Yaeko Ichikawa

2.4k total citations
33 papers, 657 citations indexed

About

Yaeko Ichikawa is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Yaeko Ichikawa has authored 33 papers receiving a total of 657 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cellular and Molecular Neuroscience, 13 papers in Molecular Biology and 13 papers in Neurology. Recurrent topics in Yaeko Ichikawa's work include Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (8 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Yaeko Ichikawa is often cited by papers focused on Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (8 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Yaeko Ichikawa collaborates with scholars based in Japan, Canada and Denmark. Yaeko Ichikawa's co-authors include Jun Goto, Shoji Tsuji, Ichiro Kanazawa, Hiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, Yasuhisa Sakurai, Toru Mannen, Guy A. Rouleau and Patrı́cia Maciel and has published in prestigious journals such as Bioinformatics, Neurology and Annals of Neurology.

In The Last Decade

Yaeko Ichikawa

31 papers receiving 647 citations

Peers

Yaeko Ichikawa
John Wolff United States
Yaeko Ichikawa
Citations per year, relative to Yaeko Ichikawa Yaeko Ichikawa (= 1×) peers John Wolff

Countries citing papers authored by Yaeko Ichikawa

Since Specialization
Citations

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

Fields of papers citing papers by Yaeko Ichikawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yaeko Ichikawa

This figure shows the co-authorship network connecting the top 25 collaborators of Yaeko Ichikawa. A scholar is included among the top collaborators of Yaeko Ichikawa 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 Yaeko Ichikawa. Yaeko Ichikawa 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.
Tokushige, Shin‐ichi, et al.. (2024). Dropped head syndrome in anti‐MuSK antibody‐positive myasthenia gravis with possible concurrent axial myopathy. Clinical and Experimental Neuroimmunology. 15(3). 137–142. 1 indexed citations
3.
Tokushige, Shin‐ichi, Shuichi Matsuda, Masayoshi Tada, et al.. (2023). Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping task. Clinical Neurophysiology. 158. 1–15. 3 indexed citations
4.
Terao, Yasuo, Motoyasu Honma, Shin‐ichi Tokushige, et al.. (2021). Time Distortion in Parkinsonism. Frontiers in Neuroscience. 15. 648814–648814. 10 indexed citations
5.
Nagashima, Yu, Tatsuo Mano, Hiroyuki Ishiura, et al.. (2021). Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the Literature. Journal of Molecular Neuroscience. 71(9). 1796–1801. 1 indexed citations
6.
Terao, Yasuo, Hideki Fukuda, Satomi Inomata‐Terada, et al.. (2015). Is multiple system atrophy with cerebellar ataxia (MSA-C) like spinocerebellar ataxia and multiple system atrophy with parkinsonism (MSA-P) like Parkinson’s disease? – A saccade study on pathophysiology. Clinical Neurophysiology. 127(2). 1491–1502. 24 indexed citations
7.
Ishiura, Hiroyuki, Yuji Takahashi, Toshihiro Hayashi, et al.. (2014). Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses. Journal of Human Genetics. 59(3). 163–172. 49 indexed citations
8.
Ichikawa, Yaeko, Hiroyuki Ishiura, Jun Mitsui, et al.. (2013). Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1. Journal of the Neurological Sciences. 331(1-2). 158–160. 4 indexed citations
9.
Ohminami, Shinya, Yasuo Terao, Yuichiro Shirota, et al.. (2012). 47. Long term potentiation/depression-like effects induced by quadripulse stimulation in Huntington’s disease. Clinical Neurophysiology. 123(9). e98–e98. 1 indexed citations
10.
Ishiura, Hiroyuki, Yuji Takahashi, Jun Mitsui, et al.. (2012). C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan. Archives of Neurology. 69(9). 1154–8. 69 indexed citations
11.
Maeda, Meiko Hashimoto, Jun Mitsui, Bing‐Wen Soong, et al.. (2011). Increased gene dosage of myelin protein zero causes Charcot‐Marie‐Tooth disease. Annals of Neurology. 71(1). 84–92. 25 indexed citations
12.
Ichikawa, Yaeko. (2010). Japan Multiple System Atrophy Research Consortium (JAMSAC). Rinsho Shinkeigaku. 50(11). 927–927.
13.
Kubota, Akatsuki, Ayumi Hida, Yaeko Ichikawa, et al.. (2009). A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations. Movement Disorders. 24(3). 441–445. 47 indexed citations
14.
Anttonen, Anna‐Kaisa, Eija Siintola, Lisbeth Tranebjærg, et al.. (2008). Novel SIL1 mutations and exclusion of functional candidate genes in Marinesco–Sjögren syndrome. European Journal of Human Genetics. 16(8). 961–969. 31 indexed citations
15.
Sakurai, Yasuhisa, Yasuo Terao, Yaeko Ichikawa, et al.. (2007). Pure alexia for kana. Characterization of alexia with lesions of the inferior occipital cortex. Journal of the Neurological Sciences. 268(1-2). 48–59. 21 indexed citations
16.
Miyashita, Mitsunori, Naomi Ito, Yuki Shirai, et al.. (2007). Attitude of outpatients with neuromuscular diseases in Japan to pain and use of analgesics. Journal of the Neurological Sciences. 267(1-2). 22–27. 10 indexed citations
17.
Ding, Jie, Yaeko Ichikawa, Takahiro Ishikawa, & Hiroyuki Shimada. (2004). Effect of formalin on extraction of mRNA from a formalin‐fixed sample: a basic investigation. Scandinavian Journal of Clinical and Laboratory Investigation. 64(3). 229–236. 8 indexed citations
18.
Fukutake, Toshio, Hitoshi Shinotoh, Hiroshi Nishino, et al.. (2002). Homozygous Machado–Joseph disease presenting as REM sleep behaviour disorder and prominent psychiatric symptoms. European Journal of Neurology. 9(1). 97–100. 39 indexed citations
19.
Ichikawa, Yaeko, Jun Goto, Masahira Hattori, et al.. (2001). The genomic structure and expression of MJD, the Machado-Joseph disease gene. Journal of Human Genetics. 46(7). 413–422. 58 indexed citations
20.
Wang, Guanghui, et al.. (1997). Machado–Joseph Disease Gene Product Identified in Lymphocytes and Brain. Biochemical and Biophysical Research Communications. 233(2). 476–479. 36 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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