Jun Mitsui

6.8k total citations
115 papers, 1.7k citations indexed

About

Jun Mitsui is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jun Mitsui has authored 115 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 37 papers in Neurology and 34 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jun Mitsui's work include Hereditary Neurological Disorders (19 papers), Neurological diseases and metabolism (17 papers) and Genetic Neurodegenerative Diseases (16 papers). Jun Mitsui is often cited by papers focused on Hereditary Neurological Disorders (19 papers), Neurological diseases and metabolism (17 papers) and Genetic Neurodegenerative Diseases (16 papers). Jun Mitsui collaborates with scholars based in Japan, United States and France. Jun Mitsui's co-authors include Shoji Tsuji, Hiroyuki Ishiura, Jun Goto, Shinichi Morishita, Yuji Takahashi, Jun Yoshimura, Takashi Matsukawa, Tatsushi Toda, Koichiro Doi and Hidetoshi Date and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and PLoS ONE.

In The Last Decade

Jun Mitsui

109 papers receiving 1.7k 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 Mitsui Japan 24 860 582 480 284 281 115 1.7k
Hiroyuki Ishiura Japan 25 844 1.0× 627 1.1× 633 1.3× 290 1.0× 383 1.4× 146 1.8k
Alessandro Malandrini Italy 26 973 1.1× 577 1.0× 591 1.2× 217 0.8× 546 1.9× 95 2.2k
Ritchie Ho United States 16 1.2k 1.4× 622 1.1× 351 0.7× 140 0.5× 376 1.3× 22 2.0k
Jianwen Deng China 19 810 0.9× 651 1.1× 395 0.8× 107 0.4× 162 0.6× 85 1.4k
Jonathan Baets Belgium 26 1.1k 1.2× 324 0.6× 1.1k 2.3× 221 0.8× 384 1.4× 80 2.2k
Sílvia Porta United States 20 1.4k 1.6× 664 1.1× 423 0.9× 124 0.4× 228 0.8× 27 2.0k
Takuya Yagi Japan 21 964 1.1× 402 0.7× 362 0.8× 99 0.3× 103 0.4× 57 1.8k
Cédric Raoul France 28 1.3k 1.5× 1.2k 2.1× 688 1.4× 191 0.7× 359 1.3× 70 2.7k
Francesco Paolo Di Giorgio Italy 14 1.5k 1.8× 637 1.1× 486 1.0× 144 0.5× 271 1.0× 26 2.3k
Youn‐Bok Lee United Kingdom 22 1.2k 1.4× 769 1.3× 360 0.8× 140 0.5× 132 0.5× 39 1.9k

Countries citing papers authored by Jun Mitsui

Since Specialization
Citations

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

Fields of papers citing papers by Jun Mitsui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jun Mitsui

This figure shows the co-authorship network connecting the top 25 collaborators of Jun Mitsui. A scholar is included among the top collaborators of Jun Mitsui 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 Mitsui. Jun Mitsui 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.
Matsukawa, Takashi, Kazutaka Shiomi, Akihiko Mitsutake, et al.. (2025). Two Japanese families with adult-onset leukoencephalopathy caused by pathogenic variants in CST3. Journal of the Neurological Sciences. 478. 123708–123708.
2.
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
3.
Matsukawa, Takashi, Yasufumi Hayashi, Akihiko Mitsutake, et al.. (2025). Vanishing White Matter Disease With EIF2B2 c.254T >A Variant. Neurology Genetics. 11(5). e200293–e200293.
4.
Ishiura, Hiroyuki, Atsushi Sudo, Kayoko Esaki, et al.. (2024). Genetic and functional analyses of SPTLC1 in juvenile amyotrophic lateral sclerosis. Journal of Neurology. 272(1). 36–36.
5.
Hamada, Yuichi, Shunsuke Kobayashi, Hiroyuki Ishiura, et al.. (2023). Noncanonical splice‐site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies. Journal of the Peripheral Nervous System. 28(3). 513–517. 1 indexed citations
6.
Mitsutake, Akihiko, Takashi Matsukawa, Atsushi Iwata, et al.. (2023). Favorable outcome of hematopoietic stem cell transplantation in late-onset Krabbe disease. Brain and Development. 45(7). 408–412. 4 indexed citations
7.
Takahashi, Akiko, Jun Mitsui, Yusuke Sugiyama, et al.. (2023). Late-onset Myoclonic Seizure in a 78-year-old Woman with Gaucher Disease. Internal Medicine. 63(6). 861–865.
8.
Kobayashi, Ryota, Shinobu Kawakatsu, Chifumi Iseki, et al.. (2022). Valosin-containing protein Asp395Gly mutation in a patient with frontotemporal dementia: a case report. BMC Neurology. 22(1). 406–406. 3 indexed citations
9.
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
10.
Enomoto, Yumi, Yoshinori Tsurusaki, Hiroaki Murakami, et al.. (2021). Divergent variant patterns among 19 patients with Rubinstein‐Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing. Clinical Genetics. 101(3). 335–345. 4 indexed citations
11.
Fukushi, Daisuke, Jun Yoshimura, Y. Suzuki, et al.. (2020). Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivation. Human Mutation. 41(8). 1447–1460. 3 indexed citations
12.
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
13.
Kobayashi, Yuta, Junichi Shindoh, Yujiro Nishioka, et al.. (2020). Germline MICA Polymorphism Is Associated with the Long-Term Outcomes in Patients Undergoing Hepatectomy for Colorectal Liver Metastases. Journal of Gastrointestinal Surgery. 24(9). 2137–2139. 1 indexed citations
14.
Ando, Masahiro, Yuji Okamoto, Akiko Yoshimura, et al.. (2020). Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan. Clinical Genetics. 99(3). 359–375. 18 indexed citations
15.
Nakano, Yumiko, Keiichiro Tsunoda, Toru Yamashita, et al.. (2019). Late presented congenital myasthenic syndrome with novel compound heterozygous CHRNE mutations mimicking seronegative myasthenia gravis. Neurology and Clinical Neuroscience. 7(5). 288–290. 1 indexed citations
16.
Nishioka, Yujiro, Junichi Shindoh, Yoshinori Inagaki, et al.. (2018). Host MICA Polymorphism as a Potential Predictive Marker in Response to Chemotherapy for Colorectal Liver Metastases. Digestive Diseases. 36(6). 437–445. 4 indexed citations
17.
Koh, Kishin, Yuta Ichinose, Hiroyuki Ishiura, et al.. (2018). PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia. Journal of Human Genetics. 64(1). 55–59. 17 indexed citations
18.
Suzuki, Yuta, Jonas Korlach, Stephen W. Turner, et al.. (2016). AgIn: measuring the landscape of CpG methylation of individual repetitive elements. Bioinformatics. 32(19). 2911–2919. 20 indexed citations
19.
Ikeda, Toshio, Rie Nagano, Hiroshi Moritake, et al.. (2016). TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophy. Journal of Human Genetics. 62(4). 473–480. 13 indexed citations
20.
Mitsui, Jun & Yasuhisa Kunimi. (1988). Effect of larval phase on susceptibility of the armyworm, Pseudaletia separata walker (Lepidoptera:Noctuidae) to an Entomogeneous Deuteromycete, Nomuraea rileyi.. Japanese Journal of Applied Entomology and Zoology. 32(2). 129–134. 13 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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