Jun Yoshimura

3.3k total citations
49 papers, 1.1k citations indexed

About

Jun Yoshimura is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Jun Yoshimura has authored 49 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Neurology and 7 papers in Genetics. Recurrent topics in Jun Yoshimura's work include Neurogenetic and Muscular Disorders Research (7 papers), Acoustic Wave Resonator Technologies (5 papers) and Genomics and Phylogenetic Studies (5 papers). Jun Yoshimura is often cited by papers focused on Neurogenetic and Muscular Disorders Research (7 papers), Acoustic Wave Resonator Technologies (5 papers) and Genomics and Phylogenetic Studies (5 papers). Jun Yoshimura collaborates with scholars based in Japan, United States and Tanzania. Jun Yoshimura's co-authors include Shinichi Morishita, Kumiko Ui‐Tei, Yuki Naito, Shoji Tsuji, Jun Mitsui, Hiroyuki Ishiura, Koichiro Doi, K. Kohra, Kazuki Ichikawa and Yuji Takahashi and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Bioinformatics.

In The Last Decade

Jun Yoshimura

47 papers receiving 1.0k 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 Yoshimura Japan 18 652 171 127 124 98 49 1.1k
Hyong Kyu Kim South Korea 21 606 0.9× 107 0.6× 52 0.4× 102 0.8× 347 3.5× 48 1.2k
Anna Pistocchi Italy 20 599 0.9× 124 0.7× 42 0.3× 44 0.4× 114 1.2× 57 1.0k
Takefumi Sone Japan 23 1.0k 1.6× 211 1.2× 287 2.3× 184 1.5× 178 1.8× 44 1.5k
Andreas Ohlenbusch Germany 20 633 1.0× 215 1.3× 25 0.2× 93 0.8× 82 0.8× 49 1.2k
Dominique Simon‐Chazottes France 22 1.1k 1.7× 427 2.5× 109 0.9× 64 0.5× 273 2.8× 53 1.8k
Yūji Takahashi Japan 15 416 0.6× 108 0.6× 316 2.5× 111 0.9× 38 0.4× 46 1.0k
Kira L. Lathrop United States 31 691 1.1× 250 1.5× 34 0.3× 35 0.3× 74 0.8× 72 2.3k
Rhys Roberts United Kingdom 18 729 1.1× 229 1.3× 58 0.5× 195 1.6× 256 2.6× 40 1.4k
Yukio Kato Japan 22 921 1.4× 346 2.0× 33 0.3× 73 0.6× 91 0.9× 123 1.9k
Tomoko Makishima United States 22 614 0.9× 100 0.6× 130 1.0× 40 0.3× 41 0.4× 37 1.3k

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-authorship network of co-authors of Jun Yoshimura

This figure shows the co-authorship network connecting the top 25 collaborators of Jun Yoshimura. A scholar is included among the top collaborators of Jun Yoshimura 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 Yoshimura. Jun Yoshimura 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.
Kimura, Shinzo, Jun Yoshimura, T. Ozawa, et al.. (2023). Overcoming complete collapse of a VBX stent graft with endovascular treatment using a bare nitinol stent. PubMed. 9(1). 66–67.
2.
Teranishi, Yu, Satoru Miyawaki, Hiroki Hongo, et al.. (2022). Early prediction of functional prognosis in neurofibromatosis type 2 patients based on genotype–phenotype correlation with targeted deep sequencing. Scientific Reports. 12(1). 9543–9543. 3 indexed citations
3.
Ishino, Kyoko, Hidetoshi Hasuwa, Jun Yoshimura, et al.. (2021). Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation. Nucleic Acids Research. 49(5). 2700–2720. 34 indexed citations
4.
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
5.
Ishiura, Hiroyuki, Jun Mitsui, Yuji Takahashi, et al.. (2020). Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population. Journal of Human Genetics. 66(3). 237–241. 11 indexed citations
6.
Yoshimura, Jun, Kazuki Ichikawa, Massa J. Shoura, et al.. (2019). Recompleting the Caenorhabditis elegans genome. Genome Research. 29(6). 1009–1022. 75 indexed citations
7.
Suzuki, Yoshihiko, Suguru Nishijima, Yoshikazu Furuta, et al.. (2019). Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut. Microbiome. 7(1). 119–119. 56 indexed citations
8.
Ishiura, Hiroyuki, Jun Mitsui, Yuji Takahashi, et al.. (2018). Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS. Journal of Neurology Neurosurgery & Psychiatry. 90(5). 537–542. 27 indexed citations
9.
Ichikawa, Kazuki, Yuta Suzuki, Ryohei Nakamura, et al.. (2017). Centromere evolution and CpG methylation during vertebrate speciation. Nature Communications. 8(1). 1833–1833. 68 indexed citations
10.
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
11.
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
12.
Fujimori, Koki, Hiroyuki Ishiura, Jun Mitsui, et al.. (2016). Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines. Molecular Brain. 9(1). 88–88. 19 indexed citations
13.
Nakatani, Yoichiro, Cecilia C. Mello, Shinichi Hashimoto, et al.. (2015). Associations between nucleosome phasing, sequence asymmetry, and tissue-specific expression in a set of inbred Medaka species. BMC Genomics. 16(1). 978–978. 3 indexed citations
14.
Nishimura, T., Amaury Herpin, Tetsuaki Kimura, et al.. (2014). Analysis of a novel gene, Sdgc , reveals sex chromosome-dependent differences of medaka germ cells prior to gonad formation. Development. 141(17). 3363–3369. 14 indexed citations
15.
Ishikawa, Tokiro, Tetsuya Okada, Tomoko Ishikawa‐Fujiwara, et al.. (2013). ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish. Molecular Biology of the Cell. 24(9). 1387–1395. 50 indexed citations
16.
Ichikawa, Yaeko, Hiroyuki Ishiura, Jun Mitsui, et al.. (2013). Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1. Journal of the Neurological Sciences. 331(1-2). 158–160. 4 indexed citations
17.
Ishii, Atsushi, Yoshiaki Saito, Jun Mitsui, et al.. (2013). Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients. PLoS ONE. 8(2). e56120–e56120. 66 indexed citations
18.
Mitsui, Jun, Takashi Matsukawa, Hiroyuki Ishiura, et al.. (2012). CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(8). 951–957. 32 indexed citations
19.
Naito, Yuki, Jun Yoshimura, Shinichi Morishita, & Kumiko Ui‐Tei. (2009). siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect. BMC Bioinformatics. 10(1). 392–392. 174 indexed citations
20.
Ozawa, T., Takashi Minakawa, Akihiko Saito, et al.. (2001). MRA Demonstration of "Periarteritis" in Tolosa-Hunt Syndrome. Acta Neurochirurgica. 143(3). 309–312. 18 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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