Wing‐Yu Fu

2.2k total citations
25 papers, 1.6k citations indexed

About

Wing‐Yu Fu is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Wing‐Yu Fu has authored 25 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in Wing‐Yu Fu's work include Neuroscience and Neuropharmacology Research (9 papers), Neuroinflammation and Neurodegeneration Mechanisms (6 papers) and Axon Guidance and Neuronal Signaling (6 papers). Wing‐Yu Fu is often cited by papers focused on Neuroscience and Neuropharmacology Research (9 papers), Neuroinflammation and Neurodegeneration Mechanisms (6 papers) and Axon Guidance and Neuronal Signaling (6 papers). Wing‐Yu Fu collaborates with scholars based in Hong Kong, China and United States. Wing‐Yu Fu's co-authors include Nancy Y. Ip, Amy K.Y. Fu, Yu Chen, Lei Shi, Kwok‐On Lai, Wing‐Ho Yung, Tom H. Cheung, Ivy Chi Wai Chan, Xiaopu Zhou and D.S.Y. Mak and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Wing‐Yu Fu

25 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wing‐Yu Fu Hong Kong 20 637 585 417 345 264 25 1.6k
Karoly Nikolich United States 18 966 1.5× 484 0.8× 434 1.0× 367 1.1× 149 0.6× 21 1.9k
Baiping Wang United States 17 730 1.1× 420 0.7× 1.1k 2.6× 479 1.4× 227 0.9× 22 1.9k
Amaia M. Arranz Spain 18 770 1.2× 447 0.8× 567 1.4× 666 1.9× 178 0.7× 23 2.0k
Sung‐Jin Jeong South Korea 22 1.2k 1.8× 653 1.1× 685 1.6× 214 0.6× 99 0.4× 33 2.1k
Sonia Franciosi Canada 26 1.0k 1.6× 869 1.5× 357 0.9× 374 1.1× 111 0.4× 63 2.0k
Pradoldej Sompol United States 23 611 1.0× 410 0.7× 435 1.0× 455 1.3× 90 0.3× 41 1.7k
Shichun Tu United States 15 1000 1.6× 953 1.6× 590 1.4× 247 0.7× 113 0.4× 29 1.9k
Sascha W. Weyer Germany 14 547 0.9× 549 0.9× 1.0k 2.5× 249 0.7× 101 0.4× 15 1.5k
Nicholas H. Varvel United States 18 584 0.9× 486 0.8× 867 2.1× 1.1k 3.1× 417 1.6× 26 2.1k
Marie‐Paule Muriel France 22 1.2k 1.9× 1.1k 1.8× 322 0.8× 415 1.2× 126 0.5× 30 2.5k

Countries citing papers authored by Wing‐Yu Fu

Since Specialization
Citations

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

Fields of papers citing papers by Wing‐Yu Fu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wing‐Yu Fu. 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 Wing‐Yu Fu. The network helps show where Wing‐Yu Fu may publish in the future.

