Deshu Lin

1.6k total citations
26 papers, 1.1k citations indexed

About

Deshu Lin is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, Deshu Lin has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Plant Science, 23 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Deshu Lin's work include Plant Molecular Biology Research (22 papers), Plant Reproductive Biology (20 papers) and Polysaccharides and Plant Cell Walls (10 papers). Deshu Lin is often cited by papers focused on Plant Molecular Biology Research (22 papers), Plant Reproductive Biology (20 papers) and Polysaccharides and Plant Cell Walls (10 papers). Deshu Lin collaborates with scholars based in China, United States and Belgium. Deshu Lin's co-authors include Zhenbiao Yang, Ying Fu, Jiřı́ Friml, Ben Scheres, Shingo Nagawa, Lingyan Cao, Pankaj Dhonukshe, Huibo Ren, Xie Dang and Tongda Xu and has published in prestigious journals such as Nature Communications, Development and PLANT PHYSIOLOGY.

In The Last Decade

Deshu Lin

26 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deshu Lin China 16 1.0k 917 118 25 19 26 1.1k
Francine M. Carland United States 15 1.5k 1.4× 1.1k 1.2× 65 0.6× 39 1.6× 18 0.9× 23 1.7k
Ushio Fujikura Japan 13 989 0.9× 813 0.9× 28 0.2× 37 1.5× 4 0.2× 17 1.1k
José Manuel Álvarez Spain 16 496 0.5× 360 0.4× 51 0.4× 46 1.8× 11 0.6× 36 666
Arata Yoneda Japan 14 691 0.7× 626 0.7× 163 1.4× 52 2.1× 4 0.2× 19 855
Christian Breuer Japan 14 941 0.9× 817 0.9× 53 0.4× 36 1.4× 2 0.1× 18 1.1k
Elke Barbez Austria 12 1.4k 1.3× 1.1k 1.2× 57 0.5× 26 1.0× 2 0.1× 18 1.5k
Urszula Piskurewicz Switzerland 14 1.3k 1.2× 652 0.7× 24 0.2× 38 1.5× 8 0.4× 17 1.4k
René Schneider Germany 17 984 0.9× 623 0.7× 172 1.5× 19 0.8× 2 0.1× 27 1.2k
Christopher Kesten Switzerland 10 673 0.6× 367 0.4× 73 0.6× 8 0.3× 4 0.2× 17 801
Victoria Mironova Russia 20 1.1k 1.0× 823 0.9× 22 0.2× 28 1.1× 3 0.2× 49 1.2k

