King‐Ho Cheung
About
King‐Ho Cheung is a scholar working on Physiology, Molecular Biology and Pharmacology.
According to data from OpenAlex, King‐Ho Cheung has authored 53 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Physiology, 21 papers in Molecular Biology and 16 papers in Pharmacology. Recurrent topics in King‐Ho Cheung's work include Alzheimer's disease research and treatments (20 papers), Cholinesterase and Neurodegenerative Diseases (14 papers) and Autophagy in Disease and Therapy (14 papers). King‐Ho Cheung is often cited by papers focused on Alzheimer's disease research and treatments (20 papers), Cholinesterase and Neurodegenerative Diseases (14 papers) and Autophagy in Disease and Therapy (14 papers). King‐Ho Cheung collaborates with scholars based in Hong Kong, China and United States. King‐Ho Cheung's co-authors include J. Kevin Foskett, Marioly Müller, Benjamin Chun‐Kit Tong, César Cárdenas, Min Li, Jun Yang, Horia Vais, Lijuan Mei, Don‐On Daniel Mak and Ian Parker and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Neuron.
In The Last Decade
King‐Ho Cheung
52 papers receiving 3.5k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| King‐Ho Cheung Hong Kong | 30 | 1.8k | 1.1k | 811 | 789 | 586 | 53 | 3.6k | ||
| Valérie Vingtdeux United States | 29 | 1.8k 1.0× | 1.7k 1.5× | 790 1.0× | 508 0.6× | 225 0.4× | 47 | 4.2k | ||
| Marioly Müller Chile | 15 | 2.4k 1.3× | 863 0.8× | 743 0.9× | 447 0.6× | 619 1.1× | 25 | 3.3k | ||
| Kenneth J. Valenzano United States | 32 | 1.4k 0.8× | 1.7k 1.5× | 1.2k 1.4× | 502 0.6× | 550 0.9× | 56 | 3.5k | ||
| Philippe Marambaud United States | 38 | 3.1k 1.7× | 2.8k 2.5× | 1.2k 1.5× | 458 0.6× | 793 1.4× | 87 | 6.6k | ||
| Jieqiong Tan China | 33 | 1.6k 0.9× | 625 0.5× | 328 0.4× | 1.1k 1.4× | 392 0.7× | 131 | 3.6k | ||
| Toshihiko Murayama Japan | 36 | 2.5k 1.4× | 912 0.8× | 728 0.9× | 160 0.2× | 457 0.8× | 208 | 5.1k | ||
| Yasunobu Okuma Japan | 35 | 1.8k 1.0× | 896 0.8× | 975 1.2× | 799 1.0× | 1.2k 2.0× | 135 | 4.5k | ||
| Agnese Secondo Italy | 35 | 1.8k 1.0× | 647 0.6× | 1.2k 1.4× | 222 0.3× | 165 0.3× | 128 | 3.5k | ||
| Julien Puyal Switzerland | 30 | 1.6k 0.9× | 439 0.4× | 668 0.8× | 1.3k 1.7× | 350 0.6× | 55 | 3.3k | ||
| Deron R. Herr United States | 35 | 3.3k 1.8× | 935 0.8× | 387 0.5× | 244 0.3× | 779 1.3× | 95 | 4.7k |
Countries citing papers authored by King‐Ho Cheung
Since
Specialization
Citations
This map shows the geographic impact of King‐Ho Cheung'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 King‐Ho Cheung with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites King‐Ho Cheung more than expected).
Fields of papers citing papers by King‐Ho Cheung
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by King‐Ho Cheung. 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 King‐Ho Cheung. The network helps show where King‐Ho Cheung may publish in the future.
Co-authorship network of co-authors of King‐Ho Cheung
This figure shows the co-authorship network connecting the top 25 collaborators of King‐Ho Cheung. A scholar is included among the top collaborators of King‐Ho Cheung 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 King‐Ho Cheung. King‐Ho Cheung is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Huang, Shiying, Benjamin Chun‐Kit Tong, Aston Jiaxi Wu, et al.. (2023). Targeting calcium signaling by inositol trisphosphate receptors: A novel mechanism for the anti-asthmatic effects of Houttuynia cordata. Biomedicine & Pharmacotherapy. 164. 114935–114935.
2.
Wu, Aston Jiaxi, Shiying Huang, Yuanyuan Yu, et al.. (2023). Exploring the Potential of Aptamers in Targeting Neuroinflammation and Neurodegenerative Disorders: Opportunities and Challenges. International Journal of Molecular Sciences. 24(14). 11780–11780.
3.
Krishnamoorthi, Senthilkumar, Ashok Iyaswamy, Sravan Gopalkrishnashetty Sreenivasmurthy, et al.. (2023). PPARɑ Ligand Caudatin Improves Cognitive Functions and Mitigates Alzheimer’s Disease Defects By Inducing Autophagy in Mice Models. Journal of Neuroimmune Pharmacology. 18(3). 509–528.
