Jiuping Ding

1.8k total citations
55 papers, 1.5k citations indexed

About

Jiuping Ding is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Jiuping Ding has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 24 papers in Cellular and Molecular Neuroscience and 21 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Jiuping Ding's work include Ion channel regulation and function (39 papers), Cardiac electrophysiology and arrhythmias (21 papers) and Neuroscience and Neuropharmacology Research (14 papers). Jiuping Ding is often cited by papers focused on Ion channel regulation and function (39 papers), Cardiac electrophysiology and arrhythmias (21 papers) and Neuroscience and Neuropharmacology Research (14 papers). Jiuping Ding collaborates with scholars based in China, United States and Canada. Jiuping Ding's co-authors include Christopher J. Lingle, Xiaoming Xia, Ying Wu, Kailai Duan, Tao Xu, Yongfeng Liu, Wenxin Li, Na Pan, Xuelin Lou and Yongming Dong and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Neuron.

In The Last Decade

Jiuping Ding

53 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jiuping Ding China 23 1.1k 499 370 281 117 55 1.5k
Julio A. Copello United States 22 1.9k 1.8× 701 1.4× 1.2k 3.2× 124 0.4× 33 0.3× 54 2.5k
David N. Bowser Australia 21 1.3k 1.2× 1.4k 2.7× 81 0.2× 352 1.3× 46 0.4× 29 2.6k
Bénédicte Dargent France 27 1.4k 1.3× 1.1k 2.2× 178 0.5× 223 0.8× 120 1.0× 42 2.2k
Baron Chanda United States 31 2.6k 2.5× 1.6k 3.3× 959 2.6× 143 0.5× 118 1.0× 75 3.1k
Maurice Gola France 27 1.5k 1.4× 1.0k 2.0× 267 0.7× 323 1.1× 13 0.1× 89 2.3k
Guillaume Sandoz France 23 1.2k 1.1× 695 1.4× 334 0.9× 149 0.5× 14 0.1× 48 1.6k
Robert S. Slaughter United States 27 1.9k 1.7× 739 1.5× 668 1.8× 198 0.7× 11 0.1× 43 2.3k
Dhasakumar Navaratnam United States 21 681 0.6× 250 0.5× 85 0.2× 190 0.7× 31 0.3× 57 1.4k
Judith A. Airey United States 30 2.1k 1.9× 991 2.0× 667 1.8× 70 0.2× 19 0.2× 44 2.8k
Mamoru Matsubara Japan 21 1.1k 1.0× 327 0.7× 137 0.4× 91 0.3× 36 0.3× 43 1.7k