Countries citing papers authored by Deshu Lin

Since Specialization
Citations

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

Fields of papers citing papers by Deshu Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deshu Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Deshu Lin. A scholar is included among the top collaborators of Deshu Lin 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 Deshu Lin. Deshu Lin 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.
Li, Yu, Yuxiang Zhang, Xiaqin Wang, et al.. (2023). Insights into cryptochrome modulation of ABA signaling to mediate dormancy regulation in Marchantia polymorpha. New Phytologist. 238(4). 1479–1497. 7 indexed citations
2.
Miao, Rui, Na Zhang, Deshu Lin, et al.. (2022). Katanin-Dependent Microtubule Ordering in Association with ABA Is Important for Root Hydrotropism. International Journal of Molecular Sciences. 23(7). 3846–3846. 6 indexed citations
3.
Dang, Xie, Yuhua Li, Yaling Li, et al.. (2022). ANGUSTIFOLIA negatively regulates resistance to Sclerotinia sclerotiorum via modulation of PTI and JA signalling pathways in Arabidopsis thaliana. Molecular Plant Pathology. 23(8). 1091–1106. 4 indexed citations
4.
Chen, Binqing, Xie Dang, Yanqiu Yang, et al.. (2022). The IPGA1‐ANGUSTIFOLIA module regulates microtubule organisation and pavement cell shape in Arabidopsis. New Phytologist. 236(4). 1310–1325. 8 indexed citations
5.
Chen, Yadi, Xiaohua Hu, Siyuan Liu, et al.. (2021). Regulation of Arabidopsis photoreceptor CRY2 by two distinct E3 ubiquitin ligases. Nature Communications. 12(1). 2155–2155. 43 indexed citations
6.
Tang, Wenxin, Wenwei Lin, Xiang Zhou, et al.. (2021). Mechano-transduction via the pectin-FERONIA complex activates ROP6 GTPase signaling in Arabidopsis pavement cell morphogenesis. Current Biology. 32(3). 508–517.e3. 90 indexed citations
7.
Zhao, Heming, Maokai Yan, Han Cheng, et al.. (2020). Comparative Expression Profiling Reveals Genes Involved in Megasporogenesis. PLANT PHYSIOLOGY. 182(4). 2006–2024. 19 indexed citations
8.
Dang, Xie, Binqing Chen, Fenglian Liu, et al.. (2020). Auxin Signaling-Mediated Apoplastic pH Modification Functions in Petal Conical Cell Shaping. Cell Reports. 30(11). 3904–3916.e3. 23 indexed citations
9.
Wang, Lulu, Yi Li, Liping Liu, et al.. (2020). Floral transcriptomes reveal gene networks in pineapple floral growth and fruit development. Communications Biology. 3(1). 500–500. 37 indexed citations
10.
Gendre, Delphine, Xie Dang, Nicolas Esnay, et al.. (2019). Rho-of-plant activated root hair formation requires Arabidopsis YIP4a/b gene function. Development. 146(5). 28 indexed citations
11.
Yang, Yanqiu, et al.. (2019). Cortical Microtubule Organization during Petal Morphogenesis in Arabidopsis. International Journal of Molecular Sciences. 20(19). 4913–4913. 10 indexed citations
12.
Yang, Yanqiu, Xie Dang, Huibo Ren, et al.. (2019). Arabidopsis IPGA1 is a microtubule-associated protein essential for cell expansion during petal morphogenesis. Journal of Experimental Botany. 70(19). 5231–5243. 14 indexed citations
13.
Dang, Xie, Yajun Li, Yanqiu Yang, et al.. (2018). Reactive oxygen species mediate conical cell shaping in Arabidopsis thaliana petals. PLoS Genetics. 14(10). e1007705–e1007705. 11 indexed citations
14.
Ren, Huibo, et al.. (2017). Spatio-temporal orientation of microtubules controls conical cell shape in Arabidopsis thaliana petals. PLoS Genetics. 13(6). e1006851–e1006851. 36 indexed citations
15.
Ren, Huibo & Deshu Lin. (2015). ROP GTPase Regulation of Auxin Transport in Arabidopsis. Molecular Plant. 8(2). 193–195. 5 indexed citations
16.
Nagawa, Shingo, Tongda Xu, Deshu Lin, et al.. (2012). ROP GTPase-Dependent Actin Microfilaments Promote PIN1 Polarization by Localized Inhibition of Clathrin-Dependent Endocytosis. PLoS Biology. 10(4). e1001299–e1001299. 158 indexed citations
17.
Li, Hongjiang, Tongda Xu, Deshu Lin, et al.. (2012). Cytokinin signaling regulates pavement cell morphogenesis in Arabidopsis. Cell Research. 23(2). 290–299. 29 indexed citations
18.
Li, Hongjiang, Deshu Lin, Pankaj Dhonukshe, et al.. (2011). Phosphorylation switch modulates the interdigitated pattern of PIN1 localization and cell expansion in Arabidopsis leaf epidermis. Cell Research. 21(6). 970–978. 50 indexed citations
19.
Wang, Airong, Chunhua Zhang, Lili Zhang, et al.. (2008). Identification of Arabidopsis Mutants with Enhanced Resistance to Sclerotinia Stem Rot Disease from an Activation‐tagged Library. Journal of Phytopathology. 157(1). 63–69. 2 indexed citations
20.
Wang, Shihua, et al.. (2007). Detection of deoxynivalenol based on a single-chain fragment variable of the antideoxynivalenol antibody. FEMS Microbiology Letters. 272(2). 214–219. 32 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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