Nopporn Sittisombut

2.4k total citations
47 papers, 1.9k citations indexed

About

Nopporn Sittisombut is a scholar working on Public Health, Environmental and Occupational Health, Infectious Diseases and Immunology. According to data from OpenAlex, Nopporn Sittisombut has authored 47 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Public Health, Environmental and Occupational Health, 30 papers in Infectious Diseases and 8 papers in Immunology. Recurrent topics in Nopporn Sittisombut's work include Mosquito-borne diseases and control (32 papers), Viral Infections and Vectors (24 papers) and Viral Infections and Outbreaks Research (10 papers). Nopporn Sittisombut is often cited by papers focused on Mosquito-borne diseases and control (32 papers), Viral Infections and Vectors (24 papers) and Viral Infections and Outbreaks Research (10 papers). Nopporn Sittisombut collaborates with scholars based in Thailand, United States and Japan. Nopporn Sittisombut's co-authors include Prida Malasit, Watchara Kasinrerk, Chunya Puttikhunt, Poonsook Keelapang, Sansanee Noisakran, Panisadee Avirutnan, Niwat Maneekarn, Pa‐thai Yenchitsomanus, Rungtawan Sriburi and Somchai Thiemmeca and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Nopporn Sittisombut

45 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nopporn Sittisombut Thailand	22	1.5k	1.3k	219	212	195	47	1.9k
Estela Escribano-Romero Spain	25	1.0k 0.7×	1.1k 0.8×	276 1.3×	233 1.1×	114 0.6×	52	1.7k
Panisadee Avirutnan Thailand	17	1.9k 1.3×	1.6k 1.2×	204 0.9×	232 1.1×	173 0.9×	50	2.3k
Chunya Puttikhunt Thailand	24	2.3k 1.5×	1.9k 1.5×	274 1.3×	309 1.5×	317 1.6×	59	2.8k
October M. Sessions Singapore	21	1.1k 0.7×	963 0.7×	234 1.1×	412 1.9×	257 1.3×	47	1.8k
Penelope Koraka Netherlands	20	1.4k 0.9×	1.3k 1.0×	191 0.9×	145 0.7×	81 0.4×	40	1.8k
К. В. Пугачев United States	23	1.1k 0.7×	1.1k 0.8×	380 1.7×	195 0.9×	117 0.6×	34	1.6k
Pornapat Surasombatpattana Thailand	10	1.2k 0.8×	936 0.7×	312 1.4×	191 0.9×	242 1.2×	11	1.5k
T J Chambers United States	13	1.4k 0.9×	1.0k 0.8×	266 1.2×	146 0.7×	255 1.3×	13	1.7k
Marie‐Pascale Frenkiel France	23	1.5k 1.0×	1.4k 1.1×	440 2.0×	309 1.5×	106 0.5×	32	2.1k
Tonya M. Colpitts United States	25	1.3k 0.8×	1.0k 0.8×	124 0.6×	320 1.5×	458 2.3×	48	1.8k

Countries citing papers authored by Nopporn Sittisombut

Since Specialization

Citations

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

Fields of papers citing papers by Nopporn Sittisombut

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nopporn Sittisombut

This figure shows the co-authorship network connecting the top 25 collaborators of Nopporn Sittisombut. A scholar is included among the top collaborators of Nopporn Sittisombut 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 Nopporn Sittisombut. Nopporn Sittisombut is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Junjhon, Jiraphan, Chunya Puttikhunt, Rungtawan Sriburi, et al.. (2021). Generation and characterization of luciferase-secreting, single-round infectious DENV-2 reporter for functional antibody assays. Journal of Virological Methods. 291. 114119–114119. 4 indexed citations

Puttikhunt, Chunya, et al.. (2021). Increased capsid oligomerization is deleterious to dengue virus particle production. Journal of General Virology. 102(8).

