Yuta Ichinose

646 total citations
28 papers, 319 citations indexed

About

Yuta Ichinose is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology. According to data from OpenAlex, Yuta Ichinose has authored 28 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cellular and Molecular Neuroscience, 8 papers in Neurology and 8 papers in Neurology. Recurrent topics in Yuta Ichinose's work include Genetic Neurodegenerative Diseases (9 papers), Neurological diseases and metabolism (7 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Yuta Ichinose is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Neurological diseases and metabolism (7 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Yuta Ichinose collaborates with scholars based in Japan, United Kingdom and Italy. Yuta Ichinose's co-authors include Yoshihisa Takiyama, Kishin Koh, Keisuke Toyama, Makoto Yonemaru, Haitian Nan, Ikuma Kasuga, Shoji Tsuji, Satoshi Kuwabara, Kazumasa Shindo and Hiroyuki Ishiura and has published in prestigious journals such as Gastroenterology, European Respiratory Journal and Journal of the Neurological Sciences.

In The Last Decade

Yuta Ichinose

28 papers receiving 313 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuta Ichinose Japan 10 119 112 82 73 59 28 319
Masakazu Kawajiri Japan 13 81 0.7× 176 1.6× 40 0.5× 22 0.3× 52 0.9× 46 408
Takahiro Iwasawa Japan 6 63 0.5× 128 1.1× 23 0.3× 61 0.8× 44 0.7× 11 336
Kathryn A. Robinson United States 7 97 0.8× 86 0.8× 19 0.2× 37 0.5× 43 0.7× 15 290
Noritaka Masahira Japan 8 71 0.6× 116 1.0× 49 0.6× 22 0.3× 49 0.8× 18 328
Alessia Perna Italy 11 124 1.0× 130 1.2× 17 0.2× 31 0.4× 24 0.4× 36 303
S Riku Japan 12 174 1.5× 210 1.9× 32 0.4× 36 0.5× 42 0.7× 26 431
Toshiko Nagashima Japan 12 114 1.0× 207 1.8× 116 1.4× 28 0.4× 21 0.4× 31 448
En‐Lin Dong China 10 119 1.0× 118 1.1× 62 0.8× 78 1.1× 7 0.1× 15 324
Bianca M. de Graaf Netherlands 9 135 1.1× 301 2.7× 31 0.4× 27 0.4× 18 0.3× 15 458
Luciana Cardoso Bonadia Brazil 11 96 0.8× 110 1.0× 124 1.5× 17 0.2× 13 0.2× 24 313

Countries citing papers authored by Yuta Ichinose

Since Specialization
Citations

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

Fields of papers citing papers by Yuta Ichinose

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuta Ichinose

This figure shows the co-authorship network connecting the top 25 collaborators of Yuta Ichinose. A scholar is included among the top collaborators of Yuta Ichinose 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 Yuta Ichinose. Yuta Ichinose 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.
Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2020). Sympathetic outflow to skin predicts central autonomic dysfunction in multiple system atrophy. Neurological Sciences. 41(8). 2241–2248. 4 indexed citations
2.
Nan, Haitian, Lihua Gao, Yuta Ichinose, et al.. (2020). A Japanese SPG4 Patient with a Confirmed <i>De Novo</i> Mutation of the <i>SPAST</i> Gene. Internal Medicine. 59(18). 2311–2315. 1 indexed citations
3.
Ichinose, Yuta, et al.. (2020). A patient with ossification of the yellow ligament and ventriculomegaly with 22q11.2 deletion syndrome undiagnosed until adulthood. Heliyon. 6(12). e05600–e05600. 4 indexed citations
4.
Nagasaka, Takamura, Kishin Koh, Mai Tsuchiya, et al.. (2019). Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene; a case report. BMC Neurology. 19(1). 125–125. 2 indexed citations
5.
Shindo, Kazumasa, et al.. (2019). Spinocerebellar ataxia type 31 associated with REM sleep behavior disorder: a case report. BMC Neurology. 19(1). 9–9. 5 indexed citations
6.
Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2019). Non-convulsive status epilepticus associated with neuronal intranuclear inclusion disease: A case report and literature review. Epilepsy & Behavior Case Reports. 11. 103–106. 10 indexed citations
7.
Ichinose, Yuta, Hiroyuki Ishiura, Masaki Tanaka, et al.. (2018). Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. Parkinsonism & Related Disorders. 61. 57–63. 6 indexed citations
8.
Koh, Kishin, Yuta Ichinose, Hiroyuki Ishiura, et al.. (2018). PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia. Journal of Human Genetics. 64(1). 55–59. 17 indexed citations
9.
Koh, Kishin, Hiroyuki Ishiura, Minako Beppu, et al.. (2018). Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment. Journal of Human Genetics. 63(9). 1009–1013. 18 indexed citations
10.
Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2017). Pre- and postganglionic vasomotor dysfunction causes distal limb coldness in multiple system atrophy. Journal of the Neurological Sciences. 380. 191–195. 4 indexed citations
11.
Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2016). Vasomotor regulation in patients with multiple system atrophy. Journal of Neural Transmission. 124(4). 477–481. 5 indexed citations
12.
Ichinose, Yuta, Kishin Koh, Takamura Nagasaka, et al.. (2016). Exome sequencing reveals a novel missense mutation in the KIAA0196 gene in a Japanese patient with SPG8. Clinical Neurology and Neurosurgery. 144. 36–38. 10 indexed citations
13.
Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2015). No relation between sympathetic outflow to muscles and respiratory function in amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 358(1-2). 66–71. 1 indexed citations
14.
Nishimoto, Yuji, Hiroko Morisaki, Osamu Yamada, Yuta Ichinose, & Norihiro Suzuki. (2014). Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p.Thr52Pro), in the ALK1/ACVRL1 gene. Neurology and Clinical Neuroscience. 2(4). 126–128. 2 indexed citations
15.
Ichinose, Yuta, et al.. (2014). Characteristic MRI findings in beta-propeller protein-associated neurodegeneration (BPAN). Neurology Clinical Practice. 4(2). 175–177. 20 indexed citations
16.
Ichinose, Yuta, et al.. (2000). Peripheral airway findings in chronic obstructive pulmonary disease using an ultrathin bronchoscope. European Respiratory Journal. 15(1). 105–108. 8 indexed citations
17.
18.
Ichinose, Yuta, et al.. (1998). [Diffuse panbronchiolitis with myeloperoxidase-specific antineutrophil cytoplasmic antibody-related vasculitis].. PubMed. 36(5). 453–8. 8 indexed citations
19.
Kasuga, Ikuma, N Yanagisawa, M. KOGA, et al.. (1997). Multiple pulmonary nodules in association with pyoderma gangrenosum. Respiratory Medicine. 91(8). 493–495. 28 indexed citations
20.
Yonemaru, Makoto, Ikuma Kasuga, Hiroyuki Kiyokawa, et al.. (1997). Elevation of antibodies to cytomegalovirus and other herpes viruses in pulmonary fibrosis. European Respiratory Journal. 10(9). 2040–2045. 59 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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