Misako Kaido

720 total citations
31 papers, 500 citations indexed

About

Misako Kaido is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Misako Kaido has authored 31 papers receiving a total of 500 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Neurology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Misako Kaido's work include Muscle Physiology and Disorders (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Misako Kaido is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Misako Kaido collaborates with scholars based in Japan and United States. Misako Kaido's co-authors include Kiichi Arahata, Eri Arikawa, Eric P. Hoffman, Harutoshi Fujimura, Takehiko Yanagihara, Hideo Sugita, Ikuya Nonaka, Saburo Sakoda, Ikuya Nonaka and H Sugita and has published in prestigious journals such as Neurology, Annals of Neurology and Scientific Reports.

In The Last Decade

Misako Kaido

29 papers receiving 489 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Misako Kaido Japan 13 369 109 105 92 77 31 500
Luca Chiveri Italy 9 291 0.8× 61 0.6× 61 0.6× 68 0.7× 199 2.6× 13 540
Marion O. Scott United States 7 380 1.0× 78 0.7× 176 1.7× 53 0.6× 25 0.3× 11 465
Toshiya Nakano Japan 11 259 0.7× 46 0.4× 94 0.9× 72 0.8× 214 2.8× 20 543
John Hildyard United Kingdom 12 775 2.1× 103 0.9× 47 0.4× 81 0.9× 18 0.2× 23 856
Rebecca Terry United Kingdom 10 391 1.1× 30 0.3× 89 0.8× 125 1.4× 19 0.2× 14 541
Raúl Juntas Morales France 10 271 0.7× 66 0.6× 98 0.9× 61 0.7× 128 1.7× 20 522
Carlos Cervera Spain 13 291 0.8× 39 0.4× 86 0.8× 61 0.7× 89 1.2× 20 465
T O'Brien United Kingdom 8 382 1.0× 48 0.4× 115 1.1× 30 0.3× 32 0.4× 11 483
Laura Jarre Italy 12 291 0.8× 58 0.5× 102 1.0× 28 0.3× 16 0.2× 18 385
Monica Traverso Italy 13 348 0.9× 61 0.6× 66 0.6× 67 0.7× 16 0.2× 32 488

