Benjaphorn Prapagdee

2.0k total citations
58 papers, 1.6k citations indexed

About

Benjaphorn Prapagdee is a scholar working on Pollution, Plant Science and Biomaterials. According to data from OpenAlex, Benjaphorn Prapagdee has authored 58 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Pollution, 24 papers in Plant Science and 18 papers in Biomaterials. Recurrent topics in Benjaphorn Prapagdee's work include Microplastics and Plastic Pollution (17 papers), Plant Stress Responses and Tolerance (16 papers) and biodegradable polymer synthesis and properties (16 papers). Benjaphorn Prapagdee is often cited by papers focused on Microplastics and Plastic Pollution (17 papers), Plant Stress Responses and Tolerance (16 papers) and biodegradable polymer synthesis and properties (16 papers). Benjaphorn Prapagdee collaborates with scholars based in Thailand, United Kingdom and Malaysia. Benjaphorn Prapagdee's co-authors include Narongrit Sombatsompop, Skorn Mongkolsuk, Skorn Mongkolsuk, Paiboon Vattanaviboon, Teerasak Markpin, Achara Ussawarujikulchai, Suchana Chavanich, James M. Dubbs, Apisit Kositchaiyong and Nopporn Thasana and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioresource Technology and FEBS Letters.

In The Last Decade

Benjaphorn Prapagdee

57 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benjaphorn Prapagdee Thailand 22 684 612 429 243 151 58 1.6k
Cesare Accinelli Italy 28 1.0k 1.5× 843 1.4× 224 0.5× 219 0.9× 111 0.7× 63 1.9k
Reeta Goel India 25 549 0.8× 712 1.2× 240 0.6× 272 1.1× 186 1.2× 71 1.7k
Motoo Koitabashi Japan 21 496 0.7× 712 1.2× 381 0.9× 332 1.4× 161 1.1× 48 1.4k
María del Carmen Vargas-García Spain 26 573 0.8× 812 1.3× 200 0.5× 305 1.3× 384 2.5× 53 2.4k
Geoff Robson United Kingdom 14 307 0.4× 382 0.6× 204 0.5× 368 1.5× 161 1.1× 23 1.1k
Alex Sivan Israel 14 915 1.3× 282 0.5× 577 1.3× 251 1.0× 161 1.1× 25 1.7k
F. Suárez‐Estrella Spain 30 764 1.1× 1.1k 1.7× 269 0.6× 344 1.4× 422 2.8× 79 3.0k
Sehroon Khan China 19 435 0.6× 487 0.8× 243 0.6× 193 0.8× 74 0.5× 43 1.2k
Vinay Mohan Pathak India 10 814 1.2× 340 0.6× 418 1.0× 165 0.7× 205 1.4× 21 1.6k

Countries citing papers authored by Benjaphorn Prapagdee

Since Specialization
Citations

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

Fields of papers citing papers by Benjaphorn Prapagdee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benjaphorn Prapagdee

