Yaoxing Wu

2.4k total citations
35 papers, 1.5k citations indexed

About

Yaoxing Wu is a scholar working on Molecular Biology, Immunology and Epidemiology. According to data from OpenAlex, Yaoxing Wu has authored 35 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Immunology and 14 papers in Epidemiology. Recurrent topics in Yaoxing Wu's work include interferon and immune responses (15 papers), Autophagy in Disease and Therapy (13 papers) and Ubiquitin and proteasome pathways (7 papers). Yaoxing Wu is often cited by papers focused on interferon and immune responses (15 papers), Autophagy in Disease and Therapy (13 papers) and Ubiquitin and proteasome pathways (7 papers). Yaoxing Wu collaborates with scholars based in China and United States. Yaoxing Wu's co-authors include Jun Cui, Shouheng Jin, Weihong Xie, Qingxiang Liu, Ling Ma, Tao Liu, Zhiyao Zhao, Shuo Tian, Shuai Yang and Yi‐Ping Li and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Yaoxing Wu

31 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yaoxing Wu China 19 693 617 507 389 329 35 1.5k
Takayuki Hishiki Japan 23 844 1.2× 620 1.0× 441 0.9× 1.0k 2.6× 313 1.0× 44 2.6k
St. Patrick Reid United States 15 512 0.7× 573 0.9× 945 1.9× 373 1.0× 94 0.3× 17 1.9k
Tony T. Wang United States 21 572 0.8× 286 0.5× 765 1.5× 196 0.5× 181 0.6× 49 1.8k
Xianwen Zhang China 15 668 1.0× 403 0.7× 1.9k 3.7× 219 0.6× 250 0.8× 49 2.5k
Marc Aumercier France 20 668 1.0× 428 0.7× 313 0.6× 306 0.8× 146 0.4× 43 1.5k
Marc P. Windisch South Korea 21 502 0.7× 226 0.4× 410 0.8× 574 1.5× 106 0.3× 57 1.6k
Shihua He Canada 28 999 1.4× 180 0.3× 703 1.4× 317 0.8× 104 0.3× 70 2.0k
Kai S. Yang China 20 532 0.8× 556 0.9× 319 0.6× 200 0.5× 48 0.1× 39 1.3k
Amie J. Eisfeld United States 22 756 1.1× 651 1.1× 496 1.0× 1.1k 2.9× 61 0.2× 34 1.9k
Mustafa Ulaşlı Türkiye 16 613 0.9× 159 0.3× 628 1.2× 299 0.8× 109 0.3× 35 1.6k

Countries citing papers authored by Yaoxing Wu

Since Specialization
Citations

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

Fields of papers citing papers by Yaoxing Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yaoxing Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Yaoxing Wu. A scholar is included among the top collaborators of Yaoxing Wu 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 Yaoxing Wu. Yaoxing Wu 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.
Jin, Shouheng, Xing He, Zheyu Wang, et al.. (2025). Oxaloacetate sensing promotes innate immune antiviral defence against influenza virus infection. Nature Microbiology. 10(10). 2521–2536.
3.
Wang, Liqiu, Mengqiu Li, Guang‐Yu Lian, et al.. (2024). Palmitoylation acts as a checkpoint for MAVS aggregation to promote antiviral innate immune responses. Journal of Clinical Investigation. 134(23). 6 indexed citations
4.
He, Xing, Haowei He, Zheyu Wang, et al.. (2024). ER-phagy restrains inflammatory responses through its receptor UBAC2. The EMBO Journal. 43(21). 5057–5084. 3 indexed citations
5.
Wu, Yaoxing, et al.. (2024). Physiologically based kinetic (PBK) modeling of propiconazole using a machine learning-enhanced read-across approach for interspecies extrapolation. Environment International. 189. 108804–108804. 4 indexed citations
6.
Cai, Sihui, Zhen Zhuang, Shengnan Zhang, et al.. (2023). Phase-separated nucleocapsid protein of SARS-CoV-2 suppresses cGAS-DNA recognition by disrupting cGAS-G3BP1 complex. Signal Transduction and Targeted Therapy. 8(1). 170–170. 30 indexed citations
7.
Yang, Shuai, Shouheng Jin, Huifang Xian, et al.. (2023). Metabolic enzyme UAP1 mediates IRF3 pyrophosphorylation to facilitate innate immune response. Molecular Cell. 83(2). 298–313.e8. 13 indexed citations
8.
Yang, Shuai, Jiajia Hu, Sihui Cai, et al.. (2023). Molecular mechanisms and cellular functions of liquid-liquid phase separation during antiviral immune responses. Frontiers in Immunology. 14. 1162211–1162211. 14 indexed citations
10.
Jin, Shouheng, Xing He, Ling Ma, et al.. (2022). Suppression of ACE2 SUMOylation protects against SARS-CoV-2 infection through TOLLIP-mediated selective autophagy. Nature Communications. 13(1). 5204–5204. 41 indexed citations
11.
Zhou, Tao, Jiajia Hu, Shouheng Jin, et al.. (2022). Targeting Selective Autophagy as a Therapeutic Strategy for Viral Infectious Diseases. Frontiers in Microbiology. 13. 889835–889835. 16 indexed citations
12.
Wu, Yaoxing, Ling Ma, Sihui Cai, et al.. (2021). RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation. Signal Transduction and Targeted Therapy. 6(1). 167–167. 115 indexed citations
13.
Tian, Shuo, Shouheng Jin, Yaoxing Wu, et al.. (2020). High-throughput screening of functional deubiquitinating enzymes in autophagy. Autophagy. 17(6). 1367–1378. 20 indexed citations
14.
Xie, Weihong, Shouheng Jin, Yaoxing Wu, et al.. (2020). Auto-ubiquitination of NEDD4-1 Recruits USP13 to Facilitate Autophagy through Deubiquitinating VPS34. Cell Reports. 30(8). 2807–2819.e4. 50 indexed citations
15.
Wu, Yaoxing, Shouheng Jin, & Jun Cui. (2019). Autophagy and Immune Tolerance. Advances in experimental medicine and biology. 1206. 635–665. 12 indexed citations
16.
Wu, Yaoxing & Jun Cui. (2019). Selective Autophagy Regulates Innate Immunity Through Cargo Receptor Network. Advances in experimental medicine and biology. 1209. 145–166. 8 indexed citations
17.
Jin, Shouheng, Shuo Tian, Man Luo, et al.. (2017). Tetherin Suppresses Type I Interferon Signaling by Targeting MAVS for NDP52-Mediated Selective Autophagic Degradation in Human Cells. Molecular Cell. 68(2). 308–322.e4. 168 indexed citations
18.
Wu, Yaoxing, Qingxiang Liu, Jie Zhou, et al.. (2017). Zika virus evades interferon-mediated antiviral response through the co-operation of multiple nonstructural proteins in vitro. Cell Discovery. 3(1). 17006–17006. 177 indexed citations
19.
Qin, Yunfei, Yaoxing Wu, Shouheng Jin, et al.. (2017). NLRP 11 disrupts MAVS signalosome to inhibit type I interferon signaling and virus‐induced apoptosis. EMBO Reports. 18(12). 2160–2171. 26 indexed citations
20.
Wang, Shanshan, Yongzhi Chen, Chunfeng Li, et al.. (2016). TRIM14 inhibits hepatitis C virus infection by SPRY domain-dependent targeted degradation of the viral NS5A protein. Scientific Reports. 6(1). 32336–32336. 62 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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