Kun Wu

2.9k total citations · 4 hit papers
19 papers, 2.0k citations indexed

About

Kun Wu is a scholar working on Molecular Biology, Physiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Kun Wu has authored 19 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Physiology and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Kun Wu's work include Ion channel regulation and function (12 papers), Erythrocyte Function and Pathophysiology (7 papers) and Cardiac electrophysiology and arrhythmias (5 papers). Kun Wu is often cited by papers focused on Ion channel regulation and function (12 papers), Erythrocyte Function and Pathophysiology (7 papers) and Cardiac electrophysiology and arrhythmias (5 papers). Kun Wu collaborates with scholars based in China, United States and South Korea. Kun Wu's co-authors include Nieng Yan, Jianlin Lei, Bailong Xiao, Huaizong Shen, Shaopeng Chi, Qiancheng Zhao, Jie Geng, Xiaojing Pan, Yanfeng Wang and Xueming Li and has published in prestigious journals such as Nature, Science and Angewandte Chemie International Edition.

In The Last Decade

Kun Wu

18 papers receiving 2.0k citations

Hit Papers

Structure and mechanogating mechanism of the Piezo1 channel 2018 2026 2020 2023 2018 2019 2018 2021 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kun Wu China 14 1.5k 731 405 326 311 19 2.0k
Christophe Vandier France 28 1.6k 1.1× 221 0.3× 384 0.9× 233 0.7× 179 0.6× 87 2.3k
Frank Wunder Germany 25 2.6k 1.7× 634 0.9× 1.5k 3.6× 1.1k 3.5× 172 0.6× 50 3.5k
Sabina Honisch Germany 20 890 0.6× 466 0.6× 355 0.9× 178 0.5× 297 1.0× 33 1.7k
Scott P. Fraser United Kingdom 32 2.2k 1.5× 219 0.3× 957 2.4× 334 1.0× 92 0.3× 66 2.9k
Shigeru Morishima Japan 21 1.3k 0.9× 249 0.3× 509 1.3× 243 0.7× 126 0.4× 57 1.7k
Tatyana I. Gudz United States 26 2.4k 1.6× 472 0.6× 422 1.0× 182 0.6× 81 0.3× 40 3.3k
Markus Waldeck‐Weiermair Austria 29 1.6k 1.1× 527 0.7× 399 1.0× 113 0.3× 47 0.2× 60 2.4k
Robert D. Harvey United States 33 2.5k 1.7× 302 0.4× 863 2.1× 1.6k 4.8× 159 0.5× 74 3.0k
Andrea Brüggemann Germany 31 1.9k 1.3× 188 0.3× 975 2.4× 993 3.0× 88 0.3× 52 2.4k
Alessandra Picollo Spain 21 1.3k 0.9× 157 0.2× 445 1.1× 294 0.9× 65 0.2× 25 1.5k

