Ping‐Chieh Chou

1.7k total citations
23 papers, 1.1k citations indexed

About

Ping‐Chieh Chou is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Ping‐Chieh Chou has authored 23 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 8 papers in Oncology and 8 papers in Cancer Research. Recurrent topics in Ping‐Chieh Chou's work include Ubiquitin and proteasome pathways (6 papers), Cancer, Hypoxia, and Metabolism (5 papers) and Cancer-related Molecular Pathways (5 papers). Ping‐Chieh Chou is often cited by papers focused on Ubiquitin and proteasome pathways (6 papers), Cancer, Hypoxia, and Metabolism (5 papers) and Cancer-related Molecular Pathways (5 papers). Ping‐Chieh Chou collaborates with scholars based in United States, China and Taiwan. Ping‐Chieh Chou's co-authors include Mong‐Hong Lee, Liem Phan, Sai‐Ching J. Yeung, Hyun Ho Choi, Lance D. Miller, Suyun Huang, Ümit Topaloĝlu, Stacey S. O’Neill, Gregory A. Hawkins and Wei Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Molecular Cell.

In The Last Decade

Ping‐Chieh Chou

23 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ping‐Chieh Chou United States 17 708 371 262 133 131 23 1.1k
Loredana Moro Italy 24 1.2k 1.7× 278 0.7× 588 2.2× 188 1.4× 101 0.8× 45 1.6k
Natalie I. Vokes United States 12 714 1.0× 228 0.6× 501 1.9× 203 1.5× 98 0.7× 46 1.1k
Latha Ramdas United States 24 1.2k 1.6× 245 0.7× 413 1.6× 94 0.7× 117 0.9× 46 1.5k
H. Artee Luchman Canada 24 850 1.2× 398 1.1× 542 2.1× 125 0.9× 147 1.1× 43 1.6k
Antonio Ramos‐Montoya United Kingdom 22 923 1.3× 388 1.0× 428 1.6× 417 3.1× 105 0.8× 38 1.4k
Cem Elbi United States 23 1.4k 2.0× 462 1.2× 219 0.8× 323 2.4× 197 1.5× 38 2.2k
J.M. Ostrem United States 6 1.9k 2.7× 818 2.2× 225 0.9× 301 2.3× 98 0.7× 8 2.4k
Flonné Wildes United States 21 849 1.2× 426 1.1× 517 2.0× 140 1.1× 111 0.8× 43 1.4k
Megan D. Hoeksema United States 13 794 1.1× 210 0.6× 552 2.1× 278 2.1× 101 0.8× 13 1.2k
Oliver N. F. King United Kingdom 14 1.9k 2.7× 194 0.5× 610 2.3× 100 0.8× 275 2.1× 20 2.4k

Countries citing papers authored by Ping‐Chieh Chou

Since Specialization
Citations

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

Fields of papers citing papers by Ping‐Chieh Chou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ping‐Chieh Chou. 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 Ping‐Chieh Chou. The network helps show where Ping‐Chieh Chou may publish in the future.

