Sukathida Ubol

3.7k total citations
75 papers, 2.8k citations indexed

About

Sukathida Ubol is a scholar working on Public Health, Environmental and Occupational Health, Infectious Diseases and Epidemiology. According to data from OpenAlex, Sukathida Ubol has authored 75 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Public Health, Environmental and Occupational Health, 42 papers in Infectious Diseases and 21 papers in Epidemiology. Recurrent topics in Sukathida Ubol's work include Mosquito-borne diseases and control (48 papers), Viral Infections and Vectors (31 papers) and Malaria Research and Control (14 papers). Sukathida Ubol is often cited by papers focused on Mosquito-borne diseases and control (48 papers), Viral Infections and Vectors (31 papers) and Malaria Research and Control (14 papers). Sukathida Ubol collaborates with scholars based in Thailand, United States and France. Sukathida Ubol's co-authors include Siripen Kalayanarooj, Scott B. Halstead, Duncan R. Smith, Naphak Modhiran, Takol Chareonsirisuthigul, Suresh Mahalingam, Mary Marovich, David M. Mosser, Weerawat Phuklia and Nitwara Wikan and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Scientific Reports.

In The Last Decade

Sukathida Ubol

73 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sukathida Ubol Thailand 28 1.8k 1.6k 463 443 409 75 2.8k
Marie‐Pascale Frenkiel France 23 1.5k 0.8× 1.4k 0.9× 309 0.7× 440 1.0× 342 0.8× 32 2.1k
Eva Lee Australia 29 1.8k 1.0× 1.5k 0.9× 450 1.0× 359 0.8× 375 0.9× 50 2.7k
Thuy T. Le Australia 26 1.1k 0.6× 1.2k 0.8× 652 1.4× 609 1.4× 783 1.9× 54 2.9k
Rosa María del Ángel Mexico 34 2.1k 1.2× 1.8k 1.1× 857 1.9× 317 0.7× 333 0.8× 108 3.3k
Florence Guivel‐Benhassine France 22 1.2k 0.7× 1.7k 1.1× 526 1.1× 519 1.2× 1.1k 2.6× 35 3.1k
Lisa Miorin United States 21 891 0.5× 1.4k 0.8× 454 1.0× 472 1.1× 661 1.6× 35 2.2k
Hwee Cheng Tan Singapore 24 1.3k 0.7× 1.4k 0.8× 336 0.7× 236 0.5× 419 1.0× 49 2.1k
Chunya Puttikhunt Thailand 24 2.3k 1.3× 1.9k 1.2× 309 0.7× 274 0.6× 251 0.6× 59 2.8k
Aleksei Lulla Estonia 21 1.3k 0.7× 1.1k 0.7× 339 0.7× 192 0.4× 365 0.9× 35 1.9k
Yiu‐Wing Kam Singapore 26 1.4k 0.8× 1.5k 0.9× 273 0.6× 313 0.7× 269 0.7× 37 2.1k

