Teerapong Buaboocha

1.6k total citations
54 papers, 1.2k citations indexed

About

Teerapong Buaboocha is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Teerapong Buaboocha has authored 54 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Plant Science, 35 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Teerapong Buaboocha's work include Plant Stress Responses and Tolerance (29 papers), Photosynthetic Processes and Mechanisms (20 papers) and Plant Molecular Biology Research (14 papers). Teerapong Buaboocha is often cited by papers focused on Plant Stress Responses and Tolerance (29 papers), Photosynthetic Processes and Mechanisms (20 papers) and Plant Molecular Biology Research (14 papers). Teerapong Buaboocha collaborates with scholars based in Thailand, United States and Japan. Teerapong Buaboocha's co-authors include Bongkoj Boonburapong, Supachitra Chadchawan, Luca Comai, Hongya Gu, Zahra Iqbal, Mohammed Shariq Iqbal, Tadao Asami, Kitiporn Plaimas, Surendra Pratap Singh and Li‐Jia Qu and has published in prestigious journals such as PLoS ONE, Applied and Environmental Microbiology and Scientific Reports.

In The Last Decade

Teerapong Buaboocha

52 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Teerapong Buaboocha Thailand 15 1.0k 536 125 30 28 54 1.2k
Chuanzhi Zhao China 24 1.3k 1.3× 810 1.5× 70 0.6× 39 1.3× 26 0.9× 75 1.5k
Jianzhong Lin China 17 1.1k 1.0× 641 1.2× 106 0.8× 34 1.1× 22 0.8× 37 1.2k
Qingjun Xie China 18 739 0.7× 473 0.9× 107 0.9× 24 0.8× 13 0.5× 46 967
Fuyou Fu China 17 1.1k 1.1× 968 1.8× 133 1.1× 12 0.4× 26 0.9× 34 1.5k
Ning Zhao China 22 1.2k 1.2× 776 1.4× 89 0.7× 20 0.7× 15 0.5× 63 1.5k
Supriya Ambawat India 9 906 0.9× 575 1.1× 129 1.0× 53 1.8× 18 0.6× 24 1.1k
David Riewe Germany 20 806 0.8× 375 0.7× 136 1.1× 28 0.9× 60 2.1× 30 1.1k
Jaewoong Yu South Korea 17 1.3k 1.3× 882 1.6× 80 0.6× 37 1.2× 22 0.8× 37 1.5k
Jiaowen Pan China 20 1.4k 1.4× 904 1.7× 86 0.7× 28 0.9× 26 0.9× 36 1.6k
Yongen Lu China 22 1.4k 1.4× 1.1k 2.1× 93 0.7× 42 1.4× 19 0.7× 47 1.8k

Countries citing papers authored by Teerapong Buaboocha

Since Specialization
Citations

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

Fields of papers citing papers by Teerapong Buaboocha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teerapong Buaboocha

