Haeng‐Soon Lee

4.4k total citations · 1 hit paper
67 papers, 3.4k citations indexed

About

Haeng‐Soon Lee is a scholar working on Molecular Biology, Plant Science and Biochemistry. According to data from OpenAlex, Haeng‐Soon Lee has authored 67 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 45 papers in Plant Science and 13 papers in Biochemistry. Recurrent topics in Haeng‐Soon Lee's work include Plant Stress Responses and Tolerance (33 papers), Photosynthetic Processes and Mechanisms (23 papers) and Plant tissue culture and regeneration (22 papers). Haeng‐Soon Lee is often cited by papers focused on Plant Stress Responses and Tolerance (33 papers), Photosynthetic Processes and Mechanisms (23 papers) and Plant tissue culture and regeneration (22 papers). Haeng‐Soon Lee collaborates with scholars based in South Korea, China and Japan. Haeng‐Soon Lee's co-authors include Sang‐Soo Kwak, Suk‐Yoon Kwon, Yun‐Hee Kim, Jae Cheol Jeong, Xiping Deng, Sun Ha Kim, Mi‐Jeong Ahn, Wenbin Wang, Young Ock Ahn and Ki-Yong Kim and has published in prestigious journals such as PLoS ONE, Scientific Reports and Frontiers in Plant Science.

In The Last Decade

Haeng‐Soon Lee

67 papers receiving 3.2k citations

Hit Papers

Analysis of antioxidant enzyme activity during germinatio... 2009 2026 2014 2020 2009 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Haeng‐Soon Lee South Korea 33 2.5k 1.9k 529 196 190 67 3.4k
Rameshwar Sharma India 30 1.8k 0.7× 1.4k 0.8× 404 0.8× 169 0.9× 185 1.0× 137 2.6k
Pengmin Li China 35 2.4k 1.0× 1.7k 0.9× 864 1.6× 339 1.7× 77 0.4× 86 3.4k
Amedeo Alpi Italy 35 4.7k 1.9× 2.5k 1.3× 288 0.5× 276 1.4× 182 1.0× 126 5.8k
Gary Creissen United Kingdom 25 3.1k 1.3× 2.4k 1.3× 255 0.5× 121 0.6× 77 0.4× 43 3.9k
Carol Wagstaff United Kingdom 32 2.1k 0.8× 1.6k 0.9× 401 0.8× 362 1.8× 112 0.6× 80 3.1k
Daqiu Zhao China 34 1.7k 0.7× 1.8k 1.0× 498 0.9× 110 0.6× 97 0.5× 113 2.8k
Rita Zrenner Germany 28 3.3k 1.3× 2.0k 1.1× 175 0.3× 433 2.2× 100 0.5× 48 4.2k
Eleonora Cominelli Italy 26 2.0k 0.8× 1.3k 0.7× 158 0.3× 160 0.8× 77 0.4× 38 2.5k
Estela M. Valle Argentina 31 2.1k 0.8× 1.6k 0.9× 182 0.3× 152 0.8× 46 0.2× 77 2.9k
Chang Kil Kim South Korea 27 1.8k 0.7× 1.5k 0.8× 299 0.6× 124 0.6× 135 0.7× 114 2.5k

Countries citing papers authored by Haeng‐Soon Lee

Since Specialization
Citations

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

Fields of papers citing papers by Haeng‐Soon Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Haeng‐Soon Lee. 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 Haeng‐Soon Lee. The network helps show where Haeng‐Soon Lee may publish in the future.

