Henry K. Yip

3.2k total citations
59 papers, 2.7k citations indexed

About

Henry K. Yip is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Henry K. Yip has authored 59 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Cellular and Molecular Neuroscience, 26 papers in Molecular Biology and 16 papers in Developmental Neuroscience. Recurrent topics in Henry K. Yip's work include Nerve injury and regeneration (33 papers), Neurogenesis and neuroplasticity mechanisms (15 papers) and Axon Guidance and Neuronal Signaling (14 papers). Henry K. Yip is often cited by papers focused on Nerve injury and regeneration (33 papers), Neurogenesis and neuroplasticity mechanisms (15 papers) and Axon Guidance and Neuronal Signaling (14 papers). Henry K. Yip collaborates with scholars based in Hong Kong, United States and China. Henry K. Yip's co-authors include Kwok‐Fai So, Eugene M. Johnson, Qi Cui, Keith M. Rich, Wutian Wu, Robert E. Schmidt, Qiang Lü, E. Marshall Johnson, Yang Du and Bing Hu and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Trends in Neurosciences.

In The Last Decade

Henry K. Yip

57 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Henry K. Yip Hong Kong 30 1.6k 1.1k 735 466 454 59 2.7k
Michael Rasminsky Canada 24 1.7k 1.0× 1.0k 0.9× 719 1.0× 204 0.4× 316 0.7× 37 2.8k
Myung‐Hoon Chun South Korea 32 1.3k 0.8× 2.1k 1.9× 262 0.4× 691 1.5× 286 0.6× 116 3.1k
Rithwick Rajagopal United States 19 944 0.6× 746 0.7× 380 0.5× 349 0.7× 194 0.4× 50 2.0k
Paulo D. Koeberle Canada 22 656 0.4× 810 0.7× 222 0.3× 299 0.6× 163 0.4× 33 1.5k
Håkan Björklund Sweden 24 875 0.5× 628 0.6× 266 0.4× 200 0.4× 165 0.4× 44 1.6k
Céline Jaillard France 23 669 0.4× 1.5k 1.3× 183 0.2× 200 0.4× 203 0.4× 37 2.4k
Francisco J. Rivera Austria 27 362 0.2× 727 0.7× 583 0.8× 106 0.2× 185 0.4× 56 2.0k
George A. Wilkinson United States 20 2.2k 1.4× 2.0k 1.8× 505 0.7× 59 0.1× 570 1.3× 28 3.7k
EM Johnson United States 25 2.1k 1.3× 1.2k 1.1× 907 1.2× 44 0.1× 421 0.9× 36 3.1k
John Grist United Kingdom 33 1.8k 1.1× 1.3k 1.2× 318 0.4× 78 0.2× 1.8k 4.0× 50 3.9k

Countries citing papers authored by Henry K. Yip

Since Specialization
Citations

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

Fields of papers citing papers by Henry K. Yip

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Henry K. Yip. 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 Henry K. Yip. The network helps show where Henry K. Yip may publish in the future.