This figure shows the co-authorship network connecting the top 25 collaborators of Benjaphorn Prapagdee. A scholar is included among the top collaborators of Benjaphorn Prapagdee 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 Benjaphorn Prapagdee. Benjaphorn Prapagdee 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.
Ussawarujikulchai, Achara, et al.. (2024). Contamination of microplastics in greenhouse soil subjected to plastic mulching. Environmental Technology & Innovation. 37. 103991–103991. 7 indexed citations
2.
Prapagdee, Benjaphorn, et al.. (2024). Enhancing heavy metal phytoremediation in landfill soil by Chrysopogon zizanioides (L.) roberty through the application of bacterial-biochar pellets. Environmental Technology & Innovation. 35. 103738–103738. 6 indexed citations
3.
Prapagdee, Benjaphorn, et al.. (2023). Bacterial-assisted phytoremediation of heavy metals: Concepts, current knowledge, and future directions. Environmental Technology & Innovation. 33. 103488–103488. 34 indexed citations
4.
Ussawarujikulchai, Achara, et al.. (2023). Seasonal variation in the abundance of microplastics in three commercial bivalves from Bandon Bay, Gulf of Thailand. Marine Pollution Bulletin. 197. 115600–115600. 20 indexed citations
5.
Prapagdee, Benjaphorn, et al.. (2023). Enhancing cadmium phytoremediation of Chlorophytum comosum (Thunb.) Jacques by applying cadmium-resistant bacterial tablet. Environmental Science and Pollution Research. 30(52). 113015–113025. 2 indexed citations
6.
Ussawarujikulchai, Achara, et al.. (2022). Microplastics in the surface seawater of Bandon Bay, Gulf of Thailand. Marine Pollution Bulletin. 179. 113664–113664. 28 indexed citations
7.
Prapagdee, Benjaphorn, et al.. (2021). Potential of a rhizobacterium on removal of heavy metals from aqueous solution and promoting plant root elongation under heavy metal toxic conditions. Environmental Technology & Innovation. 22. 101419–101419. 19 indexed citations
8.
Prapagdee, Benjaphorn, et al.. (2020). Cadmium phytoremediation performance of two species of Chlorophytum and enhancing their potentials by cadmium-resistant bacteria. Environmental Technology & Innovation. 21. 101311–101311. 21 indexed citations
9.
Sombatsompop, Narongrit, et al.. (2018). Accelerating biodegradation of PLA using microbial consortium from dairy wastewater sludge combined with PLA-degrading bacterium. International Biodeterioration & Biodegradation. 132. 74–83. 81 indexed citations
11.
Prapagdee, Benjaphorn, et al.. (2014). Efficiency of Modified Grease Trap for Domestic Wastewater Treatment. 10(2). 10–22. 5 indexed citations
12.
Boontanon, Narin, et al.. (2013). Dispersion of Cadmium-resistant Bacteria in Cadmium-contaminated Soils at Mae Sot District, Tak Province. SHILAP Revista de lepidopterología. 2 indexed citations
13.
Arunlertaree, Chumlong, et al.. (2011). Decolorization of reactive dyes and textile dyeing effluent by Pleurotus sajor-caju.. 11(1). 52–57. 7 indexed citations
14.
Prapagdee, Benjaphorn, et al.. (2010). Effects of bio-extracts on the growth of Chinese kale.. Witthayasan Kasetsat Witthayasat. 44(5). 808–815. 3 indexed citations
15.
Thasana, Nopporn, Benjaphorn Prapagdee, Nuchanart Rangkadilok, et al.. (2010). Bacillus subtilis SSE4 produces subtulene A, a new lipopeptide antibiotic possessing an unusual C15 unsaturated β‐amino acid. FEBS Letters. 584(14). 3209–3214. 50 indexed citations
16.
Prapagdee, Benjaphorn, et al.. (2008). The Role of Exopolymers in Protection of Ralstonia sp., a Cadmium-resistant Bacterium, from Cadmium Toxicity. SHILAP Revista de lepidopterología. 3 indexed citations
17.
Prapagdee, Benjaphorn, et al.. (2008). Effects of Inorganic Ions and Glucose on Hydrogen Production by Indigenous Microbes in Sewage Sludge. SHILAP Revista de lepidopterología. 1 indexed citations
18.
Prapagdee, Benjaphorn, et al.. (2008). Antifungal Potential of Extracellular Metabolites Produced by Streptomyces hygroscopicus against Phytopathogenic Fungi. International Journal of Biological Sciences. 4(5). 330–337. 194 indexed citations
19.
Prapagdee, Benjaphorn, Warawan Eiamphungporn, Panatda Saenkham, Skorn Mongkolsuk, & Paiboon Vattanaviboon. (2004). Analysis of growth phase regulated KatA and CatE and their physiological roles in determining hydrogen peroxide resistance in Agrobacterium tumefaciens. FEMS Microbiology Letters. 237(2). 219–226. 8 indexed citations
20.
Eiamphungporn, Warawan, et al.. (2003). Oxidant-inducible resistance to hydrogen peroxide killing inAgrobacterium tumefaciensrequires the global peroxide sensor-regulator OxyR and KatA. FEMS Microbiology Letters. 225(1). 167–172. 20 indexed citations

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