Jijun Wan

3.7k total citations
15 papers, 815 citations indexed

About

Jijun Wan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Jijun Wan has authored 15 papers receiving a total of 815 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Jijun Wan's work include Mitochondrial Function and Pathology (7 papers), Ion channel regulation and function (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Jijun Wan is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Ion channel regulation and function (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Jijun Wan collaborates with scholars based in United States, China and Australia. Jijun Wan's co-authors include Joanna C. Jen, Robert W. Baloh, Bruce D. Howard, Diane M. Papazian, Mu‐ming Poo, M C Graves, Janos Steffen, Qing Yue, Hafsa Mamsa and Allan F. Mock and has published in prestigious journals such as Science, Brain and Neurology.

In The Last Decade

Jijun Wan

14 papers receiving 805 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jijun Wan United States 11 530 463 145 145 101 15 815
Tine Deconinck Belgium 17 376 0.7× 376 0.8× 107 0.7× 150 1.0× 149 1.5× 28 733
Sung‐Eun Kwak South Korea 16 362 0.7× 417 0.9× 33 0.2× 189 1.3× 101 1.0× 34 718
Liana Veneziano Italy 14 564 1.1× 511 1.1× 235 1.6× 177 1.2× 69 0.7× 30 825
Nicol Birsa United Kingdom 15 786 1.5× 153 0.3× 265 1.8× 57 0.4× 57 0.6× 17 1.1k
Cécilia Marelli France 18 378 0.7× 327 0.7× 221 1.5× 34 0.2× 170 1.7× 35 682
Ana Mingorance Spain 15 331 0.6× 492 1.1× 42 0.3× 266 1.8× 81 0.8× 26 933
Romina Combi Italy 19 496 0.9× 375 0.8× 77 0.5× 349 2.4× 58 0.6× 38 1.1k
Lena E. Hjermind Denmark 18 405 0.8× 403 0.9× 388 2.7× 69 0.5× 100 1.0× 47 904
Ruth Rea United Kingdom 8 597 1.1× 444 1.0× 72 0.5× 43 0.3× 33 0.3× 10 730
Claire‐Marie Dhaenens France 23 792 1.5× 262 0.6× 166 1.1× 31 0.2× 86 0.9× 64 1.1k

Countries citing papers authored by Jijun Wan

Since Specialization
Citations

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

Fields of papers citing papers by Jijun Wan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jijun Wan

This figure shows the co-authorship network connecting the top 25 collaborators of Jijun Wan. A scholar is included among the top collaborators of Jijun Wan 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 Jijun Wan. Jijun Wan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Huang, Alden, et al.. (2024). Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genetics in Medicine. 26(11). 101218–101218.
2.
Scripture-Adams, Deirdre D., Florian Barthélémy, Richard T. Wang, et al.. (2022). Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue. Communications Biology. 5(1). 989–989. 23 indexed citations
3.
Jen, Joanna C. & Jijun Wan. (2018). Episodic ataxias. Handbook of clinical neurology. 148. 521–529. 5 indexed citations
4.
Jen, Joanna C. & Jijun Wan. (2018). Episodic ataxias. Handbook of clinical neurology. 155. 205–215. 30 indexed citations
5.
Steffen, Janos, Ajay A. Vashisht, Jijun Wan, et al.. (2017). Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria. Molecular Biology of the Cell. 28(5). 600–612. 65 indexed citations
6.
Wan, Jijun, Janos Steffen, Michael Yourshaw, et al.. (2016). Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. Brain. 139(11). 2877–2890. 69 indexed citations
7.
Hsieh, Jui-Yi, et al.. (2014). Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish. Frontiers in Neural Circuits. 8. 147–147. 31 indexed citations
8.
Vries, Boukje de, Hafsa Mamsa, Anine H Stam, et al.. (2009). Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake. Archives of Neurology. 66(1). 97–101. 99 indexed citations
9.
Jen, Joanna C., et al.. (2005). Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures. Neurology. 65(4). 529–534. 260 indexed citations
10.
Wan, Jijun, et al.. (2005). CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics. Neurology. 64(12). 2090–2097. 44 indexed citations
11.
Wan, Jijun, Janai R. Carr, Robert W. Baloh, & Joanna C. Jen. (2004). Nonconsensus intronic mutations cause episodic ataxia. Annals of Neurology. 57(1). 131–135. 10 indexed citations
12.
Maselli, Ricardo A., Jijun Wan, M C Graves, et al.. (2003). Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2. Neurology. 61(12). 1743–1748. 30 indexed citations
13.
Jen, Joanna C., Jijun Wan, M C Graves, et al.. (2001). Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission. Neurology. 57(10). 1843–1848. 105 indexed citations
14.
15.
Wan, Jijun & Mu‐ming Poo. (1999). Activity-Induced Potentiation of Developing Neuromuscular Synapses. Science. 285(5434). 1725–1728. 38 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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