Co-authorship network of co-authors of Ping‐Chieh Chou

This figure shows the co-authorship network connecting the top 25 collaborators of Ping‐Chieh Chou. A scholar is included among the top collaborators of Ping‐Chieh Chou 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 Ping‐Chieh Chou. Ping‐Chieh Chou 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.
Li, Tao, Farideh Mehraein‐Ghomi, M. Elizabeth Forbes, et al.. (2022). HSP90-CDC37 functions as a chaperone for the oncogenic FGFR3-TACC3 fusion. Molecular Therapy. 30(4). 1610–1627. 11 indexed citations
2.
Chou, Ping‐Chieh, Hyun Ho Choi, Yizhi Huang, et al.. (2021). Impact of diabetes on promoting the growth of breast cancer. Cancer Communications. 41(5). 414–431. 17 indexed citations
3.
Liu, Liang, Tamjeed Ahmed, W. Jeffrey Petty, et al.. (2020). SMARCA4 mutations in KRAS ‐mutant lung adenocarcinoma: a multi‐cohort analysis. Molecular Oncology. 15(2). 462–472. 46 indexed citations
4.
Wen, Kuo‐Chang, Pi‐Lin Sung, Alexander T.H. Wu, et al.. (2020). Neoadjuvant metformin added to conventional chemotherapy synergizes anti-proliferative effects in ovarian cancer. Journal of Ovarian Research. 13(1). 95–95. 18 indexed citations
5.
Song, Qianqian, Gregory A. Hawkins, L. James Wudel, et al.. (2019). Abstract 3391: Dissecting intratumoral cell-cell interactions in myeloid reprogramming by single cell RNA-seq. Cancer Research. 79(13_Supplement). 3391–3391. 1 indexed citations
6.
Song, Qianqian, Gregory A. Hawkins, L. James Wudel, et al.. (2019). Dissecting intratumoral myeloid cell plasticity by single cell RNA‐seq. Cancer Medicine. 8(6). 3072–3085. 108 indexed citations
7.
Li, Tao, Farideh Mehraein‐Ghomi, Qian Song, et al.. (2019). Abstract B036: Targeting Hsp90-Cdc37 complex in glioma harboring FGFR3-TACC3. Molecular Cancer Therapeutics. 18(12_Supplement). B036–B036. 1 indexed citations
8.
Chen, Tao, Jingjie Li, Mei‐Dong Xu, et al.. (2017). PKCε phosphorylates MIIP and promotes colorectal cancer metastasis through inhibition of RelA deacetylation. Nature Communications. 8(1). 939–939. 40 indexed citations
9.
Yang, Mei, M. Elizabeth Forbes, Rhonda L. Bitting, et al.. (2017). Incorporating blood-based liquid biopsy information into cancer staging: time for a TNMB system?. Annals of Oncology. 29(2). 311–323. 72 indexed citations
10.
Zhang, Xian, Binkui Li, Abdol Hossein Rezaeian, et al.. (2017). H3 ubiquitination by NEDD4 regulates H3 acetylation and tumorigenesis. Nature Communications. 8(1). 14799–14799. 35 indexed citations
11.
Li, Chien‐Feng, Ching-Yuan Wu, Xian Zhang, et al.. (2016). A hypoxia-responsive TRAF6–ATM–H2AX signalling axis promotes HIF1α activation, tumorigenesis and metastasis. Nature Cell Biology. 19(1). 38–51. 91 indexed citations
12.
Bankson, James A., Christopher M. Walker, Marc S. Ramirez, et al.. (2015). Kinetic Modeling and Constrained Reconstruction of Hyperpolarized [1-13C]-Pyruvate Offers Improved Metabolic Imaging of Tumors. Cancer Research. 75(22). 4708–4717. 70 indexed citations
13.
Jin, Guoxiang, Szu-Wei Lee, Xian Zhang, et al.. (2015). Skp2-Mediated RagA Ubiquitination Elicits a Negative Feedback to Prevent Amino-Acid-Dependent mTORC1 Hyperactivation by Recruiting GATOR1. Molecular Cell. 58(6). 989–1000. 67 indexed citations
14.
Choi, Hyun Ho, Liem Phan, Ping‐Chieh Chou, et al.. (2015). COP1 enhances ubiquitin-mediated degradation of p27Kip1 to promote cancer cell growth. Oncotarget. 6(23). 19721–19734. 25 indexed citations
15.
Chou, Ping‐Chieh, Liem Phan, Jian Chen, et al.. (2013). DNA Damage-Mediated c-Myc Degradation Requires 14-3-3 Sigma. 1(1). 3–17. 12 indexed citations
16.
Xue, Yuwen, Jian Chen, Liem Phan, et al.. (2012). HER2-Akt signaling in regulating COP9 signalsome subunit 6 and p53. Cell Cycle. 11(22). 4181–4190. 28 indexed citations
17.
Choi, Hyun Ho, Christopher Gully, Guermarie Velázquez-Torres, et al.. (2011). COP9 signalosome subunit 6 stabilizes COP1, which functions as an E3 ubiquitin ligase for 14-3-3σ. Oncogene. 30(48). 4791–4801. 44 indexed citations
18.
Steeg, Patricia S., Janet E. Price, Wen‐Tai Chiu, et al.. (2008). Molecular Basis for the Critical Role of Suppressor of Cytokine Signaling-1 in Melanoma Brain Metastasis. Cancer Research. 68(23). 9634–9642. 69 indexed citations
19.
Bao, Xinhua, Ye Wu, Lee‐Jun C. Wong, et al.. (2007). Alpers syndrome with prominent white matter changes. Brain and Development. 30(4). 295–300. 13 indexed citations
20.
Wong, Lee-Jun, Nicola Brunetti‐Pierri, Qing Zhang, et al.. (2007). Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy. Hepatology. 46(4). 1218–1227. 94 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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