Countries citing papers authored by Kun Wu

Since Specialization
Citations

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

Fields of papers citing papers by Kun Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kun Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Kun Wu. A scholar is included among the top collaborators of Kun Wu 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 Kun Wu. Kun Wu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Li, Xiaodong, Rongsong Li, Yin Chen, et al.. (2025). Baculovirus protein kinase 1 activates AMPK-protein phosphatase 5 axis to hijack transcription factor EB for self-proliferation. International Journal of Biological Macromolecules. 298. 139884–139884. 1 indexed citations
2.
Ji, Linlin, Yi Zhang, Kun Wu, et al.. (2025). Case Report: Challenges in immunotherapy for the elderly: a case of refractory ICI-induced AIHA and thrombocytopenia in advanced gastric cancer. Frontiers in Immunology. 16. 1679817–1679817.
3.
Liu, S., Xuzhong Yang, Xudong Chen, et al.. (2024). An intermediate open structure reveals the gating transition of the mechanically activated PIEZO1 channel. Neuron. 113(4). 590–604.e6. 17 indexed citations
4.
Jiang, Fan, Kunlun Yin, Kun Wu, et al.. (2021). The mechanosensitive Piezo1 channel mediates heart mechano-chemo transduction. Nature Communications. 12(1). 869–869. 178 indexed citations breakdown →
5.
Jiang, Fan, Kun Wu, Kunlun Yin, et al.. (2021). The Mechanosensitive Piezo1 Channel Mediates Heart Mechano-Chemo Transduction. Biophysical Journal. 120(3). 102a–103a. 11 indexed citations
6.
Li, Zhangqiang, Xueqin Jin, Tong Wu, et al.. (2021). Structural Basis for Pore Blockade of the Human Cardiac Sodium Channel Na v 1.5 by the Antiarrhythmic Drug Quinidine**. Angewandte Chemie International Edition. 60(20). 11474–11480. 75 indexed citations
7.
Li, Zhangqiang, Xueqin Jin, Tong Wu, et al.. (2021). Structural Basis for Pore Blockade of the Human Cardiac Sodium Channel Nav1.5 by the Antiarrhythmic Drug Quinidine**. Angewandte Chemie. 133(20). 11575–11581. 6 indexed citations
8.
Li, Tian, et al.. (2020). Structural Basis for the Modulation of Human KCNQ4 by Small-Molecule Drugs. Molecular Cell. 81(1). 25–37.e4. 62 indexed citations
9.
Zhao, Yanyu, Gaoxingyu Huang, Qiurong Wu, et al.. (2019). Cryo-EM structures of apo and antagonist-bound human Cav3.1. Nature. 576(7787). 492–497. 122 indexed citations
10.
Shen, Huaizong, et al.. (2019). Structures of human Na v 1.7 channel in complex with auxiliary subunits and animal toxins. Science. 363(6433). 1303–1308. 324 indexed citations breakdown →
11.
Wang, Yanfeng, Shaopeng Chi, Qiancheng Zhao, et al.. (2018). A Lever-Like Transduction Pathway for Long-Distance Chemical- and Mechano-Gating of the Mechanosensitive Piezo1 Channel. Biophysical Journal. 114(3). 113a–114a. 25 indexed citations
12.
Zhao, Qiancheng, Heng Zhou, Shaopeng Chi, et al.. (2018). Structure and mechanogating mechanism of the Piezo1 channel. Nature. 554(7693). 487–492. 420 indexed citations breakdown →
13.
Zhang, Yifei, Rong Hua, Fang‐Xiong Zhang, et al.. (2018). A Membrane Potential- and Calpain-Dependent Reversal of Caspase-1 Inhibition Regulates Canonical NLRP3 Inflammasome. Cell Reports. 24(9). 2356–2369.e5. 46 indexed citations
14.
Pan, Xiaojing, Zhangqiang Li, Qiang Zhou, et al.. (2018). Structure of the human voltage-gated sodium channel Na v 1.4 in complex with β1. Science. 362(6412). 318 indexed citations breakdown →
15.
Zhao, Qiancheng, Kun Wu, Shaopeng Chi, Jie Geng, & Bailong Xiao. (2017). Heterologous Expression of the Piezo1-ASIC1 Chimera Induces Mechanosensitive Currents with Properties Distinct from Piezo1. Neuron. 94(2). 274–277. 17 indexed citations
16.
Zhao, Qiancheng, Kun Wu, Jie Geng, et al.. (2016). Ion Permeation and Mechanotransduction Mechanisms of Mechanosensitive Piezo Channels. Neuron. 89(6). 1248–1263. 160 indexed citations
17.
Lan, Huan, Kun Wu, Yong Zheng, et al.. (2016). Total synthesis of mambalgin‐1/2/3 by two‐segment hydrazide‐based native chemical ligation. Journal of Peptide Science. 22(5). 320–326. 11 indexed citations
18.
Trujillo, John I., Marvin J. Meyers, David R. Anderson, et al.. (2007). Novel tetrahydro-β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2). Bioorganic & Medicinal Chemistry Letters. 17(16). 4657–4663. 130 indexed citations
19.
McKew, John C., Megan A. Foley, Paresh Thakker, et al.. (2005). Inhibition of Cytosolic Phospholipase A2α: Hit to Lead Optimization. Journal of Medicinal Chemistry. 49(1). 135–158. 63 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026