Jun Yoshimura

3.3k citations

49 papers · 1.1k indexed · h-index 18

Impact in

Aging top 5%
Molecular Biology
- Genomics and Phylogenetic Studies
- RNA Interference and Gene Delivery
- CRISPR and Genetic Engineering
- Advanced biosensing and bioanalysis techniques
- RNA modifications and cancer

Papers in ⓘ

Genetics 7
- Neurogenetic and Muscular Disorders Research 7
Aging 1

Co-authors: Shinichi Morishita (33 shared papers)Yuki Naito (1 shared paper)Kumiko Ui‐Tei (1 shared paper)Shoji Tsuji (23 shared papers)Jun Mitsui (25 shared papers)Hiroyuki Ishiura (22 shared papers)Koichiro Doi (17 shared papers)K. Kohra (2 shared papers)
Journals: Journal of Crystal Growth (5 papers)Journal of the Neurological Sciences (4 papers)Bioinformatics (3 papers)Scientific Reports (2 papers)Composite Structures (2 papers)
Partner nations: Japan United States South Korea

In The Last Decade

Jun Yoshimura

47 papers receiving 1.0k citations

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	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	174
2	Recompleting the Caenorhabditis elegans genome Genome Research ·Jun Yoshimura, Kazuki Ichikawa, Massa J. Shoura, Karen L. Artiles, Idan Gabdank, Lamia Wahba, Cheryl L. Smith, Mark L. Edgley, Ann E. Rougvie, Andrew Fire, Shinichi Morishita, Erich M. Schwarz	2019	75
3	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, Yui Uchida, Naoki Irie, Hiroyuki Takeda, Shinichi Morishita	2017	68
4	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	66
5	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	56
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	56
7	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, Jun Yoshimura, Shinichi Morishita, Atsushi Toyoda, Yoshiyuki Sakaki, Yoshihito Taniguchi, Shunichi Takeda, Kazutoshi Mori	2013	50
8	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	42
9	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
10	Measurement of local variations in spacing and orientation of lattice plane of synthetic quartz Journal of Crystal Growth ·Jun Yoshimura, Toshiki Miyazaki, Takehiko Wada, K. Kohra, Masahiro Hosaka, Tomohisa Ogawa, Sadao Taki	1979	38
11	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, Hinako Ishizaki, Harumi Masuda, Tae Kuramoto, Kuniaki Saito, Yasubumi Sakakibara, Atsushi Toyoda, Takehiko Itoh, Mikiko C. Siomi, Shinichi Morishita, Haruhiko Siomi	2021	34
12	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	32
13	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, Shinichi Morishita, Jun Goto, Tatsushi Toda, Shoji Tsuji	2018	27
14	Studies on growth defects in synthetic quartz by x-ray topography Journal of Crystal Growth ·Jun Yoshimura, K. Kohra	1976	25
15	AgIn: measuring the landscape of CpG methylation of individual repetitive elements Bioinformatics ·Yuta Suzuki, Jonas Korlach, Stephen W. Turner, Tatsuya Tsukahara, Junko Taniguchi, Wei Qü, Kazuki Ichikawa, Jun Yoshimura, Hideaki Yurino, Yuji Takahashi, Jun Mitsui, Hiroyuki Ishiura, Shoji Tsuji, Hiroyuki Takeda, Shinichi Morishita	2016	20
16	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, Miho Isoda, Ryota Hashimoto, Nubutaka Hattori, Takuya Takahashi, Shinichi Morishita, Shoji Tsuji, Wado Akamatsu, Hideyuki Okano	2016	19
17	MRA Demonstration of "Periarteritis" in Tolosa-Hunt Syndrome Acta Neurochirurgica ·T. Ozawa, Takashi Minakawa, Akihiko Saito, Yuichiro Yoneoka, Jun Yoshimura, Hajime Arai	2001	18
18	Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2 Journal of Medical Genetics ·Yu Teranishi, Satoru Miyawaki, Hiroki Hongo, Shogo Dofuku, Atsushi Okano, Shunsaku Takayanagi, Takahiro Ota, Jun Yoshimura, Wei Qü, Jun Mitsui, Hirofumi Nakatomi, Shinichi Morishita, Shoji Tsuji, Nobuhito Saito	2020	18
19	Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia The Cerebellum ·Masanori Kurihara, Hiroyuki Ishiura, Takuya Sasaki, Juuri Otsuka, Toshihiro Hayashi, Yasuo Terao, Takashi Matsukawa, Jun Mitsui, Juntaro Kaneko, Kazutoshi Nishiyama, Koichiro Doi, Jun Yoshimura, Shinichi Morishita, Jun Shimizu, Shoji Tsuji	2017	16
20	Activity-dependent distribution of protein kinase C-δ within rat cerebellar Purkinje cells following unilateral labyrinthectomy Experimental Brain Research ·Neal H. Barmack, Zuyuan Qian, Hyunsoo Kim, Jun Yoshimura	2001	15

About Jun Yoshimura

Jun Yoshimura is a scholar working on Genetics, Aging, Neurology, Clinical Biochemistry and Cellular and Molecular Neuroscience, having authored 49 papers that have together received 1.1k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (7 papers), Acoustic Wave Resonator Technologies (5 papers), Genomics and Phylogenetic Studies (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers), CRISPR and Genetic Engineering (4 papers), RNA modifications and cancer (4 papers), Mitochondrial Function and Pathology (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Aging (43 citations), Molecular Biology (652 citations), Neurology (124 citations), Neurology (66 citations) and Genetics (66 citations). Jun Yoshimura has collaborated with scholars based in Japan, United States and South Korea. Frequent co-authors include Shinichi Morishita, Yuki Naito, Kumiko Ui‐Tei, Shoji Tsuji, Jun Mitsui, Hiroyuki Ishiura, Koichiro Doi, K. Kohra, Kazuki Ichikawa and Yuji Takahashi. Their work appears in journals such as Journal of Crystal Growth, Journal of the Neurological Sciences, Bioinformatics, Scientific Reports and Composite Structures.

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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