Kunihiro Yoshida

6.2k total citations
202 papers, 4.5k citations indexed

About

Kunihiro Yoshida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Kunihiro Yoshida has authored 202 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 41 papers in Cellular and Molecular Neuroscience and 35 papers in Neurology. Recurrent topics in Kunihiro Yoshida's work include Genetic Neurodegenerative Diseases (36 papers), Mitochondrial Function and Pathology (27 papers) and Trace Elements in Health (21 papers). Kunihiro Yoshida is often cited by papers focused on Genetic Neurodegenerative Diseases (36 papers), Mitochondrial Function and Pathology (27 papers) and Trace Elements in Health (21 papers). Kunihiro Yoshida collaborates with scholars based in Japan, United States and China. Kunihiro Yoshida's co-authors include Shu‐ichi Ikeda, Akinori Nakamura, Hiroshi Morita, Nobuo Yanagisawa, Shin’ichi Takeda, Kanji Yamamoto, Kazuma Kaneko, Kenichi Furihata, Kazuhiro Fukushima and Masahiro Kato and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The EMBO Journal.

In The Last Decade

Kunihiro Yoshida

193 papers receiving 4.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Kunihiro Yoshida Japan 36 2.2k 903 863 859 671 202 4.5k
John K. Fink United States 43 1.5k 0.7× 1.3k 1.4× 685 0.8× 936 1.1× 235 0.4× 102 5.7k
Isao Hozumi Japan 33 1.4k 0.6× 575 0.6× 706 0.8× 746 0.9× 185 0.3× 142 4.1k
Takashi Inuzuka Japan 35 1.4k 0.7× 542 0.6× 538 0.6× 634 0.7× 168 0.3× 194 4.0k
Susan J. Hayflick United States 39 3.1k 1.4× 3.3k 3.7× 355 0.4× 483 0.6× 468 0.7× 94 5.3k
Laurence A. Bindoff Norway 48 6.3k 2.9× 643 0.7× 696 0.8× 269 0.3× 200 0.3× 187 8.0k
Laura Silvestri Italy 35 1.6k 0.7× 313 0.3× 794 0.9× 1.2k 1.4× 2.6k 3.9× 73 5.6k
Masakiyo Sasahara Japan 43 2.1k 0.9× 489 0.5× 594 0.7× 159 0.2× 151 0.2× 146 5.3k
Paul Gissen United Kingdom 36 1.9k 0.9× 330 0.4× 1.1k 1.3× 140 0.2× 289 0.4× 146 4.6k
Akihiko Taguchi Japan 40 2.3k 1.1× 1.6k 1.7× 778 0.9× 186 0.2× 138 0.2× 115 6.8k
Taku Sugawara Japan 36 2.0k 0.9× 1.1k 1.3× 450 0.5× 153 0.2× 203 0.3× 104 5.0k

Countries citing papers authored by Kunihiro Yoshida

Since Specialization
Citations

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

Fields of papers citing papers by Kunihiro Yoshida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kunihiro Yoshida

This figure shows the co-authorship network connecting the top 25 collaborators of Kunihiro Yoshida. A scholar is included among the top collaborators of Kunihiro Yoshida 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 Kunihiro Yoshida. Kunihiro Yoshida 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.
Matsushima, Akira, et al.. (2023). Gait training with a wearable powered robot during stroke rehabilitation: a randomized parallel-group trial. Journal of NeuroEngineering and Rehabilitation. 20(1). 54–54. 21 indexed citations
2.
3.
Kodaira, Minori, et al.. (2020). Taste disorder in facial onset sensory and motor neuronopathy: a case report. BMC Neurology. 20(1). 71–71. 9 indexed citations
4.
Shimada, Yuichi J., Tadahiro Goto, Yusuke Tsugawa, et al.. (2019). Comparative effectiveness of gastric bypass versus gastric banding on acute care use for cardiovascular disease in adults with obesity. Nutrition Metabolism and Cardiovascular Diseases. 29(5). 518–526. 1 indexed citations
5.
Yahikozawa, Hiroyuki, Satoko Miyatake, Toshiaki Sakai, et al.. (2018). A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies. The Cerebellum. 17(5). 525–530. 12 indexed citations
6.
Yoshida, Kunihiro, Satoshi Kuwabara, Katsuya Nakamura, et al.. (2017). Idiopathic cerebellar ataxia (IDCA): Diagnostic criteria and clinical analyses of 63 Japanese patients. Journal of the Neurological Sciences. 384. 30–35. 11 indexed citations
7.
Yoshinaga, Tsuneaki, Katsuya Nakamura, Tomomi Yamaguchi, et al.. (2017). A novel frameshift mutation of SYNE1 in a Japanese family with autosomal recessive cerebellar ataxia type 8. Human Genome Variation. 4(1). 17052–17052. 12 indexed citations
8.
Matsushima, Akira, Kunihiro Yoshida, Hirokazu Genno, & Shu‐ichi Ikeda. (2017). Principal component analysis for ataxic gait using a triaxial accelerometer. Journal of NeuroEngineering and Rehabilitation. 14(1). 37–37. 19 indexed citations
9.
Miyazaki, Daigo, Akinori Nakamura, Akiyo Hineno, et al.. (2016). Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis. Neurological Sciences. 37(8). 1277–1281. 22 indexed citations
10.
Yamashita, Hirofumi, et al.. (2015). A novel A792D mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids characterized by slow progression. SHILAP Revista de lepidopterología. 1(1). 7–9. 10 indexed citations
11.
Doi, Hiroshi, Kunihiro Yoshida, Takao Yasuda, et al.. (2011). Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation. The American Journal of Human Genetics. 89(2). 320–327. 57 indexed citations
12.
Miyazaki, Daigo, Akinori Nakamura, Kazuhiro Fukushima, et al.. (2011). Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers. Human Molecular Genetics. 20(9). 1787–1799. 63 indexed citations
13.
Nakamura, Akinori, Kunihiro Yoshida, Kazuhiro Fukushima, et al.. (2008). Follow-up of three patients with a large in-frame deletion of exons 45–55 in the Duchenne muscular dystrophy (DMD) gene. Journal of Clinical Neuroscience. 15(7). 757–763. 68 indexed citations
14.
Suzuki, Noriyuki, Tamio Suzuki, Katsuhiko Inagaki, et al.. (2005). Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis. Journal of Investigative Dermatology. 124(6). 1186–1192. 58 indexed citations
15.
Yamamoto, Kanji, Kunihiro Yoshida, Yuko Miyagoe, et al.. (2002). Quantitative evaluation of expression of iron-metabolism genes in ceruloplasmin-deficient mice. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1588(3). 195–202. 42 indexed citations
16.
Munakata, Koji, et al.. (1998). Examination of the Improvement of Longitudinal Resolution by Using Helical CT. Japanese Journal of Radiological Technology. 54(11). 1301–1308.
17.
Morita, Hiroshi, Shu‐ichi Ikeda, Kanji Yamamoto, et al.. (1995). Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a japanese family. Annals of Neurology. 37(5). 646–656. 195 indexed citations
18.
Yoshida, Kunihiro, et al.. (1992). Attrition survey of physiotherapists in Ontario.. PubMed. 44(2). 17–24. 11 indexed citations
19.
Yoshida, Kunihiro, et al.. (1992). Splicing defect of the glycoasparaginase gene in two Japanese siblings with apartylglucosamimiria. Human Genetics. 90(1-2). 179–80. 11 indexed citations
20.
Imai, Miki, et al.. (1986). Changes of respiratory symptom prevalence rates in relation to decrease of sulfur oxide air pollution. 36(1). 1–8. 2 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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