Keming Xu

831 total citations
29 papers, 621 citations indexed

About

Keming Xu is a scholar working on Psychiatry and Mental health, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Keming Xu has authored 29 papers receiving a total of 621 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Psychiatry and Mental health, 13 papers in Molecular Biology and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Keming Xu's work include Epilepsy research and treatment (14 papers), Neuroscience and Neuropharmacology Research (8 papers) and Metabolism and Genetic Disorders (7 papers). Keming Xu is often cited by papers focused on Epilepsy research and treatment (14 papers), Neuroscience and Neuropharmacology Research (8 papers) and Metabolism and Genetic Disorders (7 papers). Keming Xu collaborates with scholars based in China, United States and India. Keming Xu's co-authors include Husheng Wu, Yuehua Zhang, Xiru Wu, Yuwu Jiang, Xiaoyan Liu, Hong Pan, Yan Shen, Jianjun Lu, Yucai Chen and Xinhua Bao and has published in prestigious journals such as Annals of Neurology, Neuroscience Letters and Human Genetics.

In The Last Decade

Keming Xu

27 papers receiving 610 citations

Peers

Keming Xu

CMN

PMH

GENET

PPCH

Stacey B. B. Dutton United States

Aziz Mazarib Israel

Bree Hodgson Australia

Isabelle An-Gourfinkel France

Dimira Tambunan United States

Maéva Langouët United States

Jan‐Peter Ernst Germany

Goryu Fukuma Japan

Amedeo Bianchi Italy

Amy McTague United Kingdom

Stacey B. B. Dutton United States

Keming Xu

230 ×0.6

295 ×1.0

CMN

289 ×1.1

PMH

104 ×0.6

GENET

56 ×0.7

PPCH

Citations per year, relative to Keming Xu Keming Xu (= 1×) peers Stacey B. B. Dutton

Countries citing papers authored by Keming Xu

Since Specialization

Citations

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

Fields of papers citing papers by Keming Xu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keming Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Keming Xu. A scholar is included among the top collaborators of Keming Xu 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 Keming Xu. Keming Xu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Xu, Keming, et al.. (2025). A Full-Field Displacement Real-Time Reconstruction Method for Aircraft Tooling Positioner Based on Corrected Modal Superposition. IEEE Transactions on Instrumentation and Measurement. 74. 1–14.

Wu, Zhenhua, et al.. (2021). Two-stage S7 sleeve resection of the right lower lobe and S1+2 and S3 segmentectomy of the left upper lobe: a case report. Annals of Translational Medicine. 9(8). 723–723. 2 indexed citations

Cheng, Dazhi, et al.. (2020). The effect of interictal epileptiform discharges on cognitive and academic performance in children with idiopathic epilepsy. BMC Neurology. 20(1). 233–233. 14 indexed citations

Cheng, Dazhi, et al.. (2020). Oxcarbazepine monotherapy in children with benign epilepsy with centrotemporal spikes improves quality of life. Chinese Medical Journal. 133(14). 1649–1654. 5 indexed citations

Gao, Zhijie, et al.. (2018). [Glucose transporter 1 deficiency syndrome: features of movement disorders, diagnosis and treatment].. PubMed. 20(3). 209–213. 3 indexed citations

Cheng, Dazhi, et al.. (2017). Attention Contributes to Arithmetic Deficits in New-Onset Childhood Absence Epilepsy. Frontiers in Psychiatry. 8. 166–166. 8 indexed citations

Cheng, Dazhi, et al.. (2017). Common and Distinctive Patterns of Cognitive Dysfunction in Children With Benign Epilepsy Syndromes. Pediatric Neurology. 72. 36–41.e1. 28 indexed citations

Gao, Zhijie, Qian Jiang, Qian Chen, & Keming Xu. (2017). [Clinical and molecular genetic study of nonketotic hyperglycinemia in a Chinese family].. PubMed. 19(3). 268–271. 5 indexed citations

Cheng, Dazhi, et al.. (2016). Neurocognitive Profiles in Childhood Absence Epilepsy. Journal of Child Neurology. 32(1). 46–52. 19 indexed citations

10.

Jiang, Yuwu, Yuehua Zhang, Ping Zhang, et al.. (2012). NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy. Human Genetics. 131(7). 1217–1224. 30 indexed citations

11.

Chen, Qian, Guizhen Zhang, Zhijie Gao, et al.. (2010). [Emotional and behavioral comorbidities and the impact on the quality of life in epilepsy children].. PubMed. 48(5). 346–50. 8 indexed citations

12.

Zhang, Yuehua, Jianmin Liang, Xiaoyan Liu, et al.. (2008). SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus. Journal of Human Genetics. 53(8). 769–774. 56 indexed citations

13.

Zhang, Yuehua, Xiaoyan Liu, Husheng Wu, et al.. (2008). [Analysis of the GABRG2 gene mutation in a Chinese family with generalized epilepsy with febrile seizures plus].. PubMed. 25(6). 611–5. 2 indexed citations

14.

Wang, Juli, Yuehua Zhang, Jianmin Liang, et al.. (2006). CACNA1I Is Not Associated With Childhood Absence Epilepsy in the Chinese Han Population. Pediatric Neurology. 35(3). 187–190. 15 indexed citations

15.

Chen, Yucai, Jianjun Lu, Hong Pan, et al.. (2003). Association between genetic variation of CACNA1H and childhood absence epilepsy. Annals of Neurology. 54(2). 239–243. 277 indexed citations

16.

Chen, Yucai, Jianjun Lu, Yuehua Zhang, et al.. (2003). T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population. Neuroscience Letters. 341(1). 29–32. 23 indexed citations

17.

Lu, Jianjun, Yucai Chen, Hong Pan, et al.. (2003). The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han population. Neuroscience Letters. 343(3). 151–154. 7 indexed citations

18.

Lu, Jianjun, Yucai Chen, Yuehua Zhang, et al.. (2002). Mutation screen of the GABAA receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy. Neuroscience Letters. 332(2). 75–78. 13 indexed citations

19.

Xu, Keming, et al.. (2001). Screening for inborn errors of metabolism using gas chromatography–mass spectrometry. Journal of Chromatography B Biomedical Sciences and Applications. 758(1). 75–80. 14 indexed citations

20.

Xu, Keming, et al.. (2000). Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center. Journal of Chromatography B Biomedical Sciences and Applications. 746(1). 41–49. 22 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.

Explore authors with similar magnitude of impact