Ruxu Zhang

1.3k total citations
40 papers, 375 citations indexed

About

Ruxu Zhang is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Ruxu Zhang has authored 40 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cellular and Molecular Neuroscience, 14 papers in Neurology and 11 papers in Molecular Biology. Recurrent topics in Ruxu Zhang's work include Hereditary Neurological Disorders (24 papers), Neurological diseases and metabolism (13 papers) and Genetic Neurodegenerative Diseases (10 papers). Ruxu Zhang is often cited by papers focused on Hereditary Neurological Disorders (24 papers), Neurological diseases and metabolism (13 papers) and Genetic Neurodegenerative Diseases (10 papers). Ruxu Zhang collaborates with scholars based in China, United States and Switzerland. Ruxu Zhang's co-authors include Beisha Tang, Zhengmao Hu, Xiaobo Li, Kun Xia, Yongzhi Xie, Lei Liu, Xiaohong Zi, Shunxiang Huang, Lei Liu and Junling Wang and has published in prestigious journals such as PLoS ONE, Neurology and Frontiers in Immunology.

In The Last Decade

Ruxu Zhang

34 papers receiving 371 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ruxu Zhang China 11 193 190 82 72 71 40 375
Chrystian Junqueira Alves Brazil 11 161 0.8× 145 0.8× 147 1.8× 101 1.4× 53 0.7× 17 375
Katarina Stoklund Dittlau Belgium 7 154 0.8× 81 0.4× 123 1.5× 63 0.9× 45 0.6× 14 280
Michiel R. Fokkens Netherlands 9 206 1.1× 176 0.9× 64 0.8× 36 0.5× 47 0.7× 11 312
Misako Kunii Japan 10 178 0.9× 97 0.5× 90 1.1× 43 0.6× 46 0.6× 28 296
Luigi Citrigno Italy 11 160 0.8× 78 0.4× 101 1.2× 67 0.9× 71 1.0× 31 356
Chiara Scaramuzzino France 11 326 1.7× 183 1.0× 105 1.3× 86 1.2× 20 0.3× 15 461
Jiefei Yang United States 5 268 1.4× 269 1.4× 60 0.7× 36 0.5× 27 0.4× 7 434
Zoe Siemienski United States 8 214 1.1× 100 0.5× 119 1.5× 63 0.9× 88 1.2× 9 390
Lisle Blackbourn United States 4 302 1.6× 99 0.5× 138 1.7× 107 1.5× 34 0.5× 8 416
Jonathan R. Brent United States 6 181 0.9× 87 0.5× 174 2.1× 112 1.6× 34 0.5× 9 333

Countries citing papers authored by Ruxu Zhang

Since Specialization
Citations

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

Fields of papers citing papers by Ruxu Zhang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruxu Zhang

This figure shows the co-authorship network connecting the top 25 collaborators of Ruxu Zhang. A scholar is included among the top collaborators of Ruxu Zhang 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 Ruxu Zhang. Ruxu Zhang 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.
Zhang, Ruxu, Lei Shen, Huaxia Wang, Yudong Yao, & Miao Yu. (2025). Continuous phase signal modulation recognition based on combined spectral features using ResNeXt50 with channel and spatial attention mechanism. Signal Image and Video Processing. 19(4).
2.
3.
Xie, Yongzhi, Xiaobo Li, Zhiqiang Lin, et al.. (2023). Expanding the genetic and clinical spectrum of SORD‐related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement. Journal of the Peripheral Nervous System. 28(4). 608–613. 2 indexed citations
4.
Li, Xiaobo, et al.. (2023). Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot–Marie–Tooth Disease. Journal of Neurology. 271(1). 497–503. 1 indexed citations
5.
Wang, Mengli, Zhiqiang Lin, Xiaobo Li, et al.. (2023). The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies. Journal of Neurology. 270(10). 4959–4967. 1 indexed citations
6.
7.
Xie, Yongzhi, Zhiqiang Lin, Xiaobo Li, et al.. (2022). One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families. Frontiers in Neurology. 12. 736704–736704. 5 indexed citations
8.
Zhang, Ruxu, et al.. (2022). The Impact of U.S. Trade Policy Uncertainty on the Trade Margins of China’s Export to the U.S.. Sustainability. 14(22). 15101–15101. 4 indexed citations
9.
Liu, Zhen, Mengli Wang, Jie Ni, et al.. (2021). Mutation spectrum of amyotrophic lateral sclerosis in Central South China. Neurobiology of Aging. 107. 181–188. 20 indexed citations
10.
Wang, Mengli, Zhen Liu, Juan Du, et al.. (2021). Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis. Frontiers in Neurology. 12. 628710–628710. 5 indexed citations
11.
Xie, Yongzhi, Zhiqiang Lin, Xiaobo Li, et al.. (2020). Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families. Frontiers in Neurology. 11. 603003–603003. 7 indexed citations
12.
Zhang, Jiejun, Shunxiang Huang, Huadong Zhao, et al.. (2019). The electrophysiological characteristics of the four most common genotypes of Charcot-Marie-Tooth disease. Chin J Neurol. 52(1). 26–33. 1 indexed citations
13.
Wang, Binghao, Xiaobo Li, Junpu Wang, et al.. (2018). A novel AIFM1 mutation in a Chinese family with X-linked Charcot–Marie–Tooth disease type 4. Neuromuscular Disorders. 28(8). 652–659. 13 indexed citations
14.
Xie, Yongzhi, Zhengmao Hu, Xiaobo Li, et al.. (2018). Genotype–phenotype correlation and frequency of distribution in a cohort of Chinese Charcot–Marie–Tooth patients associated with GDAP1 mutations. Journal of Neurology. 265(3). 637–646. 14 indexed citations
15.
Liu, Lei, Xiaobo Li, Zhengmao Hu, et al.. (2016). IGHMBP2-related clinical and genetic features in a cohort of Chinese Charcot–Marie–Tooth disease type 2 patients. Neuromuscular Disorders. 27(2). 193–199. 20 indexed citations
16.
Xie, Yongzhi, Xiaobo Li, Lei Liu, et al.. (2016). MFN2‐related genetic and clinical features in a cohort of Chinese CMT2 patients. Journal of the Peripheral Nervous System. 21(1). 38–44. 18 indexed citations
17.
Li, Xiaobo, Zhengmao Hu, Lei Liu, et al.. (2015). A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy. Neurology. 84(24). 2430–2437. 68 indexed citations
18.
Liu, Lei & Ruxu Zhang. (2014). Intermediate Charcot-Marie-Tooth disease. Neuroscience Bulletin. 30(6). 999–1009. 18 indexed citations
19.
Liu, Lei, Xiaobo Li, Xiaohong Zi, et al.. (2013). Two novel MPZ mutations in Chinese CMT patients. Journal of the Peripheral Nervous System. 18(3). 256–260. 9 indexed citations
20.
Tang, Beisha, Xiaomin Liu, Guohua Zhao, et al.. (2005). Mutation Analysis of the Small Heat Shock Protein 27 Gene in Chinese Patients With Charcot-Marie-Tooth Disease. Archives of Neurology. 62(8). 1201–1201. 57 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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