Jun Mitsui

7.0k citations

122 papers · 1.9k · h-index 24

Impact in

Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders

Papers in

Molecular Biology 49
- RNA regulation and disease 12
Neurology 32
- Neurological diseases and metabolism 13
- Amyotrophic Lateral Sclerosis Research 12
- Parkinson's Disease Mechanisms and Treatments 9

Co-authors: Shoji Tsuji (90 shared papers)Hiroyuki Ishiura (76 shared papers)Jun Goto (23 shared papers)Shinichi Morishita (32 shared papers)Yuji Takahashi (21 shared papers)Jun Yoshimura (25 shared papers)Takashi Matsukawa (30 shared papers)Tatsushi Toda (21 shared papers)
Journals: Journal of the Neurological Sciences (10 papers)Scientific Reports (5 papers)The Cerebellum (5 papers)Neurogenetics (4 papers)Annals of Clinical and Translational Neurology (3 papers)
Partner nations: Japan United States France

In The Last Decade

Jun Mitsui

112 papers receiving 1.8k citations

Peers

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-authors

The 25 scholars most cited alongside Jun Mitsui, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jun Mitsui Line = papers co-authored together Jun Mitsui links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 122 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations for Gaucher Disease Confer High Susceptibility to Parkinson Disease Archives of Neurology ·Jun Mitsui, Ikuko Mizuta, Atsushi Toyoda, Ryo Ashida, Yūji Takahashi, Jun Goto, Y. Fukuda, Hidetoshi Date, Atsushi Iwata, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Tatsushi Toda, Shoji Tsuji	2009	155
2	Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families Neurology ·Kenju Hara, Atsushi Shiga, Hiroaki Nozaki, Jun Mitsui, Yukihiro Takahashi, Hitomi Ishiguro, Harumi Yomono, Hiroshi Kurisaki, Jun Goto, Takeshi Ikeuchi, Shoji Tsuji, M Nishizawa, Osamu Onodera	2008	112
3	Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines The American Journal of Human Genetics ·Jun Mitsui, Yuji Takahashi, Jun Goto, Hiroyuki Tomiyama, Shunpei Ishikawa, Hiroyo Yoshino, Narihiro Minami, (unknown), Suzanne Lesage, Hiroyuki Aburatani, Ichizo Nishino, Alexis Brice, Nobutaka Hattori, Shoji Tsuji	2010	79
4	C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan Archives of Neurology ·Hiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, Sohei Yoshida, Tameko Kihira, Yasumasa Kokubo, Shigeki Kuzuhara, Laura P.W. Ranum, T Tamaoki, Yaeko Ichikawa, Hidetoshi Date, Jun Goto, Shoji Tsuji	2012	74
5	Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients PLoS ONE ·Atsushi Ishii, Yoshiaki Saito, Jun Mitsui, Hiroyuki Ishiura, Jun Yoshimura, Hidee Arai, Sumimasa Yamashita, Sadami Kimura, Hirokazu Oguni, Shinichi Morishita, Shoji Tsuji, Masayuki Sasaki, Shinichi Hirose	2013	67
6	A recurrent de novo FAM111A mutation causes kenny–caffey syndrome type 2 Journal of Bone and Mineral Research ·Tsuyoshi Isojima, Koichiro Doi, Jun Mitsui, Yoichiro Oda, Etsuro Tokuhiro, Akihiro Yasoda, Tohru Yorifuji, Reiko Horikawa, Jun Yoshimura, Hiroyuki Ishiura, Shinichi Morishita, Shoji Tsuji, Sachiko Kitanaka	2013	66
7	Pathology of the sympathetic nervous system corresponding to the decreased cardiac uptake in 123I-metaiodobenzylguanidine (MIBG) scintigraphy in a patient with Parkinson disease Journal of the Neurological Sciences ·Jun Mitsui, Yuko Saito, Toshimitsu Momose, Jun Shimizu, Noritoshi Arai, Junji Shibahara, Yoshikazu Ugawa, Ichiro Kanazawa, Shoji Tsuji, Shigeo Murayama	2006	63
8	Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan Neurology ·Megumi Yamada, Masaki Tanaka, Mari Takagi, Seiju Kobayashi, Yoshiharu Taguchi, Shutaro Takashima, Kortaro Tanaka, Tetsuo Touge, Hiroyuki Hatsuta, Shigeo Murayama, Yuichi Hayashi, Masayuki Kaneko, Hiroyuki Ishiura, Jun Mitsui, (unknown), Gen Sobue, Nobuyuki Shimozawa, Takashi Inuzuka, Shoji Tsuji, Isao Hozumi	2014	58
9	The pathogenesis linked to coenzyme Q10 insufficiency in iPSC-derived neurons from patients with multiple-system atrophy Scientific Reports ·Fumiko Kusunoki Nakamoto, Satoshi Okamoto, Jun Mitsui, Takefumi Sone, Mitsuru Ishikawa, Yorihiro Yamamoto, Yumi Kanegae, Yuhki Nakatake, Kent Imaizumi, Hiroyuki Ishiura, Shoji Tsuji, Hideyuki Okano	2018	54
10	Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing Bioinformatics ·Koichiro Doi, Taku Monjo, Pham Huy Hoang, Jun Yoshimura, Hideaki Yurino, Jun Mitsui, Hiroyuki Ishiura, Yuji Takahashi, Yaeko Ichikawa, Jun Goto, Shoji Tsuji, Shinichi Morishita	2013	48
11	Development of a High-Throughput Microarray-Based Resequencing System for Neurological Disorders and Its Application to Molecular Genetics of Amyotrophic Lateral Sclerosis Archives of Neurology ·Yuji Takahashi, Naomi Seki, Hiroyuki Ishiura, Jun Mitsui, Takashi Matsukawa, Atsushi Kishino, Osamu Onodera, Masashi Aoki, Nobuyuki Shimozawa, Shigeo Murayama, Yasuto Itoyama, Yasuyuki Suzuki, Gen Sobue, Masatoyo Nishizawa, Jun Goto, Shoji Tsuji	2008	41
12	Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1 Neurogenetics ·Hiroyuki Ishiura, Y. Fukuda, Jun Mitsui, Yasuo Nakahara, Budrul Ahsan, Yuji Takahashi, Yaeko Ichikawa, Jun Goto, Tetsuo Sakai, Shoji Tsuji	2011	40
13	Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation Neurobiology of Aging ·Hiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, Hidetoshi Date, Yuji Takahashi, Takashi Matsukawa, Masaki Tanaka, Akiko Ishii, Akira Tamaoka, Keiichi Hokkoku, Masahiro Sonoo, Mari Segawa, Yoshikazu Ugawa, Koichiro Doi, Jun Yoshimura, Shinichi Morishita, Jun Goto, Shoji Tsuji	2017	39
14	Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy JAMA Neurology ·Jun Mitsui, Takashi Matsukawa, Tsutomu Yasuda, Hiroyuki Ishiura, Shoji Tsuji	2016	38
15	CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Jun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, Koichiro Higasa, Jun Yoshimura, Taro Saito, Budrul Ahsan, Yuji Takahashi, Jun Goto, Atsushi Iwata, Yuki Niimi, Yuichi Riku, Yoji Goto, Kazuo Mano, Mari Yoshida, Shinichi Morishita, Shoji Tsuji	2012	33
16	Three-Year Follow-Up of High-Dose Ubiquinol Supplementation in a Case of Familial Multiple System Atrophy with Compound Heterozygous COQ2 Mutations The Cerebellum ·Jun Mitsui, Ken Koguchi, Toshimitsu Momose, M. Takahashi, Takashi Matsukawa, Tsutomu Yasuda, Shin‐ichi Tokushige, Hiroyuki Ishiura, Jun Goto, Shigeaki Nakazaki, Tomoyoshi Kondo, Hidefumi Ito, Yorihiro Yamamoto, Shoji Tsuji	2017	33
17	Associations of pathological diagnosis and genetic abnormalities in meningiomas with the embryological origins of the meninges Scientific Reports ·Atsushi Okano, Satoru Miyawaki, Hiroki Hongo, Shogo Dofuku, Yu Teranishi, Jun Mitsui, Michihiro Tanaka, Masahiro Shin, Hirofumi Nakatomi, Nobuhito Saito	2021	30
18	Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study Journal of the Peripheral Nervous System ·Masahiro Ando, Akihiro Hashiguchi, Yuji Okamoto, Akiko Yoshimura, Yu Hiramatsu, Jun‐Hui Yuan, Yujiro Higuchi, Jun Mitsui, Hiroyuki Ishiura, Ayako Umemura, Koichi Maruyama, Takeshi Matsushige, Shinichi Morishita, Masanori Nakagawa, Shoji Tsuji, Hiroshi Takashima	2017	29
19	Clinical and mutational spectrum of Charcot–Marie–Tooth disease type 2Z caused by MORC2 variants in Japan European Journal of Neurology ·Masahiro Ando, Yuji Okamoto, Akiko Yoshimura, Jun‐Hui Yuan, Yoshihiro Hiramatsu, Yujiro Higuchi, Akihiro Hashiguchi, Jun Mitsui, Hiroyuki Ishiura, Shinobu Fukumura, Masaaki Matsushima, Nobuhiko Ochi, Jun Tsugawa, Shinichi Morishita, Shoji Tsuji, Hiroshi Takashima	2017	28
20	Increased gene dosage of myelin protein zero causes Charcot‐Marie‐Tooth disease Annals of Neurology ·Meiko Hashimoto Maeda, Jun Mitsui, Bing‐Wen Soong, Yuji Takahashi, Hiroyuki Ishiura, Shin Hayashi, Yuichiro Shirota, Yaeko Ichikawa, Hideyuki Matsumoto, Makoto Arai, Tomoko Okamoto, Sahoko Miyama, Jun Shimizu, Johji Inazawa, Jun Goto, Shoji Tsuji	2011	28

