Martin Cheung

2.9k total citations
41 papers, 2.2k citations indexed

About

Martin Cheung is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Martin Cheung has authored 41 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Martin Cheung's work include Developmental Biology and Gene Regulation (13 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Pluripotent Stem Cells Research (5 papers). Martin Cheung is often cited by papers focused on Developmental Biology and Gene Regulation (13 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Pluripotent Stem Cells Research (5 papers). Martin Cheung collaborates with scholars based in Hong Kong, China and United Kingdom. Martin Cheung's co-authors include James Briscoe, Paul J. Scotting, Muhammad Abu‐Elmagd, Kathryn S.E. Cheah, Andreas Schedl, Marie‐Christine Chaboissier, Anita Mynett, Elizabeth Hirst, Jessica Aijia Liu and Hans Clevers and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Martin Cheung

39 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Cheung Hong Kong 19 1.6k 499 389 254 212 41 2.2k
Luc Leyns Belgium 24 3.0k 1.9× 555 1.1× 150 0.4× 111 0.4× 300 1.4× 41 3.6k
Gerrit Begemann Germany 26 1.9k 1.2× 437 0.9× 170 0.4× 52 0.2× 141 0.7× 57 2.4k
Luca Gentile Germany 27 3.1k 2.0× 472 0.9× 156 0.4× 157 0.6× 414 2.0× 47 3.6k
Shinji Masui Japan 26 2.7k 1.7× 429 0.9× 236 0.6× 96 0.4× 345 1.6× 42 3.5k
Tord Hjalt Sweden 24 1.4k 0.9× 471 0.9× 150 0.4× 141 0.6× 55 0.3× 34 2.0k
Juan Larraı́n Chile 31 2.2k 1.4× 424 0.8× 231 0.6× 242 1.0× 147 0.7× 71 3.2k
Edwina M. Wright Australia 11 1.5k 0.9× 942 1.9× 742 1.9× 155 0.6× 133 0.6× 14 2.6k
Rick I. Cohen United States 19 993 0.6× 227 0.5× 150 0.4× 329 1.3× 146 0.7× 32 1.6k
Jun Motoyama Japan 27 2.2k 1.4× 682 1.4× 86 0.2× 185 0.7× 386 1.8× 39 2.8k
Verónica Palma Chile 24 1.4k 0.9× 318 0.6× 141 0.4× 285 1.1× 123 0.6× 64 2.1k

Countries citing papers authored by Martin Cheung

Since Specialization
Citations

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

Fields of papers citing papers by Martin Cheung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Cheung

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Cheung. A scholar is included among the top collaborators of Martin 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 Martin Cheung. Martin Cheung 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
2.
Chen, Yonglong, Chaoyang Fan, Stanley Sau Ching Wong, et al.. (2024). Intrinsic and extrinsic actions of human neural progenitors with SUFU inhibition promote tissue repair and functional recovery from severe spinal cord injury. npj Regenerative Medicine. 9(1). 13–13. 3 indexed citations
3.
So, Joan, Lei Peng, Lina Zhu, et al.. (2024). TSPYL1 as a Critical Regulator of TGFβ Signaling through Repression of TGFBR1 and TSPYL2. Advanced Science. 11(21). e2306486–e2306486. 3 indexed citations
4.
Yu, Jing, Stanley Sau Ching Wong, Zhiming Shan, et al.. (2024). High‐Frequency Spinal Stimulation Suppresses Microglial Kaiso‐P2X7 Receptor Axis‐Induced Inflammation to Alleviate Neuropathic Pain in Rats. Annals of Neurology. 95(5). 966–983. 5 indexed citations
5.
Wang, Xue, Feng Chen, Peikai Chen, et al.. (2024). Suppression of apoptosis impairs phalangeal joint formation in the pathogenesis of brachydactyly type A1. Nature Communications. 15(1). 2229–2229. 3 indexed citations
6.
Cheung, Martin, et al.. (2021). Urine-derived induced pluripotent/neural stem cells for modeling neurological diseases. Cell & Bioscience. 11(1). 85–85. 16 indexed citations
7.
Liu, Jessica Aijia, et al.. (2020). Fbxo9 functions downstream of Sox10 to determine neuron-glial fate choice in the dorsal root ganglia through Neurog2 destabilization. Proceedings of the National Academy of Sciences. 117(8). 4199–4210. 15 indexed citations
8.
Yang, Xintao, Feng Hu, Jessica Aijia Liu, et al.. (2020). Nuclear DLC1 exerts oncogenic function through association with FOXK1 for cooperative activation of MMP9 expression in melanoma. Oncogene. 39(20). 4061–4076. 13 indexed citations
9.
Yang, Xintao, Rui Liang, Chunxi Liu, et al.. (2019). SOX9 is a dose-dependent metastatic fate determinant in melanoma. Journal of Experimental & Clinical Cancer Research. 38(1). 17–17. 27 indexed citations
10.
Liu, Jessica Aijia, Yanxia Rao, Lo‐Kong Chan, et al.. (2017). Asymmetric localization of DLC1 defines avian trunk neural crest polarity for directional delamination and migration. Nature Communications. 8(1). 1185–1185. 15 indexed citations
11.
Wang, Yinxiang, MH Sham, Haruhiko Akiyama, et al.. (2017). Reprogramming of Dermal Fibroblasts into Osteo-Chondrogenic Cells with Elevated Osteogenic Potency by Defined Transcription Factors. Stem Cell Reports. 8(6). 1587–1599. 17 indexed citations
12.
Liu, Jessica Aijia & Martin Cheung. (2016). Neural crest stem cells and their potential therapeutic applications. Developmental Biology. 419(2). 199–216. 60 indexed citations
13.
Cheung, Martin, et al.. (2014). Homeobox b5 (Hoxb5) regulates the expression of Forkhead box D3 gene (Foxd3) in neural crest. The International Journal of Biochemistry & Cell Biology. 55. 144–152. 8 indexed citations
14.
Zheng, Fan, Tianpeng Li, Martin Cheung, Viktoriya Syrovatkina, & Chuanhai Fu. (2014). Mcp1p tracks microtubule plus ends to destabilize microtubules at cell tips. FEBS Letters. 588(6). 859–865. 5 indexed citations
15.
Tsang, Kwok Yeung, Martin Cheung, Danny Chan, & Kathryn S.E. Cheah. (2009). The developmental roles of the extracellular matrix: beyond structure to regulation. Cell and Tissue Research. 339(1). 93–110. 123 indexed citations
16.
Gao, Bo, Jianxin Hu, Sigmar Stricker, et al.. (2009). A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature. 458(7242). 1196–1200. 78 indexed citations
17.
Haines, Anthony S., Martin Cheung, & Christopher M. Thomas. (2006). Evidence that IncG (IncP-6) and IncU plasmids form a single incompatibility group. Plasmid. 55(3). 210–215. 11 indexed citations
18.
Cheung, Martin, et al.. (2002). CIC, a member of a novel subfamily of the HMG-box superfamily, is transiently expressed in developing granule neurons. Molecular Brain Research. 106(1-2). 151–156. 49 indexed citations
19.
Abu‐Elmagd, Muhammad, et al.. (2001). cSox3 Expression and Neurogenesis in the Epibranchial Placodes. Developmental Biology. 237(2). 258–269. 52 indexed citations
20.
Cheng, Yi‐Chuan, Martin Cheung, Muhammad Abu‐Elmagd, Alex Orme, & Paul J. Scotting. (2000). Chick Sox10, a transcription factor expressed in both early neural crest cells and central nervous system. Developmental Brain Research. 121(2). 233–241. 152 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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