Qi Zeng

791 total citations
21 papers, 524 citations indexed

About

Qi Zeng is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Qi Zeng has authored 21 papers receiving a total of 524 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Psychiatry and Mental health. Recurrent topics in Qi Zeng's work include Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Epilepsy research and treatment (6 papers). Qi Zeng is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Epilepsy research and treatment (6 papers). Qi Zeng collaborates with scholars based in China, United States and Australia. Qi Zeng's co-authors include Walter Hunziker, Zakir Hossain, Hui Ling Ko, Safiah Mohamed Ali, Jianliang Xu, Sathivel Ponniah, Wanjin Hong, Chee Peng Ng, Ke Guo and Yuehua Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Annals of Neurology.

In The Last Decade

Qi Zeng

21 papers receiving 516 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Qi Zeng China 11 266 228 204 127 52 21 524
Dalia Ghoneim United States 10 277 1.0× 125 0.5× 59 0.3× 33 0.3× 19 0.4× 15 409
Luigina Spaccini Italy 13 208 0.8× 159 0.7× 43 0.2× 29 0.2× 104 2.0× 47 455
Emily Tuttle United States 7 211 0.8× 113 0.5× 62 0.3× 32 0.3× 19 0.4× 10 314
Kristina Jülich United States 8 475 1.8× 116 0.5× 63 0.3× 57 0.4× 34 0.7× 14 674
Manuela Pendziwiat Germany 12 204 0.8× 103 0.5× 73 0.4× 71 0.6× 18 0.3× 21 379
Junehawk Lee South Korea 9 371 1.4× 221 1.0× 31 0.2× 46 0.4× 34 0.7× 20 569
Dimitar N. Azmanov Australia 12 191 0.7× 122 0.5× 25 0.1× 41 0.3× 53 1.0× 23 336
Sandra Whalen France 13 268 1.0× 157 0.7× 34 0.2× 13 0.1× 37 0.7× 28 417
Adeline Ngoh United Kingdom 8 136 0.5× 175 0.8× 15 0.1× 136 1.1× 35 0.7× 15 367
Emmanuelle Ranza Switzerland 12 137 0.5× 103 0.5× 19 0.1× 30 0.2× 20 0.4× 22 295

Countries citing papers authored by Qi Zeng

Since Specialization
Citations

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

Fields of papers citing papers by Qi Zeng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qi Zeng

This figure shows the co-authorship network connecting the top 25 collaborators of Qi Zeng. A scholar is included among the top collaborators of Qi Zeng 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 Qi Zeng. Qi Zeng 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.
Liu, Aijie, Xiaoli Zhang, Wenjuan Wu, et al.. (2023). Seizure course of PCDH19 clustering epilepsy in female children: A multicentre cohort study in China. Developmental Medicine & Child Neurology. 66(6). 804–815. 2 indexed citations
2.
Duan, Jing, Yan Chen, Tian Zhang, et al.. (2022). Non-convulsive Status Epilepticus in SEMA6B-Related Progressive Myoclonic Epilepsy: A Case Report With Literature Review. Frontiers in Pediatrics. 10. 859183–859183. 8 indexed citations
3.
Zeng, Qi, Ying Yang, Jing Duan, et al.. (2022). SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis. Frontiers in Molecular Neuroscience. 15. 809951–809951. 17 indexed citations
4.
Yang, Ying, Jing Zhang, Qi Zeng, et al.. (2022). Detecting genomic mosaicism in “de novo” genetic epilepsy by amplicon-based deep sequencing. Journal of Human Genetics. 68(2). 73–80. 2 indexed citations
5.
Yang, Ying, Qi Zeng, Wenshu XiangWei, et al.. (2021). GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications. Journal of Neurology. 269(5). 2649–2665. 10 indexed citations
6.
Yang, Liu, Jing Duan, Qi Zeng, et al.. (2021). Phenotypes in Children With SYNGAP1 Encephalopathy in China. Frontiers in Neuroscience. 15. 761473–761473. 13 indexed citations
7.
Zhou, Ping, et al.. (2020). A case report of microcephaly and refractory West syndrome associated with WDR62 mutation. SHILAP Revista de lepidopterología. 2(1). 2 indexed citations
8.
Zhang, Jing, et al.. (2019). Three cases of progressive myoclonic epilepsy caused by KCNC1 gene mutations and literature review. Zhonghua shiyong erke linchuang zazhi. 34(24). 1876–1881. 1 indexed citations
9.
Zhang, Jing, Aijie Liu, Liping Zhang, et al.. (2019). CHD2‐related epilepsy: novel mutations and new phenotypes. Developmental Medicine & Child Neurology. 62(5). 647–653. 20 indexed citations
10.
Burgess, Rosemary, Amy McTague, Katja Boysen, et al.. (2019). The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures. Annals of Neurology. 86(6). 821–831. 79 indexed citations
11.
Yang, Xiaoling, Xiaoxu Yang, Qi Zeng, et al.. (2019). ATP1A3 mosaicism in families with alternating hemiplegia of childhood. Clinical Genetics. 96(1). 43–52. 11 indexed citations
12.
Zhang, Jing, Qi Zeng, Liping Zhang, et al.. (2019). Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations. Seizure. 69. 228–234. 10 indexed citations
13.
Zeng, Qi, Jing Zhang, Cheng Yang, et al.. (2018). The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome. Developmental Medicine & Child Neurology. 60(6). 566–573. 26 indexed citations
14.
Zeng, Qi, et al.. (2018). [Clinical phenotypes of TBC1D24 gene related epilepsy].. PubMed. 56(9). 667–673. 4 indexed citations
15.
Zeng, Qi, et al.. (2018). [Phenotype study of SCN2A gene related epilepsy].. PubMed. 56(7). 518–523. 4 indexed citations
16.
Zeng, Qi, et al.. (2018). [Spectrum of mutations in benign familial neonatal-infantile epilepsy].. PubMed. 56(4). 267–273. 1 indexed citations
17.
Zeng, Qi, Xiaoling Yang, Jing Zhang, et al.. (2017). Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort. Journal of Human Genetics. 63(1). 9–18. 15 indexed citations
18.
Yang, Xiaoxu, Aijie Liu, Xiaojing Xu, et al.. (2017). Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort. Scientific Reports. 7(1). 15677–15677. 38 indexed citations
19.
Hossain, Zakir, Safiah Mohamed Ali, Hui Ling Ko, et al.. (2007). Glomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1. Proceedings of the National Academy of Sciences. 104(5). 1631–1636. 241 indexed citations
20.
Mullins, John J., et al.. (1988). Studies on the Regulation of Renin Genes Using Transgenic Mice. Clinical and Experimental Hypertension Part A Theory and Practice. 10(6). 1157–1167. 15 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

Breakdown of academic impact, for papers by Dalia Ghoneim Breakdown of academic impact, for papers by Luigina Spaccini Breakdown of academic impact, for papers by Emily Tuttle Breakdown of academic impact, for papers by Kristina Jülich Breakdown of academic impact, for papers by Manuela Pendziwiat Breakdown of academic impact, for papers by Junehawk Lee Breakdown of academic impact, for papers by Dimitar N. Azmanov Breakdown of academic impact, for papers by Sandra Whalen Breakdown of academic impact, for papers by Adeline Ngoh Breakdown of academic impact, for papers by Emmanuelle Ranza
Rankless by CCL
2026