Mu Yang

971 total citations
56 papers, 640 citations indexed

About

Mu Yang is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Mu Yang has authored 56 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 9 papers in Neurology and 9 papers in Genetics. Recurrent topics in Mu Yang's work include Wnt/β-catenin signaling in development and cancer (19 papers), Cancer-related gene regulation (12 papers) and Ubiquitin and proteasome pathways (10 papers). Mu Yang is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (19 papers), Cancer-related gene regulation (12 papers) and Ubiquitin and proteasome pathways (10 papers). Mu Yang collaborates with scholars based in China, United States and India. Mu Yang's co-authors include Shujin Li, Xinyan Wang, Xianjun Zhu, Yeming Yang, Zhenglin Yang, Lin Zhang, Shanshan Zhang, Wei He, Hong Zhou and Peiquan Zhao and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Mu Yang

52 papers receiving 634 citations

Peers

Mu Yang
Michael H. Farkas United States
Surasri N. Sahu United States
Gábor Keresztes United States
Mu Yang
Citations per year, relative to Mu Yang Mu Yang (= 1×) peers Xianjiang Kang

Countries citing papers authored by Mu Yang

Since Specialization
Citations

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

Fields of papers citing papers by Mu Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mu Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Mu Yang. A scholar is included among the top collaborators of Mu Yang 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 Mu Yang. Mu Yang 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
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Liu, Min, Shujin Li, Xiang Zhang, et al.. (2024). Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations. Investigative Ophthalmology & Visual Science. 65(4). 1–1. 2 indexed citations
5.
Liu, Min, Mu Yang, Shujin Li, et al.. (2024). Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation. Investigative Ophthalmology & Visual Science. 65(3). 31–31. 3 indexed citations
6.
Wang, Yuze, et al.. (2022). Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy. Genetic Testing and Molecular Biomarkers. 26(3). 146–151. 1 indexed citations
8.
You, Jianing, Hang Liu, Surong Wang, et al.. (2021). Spike Density Quantitative Trait Loci Detection and Analysis in Tetraploid and Hexaploid Wheat Recombinant Inbred Line Populations. Frontiers in Plant Science. 12. 796397–796397. 12 indexed citations
9.
Zhang, Shanshan, Xiao Li, Wenjing Liu, et al.. (2021). Whole-Exome Sequencing Identified DLG1 as a Candidate Gene for Familial Exudative Vitreoretinopathy. Genetic Testing and Molecular Biomarkers. 25(5). 309–316. 18 indexed citations
10.
Yang, Mu, Lulin Huang, Periasamy Sundaresan, et al.. (2021). Whole-Exome Sequencing Reveals Novel TSPAN12 Variants in Autosomal Dominant Familial Exudative Vitreoretinopathy. Genetic Testing and Molecular Biomarkers. 25(6). 399–404. 4 indexed citations
11.
Yang, Mu, Shujin Li, Wenjing Liu, et al.. (2021). The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis. Science China Life Sciences. 64(11). 1868–1883. 16 indexed citations
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Yang, Mu, Qing Chen, Rebecca E. Parales, et al.. (2020). Bacterial catabolism of nicotine: Catabolic strains, pathways and modules. Environmental Research. 183. 109258–109258. 43 indexed citations
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Yang, Mu, Shujin Li, Xianjun Zhu, & Zhenglin Yang. (2018). Targeted Next Generation Sequencing Reveals a Novel Frameshift MERTK Mutation in Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 59(9). 36–36. 1 indexed citations
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Yang, Mu, Shujin Li, Wenjing Liu, et al.. (2018). Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa. Genetic Testing and Molecular Biomarkers. 22(3). 165–169. 5 indexed citations
15.
Xu, Xihui, Xiaomei Liu, Long Zhang, et al.. (2018). Bioaugmentation of chlorothalonil-contaminated soil with hydrolytically or reductively dehalogenating strain and its effect on soil microbial community. Journal of Hazardous Materials. 351. 240–249. 41 indexed citations
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Li, Shujin, Mu Yang, Wenjing Liu, et al.. (2018). Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa. Genetic Testing and Molecular Biomarkers. 22(2). 109–114. 11 indexed citations
17.
Zhang, Lin, Yeming Yang, Shujin Li, et al.. (2017). Loss of Tmem30a leads to photoreceptor degeneration. Scientific Reports. 7(1). 9296–9296. 23 indexed citations
18.
Tian, Changxu, et al.. (2014). New microsatellite loci for the mandarin fish Siniperca chuatsi and their application in population genetic analysis. Genetics and Molecular Research. 13(1). 546–558. 4 indexed citations
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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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