Hong‐Shuo Sun

5.1k total citations
104 papers, 3.9k citations indexed

About

Hong‐Shuo Sun is a scholar working on Molecular Biology, Nutrition and Dietetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Hong‐Shuo Sun has authored 104 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 22 papers in Nutrition and Dietetics and 20 papers in Cellular and Molecular Neuroscience. Recurrent topics in Hong‐Shuo Sun's work include Magnesium in Health and Disease (20 papers), Ion Channels and Receptors (15 papers) and Neonatal and fetal brain pathology (15 papers). Hong‐Shuo Sun is often cited by papers focused on Magnesium in Health and Disease (20 papers), Ion Channels and Receptors (15 papers) and Neonatal and fetal brain pathology (15 papers). Hong‐Shuo Sun collaborates with scholars based in Canada, China and United States. Hong‐Shuo Sun's co-authors include Zhong‐Ping Feng, Ekaterina Turlova, Michael Tymianski, Vivian Szeto, Meihua Bao, Andrew Barszczyk, Burton B. Yang, Shuzhen Zhu, Nai‐Hong Chen and Yasuo Mori and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Nature Neuroscience.

In The Last Decade

Hong‐Shuo Sun

101 papers receiving 3.9k citations

Peers

Hong‐Shuo Sun
Michelle Aarts Canada
Valérie Vingtdeux United States
Lezanne Ooi Australia
Philippe Marambaud United States
Mark Arundine Canada
Agnese Secondo Italy
Yoon Hee Chung South Korea
Carlos Villalobos Spain
Byung Tae Choi South Korea
King‐Ho Cheung Hong Kong
Michelle Aarts Canada
Hong‐Shuo Sun
Citations per year, relative to Hong‐Shuo Sun Hong‐Shuo Sun (= 1×) peers Michelle Aarts