This figure shows the co-authorship network connecting the top 25 collaborators of Teerapong Buaboocha. A scholar is included among the top collaborators of Teerapong Buaboocha 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 Teerapong Buaboocha. Teerapong Buaboocha 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.
2.
Jakada, Bello Hassan, et al.. (2024). Rice OBF binding protein 4 (OsOBP4) participates in flowering and regulates salt stress tolerance in Arabidopsis. Environmental and Experimental Botany. 221. 105748–105748. 8 indexed citations
3.
Chadchawan, Supachitra, et al.. (2024). Association of a Specific OsCULLIN3c Haplotype with Salt Stress Responses in Local Thai Rice. International Journal of Molecular Sciences. 25(2). 1040–1040. 2 indexed citations
4.
Comai, Luca, et al.. (2023). Genome-Wide Association Study of Starch Properties in Local Thai Rice. Plants. 12(18). 3290–3290. 7 indexed citations
5.
Buaboocha, Teerapong, et al.. (2022). Salt stress responses and SNP‐based phylogenetic analysis of Thai rice cultivars. The Plant Genome. 15(1). e20189–e20189. 9 indexed citations
6.
Pongpanich, Monnat, et al.. (2022). Identification of a Negative Regulator for Salt Tolerance at Seedling Stage via a Genome-Wide Association Study of Thai Rice Populations. International Journal of Molecular Sciences. 23(3). 1842–1842. 9 indexed citations
7.
Plaimas, Kitiporn, Luca Comai, Teerapong Buaboocha, et al.. (2021). Combining Genome and Gene Co-expression Network Analyses for the Identification of Genes Potentially Regulating Salt Tolerance in Rice. Frontiers in Plant Science. 12. 704549–704549. 14 indexed citations
8.
9.
Iqbal, Zahra, Mohammed Shariq Iqbal, Surendra Pratap Singh, & Teerapong Buaboocha. (2020). Ca2+/Calmodulin Complex Triggers CAMTA Transcriptional Machinery Under Stress in Plants: Signaling Cascade and Molecular Regulation. Frontiers in Plant Science. 11. 598327–598327. 76 indexed citations
10.
Siangliw, Meechai, et al.. (2019). Physiological Mechanisms of the Seedling Stage Salt Tolerance of Near Isogenic Rice Lines with the ‘KDML105’ Genetic Background. International Journal of Agriculture and Biology. 23(5). 927–934. 3 indexed citations
11.
Buaboocha, Teerapong, et al.. (2019). OsCaM1-1 overexpression in the transgenic rice mitigated salt-induced oxidative damage. Biologia Plantarum. 63(1). 335–342. 13 indexed citations
12.
Sirikantaramas, Supaart, et al.. (2019). Isocitrate lyase plays important roles in plant salt tolerance. BMC Plant Biology. 19(1). 472–472. 43 indexed citations
13.
Qu, Li‐Jia, et al.. (2015). C-terminal extension of calmodulin-like 3 protein from <italic>Oryza sativa</italic> L.: interaction with a high mobility group target protein. Acta Biochimica et Biophysica Sinica. 47(11). 880–889. 11 indexed citations
14.
Plaimas, Kitiporn, et al.. (2014). Molecular Karyotyping and Exome Analysis of Salt‐Tolerant Rice Mutant from Somaclonal Variation. The Plant Genome. 7(3). 13 indexed citations
15.
Buaboocha, Teerapong, et al.. (2013). ผลของภาวะเคมตอการสงเคราะหดวยแสงและการเจรญเตบโตในขาวสายพนธ ทนเคมทไดจากประชากร CSSL Effect of Salt Stress on Photosynthesis and Growth in Salt-tolerant Rice Lines Obtained from CSSL Population. 1 indexed citations
16.
Limpaseni, Tipaporn, et al.. (2012). Expression analysis of calmodulin and calmodulin-like genes from rice, Oryza sativa L.. BMC Research Notes. 5(1). 625–625. 48 indexed citations
17.
Buaboocha, Teerapong, et al.. (2011). Biophysical characterization of calmodulin and calmodulin-like proteins from rice, <italic>Oryza sativa</italic> L.. Acta Biochimica et Biophysica Sinica. 43(11). 867–876. 14 indexed citations
18.
Waditee, Rungaroon, Teerapong Buaboocha, Takashi Hibino, et al.. (2006). Carboxyl-terminal hydrophilic tail of a NhaP type Na+/H+ antiporter from cyanobacteria is involved in the apparent affinity for Na+ and pH sensitivity. Archives of Biochemistry and Biophysics. 450(1). 113–121. 11 indexed citations
19.
Buaboocha, Teerapong, et al.. (2005). Calcium Signaling-mediated and Differential Induction of Calmodulin Gene Expression by Stress in Oryza sativa L.. BMB Reports. 38(4). 432–439. 35 indexed citations
20.
Buaboocha, Teerapong, Birong Liao, & Raymond E. Zielinski. (2001). Isolation of cDNA and genomic DNA clones encoding a calmodulin-binding protein related to a family of ATPases involved in cell division and vesicle fusion. Planta. 212(5-6). 774–781. 12 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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