Cuijie Wei

787 total citations
28 papers, 130 citations indexed

About

Cuijie Wei is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Cuijie Wei has authored 28 papers receiving a total of 130 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Cuijie Wei's work include Muscle Physiology and Disorders (11 papers), Neurogenetic and Muscular Disorders Research (7 papers) and RNA Research and Splicing (5 papers). Cuijie Wei is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Neurogenetic and Muscular Disorders Research (7 papers) and RNA Research and Splicing (5 papers). Cuijie Wei collaborates with scholars based in China, Belgium and United States. Cuijie Wei's co-authors include Hui Xiong, Zhiwen Liu, Xiao‐Qi Zhang, Wen‐Cai Ye, Haipo Yang, Dongdong Qin, Liwen Wu, Shuo Wang, Xiaoli Zhang and Yanling Yang and has published in prestigious journals such as The Journal of Organic Chemistry, Gene and Medicine.

In The Last Decade

Cuijie Wei

24 papers receiving 129 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cuijie Wei China 7 76 29 27 23 18 28 130
Vaibhavkumar S. Gawali Austria 12 144 1.9× 22 0.8× 17 0.6× 43 1.9× 9 0.5× 21 270
Sarah Vautier France 6 43 0.6× 21 0.7× 9 0.3× 2 0.1× 12 0.7× 8 212
Ze’e Chen China 8 117 1.5× 31 1.1× 10 0.4× 44 1.9× 6 0.3× 15 182
Lee J. Beeley United Kingdom 10 153 2.0× 9 0.3× 31 1.1× 15 0.7× 7 0.4× 13 248
Xiaoqin Zhao China 8 90 1.2× 19 0.7× 63 2.3× 10 0.4× 2 0.1× 15 227
Roger J. Melton United States 8 130 1.7× 41 1.4× 18 0.7× 4 0.2× 9 0.5× 9 223
Masaki Ueda Japan 5 47 0.6× 4 0.1× 23 0.9× 22 1.0× 12 0.7× 7 96
Peter Dove United States 8 35 0.5× 10 0.3× 60 2.2× 11 0.5× 14 0.8× 14 150
B D Potts United States 7 42 0.6× 27 0.9× 17 0.6× 9 0.4× 9 0.5× 13 168
Tetsushi Kataura Japan 8 111 1.5× 7 0.2× 8 0.3× 4 0.2× 5 0.3× 19 224

Countries citing papers authored by Cuijie Wei

Since Specialization
Citations

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

Fields of papers citing papers by Cuijie Wei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cuijie Wei

This figure shows the co-authorship network connecting the top 25 collaborators of Cuijie Wei. A scholar is included among the top collaborators of Cuijie Wei 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 Cuijie Wei. Cuijie Wei 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.
Yu, Hao, et al.. (2025). Research trends on spinal muscular atrophy from 1995 to 2023: A bibliometric analysis. Medicine. 104(13). e41801–e41801. 1 indexed citations
2.
Wei, Cuijie, Jin Xu, Yilei Zheng, et al.. (2025). Rapamycin alleviates neurodegeneration in a Drosophila model of spinocerebellar ataxia type 51. Journal of genetics and genomics. 52(10). 1259–1267.
3.
Wei, Cuijie, et al.. (2024). Q-Marker Prediction of Astragali Complanati Semen Based on Fingerprint and Network Pharmacology. Journal of AOAC International. 108(1). 78–89. 1 indexed citations
4.
5.
6.
Wei, Cuijie, Dongliang Li, Meng Zhang, et al.. (2023). Prevalence of Adeno-Associated Virus-9-Neutralizing Antibody in Chinese Patients with Duchenne Muscular Dystrophy. Human Gene Therapy. 35(1-2). 26–35. 6 indexed citations
7.
Wei, Cuijie, Yidan Liu, Yanling Yang, et al.. (2023). Case report: Muscle involvement in a Chinese patient with TRNT1-related disorder. Frontiers in Pediatrics. 11. 1160107–1160107.
8.
Huang, Xiuli, Dandan Tan, Zaiqiang Zhang, et al.. (2023). Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients. Frontiers in Neurology. 14. 1158094–1158094. 3 indexed citations
9.
Wei, Cuijie, Zhenwei Liang, Ying Wu, et al.. (2023). Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis. Orphanet Journal of Rare Diseases. 18(1). 30–30. 2 indexed citations
10.
Wei, Cuijie, et al.. (2022). Juvenile Generalized Myasthenia Gravis With AChR and MuSK Antibody Double Positivity: A Case Report With a Review of the Literature. Frontiers in Pediatrics. 10. 788353–788353. 1 indexed citations
11.
Yang, Haipo, Xiaoyu Chen, Ying Zhu, et al.. (2022). Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies. Seizure. 101. 39–47. 3 indexed citations
12.
Wei, Cuijie, Xiao Hu, Wenzhu Li, et al.. (2022). Scoliosis Orthopedic Surgery Combined With Nusinersen Intrathecal Injection Significantly Improved the Outcome of Spinal Muscular Atrophy Patient: A Case Report. Frontiers in Neurology. 13. 869230–869230. 1 indexed citations
13.
Chang, Xingzhi, Risheng Wei, Cuijie Wei, et al.. (2022). Correlation of Phenotype–Genotype and Protein Structure in RYR1-Related Myopathy. Frontiers in Neurology. 13. 870285–870285. 6 indexed citations
14.
Fan, Yanbin, Zhifei Xu, Xing Li, et al.. (2022). Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients. Frontiers in Genetics. 13. 825793–825793. 1 indexed citations
15.
Tan, Dandan, Ge Lin, Yanbin Fan, et al.. (2021). Muscle magnetic resonance imaging in patients with LAMA2-related muscular dystrophy. Neuromuscular Disorders. 31(11). 1144–1153. 4 indexed citations
16.
Zhang, Jian, Zhiwen Liu, Lijun Hu, et al.. (2019). Hunterines A–C, Three Unusual Monoterpenoid Indole Alkaloids from Hunteria zeylanica. The Journal of Organic Chemistry. 84(22). 14892–14897. 22 indexed citations
17.
Yang, Haipo, Cuijie Wei, Shuo Wang, et al.. (2016). FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies. Journal of Human Genetics. 61(12). 1013–1020. 12 indexed citations
18.
Wei, Cuijie, Haipo Yang, Aijie Liu, et al.. (2015). [Duchenne and Becker muscular dystrophy complicated with epilepsy].. PubMed. 53(4). 274–9. 2 indexed citations
19.
Xiong, Hui, Cuijie Wei, Xingzhi Chang, et al.. (2014). [Value of muscle enzyme analysis in differential diagnosis of childhood myopathic hyper-creatine kinase-emia].. PubMed. 46(1). 130–7. 1 indexed citations
20.
Xiong, Hui, Katsumi Higaki, Cuijie Wei, et al.. (2012). Genotype/phenotype of 6 Chinese cases with Niemann–Pick disease type C. Gene. 498(2). 332–335. 9 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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