Xiaolu Deng

921 total citations
35 papers, 689 citations indexed

About

Xiaolu Deng is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Xiaolu Deng has authored 35 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in Xiaolu Deng's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (7 papers) and Metabolism and Genetic Disorders (4 papers). Xiaolu Deng is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (7 papers) and Metabolism and Genetic Disorders (4 papers). Xiaolu Deng collaborates with scholars based in China, Egypt and United States. Xiaolu Deng's co-authors include Fei Yin, Jing Peng, Fang He, Lifen Yang, Ciliu Zhang, Chen Chen, Nan Pang, Shiqi Guang, Liwen Wu and Ahmed Omran and has published in prestigious journals such as Brain Research, Chemical Engineering Journal and Gene.

In The Last Decade

Xiaolu Deng

32 papers receiving 677 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiaolu Deng China 12 252 167 149 102 93 35 689
Feng Han China 18 429 1.7× 94 0.6× 106 0.7× 126 1.2× 114 1.2× 45 894
Yeping Ruan China 17 235 0.9× 41 0.2× 61 0.4× 67 0.7× 179 1.9× 42 729
Jianan Zhan United States 7 186 0.7× 187 1.1× 201 1.3× 67 0.7× 24 0.3× 17 616
Fang Shen China 16 386 1.5× 56 0.3× 99 0.7× 44 0.4× 142 1.5× 70 950
Xiaowen Li China 17 294 1.2× 58 0.3× 81 0.5× 75 0.7× 128 1.4× 44 859
Cliona O’Driscoll United States 10 259 1.0× 150 0.9× 79 0.5× 63 0.6× 104 1.1× 15 506
Jianhong Wang China 16 236 0.9× 44 0.3× 83 0.6× 51 0.5× 85 0.9× 57 827
Ming-Hong Tai Taiwan 20 321 1.3× 52 0.3× 64 0.4× 60 0.6× 205 2.2× 37 975
Geneviève Bart Finland 21 515 2.0× 35 0.2× 187 1.3× 60 0.6× 128 1.4× 40 1.2k
Wenchao Li China 14 144 0.6× 76 0.5× 73 0.5× 46 0.5× 51 0.5× 48 646

Countries citing papers authored by Xiaolu Deng

Since Specialization
Citations

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

Fields of papers citing papers by Xiaolu Deng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaolu Deng

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaolu Deng. A scholar is included among the top collaborators of Xiaolu Deng 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 Xiaolu Deng. Xiaolu Deng 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.
Deng, Xiaolu, J. Y. Zhao, Jian Li, et al.. (2025). A Case Series of Anti-Metabotropic Glutamate Receptor 2 Antibody-Related Diseases with Distinct Neurological Involvement. ImmunoTargets and Therapy. Volume 14. 465–474.
2.
Pang, Nan, Chen Chen, Lifen Yang, et al.. (2025). The genetic spectrum features of 2261 Chinese children with epilepsy and intellectual disability. BMC Medicine. 23(1). 388–388. 1 indexed citations
3.
Pang, Nan, Kuokuo Li, Meilin Chen, et al.. (2023). Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders. Gene. 897. 148071–148071. 1 indexed citations
5.
Xiong, Juan, Zhonghua Liu, Miriam Kessi, et al.. (2022). Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder. Frontiers in Pediatrics. 9. 755344–755344. 9 indexed citations
6.
Xiong, Juan, Baiyu Chen, Ciliu Zhang, et al.. (2021). Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort. Clinica Chimica Acta. 524. 179–186. 10 indexed citations
7.
Chen, Baiyu, Miriam Kessi, Juan Xiong, et al.. (2021). Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children. Frontiers in Molecular Biosciences. 8. 792319–792319. 7 indexed citations
8.
Xiong, Juan, Miriam Kessi, Fang He, et al.. (2021). Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients. BMC Medical Genomics. 14(1). 182–182. 8 indexed citations
9.
Deng, Xiaolu, Juan Xiong, Fang He, et al.. (2021). De novo variants of DEAF1 cause intellectual disability in six Chinese patients. Clinica Chimica Acta. 518. 17–21. 2 indexed citations
10.
Chen, Baiyu, Miriam Kessi, Juan Xiong, et al.. (2020). The Recommendations for the Management of Chinese Children With Epilepsy During the COVID-19 Outbreak. Frontiers in Pediatrics. 8. 495–495. 4 indexed citations
11.
Zhang, Ciliu, et al.. (2020). First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient. BMC Medical Genetics. 21(1). 235–235. 9 indexed citations
12.
Peng, Jing, Fei Yin, Xiaolu Deng, et al.. (2019). Ketogenic Diet as a Treatment for Super-Refractory Status Epilepticus in Febrile Infection-Related Epilepsy Syndrome. Frontiers in Neurology. 10. 423–423. 44 indexed citations
13.
Xiong, Juan, Nan Pang, Xiaolu Deng, et al.. (2019). Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes. Frontiers in Neuroscience. 13. 349–349. 45 indexed citations
14.
Guang, Shiqi, Nan Pang, Xiaolu Deng, et al.. (2018). Synaptopathology Involved in Autism Spectrum Disorder. Frontiers in Cellular Neuroscience. 12. 470–470. 197 indexed citations
15.
Wu, Liwen, Jing Peng, Huimin Kong, et al.. (2015). The role of ubiquitin/Nedd4-2 in the pathogenesis of mesial temporal lobe epilepsy. Physiology & Behavior. 143. 104–112. 15 indexed citations
16.
Zhang, Ciliu, Ahmed Omran, Fang He, et al.. (2013). Screening and identification of dynamin-1 interacting proteins in rat brain synaptosomes. Brain Research. 1543. 17–27. 3 indexed citations
17.
Kong, Huimin, Ahmed Omran, Na Gan, et al.. (2013). Changes in Microglial Inflammation-Related and Brain-Enriched MicroRNAs Expressions in Response to In Vitro Oxygen–Glucose Deprivation. Neurochemical Research. 39(2). 233–243. 21 indexed citations
18.
He, Fang, Jing Peng, Xiaolu Deng, et al.. (2012). Mechanisms of tumor necrosis factor-alpha-induced leaks in intestine epithelial barrier. Cytokine. 59(2). 264–272. 94 indexed citations
19.
Peng, Jing, et al.. (2012). A Retrospective Analysis of Pathological and Clinical Diagnoses: Report of 240 Pediatric Autopsies. Fetal and Pediatric Pathology. 31(2). 63–73. 2 indexed citations
20.
Peng, Jing, Fang He, Ciliu Zhang, Xiaolu Deng, & Fei Yin. (2011). Protein kinase C-α signals P115RhoGEF phosphorylation and RhoA activation in TNF-α-induced mouse brain microvascular endothelial cell barrier dysfunction. Journal of Neuroinflammation. 8(1). 28–28. 60 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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