Xiaohong Zhu

2.4k total citations
22 papers, 1.8k citations indexed

About

Xiaohong Zhu is a scholar working on Plant Science, Molecular Biology and Complementary and alternative medicine. According to data from OpenAlex, Xiaohong Zhu has authored 22 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Plant Science, 14 papers in Molecular Biology and 1 paper in Complementary and alternative medicine. Recurrent topics in Xiaohong Zhu's work include Plant Molecular Biology Research (12 papers), Plant nutrient uptake and metabolism (9 papers) and Plant Stress Responses and Tolerance (7 papers). Xiaohong Zhu is often cited by papers focused on Plant Molecular Biology Research (12 papers), Plant nutrient uptake and metabolism (9 papers) and Plant Stress Responses and Tolerance (7 papers). Xiaohong Zhu collaborates with scholars based in China, United States and Israel. Xiaohong Zhu's co-authors include Jian‐Kang Zhu, Pengcheng Wang, Yang Zhao, Yueh‐Ju Hou, Kai Tang, Guiliang Tang, Cheng‐Guo Duan, Xingang Wang, Xing Lu and Zhaobo Lang and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The EMBO Journal.

In The Last Decade

Xiaohong Zhu

21 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiaohong Zhu China 18 1.5k 1.0k 72 47 43 22 1.8k
Manuel Duval United States 11 1.1k 0.8× 651 0.6× 31 0.4× 26 0.6× 21 0.5× 19 1.4k
Xiaosan Huang China 27 2.2k 1.5× 1.7k 1.6× 19 0.3× 31 0.7× 12 0.3× 57 2.6k
Wen‐Dar Lin Taiwan 21 1.4k 0.9× 947 0.9× 20 0.3× 44 0.9× 21 0.5× 42 1.9k
Shuli Fan China 29 1.6k 1.1× 952 0.9× 15 0.2× 22 0.5× 29 0.7× 70 2.0k
Dawid Bielewicz Poland 17 1.1k 0.7× 806 0.8× 61 0.8× 13 0.3× 111 2.6× 29 1.3k
Patrice Thuleau France 23 1.6k 1.1× 972 1.0× 11 0.2× 35 0.7× 23 0.5× 35 1.9k
Naganand Rayapuram Saudi Arabia 19 717 0.5× 893 0.9× 15 0.2× 53 1.1× 12 0.3× 39 1.3k
Sung Han Ok South Korea 20 1.0k 0.7× 872 0.9× 34 0.5× 68 1.4× 8 0.2× 33 1.3k
Kiyoshi Tatematsu Japan 21 2.6k 1.8× 1.7k 1.7× 9 0.1× 34 0.7× 14 0.3× 29 2.8k
Anna Kulik Poland 16 1.0k 0.7× 516 0.5× 10 0.1× 34 0.7× 14 0.3× 22 1.2k

Countries citing papers authored by Xiaohong Zhu

Since Specialization
Citations

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

Fields of papers citing papers by Xiaohong Zhu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaohong Zhu