Co-authorship network of co-authors of Henry K. Yip

This figure shows the co-authorship network connecting the top 25 collaborators of Henry K. Yip. A scholar is included among the top collaborators of Henry K. Yip 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 Henry K. Yip. Henry K. Yip 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.
Hennigar, Randolph A., et al.. (2024). Surviving Fluid Excess: A Rare Case of Collapsing Glomerulopathy with IgM Kappa Monoclonal Gammopathy of Renal Significance. Journal of the American Society of Nephrology. 35(10S).
2.
Liu, Jingyi, Xiaoxin Chen, Haiyong Chen, et al.. (2018). Downregulation of Aquaporin 9 Exacerbates Beta-amyloid-induced Neurotoxicity in Alzheimer’s Disease Models In vitro and In vivo. Neuroscience. 394. 72–82. 13 indexed citations
3.
Yip, Henry K.. (2013). Retinal Stem Cells and Regeneration of Vision System. The Anatomical Record. 297(1). 137–160. 12 indexed citations
4.
Yip, Henry K., et al.. (2011). Neuroprotective Signaling Mechanisms of Telomerase Are Regulated by Brain-Derived Neurotrophic Factor in Rat Spinal Cord Motor Neurons. Journal of Neuropathology & Experimental Neurology. 70(7). 634–652. 43 indexed citations
5.
Du, Yang & Henry K. Yip. (2010). The expression and roles of inhibitor of DNA binding helix-loop-helix proteins in the developing and adult mouse retina. Neuroscience. 175. 367–379. 18 indexed citations
6.
Du, Yang & Henry K. Yip. (2009). Effects of bone morphogenetic protein 2 on Id expression and neuroblastoma cell differentiation. Differentiation. 79(2). 84–92. 28 indexed citations
7.
8.
Cheung, Zelda H., et al.. (2007). A Neuroprotective Herbal Mixture Inhibits Caspase-3-independent Apoptosis in Retinal Ganglion Cells. Cellular and Molecular Neurobiology. 28(1). 137–155. 30 indexed citations
9.
Zhi, Ye, Qiang Lü, Chengwu Zhang, et al.. (2005). Different optic nerve injury sites result in different responses of retinal ganglion cells to brain-derived neurotrophic factor but not neurotrophin-4/5. Brain Research. 1047(2). 224–232. 20 indexed citations
10.
Yeung, Sai‐Ching J. & Henry K. Yip. (2005). Developmental expression patterns and localization of DNA-binding protein inhibitor (Id3) in the mouse retina. Neuroreport. 16(7). 673–676. 5 indexed citations
11.
Cui, Qi, Henry K. Yip, Robert Chunhua Zhao, Kwok‐Fai So, & Alan R. Harvey. (2003). Intraocular elevation of cyclic AMP potentiates ciliary neurotrophic factor-induced regeneration of adult rat retinal ganglion cell axons. Molecular and Cellular Neuroscience. 22(1). 49–61. 219 indexed citations
12.
Cheung, Zelda H., Henry K. Yip, Wutian Wu, & Kwok‐Fai So. (2003). Axotomy induces cytochrome c release in retinal ganglion cells. Neuroreport. 14(2). 279–282. 11 indexed citations
13.
You, Si–Wei, Kuldip S. Bedi, Henry K. Yip, & Kwok‐Fai So. (2002). Axonal regeneration of retinal ganglion cells after optic nerve pre-lesions and attachment of normal or pre-degenerated peripheral nerve grafts. Visual Neuroscience. 19(5). 661–668. 6 indexed citations
14.
Yip, Henry K. & Kwok‐Fai So. (2000). Axonal regeneration of retinal ganglion cells: effect of trophic factors. Progress in Retinal and Eye Research. 19(5). 559–575. 52 indexed citations
15.
So, Kwok‐Fai, et al.. (2000). Chondroitinase ABC promotes axonal regeneration of Clarkeʼs neurons after spinal cord injury. Neuroreport. 11(5). 1063–1067. 129 indexed citations
16.
Hu, Bing, Henry K. Yip, & Kwok‐Fai So. (1999). Expression of p75 neurotrophin receptor in the injured and regenerating rat retina. Neuroreport. 10(6). 1293–1297. 22 indexed citations
17.
So, Kwok‐Fai & Henry K. Yip. (1998). Regenerative capacity of retinal ganglion cells in mammals. Vision Research. 38(10). 1525–1535. 35 indexed citations
18.
Johnson, Eugene M., Keith M. Rich, & Henry K. Yip. (1986). The role of NGF in sensory neurons in vivo. Trends in Neurosciences. 9. 33–37. 185 indexed citations
19.
Rich, Keith M., Henry K. Yip, Patricia A. Osborne, Robert E. Schmidt, & Eugene M. Johnson. (1984). Role of nerve growth factor in the adult dorsal root ganglia neuron and its response to injury. The Journal of Comparative Neurology. 230(1). 110–118. 132 indexed citations
20.
Yip, Henry K. & Bernice Grafstein. (1982). Effect of nerve growth factor on regeneration of goldfish optic axons. Brain Research. 238(2). 329–339. 42 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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