Suk‐Whan Hong

4.3k total citations · 1 hit paper
52 papers, 3.3k citations indexed

About

Suk‐Whan Hong is a scholar working on Plant Science, Molecular Biology and Ecology. According to data from OpenAlex, Suk‐Whan Hong has authored 52 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Plant Science, 39 papers in Molecular Biology and 5 papers in Ecology. Recurrent topics in Suk‐Whan Hong's work include Plant Molecular Biology Research (20 papers), Plant Stress Responses and Tolerance (18 papers) and Plant Gene Expression Analysis (15 papers). Suk‐Whan Hong is often cited by papers focused on Plant Molecular Biology Research (20 papers), Plant Stress Responses and Tolerance (18 papers) and Plant Gene Expression Analysis (15 papers). Suk‐Whan Hong collaborates with scholars based in South Korea, United States and Japan. Suk‐Whan Hong's co-authors include Elizabeth Vierling, Hojoung Lee, Susan Lindquist, Christine Queitsch, Chan Young Jeong, Ung Lee, Nguyen Hoai Nguyen, Jun Hyeok Kim, Won Je Lee and Liming Xiong and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Plant Cell and PLANT PHYSIOLOGY.

In The Last Decade

Suk‐Whan Hong

52 papers receiving 3.3k citations

Hit Papers

Heat Shock Protein 101 Plays a Crucial Role in Thermotole... 2000 2026 2008 2017 2000 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suk‐Whan Hong South Korea 29 2.4k 2.3k 150 136 108 52 3.3k
Zhen‐Hui Gong China 37 3.3k 1.3× 2.2k 0.9× 184 1.2× 160 1.2× 102 0.9× 109 4.0k
Priti Krishna Canada 28 2.9k 1.2× 2.3k 1.0× 69 0.5× 221 1.6× 127 1.2× 52 4.2k
Ayako Nishizawa‐Yokoi Japan 21 2.4k 1.0× 2.1k 0.9× 130 0.9× 141 1.0× 62 0.6× 43 3.0k
Yee‐yung Charng Taiwan 29 3.1k 1.3× 2.6k 1.1× 51 0.3× 119 0.9× 92 0.9× 42 4.0k
Dong Yul Sung United States 5 1.4k 0.6× 1.1k 0.5× 51 0.3× 111 0.8× 36 0.3× 8 1.9k
Satoshi Kidokoro Japan 32 6.2k 2.6× 3.8k 1.6× 52 0.3× 100 0.7× 98 0.9× 39 6.9k
Polydefkis Hatzopoulos Greece 30 2.0k 0.8× 1.6k 0.7× 56 0.4× 105 0.8× 63 0.6× 92 2.7k
Thomas Berberich Japan 37 3.9k 1.6× 3.4k 1.5× 34 0.2× 136 1.0× 153 1.4× 77 4.9k
Salma Balazadeh Germany 41 5.2k 2.1× 4.0k 1.7× 146 1.0× 126 0.9× 95 0.9× 77 6.0k
Lars M. Voll Germany 31 2.3k 0.9× 1.4k 0.6× 129 0.9× 79 0.6× 321 3.0× 48 2.8k

Countries citing papers authored by Suk‐Whan Hong

Since Specialization
Citations

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

Fields of papers citing papers by Suk‐Whan Hong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suk‐Whan Hong. 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 Suk‐Whan Hong. The network helps show where Suk‐Whan Hong may publish in the future.

