Ying‐Hsuan Sun

4.9k total citations
35 papers, 3.2k citations indexed

About

Ying‐Hsuan Sun is a scholar working on Molecular Biology, Plant Science and Biomedical Engineering. According to data from OpenAlex, Ying‐Hsuan Sun has authored 35 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 23 papers in Plant Science and 6 papers in Biomedical Engineering. Recurrent topics in Ying‐Hsuan Sun's work include Plant Gene Expression Analysis (18 papers), Plant Molecular Biology Research (13 papers) and Plant biochemistry and biosynthesis (5 papers). Ying‐Hsuan Sun is often cited by papers focused on Plant Gene Expression Analysis (18 papers), Plant Molecular Biology Research (13 papers) and Plant biochemistry and biosynthesis (5 papers). Ying‐Hsuan Sun collaborates with scholars based in United States, Taiwan and China. Ying‐Hsuan Sun's co-authors include Vincent L. Chiang, Shanfa Lu, Rui Shi, Laigeng Li, Ronald R. Sederoff, Quanzi Li, Catherine Clark, Shiro Suzuki, Sermsawat Tunlaya‐Anukit and Ross Whetten and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and SHILAP Revista de lepidopterología.

In The Last Decade

Ying‐Hsuan Sun

34 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ying‐Hsuan Sun United States 23 2.4k 2.2k 468 175 131 35 3.2k
Yves Martinez France 25 1.7k 0.7× 1.0k 0.5× 175 0.4× 118 0.7× 89 0.7× 43 2.2k
Tiegang Lu China 28 2.6k 1.1× 1.9k 0.9× 125 0.3× 85 0.5× 66 0.5× 69 3.3k
Eric P. Beers United States 26 2.6k 1.1× 2.1k 1.0× 110 0.2× 46 0.3× 251 1.9× 41 3.3k
Gorou Horiguchi Japan 32 4.4k 1.9× 3.9k 1.8× 172 0.4× 44 0.3× 44 0.3× 66 5.1k
Longfu Zhu China 39 4.4k 1.9× 2.7k 1.3× 89 0.2× 37 0.2× 130 1.0× 107 4.9k
Yan Xiang China 33 2.3k 1.0× 1.8k 0.8× 141 0.3× 19 0.1× 77 0.6× 133 2.9k
Jacob Krüger Jensen United States 18 1.5k 0.6× 1.0k 0.5× 394 0.8× 14 0.1× 128 1.0× 22 1.9k
Thierry Desnos France 27 4.6k 1.9× 2.3k 1.0× 147 0.3× 18 0.1× 42 0.3× 43 5.1k
Trevor H. Yeats United States 23 2.8k 1.2× 1.6k 0.7× 160 0.3× 18 0.1× 105 0.8× 29 3.6k

Countries citing papers authored by Ying‐Hsuan Sun

Since Specialization
Citations

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

Fields of papers citing papers by Ying‐Hsuan Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ying‐Hsuan Sun. 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 Ying‐Hsuan Sun. The network helps show where Ying‐Hsuan Sun may publish in the future.

