Liwen Jiang

37.6k total citations · 1 hit paper
292 papers, 13.8k citations indexed

About

Liwen Jiang is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Liwen Jiang has authored 292 papers receiving a total of 13.8k indexed citations (citations by other indexed papers that have themselves been cited), including 178 papers in Molecular Biology, 122 papers in Plant Science and 117 papers in Cell Biology. Recurrent topics in Liwen Jiang's work include Cellular transport and secretion (100 papers), Photosynthetic Processes and Mechanisms (71 papers) and Autophagy in Disease and Therapy (50 papers). Liwen Jiang is often cited by papers focused on Cellular transport and secretion (100 papers), Photosynthetic Processes and Mechanisms (71 papers) and Autophagy in Disease and Therapy (50 papers). Liwen Jiang collaborates with scholars based in Hong Kong, China and United States. Liwen Jiang's co-authors include David G. Robinson, Xiaohong Zhuang, Caiji Gao, Yong Cui, Yansong Miao, Yonglun Zeng, Jinbo Shen, Yu Ding, Stefan Hillmer and John C. Rogers and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Liwen Jiang

282 papers receiving 13.6k citations

Hit Papers

MicroRNAs Inhibit the Translation of Target mRNAs on the ... 2013 2026 2017 2021 2013 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Liwen Jiang Hong Kong 65 8.3k 7.4k 3.7k 1.6k 904 292 13.8k
Federica Brandizzí United States 57 6.4k 0.8× 5.1k 0.7× 3.9k 1.0× 784 0.5× 215 0.2× 207 9.9k
Ikuko Hara‐Nishimura Japan 73 11.1k 1.3× 10.0k 1.4× 2.9k 0.8× 726 0.5× 230 0.3× 255 16.1k
Jasper Rine United States 68 14.1k 1.7× 2.5k 0.3× 2.2k 0.6× 978 0.6× 2.0k 2.2× 203 16.8k
Chris Hawes United Kingdom 63 9.1k 1.1× 7.1k 1.0× 4.3k 1.2× 291 0.2× 182 0.2× 203 13.4k
Takashi Hashimoto Japan 69 10.4k 1.2× 7.1k 1.0× 1.7k 0.5× 246 0.2× 361 0.4× 286 13.9k
Stephen B. Shears United States 53 6.3k 0.8× 2.2k 0.3× 3.7k 1.0× 329 0.2× 408 0.5× 217 9.6k
Adolfo Saiardi United Kingdom 54 5.2k 0.6× 2.1k 0.3× 2.4k 0.7× 565 0.4× 424 0.5× 153 9.5k
David G. Robinson Germany 56 7.3k 0.9× 5.6k 0.8× 4.0k 1.1× 404 0.3× 106 0.1× 193 10.1k
Michael A. Frohman United States 70 13.5k 1.6× 1.5k 0.2× 4.6k 1.2× 897 0.6× 2.0k 2.2× 161 19.1k
Daniel F. Voytas United States 79 21.2k 2.5× 13.2k 1.8× 1.1k 0.3× 610 0.4× 3.6k 4.0× 191 25.8k

Countries citing papers authored by Liwen Jiang

Since Specialization
Citations

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

Fields of papers citing papers by Liwen Jiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liwen Jiang