Co-authorship network of co-authors of Suk‐Whan Hong

This figure shows the co-authorship network connecting the top 25 collaborators of Suk‐Whan Hong. A scholar is included among the top collaborators of Suk‐Whan Hong 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 Suk‐Whan Hong. Suk‐Whan Hong 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.
Kim, Hyun‐Jung, et al.. (2024). Antagonistic functions of CTL1 and SUH1 mediate cell wall assembly in Arabidopsis. Plant Direct. 8(3). e580–e580. 1 indexed citations
2.
Lee, Won Je, Jun‐Ho Choi, Dinh Thanh Nguyen, et al.. (2022). The Loss of Function of the NODULE INCEPTION-Like PROTEIN 7 Enhances Salt Stress Tolerance in Arabidopsis Seedlings. Frontiers in Plant Science. 12. 743832–743832. 7 indexed citations
3.
Jeong, Chan Young, et al.. (2019). Deficiency of AtGFAT1 activity impairs growth, pollen germination and tolerance to tunicamycin in Arabidopsis. Journal of Experimental Botany. 70(6). 1775–1787. 13 indexed citations
4.
Lee, Won Je, et al.. (2019). Assessment of synthetic hexaploid wheats in response to heat stress and leaf rust infection for the improvement of wheat production. Crop and Pasture Science. 70(10). 837–848. 4 indexed citations
5.
Jeong, Chan Young, et al.. (2018). Paenibacillus pabuli strain P7S promotes plant growth and induces anthocyanin accumulation in Arabidopsis thaliana. Plant Physiology and Biochemistry. 129. 264–272. 23 indexed citations
6.
Jeong, Chan Young, Won Je Lee, Kwang Yeon Hwang, et al.. (2018). Dual role of SND1 facilitates efficient communication between abiotic stress signalling and normal growth in Arabidopsis. Scientific Reports. 8(1). 10114–10114. 21 indexed citations
7.
Lee, Hyeri, Won Je Lee, Namhyun Chung, et al.. (2018). Evaluation of the plant growth-promoting activity of Pseudomonas nitroreducens in Arabidopsis thaliana and Lactuca sativa. Plant Cell Reports. 37(6). 873–885. 28 indexed citations
8.
Kim, Jihye, et al.. (2017). High accumulation of anthocyanins via the ectopic expression of AtDFR confers significant salt stress tolerance in Brassica napus L.. Plant Cell Reports. 36(8). 1215–1224. 116 indexed citations
9.
Park, Won, Kwang-Soo Kim, Young‐Lok Cha, et al.. (2017). Effect of different application levels of rapeseed meal on growth and yield components of rice. Applied Biological Chemistry. 60(4). 403–410. 11 indexed citations
10.
Nguyen, Nguyen Hoai, Jun Hyeok Kim, Jaeyoung Kwon, et al.. (2016). Characterization of Arabidopsis thaliana FLAVONOL SYNTHASE 1 (FLS1) -overexpression plants in response to abiotic stress. Plant Physiology and Biochemistry. 103. 133–142. 60 indexed citations
11.
Nguyen, Nguyen Hoai, Jun Hyeok Kim, Chan Young Jeong, Suk‐Whan Hong, & Hojoung Lee. (2013). Inhibition of histone deacetylation alters Arabidopsis root growth in response to auxin via PIN1 degradation. Plant Cell Reports. 32(10). 1625–1636. 32 indexed citations
12.
Kim, Kang‐Il, et al.. (2010). Mutation of the chitinase-like protein-encoding AtCTL2 gene enhances lignin accumulation in dark-grown Arabidopsis seedlings. Journal of Plant Physiology. 167(8). 650–658. 29 indexed citations
13.
Kim, Kang‐Il, et al.. (2009). Altered ARA2 (RABA1a) expression in Arabidopsis reveals the involvement of a Rab/YPT family member in auxin-mediated responses. Plant Molecular Biology. 70(1-2). 113–122. 14 indexed citations
14.
Hong, Suk‐Whan, et al.. (2008). The ABA Effect on the Accumulation of an Invertase Inhibitor Transcript that Is Driven by the CAMV35S Promoter in ARABIDOPSIS. Molecules and Cells. 26(3). 236–242. 7 indexed citations
15.
Chen, Hao, Jingyu Zhang, Michael M. Neff, et al.. (2008). Integration of light and abscisic acid signaling during seed germination and early seedling development. Proceedings of the National Academy of Sciences. 105(11). 4495–4500. 241 indexed citations
16.
Lee, Hee Jin, et al.. (2008). Ectopic expression of Expansin3 or Expansinβ1 causes enhanced hormone and salt stress sensitivity in Arabidopsis. Biotechnology Letters. 30(7). 1281–1288. 68 indexed citations
18.
Choi, Goh, Goh Choi, Jeong‐Il Kim, et al.. (2005). A Possible Role for NDPK2 in the Regulation of Auxin-mediated Responses for Plant Growth and Development. Plant and Cell Physiology. 46(8). 1246–1254. 34 indexed citations
20.
Liu, Zongrang, Suk‐Whan Hong, Elizabeth Vierling, et al.. (2003). Arabidopsis UVH6, a Homolog of Human XPD and Yeast RAD3 DNA Repair Genes, Functions in DNA Repair and Is Essential for Plant Growth. PLANT PHYSIOLOGY. 132(3). 1405–1414. 66 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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