Jun Mitsui

7k citations

165 papers · 5.6k · 2 hit papers · h-index 30

Impact in

Neurology top 0.5%
- Parkinson's Disease Mechanisms and Treatments
- Amyotrophic Lateral Sclerosis Research
Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders

Papers in

Cellular and Molecular Neuroscience 50
- Hereditary Neurological Disorders 39
- Genetic Neurodegenerative Diseases 14
Neurology 44
- Amyotrophic Lateral Sclerosis Research 18
- Parkinson's Disease Mechanisms and Treatments 13

Co-authors: Shoji Tsuji (101 shared papers)Hiroyuki Ishiura (85 shared papers)Jun Goto (25 shared papers)Shinichi Morishita (35 shared papers)Yuji Takahashi (23 shared papers)Takashi Matsukawa (34 shared papers)Jun Yoshimura (26 shared papers)Tatsushi Toda (26 shared papers)
Journals: Journal of the Neurological Sciences (12 papers)Scientific Reports (7 papers)The Cerebellum (6 papers)Neurogenetics (6 papers)Annals of Clinical and Translational Neurology (5 papers)
Partner nations: Japan United States France

In The Last Decade

Jun Mitsui

151 papers receiving 5.5k citations

Jun Mitsui's Hit Papers

align trajectories log scale

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease 2019 · 316 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2019 Nature Genetics
2009 New England Journal of Medicine

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 165 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease New England Journal of Medicine ·Ellen Sidransky, Mike A. Nalls, Jan Olav Aasly, Judith Aharon‐Peretz, Grazia Annesi, Egberto Reis Barbosa, Anat Bar‐Shira, Daniela Berg Hit paper breakdown →	2009	1771
2	Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease Nature Genetics ·Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, Yuta Suzuki, Wei Qü, Koichiro Doi, Junko Kanda Kikuchi, Makiko Taira Hit paper breakdown →	2019	316
3	Human genetic variation database, a reference database of genetic variations in the Japanese population Journal of Human Genetics ·Koichiro Higasa, Noriko Miyake, Jun Yoshimura, K. Okamura, Tetsuya Niihori, Hirotomo Saitsu, Koichiro Doi, Masakazu Shimizu	2016	263
4	Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy Nature Genetics ·Hiroyuki Ishiura, Koichiro Doi, Jun Mitsui, Jun Yoshimura, Asao Fujiyama, Yasuko Toyoshima, Akiyoshi Kakita, Hitoshi Takahashi	2018	233
5	CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia Nature Communications ·Kelly L. Williams, Simon D. Topp, Shu Yang, Bradley N. Smith, Jennifer A. Fifita, Sadaf T. Warraich, Katharine Y. Zhang, Natalie E. Farrawell	2016	184
6	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	2009	171
7	ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19 The American Journal of Human Genetics ·Yuji Takahashi, Y. Fukuda, Jun Yoshimura, Atsushi Toyoda, Kari J. Kurppa, Hiroyoko Moritoyo, Véronique Belzil, Patrick A. Dion	2013	119
8	Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families Neurology ·Kenju Hara, Atsushi Shiga, Hiroaki Nozaki, Jun Mitsui, Yukihiro Takahashi, Harumi Yomono, Hiroshi Kurisaki, Jun Goto	2008	116
9	The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement The American Journal of Human Genetics ·Hiroyuki Ishiura, Wataru Sako, Mari Yoshida, Toshitaka Kawarai, Osamu Tanabe, Jun Goto, Yuji Takahashi, Hidetoshi Date	2012	94
10	Variants associated with Gaucher disease in multiple system atrophy Annals of Clinical and Translational Neurology ·Jun Mitsui, Takashi Matsukawa, Hidenao Sasaki, Ichiro Yabe, Masaaki Matsushima, Alexandra Dürr, Alexis Brice, Hiroshi Takashima	2015	91
11	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	2012	86
12	Mutations inMMEcause an autosomal‐recessive Charcot–Marie–Tooth disease type 2 Annals of Neurology ·Yujiro Higuchi, Akihiro Hashiguchi, Jun‐Hui Yuan, Akiko Yoshimura, Jun Mitsui, Hiroyuki Ishiura, Masaki Tanaka, Satoshi Ishihara	2016	83
13	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, Hiroyo Yoshino, Narihiro Minami, Suzanne Lesage, Hiroyuki Aburatani	2010	82
14	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	2013	77
15	A Novel Mutation inELOVL4Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia JAMA Neurology ·Kokoro Ozaki, Hiroshi Doi, Jun Mitsui, Nozomu J. Sato, Yoichiro Iikuni, Takamasa Majima, Takashi Irioka, Hiroyuki Ishiura	2015	73
16	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	2014	71
17	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	2013	68
18	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	2006	63
19	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	2018	57
20	Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing Bioinformatics ·Koichiro Doi, Taku Monjo, Jun Yoshimura, Hideaki Yurino, Jun Mitsui, Hiroyuki Ishiura, Yuji Takahashi, Yaeko Ichikawa	2013	54

About Jun Mitsui

Jun Mitsui is a scholar working on Cellular and Molecular Neuroscience, Neurology, Genetics, Physiology and Clinical Biochemistry, having authored 165 papers that have together received 5.6k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (39 papers), Amyotrophic Lateral Sclerosis Research (18 papers), Genomics and Rare Diseases (16 papers), Genetic Neurodegenerative Diseases (14 papers), Lysosomal Storage Disorders Research (13 papers), Parkinson's Disease Mechanisms and Treatments (13 papers), Coenzyme Q10 studies and effects (9 papers) and Metabolism and Genetic Disorders (8 papers). The work is most often cited by research in Neurology (2k citations), Cellular and Molecular Neuroscience (1.1k citations), Physiology (1.1k citations), Neurology (195 citations) and Genetics (629 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, Takashi Matsukawa, Jun Yoshimura, 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

Jun Mitsui's Hit Papers

Peers

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Fields of papers citing papers by Jun Mitsui

All Works

About Jun Mitsui

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