Co-authorship network of co-authors of Ying‐Hsuan Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Ying‐Hsuan Sun. A scholar is included among the top collaborators of Ying‐Hsuan Sun 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 Ying‐Hsuan Sun. Ying‐Hsuan Sun 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.
Chiang, Yu‐Ting, et al.. (2024). Composition Characterization of Crossostephium chinense Leaf Essential Oil and Its Anti-Inflammatory Activity Mechanisms. Plants. 13(17). 2506–2506. 1 indexed citations
3.
Sun, Ying‐Hsuan, et al.. (2023). Single-cell transcriptomics unveils xylem cell development and evolution. Genome biology. 24(1). 3–3. 49 indexed citations
4.
Huang, Chun‐Lin, Jian‐Wei Liu, Ying‐Hsuan Sun, et al.. (2021). The complete plastid genome of Selaginella erythropus (Selaginellaceae), a species with distinctive giant chloroplasts. SHILAP Revista de lepidopterología. 6(12). 3369–3371. 1 indexed citations
5.
Sun, Ying‐Hsuan, Chiu‐Yueh Hung, Jie Qiu, et al.. (2017). Accumulation of high OPDA level correlates with reduced ROS and elevated GSH benefiting white cell survival in variegated leaves. Scientific Reports. 7(1). 44158–44158. 18 indexed citations
6.
Shi, Rui, Jack Wang, Ying‐Chung Jimmy Lin, et al.. (2017). Tissue and cell-type co-expression networks of transcription factors and wood component genes in Populus trichocarpa. Planta. 245(5). 927–938. 64 indexed citations
7.
Lin, Chien-Yuan, Quanzi Li, Sermsawat Tunlaya‐Anukit, et al.. (2016). A cell wall-bound anionic peroxidase, PtrPO21, is involved in lignin polymerization in Populus trichocarpa. Tree Genetics & Genomes. 12(2). 35 indexed citations
8.
Sun, Peng, Cunquan Yuan, Li Dai, et al.. (2015). Transcriptional profiles of emasculated flowers of black locust (Robinia pseudoacacia) determined using the cDNA-AFLP technique. Genetics and Molecular Research. 14(4). 15822–15838. 2 indexed citations
9.
Tsao, Nai‐Wen, Ying‐Hsuan Sun, Shih‐Chang Chien, et al.. (2015). Content and distribution of lignans in Taiwania cryptomerioides Hayata. Holzforschung. 70(6). 511–518. 8 indexed citations
10.
Lin, Ying‐Chung Jimmy, Wei Li, Hao Chen, et al.. (2014). A simple improved-throughput xylem protoplast system for studying wood formation. Nature Protocols. 9(9). 2194–2205. 81 indexed citations
11.
Lin, Ying‐Chung Jimmy, Wei Li, Ying‐Hsuan Sun, et al.. (2013). SND1 Transcription Factor-Directed Quantitative Functional Hierarchical Genetic Regulatory Network in Wood Formation in Populus trichocarpa. The Plant Cell. 25(11). 4324–4341. 109 indexed citations
12.
Shi, Rui, Christopher M. Shuford, Jack Wang, et al.. (2013). Regulation of phenylalanine ammonia-lyase (PAL) gene family in wood forming tissue of Populus trichocarpa. Planta. 238(3). 487–497. 65 indexed citations
13.
Sun, Ying‐Hsuan, Rui Shi, Xing‐Hai Zhang, Vincent L. Chiang, & Ronald R. Sederoff. (2011). MicroRNAs in trees. Plant Molecular Biology. 80(1). 37–53. 18 indexed citations
14.
Sun, Ying‐Hsuan, Shanfa Lu, Rui Shi, & Vincent L. Chiang. (2011). Computational Prediction of Plant miRNA Targets. Methods in molecular biology. 744. 175–186. 16 indexed citations
15.
Shi, Rui, Ying‐Hsuan Sun, Xing‐Hai Zhang, & Vincent L. Chiang. (2011). Poly(T) Adaptor RT-PCR. Methods in molecular biology. 822. 53–66. 39 indexed citations
17.
Lu, Shanfa, Ying‐Hsuan Sun, & Vincent L. Chiang. (2009). Adenylation of plant miRNAs. Nucleic Acids Research. 37(6). 1878–1885. 119 indexed citations
18.
Shi, Rui, Ying‐Hsuan Sun, Quanzi Li, et al.. (2009). Towards a Systems Approach for Lignin Biosynthesis in Populus trichocarpa: Transcript Abundance and Specificity of the Monolignol Biosynthetic Genes. Plant and Cell Physiology. 51(1). 144–163. 249 indexed citations
19.
Lu, Shanfa, Ying‐Hsuan Sun, Rui Shi, et al.. (2005). Novel and Mechanical Stress–Responsive MicroRNAs in Populus trichocarpa That Are Absent from Arabidopsis. The Plant Cell. 17(8). 2186–2203. 492 indexed citations
20.
Bergmann, Ben A., Ying‐Hsuan Sun, & Anne-Marie Stomp. (1997). Harvest Time and Nitrogen Source Influence In Vitro Growth of Apical Buds from Fraser Fir Seedlings. HortScience. 32(1). 125–128. 2 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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