Chen‐Ying Liu

3.9k total citations · 1 hit paper
56 papers, 3.0k citations indexed

About

Chen‐Ying Liu is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Chen‐Ying Liu has authored 56 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 22 papers in Cell Biology and 13 papers in Oncology. Recurrent topics in Chen‐Ying Liu's work include Hippo pathway signaling and YAP/TAZ (19 papers), Wnt/β-catenin signaling in development and cancer (7 papers) and Ubiquitin and proteasome pathways (6 papers). Chen‐Ying Liu is often cited by papers focused on Hippo pathway signaling and YAP/TAZ (19 papers), Wnt/β-catenin signaling in development and cancer (7 papers) and Ubiquitin and proteasome pathways (6 papers). Chen‐Ying Liu collaborates with scholars based in China, United States and Singapore. Chen‐Ying Liu's co-authors include Qun‐Ying Lei, Kun‐Liang Guan, Bin Zhao, Yue Xiong, Long Cui, Zhengyu Zha, Shimin Zhao, Q. Richard Lu, Li Li and Wei Huang and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Genes & Development.

In The Last Decade

Chen‐Ying Liu

55 papers receiving 3.0k citations

Hit Papers

Angiomotin is a novel Hippo pathway component that inhibi... 2011 2026 2016 2021 2011 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chen‐Ying Liu China 26 1.8k 1.8k 498 361 170 56 3.0k
Chunling Yi United States 19 1.4k 0.8× 1.1k 0.6× 526 1.1× 211 0.6× 138 0.8× 23 2.3k
Julien Fitamant United States 14 1.7k 0.9× 989 0.6× 648 1.3× 468 1.3× 463 2.7× 17 2.8k
Wannian Yang United States 28 1.6k 0.9× 730 0.4× 346 0.7× 236 0.7× 225 1.3× 54 2.1k
Olivier E. Pardo United Kingdom 24 1.9k 1.0× 561 0.3× 546 1.1× 552 1.5× 152 0.9× 47 2.5k
G B Mills United States 17 1.4k 0.8× 1.2k 0.7× 367 0.7× 249 0.7× 80 0.5× 19 2.5k
Qiong Lin China 23 1.4k 0.8× 459 0.3× 287 0.6× 227 0.6× 212 1.2× 59 1.8k
Michael DeRan United States 12 899 0.5× 800 0.4× 212 0.4× 150 0.4× 54 0.3× 13 1.5k
Imelda Mercado‐Uribe United States 24 1.2k 0.7× 421 0.2× 922 1.9× 756 2.1× 111 0.7× 28 2.2k
Roy Katso United Kingdom 13 1.9k 1.0× 466 0.3× 409 0.8× 206 0.6× 131 0.8× 15 2.6k
Anthony Polverino United States 18 2.3k 1.3× 463 0.3× 697 1.4× 240 0.7× 69 0.4× 29 2.8k

Countries citing papers authored by Chen‐Ying Liu

Since Specialization
Citations

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

Fields of papers citing papers by Chen‐Ying Liu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chen‐Ying Liu. 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 Chen‐Ying Liu. The network helps show where Chen‐Ying Liu may publish in the future.

