Yongbin Chen

6.9k total citations · 2 hit papers
61 papers, 4.5k citations indexed

About

Yongbin Chen is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Yongbin Chen has authored 61 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 17 papers in Cancer Research and 10 papers in Genetics. Recurrent topics in Yongbin Chen's work include Hedgehog Signaling Pathway Studies (10 papers), Epigenetics and DNA Methylation (10 papers) and Cancer-related molecular mechanisms research (8 papers). Yongbin Chen is often cited by papers focused on Hedgehog Signaling Pathway Studies (10 papers), Epigenetics and DNA Methylation (10 papers) and Cancer-related molecular mechanisms research (8 papers). Yongbin Chen collaborates with scholars based in China, United States and Hong Kong. Yongbin Chen's co-authors include Jin Jiang, Cuiping Yang, Qiuxia Xiong, Xiulin Jiang, Lincan Duan, Zhi Nie, Baiyang Liu, Zhixian Jin, Fangfang Ren and Qing Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Yongbin Chen

58 papers receiving 4.5k citations

Hit Papers

The role of m6A modifi... 2008 2026 2014 2020 2021 2008 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yongbin Chen China 28 3.5k 1.2k 996 430 411 61 4.5k
Cuiping Yang China 26 2.4k 0.7× 1.1k 0.9× 195 0.2× 503 1.2× 205 0.5× 81 3.4k
Hiroko Iwanari Japan 30 2.8k 0.8× 397 0.3× 517 0.5× 408 0.9× 399 1.0× 69 4.2k
Kyungjae Myung South Korea 42 4.9k 1.4× 995 0.8× 826 0.8× 912 2.1× 549 1.3× 147 5.9k
Feng Cong United States 34 3.8k 1.1× 408 0.3× 534 0.5× 1.4k 3.4× 443 1.1× 64 5.0k
Philip East United Kingdom 31 2.7k 0.8× 935 0.7× 395 0.4× 867 2.0× 189 0.5× 50 4.1k
Yonghao Yu United States 34 3.4k 1.0× 490 0.4× 417 0.4× 1.2k 2.9× 174 0.4× 93 4.7k
Ashwini Jambhekar United States 19 2.5k 0.7× 599 0.5× 230 0.2× 465 1.1× 171 0.4× 37 2.9k
El Bachir Affar Canada 32 4.1k 1.2× 588 0.5× 312 0.3× 1.4k 3.2× 660 1.6× 61 5.3k
Jens Peter von Kries Germany 32 5.0k 1.4× 367 0.3× 552 0.6× 878 2.0× 560 1.4× 86 6.2k
Wen‐Tai Chiu Taiwan 30 1.8k 0.5× 471 0.4× 511 0.5× 483 1.1× 159 0.4× 96 3.1k