Countries citing papers authored by Misako Kaido

Since Specialization
Citations

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

Fields of papers citing papers by Misako Kaido

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Misako Kaido

This figure shows the co-authorship network connecting the top 25 collaborators of Misako Kaido. A scholar is included among the top collaborators of Misako Kaido 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 Misako Kaido. Misako Kaido 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.
Toyooka, Keiko, Harutoshi Fujimura, Kayo Ueda, et al.. (2025). Familial ALS With p. L127S ( L126S ) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review. Neuropathology. 45(6). e70028–e70028.
2.
Kimura, Yutaka, Misako Kaido, Ryohei Kawabata, et al.. (2013). [Cases of three patients undergoing chemotherapy for gastric cancer who developed Trousseau's syndrome].. PubMed. 40(12). 2313–5. 2 indexed citations
3.
Araki, Toshiyuki, Seiichi Nagano, Minako Tateno, et al.. (2011). Misfolded SOD1 forms high-density molecular complexes with synaptic molecules in mutant SOD1-linked familial amyotrophic lateral sclerosis cases. Journal of the Neurological Sciences. 314(1-2). 92–96. 5 indexed citations
4.
Konishi, Tetsuro, Kaori Hayashi, Satoshi Ueno, et al.. (2008). Depression in Patients with Subacute Myelo-Optico- Neuropathy (SMON). Internal Medicine. 47(24). 2127–2131. 7 indexed citations
5.
Uejima, Etsuko, Kyôko Takahashi, Koichi Takahashi, et al.. (2002). Microsomal Enzyme Induction and Clinical Aggravation of Porphyria: The Evaluation of Human Urinary 6β‐Hydroxycortisol/Cortisol Ratio as the Index of Hepatic CYP3A4 Activity. The Journal of Clinical Pharmacology. 42(12). 1374–1379. 6 indexed citations
6.
Nakatsuji, Yuji, Fuminobu Sugai, Shohei Watanabe, et al.. (2000). HTLV-I-associated myelopathy manifested after renal transplantation. Journal of the Neurological Sciences. 177(2). 154–156. 29 indexed citations
7.
Konaka, Kuni, Misako Kaido, Yuki Okuda, et al.. (2000). Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease. Neuroradiology. 42(9). 662–665. 21 indexed citations
8.
Nakatsuji, Yuji, Misako Kaido, Fuminobu Sugai, et al.. (2000). Isaacs' syndrome successfully treated by immunoadsorption plasmapheresis. Acta Neurologica Scandinavica. 102(4). 271–273. 9 indexed citations
9.
Hattori, Noriaki, Misako Kaido, Toshinori Nishigaki, et al.. (1999). Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy. Neuromuscular Disorders. 9(4). 220–226. 17 indexed citations
10.
Kaido, Misako, Hironobu Fujimura, Akira Ono, et al.. (1997). Mitochondrial Abnormalities in a Murine Model of Primary Carnitine Deficiency. European Neurology. 38(4). 302–309. 19 indexed citations
11.
Fujimura, Harutoshi, Noriaki Hattori, Misako Kaido, et al.. (1997). A clinicopathological study of a patient with familial amyotrophic lateral sclerosis associated with a two base pair deletion in the copper/zinc superoxide dismutase (SOD1) gene. Acta Neuropathologica. 94(6). 617–622. 20 indexed citations
12.
Fujimura, Harutoshi, Yuji Nakatsuji, Saburo Sakoda, et al.. (1997). Demyelination in severe combined immunodeficient mice by intracisternal injection of cerebrospinal fluid cells from patients with multiple sclerosis: neuropathological investigation. Acta Neuropathologica. 93(6). 567–578. 4 indexed citations
13.
Yoshikawa, Hiroaki, Tomoya Nishimura, Misako Kaido, et al.. (1996). Cation binding at the node of Ranvier in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies. Acta Neuropathologica. 91(6). 587–594. 1 indexed citations
14.
Kaido, Misako, Harutoshi Fujimura, F. Soga, et al.. (1996). Alzheimer-type pathology in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Acta Neuropathologica. 92(3). 312–318. 28 indexed citations
15.
Mineo, Ikuo, Misako Kaido, Harutoshi Fujimura, et al.. (1995). A new variant case of muscle phosphofructokinase deficiency, coexisting with gastric ulcer, gouty arthritis, and increased hemolysis. Muscle & Nerve. 18(S14). S39–S44. 4 indexed citations
16.
Kaido, Misako, Harutoshi Fujimura, Masako Taniike, et al.. (1995). Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNAIle 4269 mutation): histochemical, immunohistochemical, and ultrastructural study. Journal of the Neurological Sciences. 131(2). 170–176. 17 indexed citations
17.
Toyooka, Keiko, Harutoshi Fujimura, Saneyoshi Ueno, et al.. (1995). Familial amyloid polyneuropathy associated with transthyretin Gly42 mutation: a quantitative light and electron microscopic study of the peripheral nervous system. Acta Neuropathologica. 90(5). 516–525. 16 indexed citations
18.
Arahata, Kiichi, Alan H. Beggs, Hideo Honda, et al.. (1991). Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy. Journal of the Neurological Sciences. 101(2). 148–156. 80 indexed citations
19.
Sunohara, N, Kiichi Arahata, Eric P. Hoffman, et al.. (1990). Quadriceps myopathy: Forme fruste of Becker muscular dystrophy. Annals of Neurology. 28(5). 634–639. 65 indexed citations
20.
Nakamura, Yusaku, et al.. (1989). Clinical utility of somatosensory evoked potentials in diabetes mellitus. Diabetes Research and Clinical Practice. 7(1). 17–23. 10 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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