Tso‐Pang Yao

11.8k total citations · 3 hit papers
64 papers, 9.6k citations indexed

About

Tso‐Pang Yao is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Tso‐Pang Yao has authored 64 papers receiving a total of 9.6k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 23 papers in Oncology and 13 papers in Genetics. Recurrent topics in Tso‐Pang Yao's work include Histone Deacetylase Inhibitors Research (32 papers), Ubiquitin and proteasome pathways (16 papers) and Peptidase Inhibition and Analysis (14 papers). Tso‐Pang Yao is often cited by papers focused on Histone Deacetylase Inhibitors Research (32 papers), Ubiquitin and proteasome pathways (16 papers) and Peptidase Inhibition and Analysis (14 papers). Tso‐Pang Yao collaborates with scholars based in United States, Japan and China. Tso‐Pang Yao's co-authors include Amaris R. Guardiola, Charlotte Hubbert, David M. Livingston, Yoshiharu Kawaguchi, Minoru Yoshida, Akihiro Ito, Xiao‐Fan Wang, Rong Shao, Andrew B. Nixon and Joo‐Yong Lee and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Tso‐Pang Yao

64 papers receiving 9.5k citations

Hit Papers

HDAC6 is a microtubule-associated deacetylase 1993 2026 2004 2015 2002 1993 2001 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tso‐Pang Yao United States 40 7.1k 2.1k 1.3k 1.3k 1.2k 64 9.6k
Tso-Pang Yao United States 23 6.3k 0.9× 1.5k 0.7× 1.2k 0.9× 515 0.4× 925 0.8× 24 8.2k
Jongkyeong Chung South Korea 50 5.0k 0.7× 1.2k 0.6× 1.2k 0.9× 1.3k 1.0× 508 0.4× 119 8.3k
Dirk Bohmann United States 49 7.7k 1.1× 1.3k 0.6× 1.4k 1.1× 1.8k 1.4× 999 0.8× 84 10.6k
Shengyun Fang United States 43 5.9k 0.8× 1.5k 0.7× 744 0.6× 835 0.7× 652 0.5× 107 8.6k
Parmjit Jat United Kingdom 44 4.6k 0.6× 1.6k 0.7× 606 0.5× 972 0.8× 1.1k 0.9× 114 7.8k
Patrick Matthias Switzerland 52 9.3k 1.3× 2.4k 1.1× 836 0.6× 3.4k 2.6× 1.7k 1.4× 109 13.6k
Sheng‐Cai Lin China 45 8.2k 1.2× 1.3k 0.6× 739 0.6× 1.6k 1.3× 1.7k 1.3× 90 11.4k
Tod Smeal United States 33 9.2k 1.3× 2.8k 1.3× 1.3k 1.0× 1.8k 1.4× 1.8k 1.4× 52 12.9k
Alberto Gulino Italy 60 7.3k 1.0× 2.4k 1.1× 720 0.6× 1.8k 1.4× 1.7k 1.4× 258 11.7k
Andrew Elia Canada 45 10.6k 1.5× 2.5k 1.2× 1.2k 0.9× 3.4k 2.7× 1.2k 0.9× 76 15.1k

Countries citing papers authored by Tso‐Pang Yao

Since Specialization
Citations

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

Fields of papers citing papers by Tso‐Pang Yao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tso‐Pang Yao. 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 Tso‐Pang Yao. The network helps show where Tso‐Pang Yao may publish in the future.

