Yoshio Hashizume

6.5k total citations · 2 hit papers
53 papers, 5.0k citations indexed

About

Yoshio Hashizume is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Yoshio Hashizume has authored 53 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Neurology, 14 papers in Cellular and Molecular Neuroscience and 11 papers in Neurology. Recurrent topics in Yoshio Hashizume's work include Amyotrophic Lateral Sclerosis Research (17 papers), Parkinson's Disease Mechanisms and Treatments (15 papers) and Neurological diseases and metabolism (8 papers). Yoshio Hashizume is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (17 papers), Parkinson's Disease Mechanisms and Treatments (15 papers) and Neurological diseases and metabolism (8 papers). Yoshio Hashizume collaborates with scholars based in Japan, United States and Italy. Yoshio Hashizume's co-authors include Mari Yoshida, Haruhiko Akiyama, Masato Hasegawa, Takashi Nonaka, Tetsuaki Arai, Kuniaki Tsuchiya, Tatsuro Oda, Kenji Ikeda, Hiroshi Mori and David Mann and has published in prestigious journals such as Journal of Biological Chemistry, Brain and Neurology.

In The Last Decade

Yoshio Hashizume

52 papers receiving 4.9k citations

Hit Papers

TDP-43 is a component of ubiquitin-positive tau-negative ... 2006 2026 2012 2019 2006 2008 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshio Hashizume Japan 30 3.3k 2.0k 1.5k 988 983 53 5.0k
William Camu France 37 3.9k 1.2× 2.3k 1.2× 2.3k 1.6× 691 0.7× 1.3k 1.3× 139 6.0k
Denise A. Figlewicz United States 33 2.7k 0.8× 2.5k 1.2× 1.7k 1.2× 585 0.6× 1.3k 1.3× 81 5.4k
Richard W. Orrell United Kingdom 36 2.2k 0.7× 1.7k 0.9× 1.2k 0.8× 688 0.7× 700 0.7× 90 4.1k
John Ravits United States 40 5.3k 1.6× 2.8k 1.4× 3.1k 2.1× 1.1k 1.1× 1.2k 1.2× 93 7.5k
Kiyomitsu Oyanagi Japan 38 1.9k 0.6× 1.2k 0.6× 423 0.3× 956 1.0× 1.1k 1.1× 173 4.2k
Marianne de Visser Netherlands 42 2.5k 0.7× 1.8k 0.9× 1.6k 1.1× 685 0.7× 707 0.7× 86 4.4k
Rickie Patani United Kingdom 35 1.7k 0.5× 2.8k 1.4× 1.3k 0.9× 749 0.8× 973 1.0× 95 5.2k
A. Prelle Italy 38 1.5k 0.5× 2.6k 1.3× 836 0.6× 683 0.7× 709 0.7× 112 4.7k
Mario Sabatelli Italy 36 2.6k 0.8× 1.3k 0.7× 997 0.7× 344 0.3× 1.4k 1.4× 179 4.0k
Séverine Boillée France 24 4.5k 1.4× 2.0k 1.0× 2.5k 1.7× 1.1k 1.1× 1.2k 1.2× 41 6.3k

Countries citing papers authored by Yoshio Hashizume

Since Specialization
Citations

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

Fields of papers citing papers by Yoshio Hashizume

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshio Hashizume

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshio Hashizume. A scholar is included among the top collaborators of Yoshio Hashizume 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 Yoshio Hashizume. Yoshio Hashizume 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.
Sako, Wataru, Hidefumi Ito, Mari Yoshida, et al.. (2012). Nuclear factor ? B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations. Clinical Neuropathology. 31(11). 418–423. 23 indexed citations
2.
Sonobe, Yoshifumi, Hideyuki Takeuchi, Hua Li, et al.. (2009). Interleukin-25 Expressed by Brain Capillary Endothelial Cells Maintains Blood-Brain Barrier Function in a Protein Kinase Cϵ-dependent Manner. Journal of Biological Chemistry. 284(46). 31834–31842. 82 indexed citations
3.
Hasegawa, Masato, Tetsuaki Arai, Takashi Nonaka, et al.. (2008). Phosphorylated TDP‐43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Annals of Neurology. 64(1). 60–70. 592 indexed citations breakdown →
4.
Arai, Tetsuaki, Masato Hasegawa, Haruhiko Akiyama, et al.. (2006). TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochemical and Biophysical Research Communications. 351(3). 602–611. 2058 indexed citations breakdown →
6.
Terao, Shin-ichi, Aiji Noda, Mari Yoshida, et al.. (2005). Respiratory failure in a patient with antecedent poliomyelitis: Amyotrophic lateral sclerosis or post-polio syndrome?. Clinical Neurology and Neurosurgery. 108(7). 670–674. 5 indexed citations
7.
Nagasaka, Takamura, et al.. (2002). Intramedullary Tuberculoma with Syringomyelia. Journal of Spinal Disorders & Techniques. 15(1). 88–90. 9 indexed citations
8.
Watanabe, Hidetaka, Fumiaki Tanaka, Manabu Doyu, et al.. (2000). Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis. Human Genetics. 107(5). 452–457. 32 indexed citations
9.
Reeves, Matthew F., Yasuhiro Ito, Michiyo Matsumoto, et al.. (1999). Tissue-Specific Somatic Mosaicism in Spinal and Bulbar Muscular Atrophy Is Dependent on CAG-Repeat Length and Androgen Receptor–Gene Expression Level. The American Journal of Human Genetics. 65(4). 966–973. 53 indexed citations
10.
Konagaya, M, Motoko Sakai, Yukihiko Matsuoka, Yoko Konagaya, & Yoshio Hashizume. (1998). Upper motor neuron predominant degeneration with frontal and temporal lobe atrophy. Acta Neuropathologica. 96(5). 532–536. 31 indexed citations
11.
Miyaishi, Osamu, et al.. (1998). Elevated expression of PDI family proteins during differentiation of mouse F9 teratocarcinoma cells. Journal of Cellular Biochemistry. 68(4). 436–445. 17 indexed citations
13.
Kato, Yoji, et al.. (1998). Immunohistochemical detection of dityrosine in lipofuscin pigments in the aged human brain. FEBS Letters. 439(3). 231–234. 78 indexed citations
15.
Maruyama, Wakako, Makoto Naoi, Toshio Kasamatsu, et al.. (1997). An Endogenous Dopaminergic Neurotoxin, N‐Methyl‐(R)‐Salsolinol, Induces DNA Damage in Human Dopaminergic Neuroblastoma SH‐SY5Y Cells. Journal of Neurochemistry. 69(1). 322–329. 77 indexed citations
16.
Makino, Mitsunori, et al.. (1996). Morphometric Study of Myelinated Fibers in Human Cervical Spinal Cord White Matter. Spine. 21(9). 1010–1016. 19 indexed citations
17.
Nakao, Naoki, Ko Sahashi, Masahiko Takahashi, Tohru Ibi, & Yoshio Hashizume. (1995). Clinical and neuropathological features of a neurodegenerative disorder in the central nervous system with progressive head drooping (Kubisagari). Acta Neuropathologica. 90(2). 208–212. 2 indexed citations
19.
Terao, Shin-ichi, Gen Sobue, Yoshio Hashizume, Noriko Shimada, & Terunori Mitsuma. (1994). Age-related changes of the myelinated fibers in the human corticospinal tract: a quantitative analysis. Acta Neuropathologica. 88(2). 137–142. 80 indexed citations
20.
Wakai, Masakazu, et al.. (1993). A histometrical study on the globus pallidus in Huntington's disease. Journal of the Neurological Sciences. 119(1). 18–27. 15 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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