Co-authorship network of co-authors of Chen‐Ying Liu

This figure shows the co-authorship network connecting the top 25 collaborators of Chen‐Ying Liu. A scholar is included among the top collaborators of Chen‐Ying Liu 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 Chen‐Ying Liu. Chen‐Ying Liu 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.
Zhu, Zhehui, Rui Ding, Wei Yu, et al.. (2025). YAP/TEAD4/SP1-induced VISTA expression as a tumor cell-intrinsic mechanism of immunosuppression in colorectal cancer. Cell Death and Differentiation. 32(5). 911–925. 3 indexed citations
2.
Xu, Weimin, Wenbo Tang, Wensong Ge, et al.. (2025). Redox‐Induced Stabilization of AMBRA1 by USP7 Promotes Intestinal Oxidative Stress and Colitis Through Antagonizing DUB3‐Mediated NRF2 Deubiquitination. Advanced Science. 12(12). e2411320–e2411320. 1 indexed citations
3.
Tang, Wenbo, Yi‐Qing Yang, Weimin Xu, et al.. (2024). The RNA helicase DDX21 activates YAP to promote tumorigenesis and is transcriptionally upregulated by β-catenin in colorectal cancer. Oncogene. 43(44). 3227–3239. 1 indexed citations
4.
Li, Lingling, Dongxian Jiang, Qiao Zhang, et al.. (2024). Comprehensive Proteogenomic Profiling Reveals the Molecular Characteristics of Colorectal Cancer at Distinct Stages of Progression. Cancer Research. 84(17). 2888–2910. 3 indexed citations
5.
Wang, Xuefei, Yuegui Guo, Jie Zhong, et al.. (2024). Computer-aided molecular design and optimization of potent inhibitors disrupting APC‒Asef interaction. Acta Pharmaceutica Sinica B. 14(6). 2631–2645. 4 indexed citations
6.
Wang, Chao, Zhen Wu, Changchun Wang, et al.. (2024). Aspirin‐Mediated Acetylation of SIRT1 Maintains Intestinal Immune Homeostasis. Advanced Science. 11(19). e2306378–e2306378. 5 indexed citations
7.
Xu, Weimin, Yaosheng Wang, Wenbo Tang, et al.. (2024). AMBRA1 promotes intestinal inflammation by antagonizing PP4R1/PP4c mediated IKK dephosphorylation in an autophagy-independent manner. Cell Death and Differentiation. 31(5). 618–634. 6 indexed citations
8.
Bao, Weilian, Yan You, Jiahui Ni, et al.. (2023). Inhibiting sorting nexin 10 promotes mucosal healing through SREBP2-mediated stemness restoration of intestinal stem cells. Science Advances. 9(35). eadh5016–eadh5016. 15 indexed citations
9.
Song, Jinglue, Xia Shen, Yun Liu, et al.. (2023). The YAP–TEAD4 complex promotes tumor lymphangiogenesis by transcriptionally upregulating CCBE1 in colorectal cancer. Journal of Biological Chemistry. 299(4). 103012–103012. 12 indexed citations
10.
Qian, Xiaolong, Yaqing Li, Chen‐Ying Liu, et al.. (2023). Effects of tumor-infiltrating lymphocytes on nonresponse rate of neoadjuvant chemotherapy in patients with invasive breast cancer. Scientific Reports. 13(1). 9256–9256. 4 indexed citations
11.
Zhong, Jie, Yuegui Guo, Shaoyong Lu, et al.. (2022). Rational design of a sensitivity-enhanced tracer for discovering efficient APC–Asef inhibitors. Nature Communications. 13(1). 4961–4961. 10 indexed citations
12.
Liu, Fangyuan, Weijun Ou, Wenbo Tang, et al.. (2021). Increased AOC1 Expression Promotes Cancer Progression in Colorectal Cancer. Frontiers in Oncology. 11. 657210–657210. 21 indexed citations
13.
Gu, Chang, Zhenyu Huang, Chen‐Ying Liu, et al.. (2020). TEAD4 promotes tumor development in patients with lung adenocarcinoma via ERK signaling pathway. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(12). 165921–165921. 45 indexed citations
14.
Wang, Yuhan, Zhehui Zhu, Zhenyu Huang, et al.. (2020). Bromodomain and Extraterminal (BET) protein inhibition suppresses tumor progression and inhibits HGF-MET signaling through targeting cancer-associated fibroblasts in colorectal cancer. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(12). 165923–165923. 7 indexed citations
15.
Wu, Tingyu, Guanghui Wang, Wei Chen, et al.. (2018). Co-inhibition of BET proteins and NF-κB as a potential therapy for colorectal cancer through synergistic inhibiting MYC and FOXM1 expressions. Cell Death and Disease. 9(3). 315–315. 35 indexed citations
16.
Liu, Chen‐Ying, et al.. (2017). ETS (E26 transformation-specific) up-regulation of the transcriptional co-activator TAZ promotes cell migration and metastasis in prostate cancer. Journal of Biological Chemistry. 292(22). 9420–9430. 43 indexed citations
17.
Wu, Tingyu, Wei Chen, Yongwang Zhong, et al.. (2016). Nuclear Export of Ubiquitinated Proteins Determines the Sensitivity of Colorectal Cancer to Proteasome Inhibitor. Molecular Cancer Therapeutics. 16(4). 717–728. 17 indexed citations
18.
Liu, Chen‐Ying, Zhengyu Zha, Xin Zhou, et al.. (2010). The Hippo Tumor Pathway Promotes TAZ Degradation by Phosphorylating a Phosphodegron and Recruiting the SCFβ-TrCP E3 Ligase. Journal of Biological Chemistry. 285(48). 37159–37169. 435 indexed citations
19.
Liu, Chen‐Ying, Tingting Li, Yanping Xu, et al.. (2010). PP1 Cooperates with ASPP2 to Dephosphorylate and Activate TAZ. Journal of Biological Chemistry. 286(7). 5558–5566. 111 indexed citations
20.
Zhang, Heng, Chen‐Ying Liu, Zhengyu Zha, et al.. (2009). TEAD Transcription Factors Mediate the Function of TAZ in Cell Growth and Epithelial-Mesenchymal Transition. Journal of Biological Chemistry. 284(20). 13355–13362. 459 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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