This figure shows the co-authorship network connecting the top 25 collaborators of Liwen Jiang. A scholar is included among the top collaborators of Liwen Jiang 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 Liwen Jiang. Liwen Jiang 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.
Zhuang, Xiaohong, Baiying Li, & Liwen Jiang. (2024). Autophagosome biogenesis and organelle homeostasis in plant cells. The Plant Cell. 36(9). 3009–3024. 8 indexed citations
2.
He, Yilin, Hailin Li, Bingyan Sun, et al.. (2024). A condensates-to-VPS41-associated phagic vacuoles conversion pathway controls autophagy degradation in plants. Developmental Cell. 59(17). 2287–2301.e6. 7 indexed citations
4.
Zeng, Yonglun, Zizhen Liang, Zhiqi Liu, et al.. (2023). Recent advances in plant endomembrane research and new microscopical techniques. New Phytologist. 240(1). 41–60. 11 indexed citations
5.
Chen, Hongfei, et al.. (2023). Photo‐Responsive Phase‐Separating Fluorescent Molecules for Intracellular Protein Delivery. Angewandte Chemie. 135(42). 5 indexed citations
6.
Ji, Peng, Liwen Jiang, Shiyu Guo, et al.. (2023). Mechanism of Action for an All-in-One Monoclonal Antibody Against Staphylococcus aureus Infection. The Journal of Infectious Diseases. 228(12). 1789–1799.
7.
Chen, Fei, et al.. (2022). Texture improvement of fermented minced pepper under vacuum impregnation with pectin methylesterase and CaCl 2 during fermentation. International Journal of Food Science & Technology. 57(6). 3477–3489. 3 indexed citations
8.
Xu, Haishan, Yuyu Chen, Shenghua Ding, et al.. (2021). Changes in texture qualities and pectin characteristics of fermented minced pepper during natural and inoculated fermentation process. International Journal of Food Science & Technology. 56(11). 6073–6085. 16 indexed citations
9.
Delgadillo, María Otilia, Jan Zouhar, Michael Sauer, et al.. (2020). MTV proteins unveil ER- and microtubule-associated compartments in the plant vacuolar trafficking pathway. Proceedings of the National Academy of Sciences. 117(18). 9884–9895. 21 indexed citations
10.
Tang, Xiao, Lina Zhang, Mo Wang, et al.. (2020). Molecular mechanisms that regulate export of the planar cell-polarity protein Frizzled-6 out of the endoplasmic reticulum. Journal of Biological Chemistry. 295(27). 8972–8987. 11 indexed citations
11.
Hu, Shuai, Hao Ye, Yong Cui, & Liwen Jiang. (2019). AtSec62 is critical for plant development and is involved in ER‐phagy in Arabidopsis thaliana. Journal of Integrative Plant Biology. 62(2). 181–200. 77 indexed citations
12.
Lai, Louis Tung Faat, et al.. (2019). Subnanometer resolution cryo-EM structure of Arabidopsis thaliana ATG9. Autophagy. 16(3). 575–583. 38 indexed citations
13.
Huang, Dingquan, Yanbiao Sun, Zhiming Ma, et al.. (2019). Salicylic acid-mediated plasmodesmal closure via Remorin-dependent lipid organization. Proceedings of the National Academy of Sciences. 116(42). 21274–21284. 111 indexed citations
14.
Koon, Alex Chun, Zhefan Stephen Chen, Shaohong Peng, et al.. (2018). Drosophila Exo70 Is Essential for Neurite Extension and Survival under Thermal Stress. Journal of Neuroscience. 38(37). 8071–8086. 11 indexed citations
15.
Belda‐Palazón, Borja, Lesia Rodríguez, Ángeles Fernández, et al.. (2016). FYVE1/FREE1 Interacts with the PYL4 ABA Receptor and Mediates Its Delivery to the Vacuolar Degradation Pathway. The Plant Cell. 28(9). 2291–2311. 140 indexed citations
16.
Zhou, Liang‐Zi, Sha Li, Qiang‐Nan Feng, et al.. (2013). PROTEIN S-ACYL TRANSFERASE10 Is Critical for Development and Salt Tolerance in Arabidopsis  . The Plant Cell. 25(3). 1093–1107. 115 indexed citations
17.
Yang, Jiangyi, Xiaobo Zhao, Ke Cheng, et al.. (2012). A Killer-Protector System Regulates Both Hybrid Sterility and Segregation Distortion in Rice. Science. 337(6100). 1336–1340. 208 indexed citations
18.
19.
Oufattole, Mohammed, Joon Ho Park, Marianne K. Poxleitner, Liwen Jiang, & John C. Rogers. (2005). Selective Membrane Protein Internalization Accompanies Movement from the Endoplasmic Reticulum to the Protein Storage Vacuole Pathway in Arabidopsis. The Plant Cell. 17(11). 3066–3080. 53 indexed citations
20.
Sohn, Eun Ju, Min Zhao, Soo Jin Kim, et al.. (2003). Rha1, an Arabidopsis Rab5 Homolog, Plays a Critical Role in the Vacuolar Trafficking of Soluble Cargo Proteins. The Plant Cell. 15(5). 1057–1070. 177 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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