Countries citing papers authored by Hong‐Shuo Sun

Since Specialization
Citations

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

Fields of papers citing papers by Hong‐Shuo Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hong‐Shuo Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Hong‐Shuo Sun. A scholar is included among the top collaborators of Hong‐Shuo 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 Hong‐Shuo Sun. Hong‐Shuo 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.
Wang, Hongyun, Ye Peng, Shasha Wang, et al.. (2025). Noncanonical role of astrocytic mitochondrial Cx43: suppressing IDH3α to sustain glycolytic homeostasis against depression. Cell Death and Disease. 17(1). 94–94.
2.
Ferreira, Ana Flávia Fernandes, Henning Ulrich, Zhong‐Ping Feng, Hong‐Shuo Sun, & Luiz Roberto Britto. (2024). Neurodegeneration and glial morphological changes are both prevented by TRPM2 inhibition during the progression of a Parkinson's disease mouse model. Experimental Neurology. 377. 114780–114780. 6 indexed citations
3.
Pörzgen, Peter, Junhao Huang, Sayuri Suzuki, et al.. (2024). Transient Receptor Potential Melastatin 7 (TRPM7) Ion Channel Inhibitors: Preliminary SAR and Conformational Studies of Xenicane Diterpenoids from the Hawaiian Soft Coral Sarcothelia edmondsoni. Journal of Natural Products. 87(4). 783–797. 2 indexed citations
4.
Ferreira, Ana Flávia Fernandes, Henning Ulrich, Yasuo Mori, et al.. (2024). Deletion of the Transient Receptor Potential Melastatin 2 Gene Mitigates the 6-Hydroxydopamine-Induced Parkinson’s Disease–Like Pathology. Molecular Neurobiology. 62(4). 5333–5346. 3 indexed citations
5.
Bin, Na‐Ryum, Ke Ma, Hidekiyo Harada, et al.. (2023). Neuronal SNAP-23 is critical for synaptic plasticity and spatial memory independently of NMDA receptor regulation. iScience. 26(5). 106664–106664. 3 indexed citations
6.
Miller, Steven P., et al.. (2023). Hypothermia combined with neuroprotective adjuvants shortens the duration of hospitalization in infants with hypoxic ischemic encephalopathy: Meta-analysis. Frontiers in Pharmacology. 13. 1037131–1037131. 9 indexed citations
7.
Wang, Shasha, Wenbin He, Zhong‐Ping Feng, et al.. (2023). A small molecule 20C from Gastrodia elata inhibits α-synuclein aggregation and prevents progression of Parkinson’s disease. Cell Death and Disease. 14(9). 594–594. 11 indexed citations
8.
Cui, Liyuan, Zhao Zhang, Zhong‐Ping Feng, et al.. (2023). A novel small-molecular CCR5 antagonist promotes neural repair after stroke. Acta Pharmacologica Sinica. 44(10). 1935–1947. 21 indexed citations
9.
Wang, Haitao, et al.. (2022). Inhibition of TRPM7 with carvacrol suppresses glioblastoma functions in vivo. European Journal of Neuroscience. 55(6). 1483–1491. 14 indexed citations
10.
Ferreira, Ana Flávia Fernandes, et al.. (2022). Inhibition of TRPM2 by AG490 Is Neuroprotective in a Parkinson’s Disease Animal Model. Molecular Neurobiology. 59(3). 1543–1559. 14 indexed citations
11.
Zhou, Xin‐Fu, Yani Zhang, Fangfang Li, et al.. (2021). Neuronal chemokine-like-factor 1 (CKLF1) up-regulation promotes M1 polarization of microglia in rat brain after stroke. Acta Pharmacologica Sinica. 43(5). 1217–1230. 34 indexed citations
12.
Zhu, Jie, Shifeng Chu, Ye Peng, et al.. (2021). Pyk2 inhibition attenuates hypoxic-ischemic brain injury in neonatal mice. Acta Pharmacologica Sinica. 43(4). 797–810. 8 indexed citations
13.
Barszczyk, Andrew, et al.. (2021). Smartphones and Video Cameras: Future Methods for Blood Pressure Measurement. Frontiers in Digital Health. 3. 770096–770096. 17 indexed citations
14.
Fleig, Andrea, et al.. (2021). Modulators of TRPM7 and its potential as a drug target for brain tumours. Cell Calcium. 101. 102521–102521. 11 indexed citations
15.
Ma, Ke, Siyan Wang, Dan Zhu, et al.. (2018). C2 Domains of Munc13-4 Are Crucial for Ca2+-Dependent Degranulation and Cytotoxicity in NK Cells. The Journal of Immunology. 201(2). 700–713. 15 indexed citations
16.
Wong, Raymond, Baofeng Xu, Feiya Li, et al.. (2018). Blockade of the swelling-induced chloride current attenuates the mouse neonatal hypoxic-ischemic brain injury in vivo. Acta Pharmacologica Sinica. 39(5). 858–865. 12 indexed citations
17.
Turlova, Ekaterina, Feiya Li, Meihua Bao, et al.. (2017). Transient receptor potential melastatin 2 channels (TRPM2) mediate neonatal hypoxic-ischemic brain injury in mice. Experimental Neurology. 296. 32–40. 49 indexed citations
18.
Dati, Lívia Mendonça Munhoz, Henning Ulrich, Caroline Cristiano Real, et al.. (2017). Carvacrol promotes neuroprotection in the mouse hemiparkinsonian model. Neuroscience. 356. 176–181. 48 indexed citations
19.
Quan, Yi, Andrew Barszczyk, Zhong‐Ping Feng, & Hong‐Shuo Sun. (2011). Current understanding of KATP channels in neonatal diseases: focus on insulin secretion disorders. Acta Pharmacologica Sinica. 32(6). 765–780. 26 indexed citations
20.
Sun, Hong‐Shuo, Zhong‐Ping Feng, Takashi Miki, Susumu Seino, & Robert J. French. (2005). Enhanced Neuronal Damage After Ischemic Insults in Mice Lacking Kir6.2-Containing ATP-Sensitive K+Channels. Journal of Neurophysiology. 95(4). 2590–2601. 73 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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