About Jun Mitsui

Jun Mitsui is a scholar working on Molecular Biology, Neurology, Cellular and Molecular Neuroscience, Genetics and Neurology, having authored 122 papers that have together received 1.9k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (17 papers), Neurological diseases and metabolism (13 papers), Genetic Neurodegenerative Diseases (13 papers), Amyotrophic Lateral Sclerosis Research (12 papers), RNA regulation and disease (12 papers), Neurogenetic and Muscular Disorders Research (11 papers), Lysosomal Storage Disorders Research (11 papers) and Parkinson's Disease Mechanisms and Treatments (9 papers). The work is most often cited by research in Neurology (549 citations), Neurology (244 citations), Cellular and Molecular Neuroscience (462 citations), Genetics (184 citations) and Molecular Biology (817 citations). Jun Mitsui has collaborated with scholars based in Japan, United States and France. Frequent co-authors include Shoji Tsuji, Hiroyuki Ishiura, Jun Goto, Shinichi Morishita, Yuji Takahashi, Jun Yoshimura, Takashi Matsukawa, Tatsushi Toda, Koichiro Doi and Hidetoshi Date. Their work appears in journals such as Journal of the Neurological Sciences, Scientific Reports, The Cerebellum, Neurogenetics and Annals of Clinical and Translational Neurology.

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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Jun Mitsui

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In The Last Decade

Jun Mitsui

Peers

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Fields of papers citing papers by Jun Mitsui

All Works

About Jun Mitsui

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