Yi‐Wu Shi

2.7k total citations · 1 hit paper
58 papers, 1.7k citations indexed

About

Yi‐Wu Shi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Yi‐Wu Shi has authored 58 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 21 papers in Genetics and 18 papers in Cellular and Molecular Neuroscience. Recurrent topics in Yi‐Wu Shi's work include Genetics and Neurodevelopmental Disorders (16 papers), Epilepsy research and treatment (15 papers) and Neuroscience and Neuropharmacology Research (13 papers). Yi‐Wu Shi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (16 papers), Epilepsy research and treatment (15 papers) and Neuroscience and Neuropharmacology Research (13 papers). Yi‐Wu Shi collaborates with scholars based in China, United States and Australia. Yi‐Wu Shi's co-authors include Wei‐Ping Liao, Yong‐Hong Yi, Na He, Zhi-Jian Lin, Xiao‐Rong Liu, Haiqing Xu, Tao Su, Jie Wang, Liu Liu and Yue‐Sheng Long and has published in prestigious journals such as Blood, Nature Neuroscience and Brain.

In The Last Decade

Yi‐Wu Shi

55 papers receiving 1.7k 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
Yi‐Wu Shi China 22 682 642 537 453 265 58 1.7k
Christopher J. Yuskaitis United States 16 914 1.3× 588 0.9× 265 0.5× 309 0.7× 98 0.4× 31 1.7k
Russell J. Buono United States 23 847 1.2× 352 0.5× 381 0.7× 723 1.6× 40 0.2× 66 1.6k
Ren‐Wu Chen United States 17 970 1.4× 294 0.5× 386 0.7× 657 1.5× 120 0.5× 20 2.0k
Adeline K. Nicholas United Kingdom 15 1.3k 1.8× 401 0.6× 70 0.1× 569 1.3× 89 0.3× 26 2.1k
Jan K. Teller United States 16 1.0k 1.5× 158 0.2× 250 0.5× 816 1.8× 137 0.5× 30 3.0k
Galila Agam Israel 25 764 1.1× 420 0.7× 388 0.7× 472 1.0× 115 0.4× 55 1.6k
Chiara Villa Italy 23 948 1.4× 145 0.2× 194 0.4× 258 0.6× 101 0.4× 76 1.9k
Luiz Miguel Camargo United States 18 1.4k 2.1× 393 0.6× 136 0.3× 516 1.1× 240 0.9× 22 2.1k
Snezana Maljevic Germany 25 1.5k 2.2× 577 0.9× 769 1.4× 1.2k 2.7× 45 0.2× 52 2.3k
Hiroko Sugiura Japan 22 1.1k 1.6× 206 0.3× 130 0.2× 713 1.6× 275 1.0× 38 2.0k

Countries citing papers authored by Yi‐Wu Shi

Since Specialization
Citations

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

Fields of papers citing papers by Yi‐Wu Shi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yi‐Wu Shi

This figure shows the co-authorship network connecting the top 25 collaborators of Yi‐Wu Shi. A scholar is included among the top collaborators of Yi‐Wu Shi 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 Yi‐Wu Shi. Yi‐Wu Shi 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.
Guo, Yutao, et al.. (2025). De novo heterozygous missense variants in ATP11A are associated with refractory focal epilepsy. Journal of Medical Genetics. 62(6). 396–404.
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.
Anderson, Alison, Yi‐Wu Shi, Ching Ching Ng, et al.. (2022). Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti‐seizure medications. Epilepsia. 63(4). 936–949. 5 indexed citations
4.
Li, Wenbin, Chao Zhang, Zongyan Li, et al.. (2022). Novel PANK2 Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype–Phenotype Correlation. Frontiers in Aging Neuroscience. 14. 848919–848919. 5 indexed citations
5.
Zhou, Xijing, Haiqing Xu, Bin Tang, et al.. (2021). Differences in SCN1A intronic variants result in diverse aberrant splicing patterns and are related to the phenotypes of epilepsy with febrile seizures. Epilepsy Research. 176. 106711–106711. 6 indexed citations
6.
Chen, Qian, Christopher A Deister, Xianhua Gao, et al.. (2020). Dysfunction of cortical GABAergic neurons leads to sensory hyper-reactivity in a Shank3 mouse model of ASD. Nature Neuroscience. 23(4). 520–532. 122 indexed citations
7.
Chen, Qian, Christopher A Deister, Xianhua Gao, et al.. (2020). Dysfunction of cortical GABAergic neurons leads to sensory hyper-reactivity in a Shank3 mouse model of ASD. DSpace@MIT (Massachusetts Institute of Technology). 2 indexed citations
8.
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
9.
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
10.
He, Na, Juan Wang, Bing Qin, et al.. (2019). HLA-B*13:01 as a Risk Allele for Antiepileptic Drugs-Induced Cutaneous Adverse Reactions: Higher Risk for Cross-Reactivity?. Frontiers in Neurology. 10. 614–614. 3 indexed citations
11.
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
12.
Xu, Xingxing, Xiao‐Rong Liu, Yi‐Wu Shi, et al.. (2017). Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy. Neuroscience Bulletin. 34(2). 237–246. 13 indexed citations
13.
Wang, Jie, Zhi-Jian Lin, Liu Liu, et al.. (2016). Epilepsy-associated genes. Seizure. 44. 11–20. 302 indexed citations breakdown →
14.
Lv, Yudan, Wei‐Ping Liao, Na He, et al.. (2013). The association between oxcarbazepine-induced maculopapular eruption and HLA-B alleles in a Northern Han Chinese population. BMC Neurology. 13(1). 75–75. 29 indexed citations
15.
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
16.
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
17.
Shi, Yi‐Wu, et al.. (2009). [Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome].. PubMed. 89(47). 3320–3. 5 indexed citations
18.
Shi, Yi‐Wu, et al.. (2007). Molecular features and expression of DAZAP2 in human multiple myeloma. Chinese Medical Journal. 120(19). 1659–1665. 8 indexed citations
19.
Tian, Jingyan, et al.. (2003). Cloning and sequence analysis of tumor-associated gene hMMTAG2 from human multiple myeloma cell line ARH-77.. PubMed. 35(2). 143–8. 2 indexed citations
20.
Shi, Yi‐Wu, Weixin Hu, & Lijun Tang. (2003). [Gene expression profile changes in human multiple myeloma].. PubMed. 28(3). 201–5. 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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