Jun Sone

2.8k total citations
54 papers, 964 citations indexed

About

Jun Sone is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Jun Sone has authored 54 papers receiving a total of 964 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Cellular and Molecular Neuroscience, 36 papers in Molecular Biology and 22 papers in Neurology. Recurrent topics in Jun Sone's work include Genetic Neurodegenerative Diseases (37 papers), Mitochondrial Function and Pathology (18 papers) and Parkinson's Disease Mechanisms and Treatments (15 papers). Jun Sone is often cited by papers focused on Genetic Neurodegenerative Diseases (37 papers), Mitochondrial Function and Pathology (18 papers) and Parkinson's Disease Mechanisms and Treatments (15 papers). Jun Sone collaborates with scholars based in Japan, United States and Netherlands. Jun Sone's co-authors include Gen Sobue, Masahisa Katsuno, Fumiaki Tanaka, Mari Yoshida, Shinsuke Ishigaki, Hirohisa Watanabe, Manabu Doyu, Shin‐ichi Yamada, Haruki Koike and Jun‐ichi Niwa and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and SHILAP Revista de lepidopterología.

In The Last Decade

Jun Sone

51 papers receiving 955 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 Sone Japan 16 594 499 452 118 114 54 964
Clara Barbot Portugal 17 892 1.5× 481 1.0× 137 0.3× 120 1.0× 43 0.4× 34 1.2k
Omar Dabbagh Saudi Arabia 10 255 0.4× 152 0.3× 479 1.1× 148 1.3× 286 2.5× 19 737
Yoshio Morimatsu Japan 15 391 0.7× 181 0.4× 102 0.2× 59 0.5× 70 0.6× 28 605
Ko Sahashi Japan 16 535 0.9× 247 0.5× 289 0.6× 41 0.3× 31 0.3× 42 857
Amber L. Rowse United States 12 287 0.5× 162 0.3× 228 0.5× 288 2.4× 44 0.4× 13 847
Annabelle Chaussenot France 16 634 1.1× 140 0.3× 101 0.2× 94 0.8× 52 0.5× 35 870
Hanna Mierzewska Poland 15 444 0.7× 105 0.2× 98 0.2× 61 0.5× 49 0.4× 57 728
Reika Wate Japan 13 319 0.5× 133 0.3× 531 1.2× 109 0.9× 263 2.3× 27 707
Alessandro Malandrini Italy 16 448 0.8× 246 0.5× 134 0.3× 130 1.1× 19 0.2× 48 734
Charlotte J. Sumner United States 12 796 1.3× 313 0.6× 152 0.3× 64 0.5× 654 5.7× 22 1.2k

Countries citing papers authored by Jun Sone

Since Specialization
Citations

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

Fields of papers citing papers by Jun Sone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jun Sone

This figure shows the co-authorship network connecting the top 25 collaborators of Jun Sone. A scholar is included among the top collaborators of Jun Sone 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 Sone. Jun Sone 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
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Miyahara, Hiroaki, Kazuhiro Takeda, Akio Akagi, et al.. (2023). Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation. Brain Pathology. 33(6). e13199–e13199. 2 indexed citations
3.
Morita, Keisuke, Takahiro Shinzato, Yuzo Endo, et al.. (2023). A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids. SHILAP Revista de lepidopterología. 11(8). e7730–e7730. 4 indexed citations
4.
Sone, Jun, Shinji Ueno, Akio Akagi, et al.. (2023). NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment. Acta Neuropathologica Communications. 11(1). 71–71. 4 indexed citations
5.
Miyamoto, Yosuke, Tetsuya Okazaki, Masami Togawa, et al.. (2022). First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing. Brain and Development. 45(1). 70–76. 5 indexed citations
6.
Tateishi, Yohei, Shunsuke Yoshimura, Teiichiro Miyazaki, et al.. (2022). Perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode: A case report. SHILAP Revista de lepidopterología. 3. 100127–100127. 3 indexed citations
7.
Sakurai, Keita, Yuto Uchida, Hideki Kato, et al.. (2022). Absence of diffusion-weighted imaging abnormalities in a patient with neuronal intranuclear inclusion disease. Neurological Sciences. 43(11). 6551–6554. 2 indexed citations
8.
Nezu, Tomohisa, Takashi Kurashige, Hiroki Ueno, et al.. (2021). Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging. Neurology Genetics. 7(4). e601–e601. 12 indexed citations
9.
Ohshita, Tomohiko, Takashi Kurashige, Hiroyuki Morino, et al.. (2021). FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report. BMC Neurology. 21(1). 396–396. 21 indexed citations
10.
Kume, Kodai, Jun Sone, Hideki Kobara, et al.. (2020). Long-term MRI findings of adult-onset neuronal intranuclear inclusion disease. Clinical Neurology and Neurosurgery. 201. 106456–106456. 8 indexed citations
11.
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Sone, Jun & Gen Sobue. (2017). [Neuronal Intranuclear Inclusion Disease].. PubMed. 69(1). 5–16. 6 indexed citations
13.
Ishida, Kyoko, Kiyofumi Mochizuki, Jun Sone, et al.. (2017). Case of adult-onset neuronal intranuclear hyaline inclusion disease with negative electroretinogram. Documenta Ophthalmologica. 134(3). 221–226. 13 indexed citations
14.
Kitagawa, Naoyuki, et al.. (2014). Neuronal Intranuclear Inclusion Disease Presenting with Resting Tremor. Case Reports in Neurology. 6(2). 176–180. 15 indexed citations
15.
Sone, Jun, Jun‐ichi Niwa, Kaori Kawai, et al.. (2009). Dorfin ameliorates phenotypes in a transgenic mouse model of amyotrophic lateral sclerosis. Journal of Neuroscience Research. 88(1). 123–135. 19 indexed citations
16.
Iguchi, Yohei, Masahisa Katsuno, Jun-ichi Niwa, et al.. (2009). TDP-43 Depletion Induces Neuronal Cell Damage through Dysregulation of Rho Family GTPases. Journal of Biological Chemistry. 284(33). 22059–22066. 83 indexed citations
17.
Yamada, Shin‐ichi, Jun‐ichi Niwa, Shinsuke Ishigaki, et al.. (2006). Archaeal Proteasomes Effectively Degrade Aggregation-prone Proteins and Reduce Cellular Toxicities in Mammalian Cells. Journal of Biological Chemistry. 281(33). 23842–23851. 10 indexed citations
18.
Ishigaki, Shinsuke, Jun‐ichi Niwa, Shin‐ichi Yamada, et al.. (2006). Dorfin-CHIP chimeric proteins potently ubiquitylate and degrade familial ALS-related mutant SOD1 proteins and reduce their cellular toxicity. Neurobiology of Disease. 25(2). 331–341. 31 indexed citations
19.
Sone, Jun, Nozomi Hishikawa, Haruki Koike, et al.. (2005). Neuronal intranuclear hyaline inclusion disease showing motor-sensory and autonomic neuropathy. Neurology. 65(10). 1538–1543. 49 indexed citations
20.
Morita, Koji, Chie Hasegawa, Masakatsu Kaneko, et al.. (2001). 2'-O, 4'-C-Ethylene-bridged nucleic acids (ENA) with nuclease-resistance and high affnity for RNA. Nucleic Acids Symposium Series. 1(1). 241–242. 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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