Akihiro Hashiguchi

2.6k total citations
79 papers, 822 citations indexed

About

Akihiro Hashiguchi is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Akihiro Hashiguchi has authored 79 papers receiving a total of 822 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Cellular and Molecular Neuroscience, 32 papers in Molecular Biology and 18 papers in Neurology. Recurrent topics in Akihiro Hashiguchi's work include Hereditary Neurological Disorders (40 papers), Neurological diseases and metabolism (17 papers) and Genetic Neurodegenerative Diseases (16 papers). Akihiro Hashiguchi is often cited by papers focused on Hereditary Neurological Disorders (40 papers), Neurological diseases and metabolism (17 papers) and Genetic Neurodegenerative Diseases (16 papers). Akihiro Hashiguchi collaborates with scholars based in Japan, United States and Italy. Akihiro Hashiguchi's co-authors include Hiroshi Takashima, Yujiro Higuchi, Akiko Yoshimura, Yuji Okamoto, Jun‐Hui Yuan, Tomonori Nakamura, Yusuke Sakiyama, Masahiro Ando, Masanori Nakagawa and Eiji Matsuura and has published in prestigious journals such as Neurology, Journal of Neurology Neurosurgery & Psychiatry and Journal of Clinical Pathology.

In The Last Decade

Akihiro Hashiguchi

72 papers receiving 814 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Akihiro Hashiguchi Japan 16 498 317 204 178 111 79 822
Jean‐Michel Vallat France 16 377 0.8× 485 1.5× 107 0.5× 134 0.8× 172 1.5× 28 807
María José Chumillas Spain 12 525 1.1× 246 0.8× 229 1.1× 263 1.5× 97 0.9× 14 766
Nina Barišić Croatia 17 261 0.5× 396 1.2× 76 0.4× 161 0.9× 121 1.1× 61 860
G. Tennekoon United States 15 304 0.6× 472 1.5× 63 0.3× 141 0.8× 110 1.0× 31 1.0k
Elke Ydens Belgium 8 295 0.6× 217 0.7× 147 0.7× 103 0.6× 58 0.5× 8 666
H. Grehl Germany 12 325 0.7× 215 0.7× 118 0.6× 245 1.4× 66 0.6× 32 616
Pascale Bomont France 19 484 1.0× 627 2.0× 231 1.1× 242 1.4× 532 4.8× 26 1.3k
Anne‐Sophie Lia France 13 332 0.7× 298 0.9× 70 0.3× 85 0.5× 60 0.5× 40 577
Mutsuo Oyake Japan 15 737 1.5× 678 2.1× 73 0.4× 455 2.6× 35 0.3× 40 1.0k
Mingyan Fang China 17 177 0.4× 615 1.9× 70 0.3× 207 1.2× 139 1.3× 49 1.2k

Countries citing papers authored by Akihiro Hashiguchi

Since Specialization
Citations

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

Fields of papers citing papers by Akihiro Hashiguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Akihiro Hashiguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Akihiro Hashiguchi. A scholar is included among the top collaborators of Akihiro Hashiguchi 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 Akihiro Hashiguchi. Akihiro Hashiguchi 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.
2.
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.
3.
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
4.
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.
5.
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
6.
Matsuura, Eiji, Satoshi Nozuma, Tomonori Nakamura, et al.. (2023). HTLV-1-associated myelopathy/tropical spastic paraplegia with sporadic late-onset nemaline myopathy: a case report. BMC Musculoskeletal Disorders. 24(1). 355–355. 2 indexed citations
7.
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.
8.
Sasaki, Ryo, Namiko Matsumoto, Koh Tadokoro, et al.. (2022). A case of successful renal transplantation of Charcot‐Marie‐Tooth disease associated with FSGS due to mutation of the INF2 gene. Neurology and Clinical Neuroscience. 10(5). 252–254.
9.
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
10.
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
11.
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
12.
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
13.
Hashiguchi, Akihiro, Tomoya Moribayashi, Kimiyoshi Koshi, et al.. (2017). 結晶欠陥をもつ(001)β-Ga 2 O 3 基板上に作製したSchottky障壁ダイオードの電気的性質. Japanese Journal of Applied Physics. 56(8). 1–86501. 1 indexed citations
14.
Yamashita, Sumimasa, Mio Tanaka, Yukichi Tanaka, et al.. (2017). Peripheral nerve pathology at fixed stage in spinal muscular atrophy with respiratory distress type 1. Brain and Development. 40(2). 155–158. 1 indexed citations
15.
Maruyama, Koichi, N. Kurahashi, Keitaro Yamada, et al.. (2016). Arts syndrome with a novel missense mutation in the PRPS1 gene: A case report. Brain and Development. 38(10). 954–958. 9 indexed citations
16.
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
17.
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
18.
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
19.
Iguchi, Masahiro, Akihiro Hashiguchi, Eiichi Ito, et al.. (2012). Charcot‐marie‐tooth disease type 4C in Japan: Report of a case. Muscle & Nerve. 47(2). 283–286. 3 indexed citations
20.
Shiga, Kensuke, Yu‐ichi Noto, Ikuko Mizuta, et al.. (2012). A novel EGR2 mutation within a family with a mild demyelinating form of Charcot‐Marie‐Tooth disease. Journal of the Peripheral Nervous System. 17(2). 206–209. 8 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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