Na Sui

7.1k total citations · 3 hit papers
105 papers, 5.1k citations indexed

About

Na Sui is a scholar working on Plant Science, Molecular Biology and Biochemistry. According to data from OpenAlex, Na Sui has authored 105 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Plant Science, 71 papers in Molecular Biology and 9 papers in Biochemistry. Recurrent topics in Na Sui's work include Plant Stress Responses and Tolerance (55 papers), Photosynthetic Processes and Mechanisms (37 papers) and Plant Molecular Biology Research (29 papers). Na Sui is often cited by papers focused on Plant Stress Responses and Tolerance (55 papers), Photosynthetic Processes and Mechanisms (37 papers) and Plant Molecular Biology Research (29 papers). Na Sui collaborates with scholars based in China, United Kingdom and United States. Na Sui's co-authors include Guoliang Han, Hongxiang Zheng, Jinlu Li, Xi Sun, Zhen Yang, Baoshan Wang, Xiansheng Zhang, Jie Song, Lu‐Ning Liu and Simin Li and has published in prestigious journals such as The Plant Cell, PLANT PHYSIOLOGY and Journal of Agricultural and Food Chemistry.

In The Last Decade

Na Sui

102 papers receiving 5.0k citations

Hit Papers

C2H2 Zinc Finger Proteins: Master Regulators of Abiotic S... 2020 2026 2022 2024 2020 2020 2024 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Na Sui China 47 4.1k 2.5k 241 234 233 105 5.1k
Laurent Nussaume France 48 8.8k 2.2× 4.3k 1.7× 211 0.9× 201 0.9× 202 0.9× 88 10.2k
Toshihiro Obata Germany 41 3.7k 0.9× 3.3k 1.3× 214 0.9× 122 0.5× 347 1.5× 111 5.8k
Paul E. Verslues Taiwan 37 6.4k 1.6× 3.0k 1.2× 198 0.8× 198 0.8× 94 0.4× 55 7.1k
László Szabados Hungary 38 7.8k 1.9× 4.2k 1.7× 302 1.3× 296 1.3× 168 0.7× 91 9.3k
Maki Kawai‐Yamada Japan 42 4.0k 1.0× 3.0k 1.2× 200 0.8× 78 0.3× 221 0.9× 148 5.5k
Tomasz Czechowski Germany 16 4.5k 1.1× 3.0k 1.2× 154 0.6× 207 0.9× 148 0.6× 22 5.9k
Filip Rolland Belgium 36 7.6k 1.9× 4.7k 1.9× 237 1.0× 146 0.6× 175 0.8× 49 9.3k
Liming Xiong United States 46 10.8k 2.6× 6.7k 2.7× 257 1.1× 209 0.9× 231 1.0× 84 12.6k
Nicolas L. Taylor Australia 45 3.6k 0.9× 3.7k 1.5× 397 1.6× 322 1.4× 368 1.6× 166 6.3k
Shaojun Dai China 33 3.7k 0.9× 2.3k 0.9× 339 1.4× 102 0.4× 75 0.3× 117 4.6k

Countries citing papers authored by Na Sui

Since Specialization
Citations

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

Fields of papers citing papers by Na Sui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Na Sui