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

Keelapang, Poonsook, et al.. (2017). Codon optimization of the prM-E coding region generates stable genome-length cDNA clone for a chimeric dengue 2/3 virus that can be propagated in Escherichia coli. 56(3). 1 indexed citations

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

Keelapang, Poonsook, Narong Nitatpattana, Rungtawan Sriburi, et al.. (2013). Generation and preclinical evaluation of a DENV-1/2 prM+E chimeric live attenuated vaccine candidate with enhanced prM cleavage. Vaccine. 31(44). 5134–5140. 13 indexed citations

Junjhon, Jiraphan, Sansanee Noisakran, Adisak Songjaeng, et al.. (2008). Differential Modulation of prM Cleavage, Extracellular Particle Distribution, and Virus Infectivity by Conserved Residues at Nonfurin Consensus Positions of the Dengue Virus pr-M Junction. Journal of Virology. 82(21). 10776–10791. 95 indexed citations

Tovanabutra, Sodsai, Mark de Souza, Nopporn Sittisombut, et al.. (2007). HIV-1 genetic diversity and compartmentalization in mother/infant pairs infected with CRF01_AE. AIDS. 21(8). 1050–1053. 9 indexed citations

Limjindaporn, Thawornchai, Janjuree Netsawang, Sansanee Noisakran, et al.. (2007). Sensitization to Fas-mediated apoptosis by dengue virus capsid protein. Biochemical and Biophysical Research Communications. 362(2). 334–339. 49 indexed citations

10.

Avirutnan, Panisadee, Nuntaya Punyadee, Sansanee Noisakran, et al.. (2006). Vascular Leakage in Severe Dengue Virus Infections: A Potential Role for the Nonstructural Viral Protein NS1 and Complement. The Journal of Infectious Diseases. 193(8). 1078–1088. 384 indexed citations

11.

Wiriyarat, Witthawat, Sanya Sukpanichnant, Nopporn Sittisombut, et al.. (2005). Specific immune response and pathological findings in BALB/c mice inoculated with recombinant BCG expressing HIV-1 antigen.. PubMed. 23(1). 41–51. 1 indexed citations

12.

Utaipat, Utaiwan, Ann Duerr, Donna L. Rudolph, et al.. (2002). Coreceptor Utilization of HIV Type 1 Subtype E Viral Isolates from Thai Men with HIV Type 1-Infected and Uninfected Wives. AIDS Research and Human Retroviruses. 18(1). 1–11. 14 indexed citations

13.

Sriburi, Rungtawan, Poonsook Keelapang, Thaneeya Duangchinda, et al.. (2001). Construction of infectious dengue 2 virus cDNA clones using high copy number plasmid. Journal of Virological Methods. 92(1). 71–82. 40 indexed citations

14.

Pruksakorn, Sumalee, et al.. (2000). Epidemiological Analysis of Non-M-Typeable Group A Streptococcus Isolates from a Thai Population in Northern Thailand. Journal of Clinical Microbiology. 38(3). 1250–1254. 41 indexed citations

15.

Vanittanakom, Nongnuch, William G. Merz, Nopporn Sittisombut, et al.. (1998). Specific identification ofPenicillium marneffeiby a polymerase chain reaction/hybridization technique. Medical Mycology. 36(3). 169–175. 25 indexed citations

16.

Kasinrerk, Watchara, et al.. (1994). Enhancement of human lymphocyte proliferative response to purified protein derivative by an anti-interleukin-2 receptor alpha chain antibody (CD25).. PubMed. 83(1). 33–7. 2 indexed citations

17.

Honoré, Nadine, Staffan Bergh, S Chanteau, et al.. (1993). Nucleotide sequence of the first cosmid from the Mycobacterium leprae genome project: structure and function of the Rif‐Str regions. Molecular Microbiology. 7(2). 207–214. 89 indexed citations

18.

Spieker-Polet, H, et al.. (1990). RABBIT MAJOR HISTOCOMPATIBILITY COMPLEX IV. EXPRESSION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS II GENES. International Journal of Immunogenetics. 17(1-2). 123–132. 7 indexed citations

19.

Sittisombut, Nopporn, et al.. (1989). RABBIT MAJOR HISTOCOMPATIBILITY COMPLEX.: III. MULTIPLE CLASS II DRβ GENES AND RESTRICTION FRAGMENT LENGTH POLYMORPHISM OF THE CLASS II α AND β GENES. International Journal of Immunogenetics. 16(1). 63–75. 7 indexed citations

20.

Sittisombut, Nopporn, et al.. (1988). Rabbit MHC. II. Sequence analysis of the R-DP alpha - and beta -genes.. The Journal of Immunology. 140(9). 3237–3243. 18 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