Yong‐Hong Yi

3.1k total citations · 1 hit paper
83 papers, 1.9k citations indexed

About

Yong‐Hong Yi is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Yong‐Hong Yi has authored 83 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 39 papers in Molecular Biology and 22 papers in Psychiatry and Mental health. Recurrent topics in Yong‐Hong Yi's work include Genetics and Neurodevelopmental Disorders (43 papers), Epilepsy research and treatment (22 papers) and Genomics and Rare Diseases (21 papers). Yong‐Hong Yi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (43 papers), Epilepsy research and treatment (22 papers) and Genomics and Rare Diseases (21 papers). Yong‐Hong Yi collaborates with scholars based in China, United States and India. Yong‐Hong Yi's co-authors include Wei‐Ping Liao, Yi‐Wu Shi, Na He, Tao Su, Xiao‐Rong Liu, Zhi-Jian Lin, Yue‐Sheng Long, Haiqing Xu, Liu Liu and Jie Wang and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Yong‐Hong Yi

80 papers receiving 1.9k citations

Hit Papers

Epilepsy-associated genes 2016 2026 2019 2022 2016 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yong‐Hong Yi China 23 978 915 676 400 218 83 1.9k
Arvid Suls Belgium 22 866 0.9× 1.0k 1.1× 1.1k 1.7× 627 1.6× 94 0.4× 44 2.4k
Russell J. Buono United States 23 352 0.4× 847 0.9× 381 0.6× 723 1.8× 109 0.5× 66 1.6k
Guang Chen China 16 196 0.2× 570 0.6× 339 0.5× 285 0.7× 71 0.3× 38 1.3k
Sanjay N. Rakhade United States 15 139 0.1× 466 0.5× 526 0.8× 766 1.9× 195 0.9× 19 1.3k
Frédéric de Bock France 22 147 0.2× 612 0.7× 262 0.4× 677 1.7× 60 0.3× 35 1.7k
Joan Liu United Kingdom 22 129 0.1× 350 0.4× 606 0.9× 483 1.2× 129 0.6× 35 1.4k
Alberto Arregui Peru 24 385 0.4× 671 0.7× 122 0.2× 611 1.5× 90 0.4× 32 1.7k
John Kauwe United States 24 359 0.4× 659 0.7× 289 0.4× 111 0.3× 47 0.2× 53 1.7k
Jacqueline Rimmler United States 14 272 0.3× 709 0.8× 476 0.7× 307 0.8× 106 0.5× 17 2.3k

Countries citing papers authored by Yong‐Hong Yi

Since Specialization
Citations

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

Fields of papers citing papers by Yong‐Hong Yi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yong‐Hong Yi. 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 Yong‐Hong Yi. The network helps show where Yong‐Hong Yi may publish in the future.

Co-authorship network of co-authors of Yong‐Hong Yi

This figure shows the co-authorship network connecting the top 25 collaborators of Yong‐Hong Yi. A scholar is included among the top collaborators of Yong‐Hong Yi 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 Yong‐Hong Yi. Yong‐Hong Yi 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.
Meng, Xianghong, Wuchen Wu, Jing Guo, et al.. (2025). De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum. Epilepsia. 67(2). 846–861.
2.
Luo, Sheng, Wenjun Zhang, Lei Liu, et al.. (2025). De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy. Epilepsia. 66(7). 2365–2378. 3 indexed citations
3.
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
4.
Jin, Liang, Sheng Luo, Qian Peng, et al.. (2023). Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders. Seizure. 111. 172–177. 7 indexed citations
5.
Zhang, Mengwen, Xiaoyu Liang, Jie Wang, et al.. (2023). Epilepsy-associated genes: an update. Seizure. 116. 4–13. 32 indexed citations
6.
Lu, Qiang, Zan Wang, Wei Yue, et al.. (2023). Efficacy and safety of perampanel as early add-on therapy in Chinese patients with focal-onset seizures: a multicenter, open-label, single-arm study. Frontiers in Neurology. 14. 1236046–1236046. 3 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.
Chen, Zirong, Heng Meng, Liu Liu, et al.. (2018). Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlation. Seizure. 69. 180–185. 9 indexed citations
9.
He, Na, Zhi-Jian Lin, Jie Wang, et al.. (2018). Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies. Genetics in Medicine. 21(1). 17–27. 37 indexed citations
10.
Yan, Limin, Tao Su, Na He, et al.. (2017). Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy. Neuroscience Bulletin. 33(4). 455–477. 98 indexed citations
11.
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
12.
Chen, Shengqiang, et al.. (2016). Alpha-asarone improves striatal cholinergic function and locomotor hyperactivity in Fmr1 knockout mice. Behavioural Brain Research. 312. 212–218. 11 indexed citations
13.
Yang, Haixuan, Qi‐Hua Zhao, Mei‐Mei Gao, et al.. (2016). Involvement of FMRP in Primary MicroRNA Processing via Enhancing Drosha Translation. Molecular Neurobiology. 54(4). 2585–2594. 18 indexed citations
14.
Lin, Guo‐Wang, Tao Zeng, Huiling Tang, et al.. (2016). GAPDH-mediated posttranscriptional regulations of sodium channel Scn1a and Scn3a genes under seizure and ketogenic diet conditions. Neuropharmacology. 113(Pt A). 480–489. 12 indexed citations
15.
Liu, Ting, Shujing Liu, Qi‐Hua Zhao, et al.. (2014). A MicroRNA Profile in Fmr1 Knockout Mice Reveals MicroRNA Expression Alterations with Possible Roles in Fragile X Syndrome. Molecular Neurobiology. 51(3). 1053–1063. 29 indexed citations
16.
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
17.
Qin, Jiaming, Tao Su, Qi‐Hua Zhao, et al.. (2011). Promoter Analysis of Mouse Scn3a Gene and Regulation of the Promoter Activity by GC Box and CpG Methylation. Journal of Molecular Neuroscience. 44(2). 115–121. 7 indexed citations
18.
Shi, Yi‐Wu, Mei‐Mei Gao, Xiao‐Rong Liu, et al.. (2010). Milder phenotype with SCN1A truncation mutation other than SMEI. Seizure. 19(7). 443–445. 19 indexed citations
19.
Yi, Yong‐Hong, Wen‐Chao Guo, Weiwen Sun, et al.. (2008). Neuroprotection of lamotrigine on hypoxic-ischemic brain damage in neonatal rats: Relations to administration time and doses. SHILAP Revista de lepidopterología. 2 indexed citations
20.
Yi, Yong‐Hong. (2008). Research on Earthquake Forecast. Microelectronics & Computer. 2 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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