Countries citing papers authored by Yongbin Chen

Since Specialization
Citations

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

Fields of papers citing papers by Yongbin Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yongbin Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Yongbin Chen. A scholar is included among the top collaborators of Yongbin Chen 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 Yongbin Chen. Yongbin Chen 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.
Wang, Qingbo, Xingming Chen, Zisheng Yang, et al.. (2025). Rechallenge with Immune Checkpoint Inhibitors in Patients with Hepatocellular Carcinoma: A Narrative Review. Liver Cancer. 1–20. 1 indexed citations
2.
Shi, Yulin, Zhi Nie, Li Yao, et al.. (2023). Sertindole inhibits autophagic flux and glioma progression. SHILAP Revista de lepidopterología. 2(2). 1 indexed citations
3.
Shen, Qiushuo, Yanfei Han, Kai Wu, et al.. (2022). MrgprF acts as a tumor suppressor in cutaneous melanoma by restraining PI3K/Akt signaling. Signal Transduction and Targeted Therapy. 7(1). 147–147. 29 indexed citations
4.
Li, Jingyi, Xiaoyu Liao, Tao He, et al.. (2022). RIOX1-demethylated cGAS regulates ionizing radiation-elicited DNA repair. Bone Research. 10(1). 19–19. 10 indexed citations
5.
Liu, Kun, Liping Jiang, Yulin Shi, et al.. (2022). Hypoxia-induced GLT8D1 promotes glioma stem cell maintenance by inhibiting CD133 degradation through N-linked glycosylation. Cell Death and Differentiation. 29(9). 1834–1849. 43 indexed citations
6.
Yuan, Jian, Guodong Zheng, Yongbin Chen, et al.. (2021). Enhanced 1.5 μm emission from Yb3+/Er3+ codoped tungsten tellurite glasses for broadband near-infrared optical fiber amplifiers and tunable fiber lasers. RSC Advances. 11(45). 27992–27999. 25 indexed citations
7.
Jiang, Xiulin, Baiyang Liu, Zhi Nie, et al.. (2021). The role of m6A modification in the biological functions and diseases. Signal Transduction and Targeted Therapy. 6(1). 74–74. 1430 indexed citations breakdown →
8.
Han, Yuhong, Bing Wang, Yong Suk Cho, et al.. (2019). Phosphorylation of Ci/Gli by Fused Family Kinases Promotes Hedgehog Signaling. Developmental Cell. 50(5). 610–626.e4. 50 indexed citations
9.
Yang, Cuiping, Xiaoyan Li, Yong Wu, et al.. (2018). Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes. Nature Communications. 9(1). 838–838. 73 indexed citations
10.
Jiang, Liping, Songqing Fan, Qiuxia Xiong, et al.. (2018). GRK5 functions as an oncogenic factor in non-small-cell lung cancer. Cell Death and Disease. 9(3). 295–295. 34 indexed citations
11.
Wang, Feng, Peng Gao, Ling T. Guo, et al.. (2017). Radio-protective effect and mechanism of 4-Acetamido-2,2,6,6- tetramethylpiperidin-1-oxyl in HUVEC cells. Environmental Health and Preventive Medicine. 22(1). 14–14. 6 indexed citations
12.
Jiang, Liping, Qiushuo Shen, Qiuxia Xiong, et al.. (2017). NCAPH plays important roles in human colon cancer. Cell Death and Disease. 8(3). e2680–e2680. 65 indexed citations
13.
Li, Shuangxi, Shuang Li, Yuhong Han, et al.. (2016). Regulation of Smoothened Phosphorylation and High-Level Hedgehog Signaling Activity by a Plasma Membrane Associated Kinase. PLoS Biology. 14(6). e1002481–e1002481. 42 indexed citations
14.
15.
Yang, Zuozhang, Yongbin Chen, Yu Fu, et al.. (2014). Meta-analysis of differentially expressed genes in osteosarcoma based on gene expression data. BMC Medical Genetics. 15(1). 80–80. 57 indexed citations
16.
Ren, Fangfang, Qing Shi, Yongbin Chen, et al.. (2013). Drosophila Myc integrates multiple signaling pathways to regulate intestinal stem cell proliferation during midgut regeneration. Cell Research. 23(9). 1133–1146. 50 indexed citations
17.
Li, Shuang, Yongbin Chen, Qing Shi, et al.. (2012). Hedgehog-Regulated Ubiquitination Controls Smoothened Trafficking and Cell Surface Expression in Drosophila. PLoS Biology. 10(1). e1001239–e1001239. 94 indexed citations
18.
Yang, Cuiping, Wenlin Chen, Yongbin Chen, & Jin Jiang. (2012). Smoothened transduces Hedgehog signal by forming a complex with Evc/Evc2. Cell Research. 22(11). 1593–1604. 82 indexed citations
19.
Ding, Li, et al.. (2012). A multilayered approach of Si/SiO to promote carrier transport in electroluminescence of Si nanocrystals. Nanoscale Research Letters. 7(1). 200–200. 10 indexed citations
20.
Zhang, Lei, Fangfang Ren, Qing Zhang, et al.. (2008). The TEAD/TEF Family of Transcription Factor Scalloped Mediates Hippo Signaling in Organ Size Control. Developmental Cell. 14(3). 377–387. 529 indexed citations breakdown →

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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