Co-authorship network of co-authors of Wing‐Yu Fu

This figure shows the co-authorship network connecting the top 25 collaborators of Wing‐Yu Fu. A scholar is included among the top collaborators of Wing‐Yu Fu 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 Wing‐Yu Fu. Wing‐Yu Fu 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.
Fu, Wing‐Yu, et al.. (2025). Impact of iris pigmented naevus on pupil tracking during femtosecond LASIK surgery. Clinical and Experimental Optometry. 1–4. 1 indexed citations
2.
Fu, Wing‐Yu & Nancy Y. Ip. (2022). The role of genetic risk factors of Alzheimer's disease in synaptic dysfunction. Seminars in Cell and Developmental Biology. 139. 3–12. 31 indexed citations
3.
Tian, Min, Yang Shen, Shun‐Fat Lau, et al.. (2021). Melanocortin receptor activation alleviates amyloid pathology and glial reactivity in an Alzheimer’s disease transgenic mouse model. Scientific Reports. 11(1). 4359–4359. 15 indexed citations
4.
Lau, Shun‐Fat, Congping Chen, Wing‐Yu Fu, et al.. (2020). IL-33-PU.1 Transcriptome Reprogramming Drives Functional State Transition and Clearance Activity of Microglia in Alzheimer’s Disease. Cell Reports. 31(3). 107530–107530. 80 indexed citations
5.
Li, Ouyang, Yu Chen, Ye Wang, et al.. (2020). p39-associated Cdk5 activity regulates dendritic morphogenesis. Scientific Reports. 10(1). 18746–18746. 11 indexed citations
6.
Gu, Shuo, Wing‐Yu Fu, Amy K.Y. Fu, et al.. (2018). Identification of new EphA4 inhibitors by virtual screening of FDA-approved drugs. Scientific Reports. 8(1). 7377–7377. 23 indexed citations
7.
Fu, Amy K.Y., Xiaopu Zhou, D.S.Y. Mak, et al.. (2016). IL-33 ameliorates Alzheimer’s disease-like pathology and cognitive decline. Proceedings of the National Academy of Sciences. 113(19). E2705–13. 294 indexed citations
8.
Chen, Yu, Zhuoyi Liang, Erkang Fei, et al.. (2015). Axin Regulates Dendritic Spine Morphogenesis through Cdc42-Dependent Signaling. PLoS ONE. 10(7). e0133115–e0133115. 21 indexed citations
9.
Zhang, Peng, Wing‐Yu Fu, Amy K.Y. Fu, & Nancy Y. Ip. (2015). S-nitrosylation-dependent proteasomal degradation restrains Cdk5 activity to regulate hippocampal synaptic strength. Nature Communications. 6(1). 8665–8665. 31 indexed citations
10.
Ip, Fanny C.F., et al.. (2015). Anemoside A3 Enhances Cognition through the Regulation of Synaptic Function and Neuroprotection. Neuropsychopharmacology. 40(8). 1877–1887. 24 indexed citations
11.
Zhao, Xiaosu, et al.. (2014). p35 Regulates the CRM1-Dependent Nucleocytoplasmic Shuttling of Nuclear Hormone Receptor Coregulator-Interacting Factor 1 (NIF-1). PLoS ONE. 9(10). e110584–e110584. 3 indexed citations
12.
Shen, Yang, Wing‐Yu Fu, Elaine Cheng, Amy K.Y. Fu, & Nancy Y. Ip. (2013). Melanocortin-4 Receptor Regulates Hippocampal Synaptic Plasticity through a Protein Kinase A-Dependent Mechanism. Journal of Neuroscience. 33(2). 464–472. 70 indexed citations
13.
Fu, Amy K.Y., et al.. (2012). Cdk5 Phosphorylates a Component of the HDAC Complex and Regulates Histone Acetylation during Neuronal Cell Death. Neurosignals. 21(1-2). 55–60. 7 indexed citations
14.
Fu, Wing‐Yu, Kai Cheng, Amy K.Y. Fu, & Nancy Y. Ip. (2011). Cyclin-dependent kinase 5-dependent phosphorylation of Pctaire1 regulates dendrite development. Neuroscience. 180. 353–359. 19 indexed citations
15.
Ip, Jacque Pak Kan, Lei Shi, Yu Chen, et al.. (2011). α2-chimaerin controls neuronal migration and functioning of the cerebral cortex through CRMP-2. Nature Neuroscience. 15(1). 39–47. 70 indexed citations
16.
Fu, Amy K.Y., Wing‐Yu Fu, Chong Shen, et al.. (2010). APCCdh1 mediates EphA4-dependent downregulation of AMPA receptors in homeostatic plasticity. Nature Neuroscience. 14(2). 181–189. 144 indexed citations
17.
Zhang, Peng, Pei-Chun Yu, Anthony H. Tsang, et al.. (2010). S-Nitrosylation of Cyclin-Dependent Kinase 5 (Cdk5) Regulates Its Kinase Activity and Dendrite Growth During Neuronal Development. Journal of Neuroscience. 30(43). 14366–14370. 55 indexed citations
18.
Fu, Wing‐Yu, Yu Chen, Mustafa Şahin, et al.. (2006). Cdk5 regulates EphA4-mediated dendritic spine retraction through an ephexin1-dependent mechanism. Nature Neuroscience. 10(1). 67–76. 257 indexed citations
19.
Fu, Wing‐Yu, et al.. (2002). Expression of Cdk5 and its activators in NT2 cells during neuronal differentiation. Journal of Neurochemistry. 81(3). 646–654. 20 indexed citations
20.
Cheng, Kai, Zhen Li, Wing‐Yu Fu, et al.. (2002). Pctaire1 Interacts with p35 and Is a Novel Substrate for Cdk5/p35. Journal of Biological Chemistry. 277(35). 31988–31993. 50 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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