024). Dirus complex species identification PCR (DiCSIP) improves the identification of Anopheles dirus complex from the Greater Mekong Subregion. Parasites & Vectors. 17(1). 260–260. 3 indexed citations
6.
Jupatanakul, Natapong, et al.. (2024). Overview of national and local efforts to eliminate malaria in Thailand. Trends in Parasitology. 41(1). 52–65. 2 indexed citations
7.
Saeung, Atiporn, et al.. (2021). New Insights into Antimalarial Chemopreventive Activity of Antifolates. Antimicrobial Agents and Chemotherapy. 66(2). e0153821–e0153821. 11 indexed citations
8.
Prommana, Parichat, et al.. (2021). Transgenic pyrimethamine-resistant plasmodium falciparum reveals transmission-blocking potency of P218, a novel antifolate candidate drug. International Journal for Parasitology. 51(8). 635–642. 8 indexed citations
9.
Dada, Nsa, Natapong Jupatanakul, Guillaume Minard, et al.. (2021). Considerations for mosquito microbiome research from the Mosquito Microbiome Consortium. Microbiome. 9(1). 36–36. 26 indexed citations
10.
Jupatanakul, Natapong, et al.. (2020). Serratia marcescens secretes proteases and chitinases with larvicidal activity against Anopheles dirus. Acta Tropica. 212. 105686–105686. 22 indexed citations
11.
Duangchinda, Thaneeya, et al.. (2018). Multi-color fluorescent reporter dengue viruses with improved stability for analysis of a multi-virus infection. PLoS ONE. 13(3). e0194399–e0194399. 22 indexed citations
12.
Angleró-Rodríguez, Yesseinia, Octávio A. C. Talyuli, Benjamin J. Blumberg, et al.. (2017). An Aedes aegypti-associated fungus increases susceptibility to dengue virus by modulating gut trypsin activity. eLife. 6. 79 indexed citations
13.
Angleró-Rodríguez, Yesseinia, Hannah J. MacLeod, Seokyoung Kang, et al.. (2017). Aedes aegypti Molecular Responses to Zika Virus: Modulation of Infection by the Toll and Jak/Stat Immune Pathways and Virus Host Factors. Frontiers in Microbiology. 8. 2050–2050. 98 indexed citations
14.
Jupatanakul, Natapong, et al.. (2017). Molecular analysis of Culex quinquefasciatus larvae responses to Lysinibacillus sphaericus Bin toxin. PLoS ONE. 12(4). e0175473–e0175473. 12 indexed citations
15.
Jupatanakul, Natapong, et al.. (2016). The DNA chaperone HMGB1 potentiates the transcriptional activity of Rel1A in the mosquito Aedes aegypti. Insect Biochemistry and Molecular Biology. 80. 32–41. 11 indexed citations
16.
Dennison, Nathan, Natapong Jupatanakul, & George Dimopoulos. (2014). The mosquito microbiota influences vector competence for human pathogens. Current Opinion in Insect Science. 3. 6–13. 164 indexed citations
17.
Kang, Seokyoung, et al.. (2014). Suppressing Dengue-2 Infection by Chemical Inhibition of Aedes aegypti Host Factors. PLoS neglected tropical diseases. 8(8). e3084–e3084. 39 indexed citations
18.
Sim, Shuzhen, Natapong Jupatanakul, José L. Ramírez, et al.. (2013). Transcriptomic Profiling of Diverse Aedes aegypti Strains Reveals Increased Basal-level Immune Activation in Dengue Virus-refractory Populations and Identifies Novel Virus-vector Molecular Interactions. PLoS neglected tropical diseases. 7(7). e2295–e2295. 124 indexed citations
19.
Jupatanakul, Natapong, Shuzhen Sim, & George Dimopoulos. (2013). Aedes aegypti ML and Niemann-Pick type C family members are agonists of dengue virus infection. Developmental & Comparative Immunology. 43(1). 1–9. 56 indexed citations
20.
Jupatanakul, Natapong, et al.. (2010). Cloning and expression of recombinant shrimp PmRab7 (a virus-binding protein) in Pichia pastoris. Protein Expression and Purification. 76(1). 1–6. 5 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

Breakdown of academic impact, for papers by Seokyoung Kang Breakdown of academic impact, for papers by Luc Abate Breakdown of academic impact, for papers by Eric P. Caragata Breakdown of academic impact, for papers by Majoline T. Tchioffo Breakdown of academic impact, for papers by Sandrine E. Nsango Breakdown of academic impact, for papers by Margus Varjak Breakdown of academic impact, for papers by Claire L. Donald Breakdown of academic impact, for papers by Kerri L. Coon Breakdown of academic impact, for papers by Jaclyn C. Scott Breakdown of academic impact, for papers by Charles B. Pumpuni
Rankless by CCL
2026