This figure shows the co-authorship network connecting the top 25 collaborators of Na Sui. A scholar is included among the top collaborators of Na Sui 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 Na Sui. Na Sui 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.
Xue, Xin, et al.. (2024). Halotolerant Bacillus sp. strain RA coordinates myo‐inositol metabolism to confer salt tolerance to tomato. Journal of Integrative Plant Biology. 66(9). 1871–1885. 13 indexed citations
2.
Liu, Ranran, Qiong Yu, Jianrong Guo, et al.. (2024). Combined genome and transcriptome provides insight into the genetic evolution of an edible halophyte Suaeda salsa adaptation to high salinity. Molecular Ecology. 34(15). e17457–e17457. 6 indexed citations
3.
Zheng, Hongxiang, et al.. (2023). Characterization of the m6A gene family in sorghum and its function in growth, development and stress resistance. Industrial Crops and Products. 198. 116625–116625. 6 indexed citations
4.
Lu, Mei, Jinlu Li, Jingyi Wang, et al.. (2023). Identification of the MYB gene family in Sorghum bicolor and functional analysis of SbMYBAS1 in response to salt stress. Plant Molecular Biology. 113(4-5). 249–264. 12 indexed citations
5.
Zheng, Hongxiang, Yi Sui, Xuemei Wang, et al.. (2023). R2R3 MYB transcription factor SbMYBHv33 negatively regulates sorghum biomass accumulation and salt tolerance. Theoretical and Applied Genetics. 136(1). 5–5. 19 indexed citations
6.
Zheng, Hongxiang, Xiansheng Zhang, & Na Sui. (2020). Advances in the profiling of N6-methyladenosine (m6A) modifications. Biotechnology Advances. 45. 107656–107656. 74 indexed citations
7.
Sui, Na, Fang Huang, & Lu‐Ning Liu. (2020). Photosynthesis in Phytoplankton: Insights from the Newly Discovered Biological Inorganic Carbon Pumps. Molecular Plant. 13(7). 949–951. 15 indexed citations
8.
Chen, Meng, Minmin Yang, Yixuan Wang, et al.. (2020). SlWHY2 interacts with SlRECA2 to maintain mitochondrial function under drought stress in tomato. Plant Science. 301. 110674–110674. 17 indexed citations
9.
Sun, Xi, Guoliang Han, Zhe Meng, Lin Lin, & Na Sui. (2019). Roles of malic enzymes in plant development and stress responses. Plant Signaling & Behavior. 14(10). e1644596–e1644596. 63 indexed citations
10.
Han, Guoliang, Xiaocen Wei, Xinxiu Dong, et al.. (2019). Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes. The Plant Cell. 32(1). 206–225. 83 indexed citations
11.
Li, Meng, Lin Lin, Yuanhu Zhang, & Na Sui. (2019). ZmMYB31, a R2R3-MYB transcription factor in maize, positively regulates the expression of CBF genes and enhances resistance to chilling and oxidative stress. Molecular Biology Reports. 46(4). 3937–3944. 55 indexed citations
12.
Chen, Meng & Na Sui. (2018). Overexpression of maize MYB-IF35 increases chilling tolerance in Arabidopsis. Plant Physiology and Biochemistry. 135. 167–173. 32 indexed citations
13.
Sun, Xi, Lin Lin, & Na Sui. (2018). Regulation mechanism of microRNA in plant response to abiotic stress and breeding. Molecular Biology Reports. 46(1). 1447–1457. 66 indexed citations
14.
Chen, Weiyang, Xiahe Huang, Haitao Ge, et al.. (2018). Systematic identification of light-regulated cold-responsive proteome in a model cyanobacterium. Journal of Proteomics. 179. 100–109. 7 indexed citations
15.
Xu, Yange, et al.. (2017). Transcriptomic profiling of genes in matured dimorphic seeds of euhalophyte Suaeda salsa. BMC Genomics. 18(1). 727–727. 22 indexed citations
16.
Guo, Yuanyuan, et al.. (2016). Responses of Unsaturated Fatty Acid in Membrane Lipid and Antioxidant Enzymes to Chilling Stress in Sweet Sorghum (Sorghum bicolor (L.) Moench) Seedling. Journal of Agricultural Science. 8(9). 71–71. 11 indexed citations
17.
Sui, Na, Zhen Yang, Mingli Liu, & Baoshan Wang. (2015). Identification and transcriptomic profiling of genes involved in increasing sugar content during salt stress in sweet sorghum leaves. BMC Genomics. 16(1). 534–534. 130 indexed citations
18.
Zhou, Jie, et al.. (2014). The role of salinity in seed maturation of the euhalophyte Suaeda salsa. Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology. 150(1). 83–90. 66 indexed citations
19.
Liu, Jinping, et al.. (2010). Effects of salt stress on photosynthesis and ion accumulation patterns of Suaeda salsa under different habitats.. 34(6). 671–677. 8 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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