Countries citing papers authored by Jiuping Ding

Since Specialization
Citations

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

Fields of papers citing papers by Jiuping Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiuping Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Jiuping Ding. A scholar is included among the top collaborators of Jiuping Ding 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 Jiuping Ding. Jiuping Ding 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.
Shan, Baoqing, et al.. (2025). Achieving Dual-Color Luminescence via Halogen Regulation in Copper-Based Halides for Anticounterfeiting. Inorganic Chemistry. 64(34). 17561–17568. 1 indexed citations
2.
Neely, Alan, et al.. (2021). Fast inactivation of Nav current in rat adrenal chromaffin cells involves two independent inactivation pathways. The Journal of General Physiology. 153(4). 6 indexed citations
3.
Hu, Bin, et al.. (2019). A conserved arginine/lysine-based motif promotes ER export of KCNE1 and KCNE2 to regulate KCNQ1 channel activity. Channels. 13(1). 483–497. 5 indexed citations
4.
Chai, Zuying, Changhe Wang, Rong Huang, et al.. (2017). CaV2.2 Gates Calcium-Independent but Voltage-Dependent Secretion in Mammalian Sensory Neurons. Neuron. 96(6). 1317–1326.e4. 39 indexed citations
5.
Hou, Panpan, Haowen Liu, Ming Yuchi, et al.. (2016). Extrapolating microdomain Ca2+ dynamics using BK channels as a Ca2+ sensor. Scientific Reports. 6(1). 17343–17343. 6 indexed citations
6.
Yan, Zhenzhen, Bin Hu, Zhigang Huang, et al.. (2016). Single Channel Recordings Reveal Differential β2 Subunit Modulations Between Mammalian and Drosophila BKCa(β2) Channels. PLoS ONE. 11(10). e0163308–e0163308.
7.
Ding, Jiuping, et al.. (2015). Cytotoxic effect of Quinidine on testicular tissues, sperm parameters and Ca2+ level in mice sperms; as an option of male contraception. Journals & Books Hosting (International Knowledge Sharing Platform). 30. 70–76.
8.
Yang, Yi, Wei Wang, Michael J. Fedchyshyn, et al.. (2014). Enhancing the fidelity of neurotransmission by activity-dependent facilitation of presynaptic potassium currents. Nature Communications. 5(1). 4564–4564. 38 indexed citations
9.
10.
Lu, Jie, Zhengwang Chen, Ying Wu, et al.. (2014). An ATPase inhibitory peptide with antibacterial and ion current effects. Biochemical and Biophysical Research Communications. 446(2). 519–522. 7 indexed citations
11.
Hou, Panpan, Wenping Zeng, Geliang Gan, et al.. (2013). Inter-α/β subunits coupling mediating pre-inactivation and augmented activation of BKCa(β2). Scientific Reports. 3(1). 1666–1666. 14 indexed citations
12.
Wang, Wei, Panpan Hou, Yi Yang, et al.. (2013). Native Gating Behavior of Ion Channels in Neurons with Null-Deviation Modeling. PLoS ONE. 8(10). e77105–e77105. 4 indexed citations
13.
Wu, Ying, Hong Yi, Hui Li, et al.. (2009). Intersubunit Coupling in the Pore of BK Channels. Journal of Biological Chemistry. 284(35). 23353–23363. 22 indexed citations
14.
Chen, Maorong, Geliang Gan, Ying Wu, et al.. (2008). Lysine-Rich Extracellular Rings Formed by hβ2 Subunits Confer the Outward Rectification of BK Channels. PLoS ONE. 3(5). e2114–e2114. 18 indexed citations
15.
Sun, Xiaohui, Jiuping Ding, Hui Li, et al.. (2007). Activation of Large-Conductance Calcium-Activated Potassium Channels by Puerarin: The Underlying Mechanism of Puerarin-Mediated Vasodilation. Journal of Pharmacology and Experimental Therapeutics. 323(1). 391–397. 64 indexed citations
16.
Chen, Maorong, et al.. (2007). Four-turn α-Helical Segment Prevents Surface Expression of the Auxiliary hβ2 Subunit of BK-type Channel. Journal of Biological Chemistry. 283(5). 2709–2715. 10 indexed citations
17.
Xie, Li, Ming Zhang, Wei Zhou, et al.. (2006). Extracellular ATP Stimulates Exocytosis via Localized Ca2+ Release from Acidic Stores in Rat Pancreatic β Cells. Traffic. 7(4). 429–439. 29 indexed citations
18.
Zhang, Zhe, Yu Zhou, Jiuping Ding, Xiaoming Xia, & Christopher J. Lingle. (2006). A Limited Access Compartment between the Pore Domain and Cytosolic Domain of the BK Channel. Journal of Neuroscience. 26(46). 11833–11843. 17 indexed citations
19.
Yao, Jing, Xiang Chen, Hui Li, et al.. (2005). BmP09, a “Long Chain” Scorpion Peptide Blocker of BK Channels. Journal of Biological Chemistry. 280(15). 14819–14828. 35 indexed citations
20.
Solaro, Christopher R., et al.. (1997). The cytosolic inactivation domains of BKi channels in rat chromaffin cells do not behave like simple, open-channel blockers. Biophysical Journal. 73(2). 819–830. 29 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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