Yujiro Higuchi

1.1k total citations
53 papers, 551 citations indexed

About

Yujiro Higuchi is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Yujiro Higuchi has authored 53 papers receiving a total of 551 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Cellular and Molecular Neuroscience, 23 papers in Molecular Biology and 14 papers in Neurology. Recurrent topics in Yujiro Higuchi's work include Hereditary Neurological Disorders (31 papers), Genetic Neurodegenerative Diseases (16 papers) and Neurological diseases and metabolism (14 papers). Yujiro Higuchi is often cited by papers focused on Hereditary Neurological Disorders (31 papers), Genetic Neurodegenerative Diseases (16 papers) and Neurological diseases and metabolism (14 papers). Yujiro Higuchi collaborates with scholars based in Japan, United States and Italy. Yujiro Higuchi's co-authors include Hiroshi Takashima, Akihiro Hashiguchi, Akiko Yoshimura, Jun‐Hui Yuan, Yuji Okamoto, Tomonori Nakamura, Masahiro Ando, Masanori Nakagawa, Yusuke Sakiyama and Eiji Matsuura and has published in prestigious journals such as Neurology, Journal of Neurology Neurosurgery & Psychiatry and Frontiers in Immunology.

In The Last Decade

Yujiro Higuchi

46 papers receiving 547 citations

Peers

Yujiro Higuchi

CMN

NEURO

J. Blake United Kingdom

Ilaria Cabrini Italy

Jun‐Hui Yuan Japan

Andrzej Kochański Poland

María José Chumillas Spain

Dagmara Kabzińska Poland

Paola S. Denora Italy

Alleene V. Strickland United States

Michel Gugenheim France

Rhona McGonigal United Kingdom

J. Blake United Kingdom

Yujiro Higuchi

468 ×1.2

CMN

250 ×1.2

124 ×0.8

NEURO

279 ×2.1

NEURO

90 ×1.1

Citations per year, relative to Yujiro Higuchi Yujiro Higuchi (= 1×) peers J. Blake

Countries citing papers authored by Yujiro Higuchi

Since Specialization

Citations

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

Fields of papers citing papers by Yujiro Higuchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yujiro Higuchi

This figure shows the co-authorship network connecting the top 25 collaborators of Yujiro Higuchi. A scholar is included among the top collaborators of Yujiro Higuchi 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 Yujiro Higuchi. Yujiro Higuchi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Matsuura, Eiji, Tomonori Nakamura, Akira Sonoda, et al.. (2025). Visual evoked potential in myelin oligodendrocyte glycoprotein antibody-associated disease. Multiple Sclerosis and Related Disorders. 98. 106408–106408.

Ando, Masahiro, Yujiro Higuchi, Jun‐Hui Yuan, et al.. (2025). SOD1-related inherited peripheral neuropathies in a Japanese cohort: genetic variants and clinical insights. Journal of Neurology. 272(3). 191–191. 1 indexed citations

Pruksaphon, Kritsada, et al.. (2025). Exploring the structural basis and functional immunodynamics of immunoglobulin M in host defense against fungal pathogens. Frontiers in Immunology. 16. 1666690–1666690.

Okamoto, Yuji, Masahiro Ando, Yujiro Higuchi, et al.. (2024). A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review. Neurogenetics. 25(2). 149–156.

Ito, Miwa, Atsuhiko Sugiyama, Yujiro Higuchi, et al.. (2023). Writer's Cramps as an Initial Symptom of Spinocerebellar Ataxia Type 14. Internal Medicine. 63(15). 2183–2186.

Yuan, Jun‐Hui, Xiaoyang Cheng, Eiji Matsuura, et al.. (2023). Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders. Journal of the Peripheral Nervous System. 28(4). 597–607. 4 indexed citations

Hosokawa, Takafumi, Shimon Ishida, Yujiro Higuchi, et al.. (2023). Spatial Fluctuation of Central Nervous System Lesions in X-linked Charcot-Marie-Tooth Disease with a Novel <i>GJB1</i> Mutation. Internal Medicine. 63(4). 571–576.

Takahashi, Nobutaka, Takayasu Mishima, Shinsuke Fujioka, et al.. (2023). Siblings with Cockayne Syndrome B Type III Presenting with Slowly Progressive Cerebellar Ataxia. Internal Medicine. 62(15). 2253–2259. 1 indexed citations

Inoue, Kimiko, et al.. (2023). Involvement of autonomic nervous system since middle age in elderly patient with giant axonal neuropathy caused by novel genetic mutation. Rinsho Shinkeigaku. 63(9). 566–571.

10.

Ando, Masahiro, Yujiro Higuchi, Yuji Okamoto, et al.. (2022). An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families. Journal of Human Genetics. 67(7). 399–403. 5 indexed citations

11.

Higuchi, Yujiro, Masahiro Ando, Akiko Yoshimura, et al.. (2021). Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan. The Cerebellum. 21(5). 851–860. 10 indexed citations

12.

Ishihara, Satoshi, Yuji Okamoto, Hajime Tanabe, et al.. (2020). Clinical features of inherited neuropathy with BSCL2 mutations in Japan. Journal of the Peripheral Nervous System. 25(2). 125–131. 10 indexed citations

13.

Ando, Masahiro, Yuji Okamoto, Akiko Yoshimura, et al.. (2020). Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan. Clinical Genetics. 99(3). 359–375. 18 indexed citations

14.

Yamagata, Takanori, Jun Matsui, Chihiro Sawai, et al.. (2018). X-linked Charcot–Marie–Tooth disease type 5 with recurrent weakness after febrile illness. Brain and Development. 41(2). 201–204. 9 indexed citations

15.

Yoshimura, Akiko, Jun‐Hui Yuan, Akihiro Hashiguchi, et al.. (2018). Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan. Journal of Neurology Neurosurgery & Psychiatry. 90(2). 195–202. 62 indexed citations

16.

Yuan, Jun‐Hui, Akihiro Hashiguchi, Akiko Yoshimura, et al.. (2017). Clinical diversity caused by novel IGHMBP2 variants. Journal of Human Genetics. 62(6). 599–604. 20 indexed citations

17.

Noto, Yu‐ichi, Kensuke Shiga, Yukiko Tsuji, et al.. (2014). Nerve ultrasound depicts peripheral nerve enlargement in patients with genetically distinct Charcot-Marie-Tooth disease. Journal of Neurology Neurosurgery & Psychiatry. 86(4). 378–384. 60 indexed citations

18.

Yuan, Jun‐Hui, Yusuke Sakiyama, Itsuro Higuchi, et al.. (2013). Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation. Journal of Clinical Pathology. 66(8). 659–664. 11 indexed citations

19.

Yuan, Jun‐Hui, Yujiro Higuchi, Satoshi Nozuma, et al.. (2013). Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE. Journal of the Peripheral Nervous System. 18(1). 89–93. 27 indexed citations

20.

Higuchi, Yujiro, Yusuke Sakiyama, Yasushi Nishihira, et al.. (2012). An autopsy case of coexisting Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyradiculoneuropathy, later associated with amyotrophic lateral sclerosis. Rinsho Shinkeigaku. 52(10). 750–756. 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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