Countries citing papers authored by Sukathida Ubol

Since Specialization
Citations

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

Fields of papers citing papers by Sukathida Ubol

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sukathida Ubol

This figure shows the co-authorship network connecting the top 25 collaborators of Sukathida Ubol. A scholar is included among the top collaborators of Sukathida Ubol 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 Sukathida Ubol. Sukathida Ubol 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.
Casadémont, Isabelle, Naphak Modhiran, Matthieu Prot, et al.. (2025). miRNome analysis reveals mir-155-5p as a protective factor to dengue infection in a resistant Thai cohort. Medical Microbiology and Immunology. 214(1). 13–13. 1 indexed citations
2.
Sunintaboon, Panya, et al.. (2024). Ag/Au-incorporated trimethyl chitosan-shell hybrid particles as reinforcing and antioxidant fillers for trimethyl chitosan hydrogel. Carbohydrate Polymers. 337. 122132–122132. 4 indexed citations
3.
Chawengkirttikul, Runglawan, et al.. (2021). Intranasal Administration of RBD Nanoparticles Confers Induction of Mucosal and Systemic Immunity against SARS-CoV-2. Vaccines. 9(7). 768–768. 49 indexed citations
4.
Intra, Bungonsiri, Sukathida Ubol, Atchareeya A-nuegoonpipat, et al.. (2019). <i>In vitro</i> antiviral activity of spirotetronate compounds against dengue virus serotype 2. The Journal of General and Applied Microbiology. 65(4). 197–203. 7 indexed citations
5.
Suksatu, Ampa, et al.. (2019). Insect anionic septapeptides suppress DENV replication by activating antiviral cytokines and miRNAs in primary human monocytes. Antiviral Research. 168. 1–8. 8 indexed citations
6.
Yoksan, Sutee, et al.. (2017). Small plaque size variant of chikungunya primary isolate showed reduced virulence in mice. Asian Pacific Journal of Allergy and Immunology. 36(3). 201–205. 9 indexed citations
7.
Yoksan, Sutee, et al.. (2017). The synergistic effect of nsP2-L618, nsP3-R117, and E2-K187 on the large plaque phenotype of chikungunya virus. Virus Genes. 54(1). 48–56. 5 indexed citations
8.
Saisawang, Chonticha, Atichat Kuadkitkan, Duncan R. Smith, Sukathida Ubol, & Albert J. Ketterman. (2016). Glutathionylation of chikungunya nsP2 protein affects protease activity. Biochimica et Biophysica Acta (BBA) - General Subjects. 1861(2). 106–111. 11 indexed citations
9.
Saisawang, Chonticha, et al.. (2015). Chikungunya nsP2 protease is not a papain-like cysteine protease and the catalytic dyad cysteine is interchangeable with a proximal serine. Scientific Reports. 5(1). 17125–17125. 18 indexed citations
10.
Wintachai, Phitchayapak, Parveen Kaur, Regina Ching Hua Lee, et al.. (2015). Activity of andrographolide against chikungunya virus infection. Scientific Reports. 5(1). 14179–14179. 120 indexed citations
11.
Hunsawong, Taweewun, Panya Sunintaboon, Saradee Warit, et al.. (2015). Immunogenic Properties of a BCG Adjuvanted Chitosan Nanoparticle-Based Dengue Vaccine in Human Dendritic Cells. PLoS neglected tropical diseases. 9(9). e0003958–e0003958. 29 indexed citations
12.
Kuadkitkan, Atichat, Nitwara Wikan, Phitchayapak Wintachai, et al.. (2014). Involvement of ATP synthase β subunit in chikungunya virus entry into insect cells. Archives of Virology. 159(12). 3353–3364. 47 indexed citations
13.
Wintachai, Phitchayapak, Nitwara Wikan, Atichat Kuadkitkan, et al.. (2012). Identification of prohibitin as a Chikungunya virus receptor protein. Journal of Medical Virology. 84(11). 1757–1770. 150 indexed citations
14.
Wikan, Nitwara, et al.. (2012). Chikungunya Virus Infection of Cell Lines: Analysis of the East, Central and South African Lineage. PLoS ONE. 7(1). e31102–e31102. 76 indexed citations
15.
Halstead, Scott B., Suresh Mahalingam, Mary Marovich, Sukathida Ubol, & David M. Mosser. (2010). Intrinsic antibody-dependent enhancement of microbial infection in macrophages: disease regulation by immune complexes. The Lancet Infectious Diseases. 10(10). 712–722. 317 indexed citations
16.
Modhiran, Naphak, Siripen Kalayanarooj, & Sukathida Ubol. (2010). Subversion of Innate Defenses by the Interplay between DENV and Pre-Existing Enhancing Antibodies: TLRs Signaling Collapse. PLoS neglected tropical diseases. 4(12). e924–e924. 76 indexed citations
17.
Chareonsirisuthigul, Takol, Siripen Kalayanarooj, & Sukathida Ubol. (2007). Dengue virus (DENV) antibody-dependent enhancement of infection upregulates the production of anti-inflammatory cytokines, but suppresses anti-DENV free radical and pro-inflammatory cytokine production, in THP-1 cells. Journal of General Virology. 88(2). 365–375. 185 indexed citations
18.
Kantachuvesiri, Surasak, et al.. (2006). Partial construction of apoptotic pathway in PBMC obtained from active SLE patients and the significance of plasma TNF-α on this pathway. Clinical Rheumatology. 25(5). 705–714. 20 indexed citations
19.
Ubol, Sukathida, et al.. (1998). Apoptosis induction in brain during the fixed strain of rabies virus infection correlates with onset and severity of illness. Journal of NeuroVirology. 4(4). 407–414. 57 indexed citations
20.
Griffin, Diane E., Beth Levine, William R. Tyor, Sukathida Ubol, & Philippe Desprès. (1997). The role of antibody in recovery from alphavirus encephalitis. Immunological Reviews. 159(1). 155–161. 92 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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