Jun Yoshimura

3.0k citations

49 papers · 2.2k · 1 hit paper · h-index 21

Impact in

Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 5%
- Amyotrophic Lateral Sclerosis Research

Papers in

Cellular and Molecular Neuroscience 9
- Genetic Neurodegenerative Diseases 5
- Hereditary Neurological Disorders 4
Neurology 8
- Amyotrophic Lateral Sclerosis Research 6
- Neurofibromatosis and Schwannoma Cases 2

Co-authors: Shinichi Morishita (34 shared papers)Yuki Naito (1 shared paper)Kumiko Ui‐Tei (1 shared paper)Shoji Tsuji (25 shared papers)Jun Mitsui (26 shared papers)Hiroyuki Ishiura (23 shared papers)Koichiro Doi (18 shared papers)Yuji Takahashi (9 shared papers)
Journals: Journal of the Neurological Sciences (4 papers)Bioinformatics (3 papers)Scientific Reports (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Nature Genetics (2 papers)
Partner nations: Japan United States France

In The Last Decade

Jun Yoshimura

48 papers receiving 2.2k citations

Jun Yoshimura'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

Peers

Countries citing papers authored by Jun Yoshimura

Since Specialization

Citations

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

Fields of papers citing papers by Jun Yoshimura

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jun Yoshimura, 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 Yoshimura Line = papers co-authored together Jun Yoshimura 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 49 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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
2	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
3	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
4	siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect BMC Bioinformatics ·Yuki Naito, Jun Yoshimura, Shinichi Morishita, Kumiko Ui‐Tei	2009	201
5	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
6	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
7	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
8	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
9	Centromere evolution and CpG methylation during vertebrate speciation Nature Communications ·Kazuki Ichikawa, Shingo Tomioka, Yuta Suzuki, Ryohei Nakamura, Koichiro Doi, Jun Yoshimura, Masahiko Kumagai, Yusuke Inoue	2017	67
10	Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut Microbiome ·Yoshihiko Suzuki, Suguru Nishijima, Yoshikazu Furuta, Jun Yoshimura, Wataru Suda, Kenshiro Oshima, Masahira Hattori, Shinichi Morishita	2019	64
11	ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish Molecular Biology of the Cell ·Tokiro Ishikawa, Tetsuya Okada, Tomoko Ishikawa‐Fujiwara, Takeshi Todo, Yasuhiro Kamei, Shuji Shigenobu, Minoru Tanaka, Taro Saito	2013	55
12	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
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	2017	45
14	Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency PLoS Genetics ·Masahito Kawazu, Shinya Kojima, Toshihide Ueno, Yasushi Totoki, Hiromi K. Nakamura, Akiko Kunita, Wei Qü, Jun Yoshimura	2017	43
15	Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy Brain ·Yujiro Higuchi, Ryuta Okunushi, Taichi Hara, Akihiro Hashiguchi, Jun‐Hui Yuan, Akiko Yoshimura, Kei Murayama, Akira Ohtake	2018	40
16	Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation Nucleic Acids Research ·Kyoko Ishino, Hidetoshi Hasuwa, Jun Yoshimura, Yuka W. Iwasaki, Hidenori Nishihara, Naomi M. Seki, Takamasa Hirano, Marie Tsuchiya	2021	38
17	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	2012	37
18	Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS Journal of Neurology Neurosurgery & Psychiatry ·Hiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, Yuji Takahashi, Takashi Matsukawa, Masaki Tanaka, Koichiro Doi, Jun Yoshimura	2018	30
19	Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines Molecular Brain ·Koki Fujimori, Toshiki Tezuka, Hiroyuki Ishiura, Jun Mitsui, Koichiro Doi, Jun Yoshimura, Hirobumi Tada, Takuya Matsumoto	2016	26
20	AgIn: measuring the landscape of CpG methylation of individual repetitive elements Bioinformatics ·Yuta Suzuki, Jonas Korlach, Stephen W. Turner, Tatsuya Tsukahara, Wei Qü, Kazuki Ichikawa, Jun Yoshimura, Hideaki Yurino	2016	25

About Jun Yoshimura

Jun Yoshimura is a scholar working on Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry, Molecular Biology and Genetics, having authored 49 papers that have together received 2.2k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (6 papers), Genetic Neurodegenerative Diseases (5 papers), Hereditary Neurological Disorders (4 papers), Genomics and Rare Diseases (3 papers), Metabolism and Genetic Disorders (2 papers), Neurofibromatosis and Schwannoma Cases (2 papers), Genomics and Phylogenetic Studies (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (370 citations), Neurology (263 citations), Genetics (196 citations), Psychiatry and Mental health (119 citations) and Molecular Biology (327 citations). Jun Yoshimura has collaborated with scholars based in Japan, United States and France. Frequent co-authors include Shinichi Morishita, Yuki Naito, Kumiko Ui‐Tei, Shoji Tsuji, Jun Mitsui, Hiroyuki Ishiura, Koichiro Doi, Yuji Takahashi, Jun Goto and Takashi Matsukawa. Their work appears in journals such as Journal of the Neurological Sciences, Bioinformatics, Scientific Reports, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Nature Genetics.

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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In The Last Decade

Jun Yoshimura

Jun Yoshimura's Hit Papers

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Fields of papers citing papers by Jun Yoshimura

All Works

About Jun Yoshimura

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