Reika Wate

950 total citations
27 papers, 707 citations indexed

About

Reika Wate is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Reika Wate has authored 27 papers receiving a total of 707 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Neurology, 13 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Reika Wate's work include Amyotrophic Lateral Sclerosis Research (15 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (8 papers). Reika Wate is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (15 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (8 papers). Reika Wate collaborates with scholars based in Japan, China and United States. Reika Wate's co-authors include Hidefumi Ito, Hirofumi Kusaka, Satoshi Nakano, Satoshi Kaneko, Hisashi Ito, Masataka Nakamura, Kengo Fujita, Asao Hirano, Yoshimi Kinoshita and Hideshi Kawakami and has published in prestigious journals such as Neurology, Brain Research and Experimental Neurology.

In The Last Decade

Reika Wate

27 papers receiving 698 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Reika Wate Japan 13 531 319 263 133 109 27 707
Anissa Fergani France 10 635 1.2× 271 0.8× 373 1.4× 157 1.2× 85 0.8× 10 843
Javier H. Jara United States 14 434 0.8× 249 0.8× 271 1.0× 175 1.3× 140 1.3× 15 677
Christine Bareil Canada 8 464 0.9× 412 1.3× 241 0.9× 78 0.6× 128 1.2× 8 750
Maria Rosaria Monsurrò Italy 12 424 0.8× 248 0.8× 269 1.0× 96 0.7× 92 0.8× 14 604
Laurie Destroismaisons Canada 8 431 0.8× 525 1.6× 252 1.0× 92 0.7× 110 1.0× 10 857
Jenna M. Gregory United Kingdom 15 474 0.9× 346 1.1× 229 0.9× 99 0.7× 113 1.0× 38 739
Omar Dabbagh Saudi Arabia 10 479 0.9× 255 0.8× 286 1.1× 152 1.1× 148 1.4× 19 737
Elizabeth C. Lopes Australia 13 432 0.8× 251 0.8× 247 0.9× 211 1.6× 84 0.8× 17 680
Paola Zago Italy 5 449 0.8× 409 1.3× 223 0.8× 67 0.5× 95 0.9× 7 671
Shashirekha S. Markandaiah United States 7 426 0.8× 291 0.9× 248 0.9× 131 1.0× 89 0.8× 10 644

Countries citing papers authored by Reika Wate

Since Specialization
Citations

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

Fields of papers citing papers by Reika Wate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reika Wate

