Jun‐Hui Yuan

1.0k total citations
48 papers, 522 citations indexed

About

Jun‐Hui Yuan is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Jun‐Hui Yuan has authored 48 papers receiving a total of 522 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 21 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Jun‐Hui Yuan's work include Hereditary Neurological Disorders (21 papers), Genetic Neurodegenerative Diseases (10 papers) and Neurological diseases and metabolism (8 papers). Jun‐Hui Yuan is often cited by papers focused on Hereditary Neurological Disorders (21 papers), Genetic Neurodegenerative Diseases (10 papers) and Neurological diseases and metabolism (8 papers). Jun‐Hui Yuan collaborates with scholars based in Japan, United States and China. Jun‐Hui Yuan's co-authors include Hiroshi Takashima, Akiko Yoshimura, Akihiro Hashiguchi, Yujiro Higuchi, Yuji Okamoto, Tomonori Nakamura, Masahiro Ando, Stephen G. Waxman, Yusuke Sakiyama and Sulayman D. Dib‐Hajj and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Journal of Neurophysiology.

In The Last Decade

Jun‐Hui Yuan

44 papers receiving 518 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jun‐Hui Yuan Japan 13 314 210 133 93 90 48 522
Tae‐Ryong Riew South Korea 11 92 0.3× 178 0.8× 74 0.6× 38 0.4× 78 0.9× 32 378
Antonio Berretta United Kingdom 11 158 0.5× 156 0.7× 122 0.9× 154 1.7× 46 0.5× 15 486
Robyn Labrum United Kingdom 14 400 1.3× 488 2.3× 62 0.5× 175 1.9× 32 0.4× 21 772
Jennifer Müller vom Hagen Germany 12 117 0.4× 169 0.8× 51 0.4× 150 1.6× 152 1.7× 15 440
Hao Chiang Taiwan 13 108 0.3× 196 0.9× 29 0.2× 62 0.7× 202 2.2× 15 451
Gavin Charlesworth United Kingdom 14 356 1.1× 176 0.8× 93 0.7× 472 5.1× 63 0.7× 18 658
Elena Giusto United Kingdom 10 94 0.3× 203 1.0× 102 0.8× 74 0.8× 61 0.7× 16 438
Gautam Wali Australia 12 169 0.5× 119 0.6× 77 0.6× 103 1.1× 30 0.3× 30 363
Yujiro Higuchi Japan 13 381 1.2× 206 1.0× 161 1.2× 135 1.5× 47 0.5× 53 551
Anthony Crawley United States 9 233 0.7× 166 0.8× 105 0.8× 455 4.9× 116 1.3× 9 677

Countries citing papers authored by Jun‐Hui Yuan

Since Specialization
Citations

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

Fields of papers citing papers by Jun‐Hui Yuan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jun‐Hui Yuan. 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 Jun‐Hui Yuan. The network helps show where Jun‐Hui Yuan may publish in the future.