Co-authorship network of co-authors of Haeng‐Soon Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Haeng‐Soon Lee. A scholar is included among the top collaborators of Haeng‐Soon Lee 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 Haeng‐Soon Lee. Haeng‐Soon Lee 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.
Kang, Le, Chang Yoon Ji, Sun Ha Kim, et al.. (2017). Suppression of the β-carotene hydroxylase gene increases β-carotene content and tolerance to abiotic stress in transgenic sweetpotato plants. Plant Physiology and Biochemistry. 117. 24–33. 59 indexed citations
2.
Park, Seyeon, Ho Soo Kim, Young Jun Jung, et al.. (2016). Orange protein has a role in phytoene synthase stabilization in sweetpotato. Scientific Reports. 6(1). 33563–33563. 104 indexed citations
3.
Ke, Qingbo, Zhi Wang, Chang Yoon Ji, et al.. (2016). Transgenic poplar expressing codA exhibits enhanced growth and abiotic stress tolerance. Plant Physiology and Biochemistry. 100. 75–84. 26 indexed citations
4.
Wang, Zhi, Qingbo Ke, Myoung Duck Kim, et al.. (2015). Transgenic Alfalfa Plants Expressing the Sweetpotato Orange Gene Exhibit Enhanced Abiotic Stress Tolerance. PLoS ONE. 10(5). e0126050–e0126050. 71 indexed citations
5.
Ke, Qingbo, Zhi Wang, Chang Yoon Ji, et al.. (2015). Transgenic poplar expressing Arabidopsis YUCCA6 exhibits auxin-overproduction phenotypes and increased tolerance to abiotic stress. Plant Physiology and Biochemistry. 94. 19–27. 95 indexed citations
6.
Lee, Jeung Joo, Yun‐Hee Kim, Youn‐Sig Kwak, et al.. (2014). A comparative study of proteomic differences between pencil and storage roots of sweetpotato (Ipomoea batatas (L.) Lam.). Plant Physiology and Biochemistry. 87. 92–101. 19 indexed citations
7.
Park, Sung‐Chul, Sun Ha Kim, Seyeon Park, et al.. (2014). Enhanced accumulation of carotenoids in sweetpotato plants overexpressing IbOr-Ins gene in purple-fleshed sweetpotato cultivar. Plant Physiology and Biochemistry. 86. 82–90. 78 indexed citations
8.
Lee, Young-Pyo, et al.. (2013). Improved tolerance of Cu/Zn superoxide dismutase and ascorbate peroxidase expressing transgenic tobacco seeds and seedlings against multiple abiotic stresses.. International Journal of Agriculture and Biology. 15(4). 725–730. 13 indexed citations
9.
Kim, Sun Ha, Young Ock Ahn, Mi‐Jeong Ahn, et al.. (2013). Cloning and characterization of an Orange gene that increases carotenoid accumulation and salt stress tolerance in transgenic sweetpotato cultures. Plant Physiology and Biochemistry. 70. 445–454. 107 indexed citations
10.
Lee, Jeung Joo, Kee Woong Park, Youn‐Sig Kwak, et al.. (2012). Comparative proteomic study between tuberous roots of light orange- and purple-fleshed sweetpotato cultivars. Plant Science. 193-194. 120–129. 29 indexed citations
11.
Kim, Sun Ha, Young Ock Ahn, Mi‐Jeong Ahn, Haeng‐Soon Lee, & Sang‐Soo Kwak. (2011). Down-regulation of β-carotene hydroxylase increases β-carotene and total carotenoids enhancing salt stress tolerance in transgenic cultured cells of sweetpotato. Phytochemistry. 74. 69–78. 126 indexed citations
12.
Kim, Cha Young, Young Ock Ahn, Sun Ha Kim, et al.. (2010). The sweet potatoIbMYB1gene as a potential visible marker for sweet potato intragenic vector system. Physiologia Plantarum. 139(3). 229–40. 52 indexed citations
13.
Park, Sung‐Chul, Yunhee Kim, Jae Cheol Jeong, et al.. (2010). Sweetpotato late embryogenesis abundant 14 (IbLEA14) gene influences lignification and increases osmotic- and salt stress-tolerance of transgenic calli. Planta. 233(3). 621–634. 123 indexed citations
14.
Kim, Yun‐Hee, Sim-Hee Han, Jae‐Cheon Lee, et al.. (2007). Differential expression of 10 sweetpotato peroxidases in response to sulfur dioxide, ozone, and ultraviolet radiation. Plant Physiology and Biochemistry. 45(12). 908–914. 44 indexed citations
15.
Kim, Yun‐Hee, Kee-Yeun Kim, Wankeun Song, et al.. (2007). Molecular characterization of a cDNA encoding DRE-binding transcription factor from dehydration-treated fibrous roots of sweetpotato. Plant Physiology and Biochemistry. 46(2). 196–204. 17 indexed citations
16.
Kim, Yun‐Hee, Cha Young Kim, Wankeun Song, et al.. (2007). Overexpression of sweetpotato swpa4 peroxidase results in increased hydrogen peroxide production and enhances stress tolerance in tobacco. Planta. 227(4). 867–881. 116 indexed citations
17.
Lee, Young-Pyo, Sun‐Hyung Kim, Jae-Wook Bang, et al.. (2007). Enhanced tolerance to oxidative stress in transgenic tobacco plants expressing three antioxidant enzymes in chloroplasts. Plant Cell Reports. 26(5). 591–598. 173 indexed citations
18.
Tang, Li, Myoung Duck Kim, Suk‐Yoon Kwon, et al.. (2007). Enhanced tolerance of transgenic potato plants overexpressing nucleoside diphosphate kinase 2 against multiple environmental stresses. Transgenic Research. 17(4). 705–715. 80 indexed citations
19.
Shin, Seung-Yong, et al.. (2005). Molecular characterization of a cDNA encoding copper/zinc superoxide dismutase from cultured cells of Manihot esculenta. Plant Physiology and Biochemistry. 43(1). 55–60. 27 indexed citations
20.
Kwon, Suk‐Yoon, et al.. (2003). High expression of a human lactoferrin in transgenic tobacco cell cultures. Biotechnology Letters. 25(3). 213–218. 35 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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