Xiru Wu

5.1k total citations
201 papers, 3.6k citations indexed

About

Xiru Wu is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Xiru Wu has authored 201 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Molecular Biology, 55 papers in Genetics and 40 papers in Psychiatry and Mental health. Recurrent topics in Xiru Wu's work include Genetics and Neurodevelopmental Disorders (44 papers), Epilepsy research and treatment (40 papers) and Neuroscience and Neuropharmacology Research (31 papers). Xiru Wu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (44 papers), Epilepsy research and treatment (40 papers) and Neuroscience and Neuropharmacology Research (31 papers). Xiru Wu collaborates with scholars based in China, United States and Japan. Xiru Wu's co-authors include Yuwu Jiang, Yuehua Zhang, Xinhua Bao, Xuanju Dang, Jingmin Wang, Hong Pan, Ye Wu, Hui Jiang, Yaonan Wang and Yucai Chen and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Annals of Neurology.

In The Last Decade

Xiru Wu

192 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiru Wu China 31 1.6k 1.0k 845 717 341 201 3.6k
Frédéric Dubas France 27 888 0.5× 279 0.3× 436 0.5× 212 0.3× 158 0.5× 123 3.1k
Hyungju Park South Korea 23 1.2k 0.7× 170 0.2× 2.0k 2.4× 128 0.2× 519 1.5× 64 4.0k
Edward A. Burton United States 37 1.7k 1.0× 406 0.4× 1000 1.2× 29 0.0× 104 0.3× 74 4.0k
Hideki Hayakawa Japan 25 522 0.3× 96 0.1× 400 0.5× 69 0.1× 193 0.6× 79 2.0k
Marvin E. Adams United States 34 3.7k 2.3× 292 0.3× 1.2k 1.5× 101 0.1× 59 0.2× 63 4.8k
Christian Winkler Germany 35 1.4k 0.9× 233 0.2× 2.8k 3.3× 55 0.1× 507 1.5× 126 5.1k
Qiping Chen China 20 1.2k 0.7× 53 0.1× 998 1.2× 26 0.0× 37 0.1× 106 4.1k
Marek Pawlikowski Poland 27 611 0.4× 212 0.2× 347 0.4× 77 0.1× 77 0.2× 251 3.2k
Ying Lee United States 17 495 0.3× 228 0.2× 152 0.2× 74 0.1× 158 0.5× 48 2.0k
Fangang Meng China 28 659 0.4× 78 0.1× 635 0.8× 414 0.6× 568 1.7× 163 2.8k

Countries citing papers authored by Xiru Wu

Since Specialization
Citations

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

Fields of papers citing papers by Xiru Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiru Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Xiru Wu. A scholar is included among the top collaborators of Xiru Wu 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 Xiru Wu. Xiru Wu 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.
Yuan, Xiaofang, et al.. (2025). Learn Once Plan Arbitrarily (LOPA): Dynamic Observation-Based Deep Reinforcement Learning Method for Global Path Planning in Mountainous Terrain Environment. IEEE Transactions on Artificial Intelligence. 7(2). 1168–1184. 1 indexed citations
2.
3.
Zhu, Jiang, et al.. (2023). A Lightweight Network for Defect Detection in Nickel-Plated Punched Steel Strip Images. IEEE Transactions on Instrumentation and Measurement. 72. 1–15. 20 indexed citations
4.
Wang, Jiaping, Qingping Zhang, Yan Chen, et al.. (2018). Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation. BMC Medical Genetics. 19(1). 191–191. 20 indexed citations
5.
Zeng, Qi, Jing Zhang, Cheng Yang, et al.. (2018). The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome. Developmental Medicine & Child Neurology. 60(6). 566–573. 26 indexed citations
6.
Dang, Xuanju, et al.. (2018). Torque ripple suppression for switched reluctance motors based on current self-adaptive control. 37(3). 66–71. 1 indexed citations
7.
Zhang, Qingping, Jiaping Wang, Jiarui Li, et al.. (2017). Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation. BMC Medical Genetics. 18(1). 96–96. 8 indexed citations
8.
Wang, Jiaping, Hua Gao, Xinhua Bao, et al.. (2017). SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures. BMC Medical Genetics. 18(1). 104–104. 28 indexed citations
9.
Yang, Haipo, Shuo Wang, Aijie Liu, et al.. (2017). Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing. Scientific Reports. 7(1). 7056–7056. 4 indexed citations
10.
Dang, Xuanju, et al.. (2015). Open-Circuit Voltage-Based State of Charge Estimation of Lithium-ion Battery Using Dual Neural Network Fusion Battery Model. Electrochimica Acta. 188. 356–366. 165 indexed citations
11.
Oda, Tetsuya, Hui Xiong, Kazuhiro Kobayashi, et al.. (2015). A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy. Human Genome Variation. 2(1). 15022–15022. 5 indexed citations
12.
Chen, Xiaoli, Jingmin Wang, Hua Xie, et al.. (2015). Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder. BMC Pediatrics. 15(1). 77–77. 10 indexed citations
13.
Zhang, Yujia, Yang Gao, Xiaoyan Liu, et al.. (2015). Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities. PLoS ONE. 10(11). e0141782–e0141782. 71 indexed citations
14.
Li, Dongxiao, Ye Wu, Taoyun Ji, et al.. (2014). Clinical and molecular genetic analysis of three pedigrees with Pelizaeus-Merzbacher-like disease. Zhonghua shiyong erke linchuang zazhi. 29(16). 1240–1245. 1 indexed citations
15.
Wu, Ye, Taoyun Ji, Jingmin Wang, et al.. (2010). Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation. BMC Medical Genetics. 11(1). 72–72. 53 indexed citations
16.
Zhang, Yuehua, Zhixian Yang, Xiaoyan Liu, et al.. (2010). Childhood absence epilepsy: Elctroclinical features and diagnostic criteria. Brain and Development. 33(2). 114–119. 17 indexed citations
17.
Wu, Ye, Li Du, Jingmin Wang, et al.. (2009). Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease. Journal of Human Genetics. 54(2). 74–77. 22 indexed citations
18.
Wu, Xiru. (2008). Treatment and prognosis of childhood absence epilepsy in 240 patients:Application of modified diagnostic criteria of childhood absence epilepsy 1989. 1 indexed citations
19.
Li, Meirong, Hong Pan, Xinhua Bao, Yuzhi Zhang, & Xiru Wu. (2006). MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome. Journal of Human Genetics. 52(1). 38–47. 37 indexed citations
20.
Wu, Xiru. (2004). Long-term effect of early seizure-like discharge on MTT metabolic rate in developing cortical neurons of rat. 1 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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