Co-authorship network of co-authors of Jun‐Hui Yuan

This figure shows the co-authorship network connecting the top 25 collaborators of Jun‐Hui Yuan. A scholar is included among the top collaborators of Jun‐Hui Yuan 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 Jun‐Hui Yuan. Jun‐Hui Yuan 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.
Ando, Masahiro, Yujiro Higuchi, Jun‐Hui Yuan, et al.. (2025). SOD1-related inherited peripheral neuropathies in a Japanese cohort: genetic variants and clinical insights. Journal of Neurology. 272(3). 191–191. 1 indexed citations
2.
Higuchi, Yujiro, Mari Yoshida, Masahito Suehara, et al.. (2024). Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications. Acta Neuropathologica Communications. 12(1). 136–136. 3 indexed citations
3.
4.
Okamoto, Yuji, Masahiro Ando, Yujiro Higuchi, et al.. (2024). A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review. Neurogenetics. 25(2). 149–156.
5.
Ghovanloo, Mohammad‐Reza, Philip R. Effraim, Xiaoyang Cheng, et al.. (2024). TRPM8 Mutations Associated With Persistent Pain After Surgical Injury of Corneal Trigeminal Axons. Neurology Genetics. 10(6). e200206–e200206.
6.
Gualdani, Roberta, Jun‐Hui Yuan, Deborah S. Jacobs, et al.. (2024). TRPV1 corneal neuralgia mutation: Enhanced pH response, bradykinin sensitization, and capsaicin desensitization. Proceedings of the National Academy of Sciences. 121(37). e2406186121–e2406186121. 2 indexed citations
7.
Ghovanloo, Mohammad‐Reza, Philip R. Effraim, Jun‐Hui Yuan, et al.. (2023). Nav1.7 P610T mutation in two siblings with persistent ocular pain after corneal axon transection: impaired slow inactivation and hyperexcitable trigeminal neurons. Journal of Neurophysiology. 129(3). 609–618. 9 indexed citations
8.
Yuan, Jun‐Hui, Xiaoyang Cheng, Eiji Matsuura, et al.. (2023). Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders. Journal of the Peripheral Nervous System. 28(4). 597–607. 4 indexed citations
9.
Ando, Masahiro, Yujiro Higuchi, Jun‐Hui Yuan, et al.. (2023). Clinical phenotypic diversity ofNOTCH2NLC-related disease in the largest case series of inherited peripheral neuropathy in Japan. Journal of Neurology Neurosurgery & Psychiatry. 94(8). 622–630. 8 indexed citations
10.
Higuchi, Yujiro, Masahiro Ando, Akiko Yoshimura, et al.. (2023). Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation. Frontiers in Neurology. 14. 1241678–1241678. 3 indexed citations
11.
Yuan, Jun‐Hui, Yujiro Higuchi, Akihiro Hashiguchi, et al.. (2023). Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan. Frontiers in Neurology. 14. 1078195–1078195. 2 indexed citations
12.
Ando, Masahiro, Yujiro Higuchi, Yuji Okamoto, et al.. (2022). An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families. Journal of Human Genetics. 67(7). 399–403. 5 indexed citations
13.
Gualdani, Roberta, Philippe Gailly, Jun‐Hui Yuan, et al.. (2022). A TRPM7 mutation linked to familial trigeminal neuralgia: Omega current and hyperexcitability of trigeminal ganglion neurons. Proceedings of the National Academy of Sciences. 119(38). e2119630119–e2119630119. 16 indexed citations
14.
Yuan, Jun‐Hui, Yujiro Higuchi, Akihiro Hashiguchi, et al.. (2022). Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series study. Journal of Neurology. 269(12). 6406–6415. 3 indexed citations
15.
Ishihara, Satoshi, Yuji Okamoto, Hajime Tanabe, et al.. (2020). Clinical features of inherited neuropathy with BSCL2 mutations in Japan. Journal of the Peripheral Nervous System. 25(2). 125–131. 10 indexed citations
16.
Yoshimura, Akiko, Jun‐Hui Yuan, Akihiro Hashiguchi, et al.. (2018). Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan. Journal of Neurology Neurosurgery & Psychiatry. 90(2). 195–202. 62 indexed citations
17.
Yuan, Jun‐Hui, Akihiro Hashiguchi, Akiko Yoshimura, et al.. (2017). Clinical diversity caused by novel IGHMBP2 variants. Journal of Human Genetics. 62(6). 599–604. 20 indexed citations
18.
Yuan, Jun‐Hui, Yusuke Sakiyama, Itsuro Higuchi, et al.. (2013). Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation. Journal of Clinical Pathology. 66(8). 659–664. 11 indexed citations
19.
Yuan, Jun‐Hui, Eiji Matsuura, Yujiro Higuchi, et al.. (2013). Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation. Neurology. 80(18). 1641–1649. 51 indexed citations
20.
Yuan, Jun‐Hui, et al.. (2008). Genetically Confirmed Patients with Merosin-deficient Congenital Muscular Dystrophy in China. Neuropediatrics. 39(5). 264–267. 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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