Bing-Mei Li

694 total citations
22 papers, 360 citations indexed

About

Bing-Mei Li is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Bing-Mei Li has authored 22 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Psychiatry and Mental health. Recurrent topics in Bing-Mei Li's work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (9 papers) and Epilepsy research and treatment (8 papers). Bing-Mei Li is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (9 papers) and Epilepsy research and treatment (8 papers). Bing-Mei Li collaborates with scholars based in China and United States. Bing-Mei Li's co-authors include Wei‐Ping Liao, Xiao‐Rong Liu, Yong‐Hong Yi, Tao Su, Yi‐Wu Shi, Yuhong Deng, Xin Zou, Na He, Bin Tang and Peng Zhou and has published in prestigious journals such as Journal of Medical Genetics, Frontiers in Neuroscience and Molecular Neurobiology.

In The Last Decade

Bing-Mei Li

21 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bing-Mei Li China 11 193 136 122 78 53 22 360
Zhi-Jian Lin China 5 237 1.2× 198 1.5× 189 1.5× 126 1.6× 25 0.5× 6 456
Dora Steel United Kingdom 9 107 0.6× 131 1.0× 105 0.9× 111 1.4× 17 0.3× 17 360
Evan E. Eichler United States 2 270 1.4× 338 2.5× 150 1.2× 142 1.8× 23 0.4× 3 538
Maéva Langouët United States 8 226 1.2× 253 1.9× 164 1.3× 114 1.5× 13 0.2× 9 462
Jue Ji China 12 148 0.8× 177 1.3× 89 0.7× 68 0.9× 37 0.7× 27 378
Lutz Priebe Germany 11 170 0.9× 159 1.2× 89 0.7× 40 0.5× 21 0.4× 13 373
Wenshu XiangWei China 10 169 0.9× 227 1.7× 78 0.6× 187 2.4× 45 0.8× 13 399
Liri Jin China 11 60 0.3× 141 1.0× 151 1.2× 140 1.8× 41 0.8× 34 391
Susanne Ruf Germany 5 112 0.6× 103 0.8× 83 0.7× 74 0.9× 27 0.5× 6 221
Mathieu Lachance Canada 6 143 0.7× 124 0.9× 97 0.8× 152 1.9× 65 1.2× 9 330

Countries citing papers authored by Bing-Mei Li

Since Specialization
Citations

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

Fields of papers citing papers by Bing-Mei Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bing-Mei Li. 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 Bing-Mei Li. The network helps show where Bing-Mei Li may publish in the future.

Co-authorship network of co-authors of Bing-Mei Li

This figure shows the co-authorship network connecting the top 25 collaborators of Bing-Mei Li. A scholar is included among the top collaborators of Bing-Mei Li 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 Bing-Mei Li. Bing-Mei Li 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.
He, Ye, Xiaoyu Liang, Siqi Zhang, et al.. (2024). CCDC22 variants caused X-linked focal epilepsy and focal cortical dysplasia. Seizure. 123. 1–8. 8 indexed citations
2.
Li, Bing-Mei, Jie Wang, Na He, et al.. (2024). NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation. Molecular Neurobiology. 61(11). 8518–8530.
3.
Liu, Lihong, Juan Wang, Jiajun Guo, et al.. (2024). ZFHX3variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. Journal of Medical Genetics. 61(7). 652–660. 11 indexed citations
4.
Liu, Wenhui, Sheng Luo, Xin Li, et al.. (2024). De novo GABRA1 variants in childhood epilepsies and the molecular subregional effects. Frontiers in Molecular Neuroscience. 16. 1321090–1321090. 10 indexed citations
5.
Luo, Sheng, Xingguang Ye, Liang Jin, et al.. (2023). SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation. Frontiers in Molecular Neuroscience. 16. 1162408–1162408. 11 indexed citations
6.
Li, Xiaoyan, Xinguo Lu, Mengwen Zhang, et al.. (2023). Association of FAT1 with focal epilepsy and correlation between seizure relapse and gene expression stage. Seizure. 116. 37–44. 9 indexed citations
7.
Li, Zongjun, Jie Wang, Sheng Luo, et al.. (2022). SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges. Frontiers in Molecular Neuroscience. 15. 862480–862480. 5 indexed citations
8.
Luo, Sheng, Bin Li, Lihong Liu, et al.. (2022). PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation. Frontiers in Neurology. 13. 836048–836048. 2 indexed citations
9.
Ye, Tingting, Jiwei Zhang, Jie Wang, et al.. (2022). Variants inBSNgene associated with epilepsy with favourable outcome. Journal of Medical Genetics. 60(8). 776–783. 9 indexed citations
10.
Li, Xuelian, Zongjun Li, Xiaoyu Liang, et al.. (2022). CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications. Frontiers in Molecular Neuroscience. 15. 860662–860662. 18 indexed citations
11.
Luo, Sheng, Zhigang Liu, Juan Wang, et al.. (2022). Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy. Frontiers in Molecular Neuroscience. 15. 825390–825390. 19 indexed citations
12.
Li, Xiang, Xiao‐Rong Liu, Jie Wang, et al.. (2022). BCOR variants are associated with X-linked recessive partial epilepsy. Epilepsy Research. 187. 107036–107036. 11 indexed citations
13.
Liu, Xiao‐Rong, Yuan Wu, Jie Wang, et al.. (2021). RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia. Frontiers in Neuroscience. 15. 629610–629610. 20 indexed citations
14.
Liu, Xiao‐Rong, Xingxing Xu, Tingting Ye, et al.. (2021). GRIN2A Variants Associated With Idiopathic Generalized Epilepsies. Frontiers in Molecular Neuroscience. 14. 720984–720984. 16 indexed citations
15.
Wang, Jie, Sarah Poliquin, Jaclyn M. Eissman, et al.. (2020). Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism. Molecular Brain. 13(1). 76–76. 30 indexed citations
16.
Liu, Xiao‐Rong, Jie Wang, Tingting Ye, et al.. (2020). Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance. Frontiers in Genetics. 11. 559080–559080. 6 indexed citations
17.
Zeng, Yang, Bing Qin, Yi‐Wu Shi, et al.. (2020). Ilepcimide inhibited sodium channel activity in mouse hippocampal neurons. Epilepsy Research. 170. 106533–106533. 6 indexed citations
18.
Wang, Jingyang, Peng Zhou, Jie Wang, et al.. (2017). ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation. Neurogenetics. 19(1). 9–16. 42 indexed citations
19.
He, Na, Yi‐Wu Shi, Jing Guo, et al.. (2012). Cutaneous reactions induced by oxcarbazepine in Southern Han Chinese: Incidence, features, risk factors and relation to HLA-B alleles. Seizure. 21(8). 614–618. 32 indexed citations
20.
Li, Bing-Mei, Xiao‐Rong Liu, Yong‐Hong Yi, et al.. (2011). Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation. Epilepsy & Behavior. 21(3). 291–295. 92 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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