Mugen Liu

5.0k total citations · 1 hit paper
102 papers, 2.7k citations indexed

About

Mugen Liu is a scholar working on Molecular Biology, Cell Biology and Ophthalmology. According to data from OpenAlex, Mugen Liu has authored 102 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 22 papers in Cell Biology and 20 papers in Ophthalmology. Recurrent topics in Mugen Liu's work include Retinal Development and Disorders (22 papers), Connexins and lens biology (16 papers) and Retinal Diseases and Treatments (13 papers). Mugen Liu is often cited by papers focused on Retinal Development and Disorders (22 papers), Connexins and lens biology (16 papers) and Retinal Diseases and Treatments (13 papers). Mugen Liu collaborates with scholars based in China, United States and United Kingdom. Mugen Liu's co-authors include Colin J. Barnstable, David T.L. Liu, Wai Man Chan, Stephen E. Hartman, Pancy O. S. Tam, Samuel Shao-Min Zhang, Dennis S.C. Lam, Andrew T. DeWan, Connie Zhao and M Snyder and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Mugen Liu

99 papers receiving 2.6k citations

Hit Papers

HTRA1 Promoter Polymorphism in Wet Age-Related Macular De... 2006 2026 2012 2019 2006 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mugen Liu China 26 1.6k 762 425 408 312 102 2.7k
Ricardo P. Casaroli‐Marano Spain 24 832 0.5× 747 1.0× 159 0.4× 584 1.4× 399 1.3× 139 2.2k
Małgorzata Rydzanicz Poland 27 1.3k 0.8× 247 0.3× 400 0.9× 413 1.0× 131 0.4× 171 2.4k
Nady Golestaneh United States 22 1.4k 0.9× 547 0.7× 304 0.7× 186 0.5× 87 0.3× 41 2.2k
Robert J. Wordinger United States 35 2.0k 1.2× 2.3k 3.1× 333 0.8× 1.0k 2.5× 529 1.7× 104 4.1k
Elisabeth Rungger‐Brändle Switzerland 23 1.1k 0.7× 1.0k 1.4× 134 0.3× 607 1.5× 562 1.8× 44 2.7k
Qingxian Lu United States 27 1.2k 0.7× 227 0.3× 185 0.4× 142 0.3× 259 0.8× 53 3.3k
John Danias United States 30 1.6k 1.0× 2.1k 2.8× 154 0.4× 782 1.9× 263 0.8× 73 3.3k
Muriel I. Kaiser‐Kupfer United States 41 2.0k 1.2× 1.3k 1.7× 566 1.3× 413 1.0× 620 2.0× 103 4.9k
H Inomata Japan 20 934 0.6× 523 0.7× 179 0.4× 345 0.8× 190 0.6× 68 1.7k
Jennifer L. Kielczewski United States 21 944 0.6× 709 0.9× 133 0.3× 235 0.6× 78 0.3× 27 1.7k

Countries citing papers authored by Mugen Liu

Since Specialization
Citations

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

Fields of papers citing papers by Mugen Liu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mugen Liu

This figure shows the co-authorship network connecting the top 25 collaborators of Mugen Liu. A scholar is included among the top collaborators of Mugen 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 Mugen Liu. Mugen 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.
Hu, Hualei, Yayun Qin, Zhen Qu, et al.. (2024). The Zpr-3 Antibody Recognizes the 320–354 Region of Rho and Labels Both Rods and Green Cones in Zebrafish. Zebrafish. 21(6). 394–400.
2.
Luo, Yi, et al.. (2024). Deficiency of copper responsive gene stmn4 induces retinal developmental defects. Cell Biology and Toxicology. 40(1). 2–2. 4 indexed citations
4.
Zhang, Jing, et al.. (2023). HSF4 Transcriptionally Activates Autophagy by Regulating ATG9a During Lens Terminal Differentiation. Investigative Ophthalmology & Visual Science. 64(7). 5–5. 4 indexed citations
5.
Liu, Fei, Yayun Qin, Yuwen Huang, et al.. (2022). Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration. PLoS Genetics. 18(3). e1009841–e1009841. 13 indexed citations
6.
Yu, Shanshan, Jingzhen Li, Yangjun Zhang, et al.. (2022). Dhx38 is required for the maintenance and differentiation of erythro-myeloid progenitors and hematopoietic stem cells by alternative splicing. Development. 149(17). 6 indexed citations
7.
Sun, Hao, Xuan Xu, Junyu Luo, et al.. (2022). Mechanisms of PiT2-loop7 Missense Mutations Induced Pi Dyshomeostasis. Neuroscience Bulletin. 39(1). 57–68. 2 indexed citations
8.
Cui, Xiukun, Dandan Wu, Jing Zhang, et al.. (2021). Deficiency of heat shock factor 4 promotes lens epithelial cell senescence through upregulating p21cip1 expression. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1867(11). 166233–166233. 7 indexed citations
9.
Zhang, Jing, Yu-Wen Huang, Weikang Huang, et al.. (2020). Knockout of DNase1l1l abrogates lens denucleation process and causes cataract in zebrafish. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(5). 165724–165724. 15 indexed citations
10.
Yang, Yujie, Junyu Luo, Teng Liu, et al.. (2019). A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate. Genetic Testing and Molecular Biomarkers. 23(11). 759–765. 7 indexed citations
11.
Yu, Shanshan, et al.. (2018). A PCR-Based Method for RNA Probes and Applications in Neuroscience. Frontiers in Neuroscience. 12. 266–266. 29 indexed citations
12.
Liu, Fei, Yayun Qin, Shanshan Yu, et al.. (2017). Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafish. Journal of Biological Chemistry. 292(15). 6225–6239. 13 indexed citations
13.
Lu, Zhaojing, Xuebin Hu, Fei Liu, et al.. (2017). Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy. Scientific Reports. 7(1). 46098–46098. 49 indexed citations
14.
Wang, Dengke, Ying Liu, Jiamin Li, et al.. (2015). Effects of Nt-truncation and coexpression of isolated Nt domains on the membrane trafficking of electroneutral Na+/HCO3– cotransporters. Scientific Reports. 5(1). 12241–12241. 11 indexed citations
15.
Liao, Shengjie, Lei Wang, Zhen Qu, et al.. (2015). BCAS2 interacts with HSF4 and negatively regulates its protein stability via ubiquitination. The International Journal of Biochemistry & Cell Biology. 68. 78–86. 10 indexed citations
16.
Cui, Xiukun, Lei Wang, Jing Zhang, et al.. (2013). HSF4 regulates DLAD expression and promotes lens de-nucleation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832(8). 1167–1172. 41 indexed citations
17.
Xu, Zhenping, Yulei Li, Xiangyang Zhang, et al.. (2011). Identification and molecular characterization of two novel mutations in COL1A2 in two Chinese families with osteogenesis imperfecta. Journal of genetics and genomics. 38(4). 149–156. 3 indexed citations
18.
Li, Hui, Chang Li, Qiulun Lu, et al.. (2008). Cataract mutation P20S of αB-crystallin impairs chaperone activity of αA-crystallin and induces apoptosis of human lens epithelial cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1782(5). 303–309. 29 indexed citations
19.
Yang, Tao, et al.. (2008). A novel mutation in the ATP2C1 gene is associated with Hailey–Hailey disease in a Chinese family. International Journal of Dermatology. 48(1). 47–51. 7 indexed citations
20.
Liu, Mugen, Zhou Cai, Zhaohui Tang, et al.. (2006). A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family. Journal of Human Genetics. 51(8). 727–731. 25 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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