This figure shows the co-authorship network connecting the top 25 collaborators of Reika Wate. A scholar is included among the top collaborators of Reika Wate 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 Reika Wate. Reika Wate 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.
Nakamura, Masataka, Reika Wate, Satoshi Kaneko, et al.. (2021). Efficacy and safety of tacrolimus as long-term monotherapy for myasthenia gravis. Neuromuscular Disorders. 31(6). 512–518. 6 indexed citations
2.
Kaneko, Satoshi, Norihiro Takenouchi, Takanori Hashizume, et al.. (2017). Zonisamide ameliorates levodopa-induced dyskinesia and reduces expression of striatal genes in Parkinson model rats. Neuroscience Research. 122. 45–50. 18 indexed citations
3.
Ayaki, Takashi, Hidefumi Ito, Osamu Komure, et al.. (2017). Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations. Journal of Neuropathology & Experimental Neurology. 77(2). 128–138. 21 indexed citations
4.
Nakamura, Masataka, et al.. (2015). Successful treatment of paroxysmal tonic spasms with topiramate in a patient with neuromyelitis optica. Multiple Sclerosis and Related Disorders. 4(5). 457–459. 8 indexed citations
5.
Wate, Reika, Satoshi Kaneko, Masabumi Nagashima, et al.. (2013). Levodopa challenge test and123I-metaiodobenzylguanidine scintigraphy for diagnosing Parkinson's disease. Acta Neurologica Scandinavica. 128(3). 160–165. 10 indexed citations
6.
Nakamura, Masataka, Satoshi Kaneko, Reika Wate, et al.. (2012). Regionally different immunoreactivity for Smurf2 and pSmad2/3 in TDP‐43‐positive inclusions of amyotrophic lateral sclerosis. Neuropathology and Applied Neurobiology. 39(2). 144–156. 9 indexed citations
7.
Nakamura, Masataka, Satoshi Kaneko, Hidefumi Ito, et al.. (2012). Activation of Transforming Growth Factor-β/Smad Signaling Reduces Aggregate Formation of Mislocalized TAR DNA-Binding Protein-43. Neurodegenerative Diseases. 11(4). 182–193. 12 indexed citations
8.
Ito, Hidefumi, Masataka Nakamura, Osamu Komure, et al.. (2011). Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation. Acta Neuropathologica. 122(2). 223–229. 50 indexed citations
9.
Nakano, Satoshi, et al.. (2011). Myonuclear breakdown in sporadic inclusion body myositis is accompanied by DNA double strand breaks. Neuromuscular Disorders. 21(5). 345–352. 11 indexed citations
10.
Nakamura, Masataka, Hidefumi Ito, Yoshimi Nakamura, et al.. (2010). Smad ubiquitination regulatory factor-2 in progressive supranuclear palsy. Neuropathology and Applied Neurobiology. 37(3). 307–314. 3 indexed citations
11.
12.
Kunieda, Takenobu, Yoshimi Kinoshita, Reika Wate, et al.. (2009). The first Japanese patient with variant Creutzfeldt‐Jakob disease (vCJD). Neuropathology. 29(6). 713–719. 6 indexed citations
13.
Kamada, Masaki, Hirofumi Maruyama, Eiji Tanaka, et al.. (2009). Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 284(1-2). 69–71. 38 indexed citations
14.
Kinoshita, Yoshimi, Hidefumi Ito, Asao Hirano, et al.. (2009). Nuclear Contour Irregularity and Abnormal Transporter Protein Distribution in Anterior Horn Cells in Amyotrophic Lateral Sclerosis. Journal of Neuropathology & Experimental Neurology. 68(11). 1184–1192. 81 indexed citations
15.
Wate, Reika, et al.. (2009). A case of cerebellar syndrome associated with HIV infection. Rinsho Shinkeigaku. 49(10). 651–655. 2 indexed citations
16.
Ito, Hidefumi, Hidefumi Ito, Reika Wate, et al.. (2008). Treatment with edaravone, initiated at symptom onset, slows motor decline and decreases SOD1 deposition in ALS mice. Experimental Neurology. 213(2). 448–455. 155 indexed citations
17.
Fujita, Kengo, Hidefumi Ito, Satoshi Nakano, et al.. (2008). Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease. Acta Neuropathologica. 116(4). 439–445. 50 indexed citations
18.
Zhang, Jianhua, et al.. (2006). Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis. Acta Neuropathologica. 112(6). 673–680. 46 indexed citations
19.
Ito, Hidefumi, Hideshi Kawakami, Reika Wate, et al.. (2006). Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats. Neurology. 67(8). 1479–1481. 28 indexed citations
20.
Wate, Reika, Sentaro Takahashi, Hidefumi Ito, et al.. (2005). Radio-sensitivity of the Cells from Amyotrophic Lateral Sclerosis Model Mice Transfected with Human Mutant SOD1. Journal of Radiation Research. 46(1). 67–73. 5 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Anissa Fergani Breakdown of academic impact, for papers by Javier H. Jara Breakdown of academic impact, for papers by Christine Bareil Breakdown of academic impact, for papers by Maria Rosaria Monsurrò Breakdown of academic impact, for papers by Laurie Destroismaisons Breakdown of academic impact, for papers by Jenna M. Gregory Breakdown of academic impact, for papers by Omar Dabbagh Breakdown of academic impact, for papers by Elizabeth C. Lopes Breakdown of academic impact, for papers by Paola Zago Breakdown of academic impact, for papers by Shashirekha S. Markandaiah
Rankless by CCL
2026