Co-authorship network of co-authors of Tso‐Pang Yao

This figure shows the co-authorship network connecting the top 25 collaborators of Tso‐Pang Yao. A scholar is included among the top collaborators of Tso‐Pang Yao 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 Tso‐Pang Yao. Tso‐Pang Yao 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.
Lin, Chao‐Chieh, Jin Yan, Meghan Kapur, et al.. (2022). Parkin coordinates mitochondrial lipid remodeling to execute mitophagy. EMBO Reports. 23(12). e55191–e55191. 14 indexed citations
2.
Lin, Chao‐Chieh, Nathaniel W. Mabe, Yi-Tzu Lin, et al.. (2020). RIPK3 upregulation confers robust proliferation and collateral cystine-dependence on breast cancer recurrence. Cell Death and Differentiation. 27(7). 2234–2247. 45 indexed citations
3.
4.
Lin, Chao‐Chieh, Mayumi Kitagawa, Xiaohu Tang, et al.. (2018). CoA synthase regulates mitotic fidelity via CBP-mediated acetylation. Nature Communications. 9(1). 1039–1039. 35 indexed citations
5.
Choi, Su Jin, Hyun‐Cheol Lee, Jaehoon Kim, et al.. (2016). HDAC 6 regulates cellular viral RNA sensing by deacetylation of RIG ‐I. The EMBO Journal. 35(4). 429–442. 106 indexed citations
6.
Lee, Joo‐Yong, Yoshiharu Kawaguchi, Ming Li, et al.. (2015). Uncoupling of Protein Aggregation and Neurodegeneration in a Mouse Amyotrophic Lateral Sclerosis Model. Neurodegenerative Diseases. 15(6). 339–349. 21 indexed citations
7.
Kim, Nam Chul, Emilie Tresse, Regina‐Maria Kolaitis, et al.. (2013). VCP Is Essential for Mitochondrial Quality Control by PINK1/Parkin and this Function Is Impaired by VCP Mutations. Neuron. 78(2). 403–403. 6 indexed citations
8.
Fukada, Masahide, Atsuo Nakayama, Takayoshi Suzuki, et al.. (2012). Loss of Deacetylation Activity of Hdac6 Affects Emotional Behavior in Mice. PLoS ONE. 7(2). e30924–e30924. 97 indexed citations
9.
Gao, Ya‐sheng, Charlotte Hubbert, & Tso‐Pang Yao. (2010). The Microtubule-associated Histone Deacetylase 6 (HDAC6) Regulates Epidermal Growth Factor Receptor (EGFR) Endocytic Trafficking and Degradation. Journal of Biological Chemistry. 285(15). 11219–11226. 136 indexed citations
10.
Lee, Joo‐Yong & Tso‐Pang Yao. (2010). Quality control autophagy: A joint effort of ubiquitin, protein deacetylase and actin cytoskeleton. Autophagy. 6(4). 555–557. 39 indexed citations
11.
Lee, Yi-Shan, Kian‐Huat Lim, Xingrong Guo, et al.. (2008). The Cytoplasmic Deacetylase HDAC6 Is Required for Efficient Oncogenic Tumorigenesis. Cancer Research. 68(18). 7561–7569. 220 indexed citations
12.
Shan, Bin, Tso‐Pang Yao, Hong T. Nguyen, et al.. (2008). Requirement of HDAC6 for Transforming Growth Factor-β1-induced Epithelial-Mesenchymal Transition. Journal of Biological Chemistry. 283(30). 21065–21073. 149 indexed citations
13.
Kamemura, Kazuo, Akihiro Ito, Tadahiro Shimazu, et al.. (2008). Effects of downregulated HDAC6 expression on the proliferation of lung cancer cells. Biochemical and Biophysical Research Communications. 374(1). 84–89. 27 indexed citations
14.
Kovacs, Jeffrey J., Todd J. Cohen, & Tso‐Pang Yao. (2005). Chaperoning steroid hormone signaling via reversible acetylation. PubMed. 3(1). e004–e004. 27 indexed citations
15.
Yang, Chih‐Sheng, Hsiao-Ching Chuang, Ching‐Wen Chang, et al.. (2005). FBW2 Targets GCMa to the Ubiquitin-Proteasome Degradation System. Journal of Biological Chemistry. 280(11). 10083–10090. 45 indexed citations
16.
Hubbert, Charlotte, et al.. (2004). The HDAC Complex and Cytoskeleton. Novartis Foundation symposium. 259. 170–181. 11 indexed citations
17.
Guardiola, Amaris R. & Tso‐Pang Yao. (2002). Molecular Cloning and Characterization of a Novel Histone Deacetylase HDAC10. Journal of Biological Chemistry. 277(5). 3350–3356. 202 indexed citations
18.
Tsai, Chih‐Cheng, Hung‐Ying Kao, Tso‐Pang Yao, Mick McKeown, & Ronald M. Evans. (1999). SMRTER, a Drosophila Nuclear Receptor Coregulator, Reveals that EcR-Mediated Repression Is Critical for Development. Molecular Cell. 4(2). 175–186. 177 indexed citations
19.
Kawasaki, Hiroaki, Richard Eckner, Tso‐Pang Yao, et al.. (1998). Distinct roles of the co-activators p300 and CBP in retinoic-acid-induced F9-cell differentiation. Nature. 393(6682). 284–289. 273 indexed citations
20.
Zelhof, Andrew C., et al.. (1995). Seven-up Inhibits Ultraspiracle-Based Signaling Pathways In Vitro and In Vivo. Molecular and Cellular Biology. 15(12). 6736–6745. 75 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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