4.
Guan, Xinjie, Ashok Iyaswamy, Sravan Gopalkrishnashetty Sreenivasmurthy, et al.. (2022). Mechanistic Insights into Selective Autophagy Subtypes in Alzheimer’s Disease. International Journal of Molecular Sciences. 23(7). 3609–3609.
5.
Sreenivasmurthy, Sravan Gopalkrishnashetty, Ashok Iyaswamy, Senthilkumar Krishnamoorthi, et al.. (2022). Bromo-protopine, a novel protopine derivative, alleviates tau pathology by activating chaperone-mediated autophagy for Alzheimer’s disease therapy. Frontiers in Molecular Biosciences. 9. 1030534–1030534.
6.
Iyaswamy, Ashok, Xueli Wang, Senthilkumar Krishnamoorthi, et al.. (2022). Theranostic F-SLOH mitigates Alzheimer's disease pathology involving TFEB and ameliorates cognitive functions in Alzheimer's disease models. Redox Biology. 51. 102280–102280.
7.
Tong, Benjamin Chun‐Kit, Aston Jiaxi Wu, Shiying Huang, et al.. (2021). Lysosomal TPCN (two pore segment channel) inhibition ameliorates beta-amyloid pathology and mitigates memory impairment in Alzheimer disease. Autophagy. 18(3). 624–642.
8.
Cai, Cui-Zan, Chuanbin Yang, Xu‐Xu Zhuang, et al.. (2020). NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradation. Autophagy. 17(5). 1112–1130.
9.
Wang, Ziying, Chuanbin Yang, Jia Liu, et al.. (2020). A Curcumin Derivative Activates TFEB and Protects Against Parkinsonian Neurotoxicity in Vitro. International Journal of Molecular Sciences. 21(4). 1515–1515.
10.
Iyaswamy, Ashok, Senthilkumar Krishnamoorthi, Ju‐Xian Song, et al.. (2020). Yuan-Hu Zhi Tong Prescription Mitigates Tau Pathology and Alleviates Memory Deficiency in the Preclinical Models of Alzheimer’s Disease. Frontiers in Pharmacology. 11. 584770–584770.
11.
Iyaswamy, Ashok, Ju‐Xian Song, Chuanbin Yang, et al.. (2019). NeuroDefend, a novel Chinese medicine, attenuates amyloid-β and tau pathology in experimental Alzheimer's disease models. Journal of Food and Drug Analysis. 28(1). 132–146.
12.
Yang, Long, Wenwen Gu, King‐Ho Cheung, et al.. (2018). InsP3R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca2+ elevation and TBK1 activity. BMC Biology. 16(1). 158–158.
13.
Mak, Don‐On Daniel, et al.. (2015). Analyzing and Quantifying the Gain-of-Function Enhancement of IP3 Receptor Gating by Familial Alzheimer’s Disease-Causing Mutants in Presenilins. PLoS Computational Biology. 11(10). e1004529–e1004529.
14.
Liao, Song-Yan, et al.. (2013). Adrenomedullin Increased the Short-Circuit Current in the Pig Oviduct Through Chloride Channels via the CGRP Receptor: Mediation by cAMP and Calcium Ions But Not by Nitric Oxide1. Biology of Reproduction. 89(4). 99–99.
15.
Ye, Yiqing, Yingying Xu, Wanling Liang, et al.. (2013). DNA-loaded chitosan oligosaccharide nanoparticles with enhanced permeability across Calu-3 cells. Journal of drug targeting. 21(5). 474–486.
16.
Mak, Don‐On Daniel, Horia Vais, King‐Ho Cheung, & J. Kevin Foskett. (2013). Isolating Nuclei from Cultured Cells for Patch-Clamp Electrophysiology of Intracellular Ca2+ Channels. Cold Spring Harbor Protocols. 2013(9). pdb.prot073056–pdb.prot073056.
17.
Bozym, Rebecca A., Kunal P. Patel, Carl White, et al.. (2011). Calcium signals and calpain-dependent necrosis are essential for release of coxsackievirus B from polarized intestinal epithelial cells. Molecular Biology of the Cell. 22(17). 3010–3021.
18.
Müller, Marioly, King‐Ho Cheung, & J. Kevin Foskett. (2010). Enhanced ROS Generation Mediated by Alzheimer's Disease Presenilin Regulation of InsP 3 R Ca 2+ Signaling. Antioxidants and Redox Signaling. 14(7). 1225–1235.
19.
Cárdenas, César, Russell Miller, Ian F. Smith, et al.. (2010). Essential Regulation of Cell Bioenergetics by Constitutive InsP3 Receptor Ca2+ Transfer to Mitochondria. Cell. 142(2). 270–283.
20.
Cheung, King‐Ho, et al.. (2006). Graded recruitment and inactivation of single InsP3 receptor Ca2+‐release channels: implications for quartal Ca2+release. The Journal of Physiology. 573(3). 645–662.
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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