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaohong Zhu. A scholar is included among the top collaborators of Xiaohong Zhu 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 Xiaohong Zhu. Xiaohong Zhu 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.
Shen, Shiying, Xin Liu, Jing Zeng, et al.. (2025). From virtual to reality: innovative practices of digital twins in tumor therapy. Journal of Translational Medicine. 23(1). 348–348. 17 indexed citations
2.
Shi, Danfeng, et al.. (2024). Catalytic mechanism study of ATP-citrate lyase during citryl-CoA synthesis process. iScience. 27(9). 110605–110605. 1 indexed citations
3.
Sun, Shujing, et al.. (2021). Screening for Arabidopsis mutants with altered Ca2+ signal response using aequorin-based Ca2+ reporter system. STAR Protocols. 2(2). 100558–100558. 9 indexed citations
4.
Yan, Jun, Pengcheng Wang, Bangshing Wang, et al.. (2017). The SnRK2 kinases modulate miRNA accumulation in Arabidopsis. PLoS Genetics. 13(4). e1006753–e1006753. 83 indexed citations
5.
Yan, Jun, Chunzhao Zhao, Jianping Zhou, et al.. (2016). The miR165/166 Mediated Regulatory Module Plays Critical Roles in ABA Homeostasis and Response in Arabidopsis thaliana. PLoS Genetics. 12(11). e1006416–e1006416. 103 indexed citations
6.
Hou, Yueh‐Ju, Yingfang Zhu, Pengcheng Wang, et al.. (2016). Type One Protein Phosphatase 1 and Its Regulatory Protein Inhibitor 2 Negatively Regulate ABA Signaling. PLoS Genetics. 12(3). e1005835–e1005835. 68 indexed citations
7.
Li, Yan, Cheng‐Guo Duan, Xiaohong Zhu, Weiqiang Qian, & Jian‐Kang Zhu. (2015). A DNA ligase required for active DNA demethylation and genomic imprinting in Arabidopsis. Cell Research. 25(6). 757–760. 27 indexed citations
8.
Li, Yan, Dolores Córdoba‐Cañero, Weiqiang Qian, et al.. (2015). An AP Endonuclease Functions in Active DNA Demethylation and Gene Imprinting in Arabidopsis. PLoS Genetics. 11(1). e1004905–e1004905. 50 indexed citations
9.
Liu, Wen‐Shan, Xiaohong Zhu, Mingguang Lei, et al.. (2015). A detailed procedure for CRISPR/Cas9-mediated gene editing in Arabidopsis thaliana. Science Bulletin. 60(15). 1332–1347. 36 indexed citations
10.
Wan, Yizhen, Kai Tang, Dayong Zhang, et al.. (2015). Transcriptome-wide high-throughput deep m6A-seq reveals unique differential m6A methylation patterns between three organs in Arabidopsis thaliana. Genome biology. 16(1). 272–272. 151 indexed citations
11.
Duan, Cheng‐Guo, Huiming Zhang, Kai Tang, et al.. (2014). Specific but interdependent functions for A rabidopsis AGO 4 and AGO 6 in RNA ‐directed DNA methylation. The EMBO Journal. 34(5). 581–592. 86 indexed citations
12.
Qian, Weiqiang, Daisuke Miki, Mingguang Lei, et al.. (2014). Regulation of Active DNA Demethylation by an α-Crystallin Domain Protein in Arabidopsis. Molecular Cell. 55(3). 361–371. 40 indexed citations
13.
Zhang, Huiming, Kai Tang, Weiqiang Qian, et al.. (2014). An Rrp6-like Protein Positively Regulates Noncoding RNA Levels and DNA Methylation in Arabidopsis. Molecular Cell. 54(3). 418–430. 41 indexed citations
14.
Wang, Pengcheng, Yanyan Du, Yueh‐Ju Hou, et al.. (2014). Nitric oxide negatively regulates abscisic acid signaling in guard cells by S-nitrosylation of OST1. Proceedings of the National Academy of Sciences. 112(2). 613–618. 284 indexed citations
15.
Zhao, Yang, Xing Lu, Xingang Wang, et al.. (2014). The ABA Receptor PYL8 Promotes Lateral Root Growth by Enhancing MYB77-Dependent Transcription of Auxin-Responsive Genes. Science Signaling. 7(328). ra53–ra53. 278 indexed citations
16.
Zhu, Xiaohong, et al.. (2013). Aequorin-Based Luminescence Imaging Reveals Stimulus- and Tissue-Specific Ca2+ Dynamics in Arabidopsis Plants. Molecular Plant. 6(2). 444–455. 67 indexed citations
17.
Stepansky, Asya, et al.. (2006). Lysine catabolism, an effective versatile regulator of lysine level in plants. Amino Acids. 30(2). 121–125. 53 indexed citations
18.
Galili, Gad, Guiliang Tang, Xiaohong Zhu, & Bertrand Gakière. (2001). Lysine catabolism: a stress and development super-regulated metabolic pathway. Current Opinion in Plant Biology. 4(3). 261–266. 135 indexed citations
19.
Tang, Guiliang, Xiaohong Zhu, Xiaohu Tang, & Gad Galili. (2000). A novel composite locus of Arabidopsis encoding two polypeptides with metabolically related but distinct functions in lysine catabolism. The Plant Journal. 23(2). 195–203. 21 indexed citations
20.
Song, Ping, et al.. (1996). Regulation of gibberellin-binding proteins on dwarfism of rice (Oryza sativa L.). Zuo wu xue bao. 22(6). 652–656.

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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