Chizu Wada

413 total citations
20 papers, 217 citations indexed

About

Chizu Wada is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Chizu Wada has authored 20 papers receiving a total of 217 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 9 papers in Neurology and 7 papers in Molecular Biology. Recurrent topics in Chizu Wada's work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Chizu Wada is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Chizu Wada collaborates with scholars based in Japan, United States and France. Chizu Wada's co-authors include Itaru Toyoshima, Masashiro Sugawara, Osamu Masamune, Michael P. Sheetz, Kazuko Hasegawa, Hisayuki Kowa, Masanori Takahashi, Shugo Suwazono, Michio Kobayashi and Kozo Matsubayashi and has published in prestigious journals such as Journal of the Neurological Sciences, Muscle & Nerve and Neuroscience Letters.

In The Last Decade

Chizu Wada

20 papers receiving 214 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chizu Wada Japan 10 87 79 78 37 22 20 217
Ailian Du China 8 28 0.3× 41 0.5× 62 0.8× 11 0.3× 10 0.5× 16 159
Andrew B. Singleton United States 5 36 0.4× 10 0.1× 93 1.2× 35 0.9× 57 2.6× 6 187
Vittorio Riso Italy 9 110 1.3× 80 1.0× 284 3.6× 19 0.5× 28 1.3× 15 393
Sarah Pan United States 7 20 0.2× 57 0.7× 47 0.6× 8 0.2× 56 2.5× 9 254
Luís Velázquez Cuba 10 226 2.6× 110 1.4× 202 2.6× 6 0.2× 66 3.0× 19 345
Moran Hausman‐Kedem Israel 8 53 0.6× 26 0.3× 39 0.5× 6 0.2× 9 0.4× 30 223
Yosef Berlyand United States 8 45 0.5× 127 1.6× 91 1.2× 14 0.4× 61 2.8× 17 272
Janet Brooks United States 7 55 0.6× 104 1.3× 52 0.7× 7 0.2× 32 1.5× 13 196
G. Baldwin Brown United Kingdom 7 25 0.3× 25 0.3× 97 1.2× 54 1.5× 20 0.9× 9 313
Carmen Marrero Spain 6 85 1.0× 160 2.0× 74 0.9× 11 0.3× 31 1.4× 11 296

Countries citing papers authored by Chizu Wada

Since Specialization
Citations

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

Fields of papers citing papers by Chizu Wada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chizu Wada

This figure shows the co-authorship network connecting the top 25 collaborators of Chizu Wada. A scholar is included among the top collaborators of Chizu Wada 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 Chizu Wada. Chizu Wada 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.
Itoh, Hideki, Takashi Hisamatsu, Toshiaki Takahashi, et al.. (2024). CTG repeat length underlying cardiac events and sudden death in myotonic dystrophy type 1. European Heart Journal Open. 4(5). oeae078–oeae078. 2 indexed citations
2.
Yokoi, Kayoko, Hiroto Takahashi, Tomoyuki Hatakeyama, et al.. (2021). Visual illusions in Parkinson's disease: an interview survey of symptomatology. Psychogeriatrics. 22(1). 38–48. 8 indexed citations
3.
Itoh, Hideki, Takashi Hisamatsu, Toshiaki Takahashi, et al.. (2020). Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1. Journal of the American Heart Association. 9(17). e015709–e015709. 11 indexed citations
4.
Satake, Masahiro, et al.. (2018). Approaches to Cough Peak Flow Measurement With Duchenne Muscular Dystrophy. Respiratory Care. 63(12). 1514–1519. 8 indexed citations
5.
Fujino, Haruo, Shugo Suwazono, Yukihiko Ueda, et al.. (2017). Cognitive impairment and quality of life in patients with myotonic dystrophy type 1. Muscle & Nerve. 57(5). 742–748. 29 indexed citations
6.
Sugawara, Masashiro, Chizu Wada, Satoshi Okawa, et al.. (2010). Long-term follow up of thymus in patients with myasthenia gravis. Journal of Neuroimmunology. 221(1-2). 121–124. 5 indexed citations
7.
Sugawara, Masashiro, Chizu Wada, Satoshi Okawa, et al.. (2007). Purkinje Cell Loss in the Cerebellar Flocculus in Patients with Ataxia with Ocular Motor Apraxia Type 1/Early-Onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia. European Neurology. 59(1-2). 18–23. 13 indexed citations
8.
Obara, Koji, Chizu Wada, Toshiaki Yoshioka, et al.. (2007). Acute encephalopathy associated with ingestion of a mushroom, Pleurocybella porrigens (angel's wing), in a patient with chronic renal failure. Neuropathology. 28(2). 151–156. 9 indexed citations
9.
10.
Fujishima, Naohito, Makoto Hirokawa, Masumi Fujishima, et al.. (2006). Oligoclonal T cell expansion in blood but not in the thymus from a patient with thymoma-associated pure red cell aplasia.. PubMed. 91(12 Suppl). ECR47–ECR47. 17 indexed citations
11.
Matsubayashi, Kozo, Kiyohito Okumiya, Taizo Wada, et al.. (2005). Comprehensive geriatric assessment for community‐dwelling elderly in Asia compared with those in Japan: I. Singapore. Geriatrics and gerontology international. 5(2). 99–106. 11 indexed citations
12.
Wada, Taizo, Chizu Wada, Masayuki Ishine, et al.. (2005). Comprehensive geriatric assessment for community‐dwelling elderly in Asia compared with those in Japan: V. West Java in Indonesia. Geriatrics and gerontology international. 5(3). 168–175. 16 indexed citations
13.
Toyoshima, Itaru, et al.. (2002). Two Kinetic Patterns of Axonal Swelling in Chick Spinal Cord and Sacral Plexus with β,β'-Iminodipropionitrile(IDPN) Intoxication. 29(1). 13–21. 1 indexed citations
14.
Toyoshima, Itaru, Masashiro Sugawara, Chizu Wada, et al.. (2002). Time course of polyglutamine aggregate body formation and cell death: Enhanced growth in nucleus and an interval for cell death. Journal of Neuroscience Research. 68(4). 442–448. 6 indexed citations
15.
Toyoshima, Itaru, Masashiro Sugawara, Chizu Wada, et al.. (2000). Massive accumulation of M and H subunits of neurofilament proteins in spinal motor neurons of neurofilament deficient Japanese quail, Quv. Neuroscience Letters. 287(3). 175–178. 7 indexed citations
16.
Sugawara, Masashiro, Itaru Toyoshima, Chizu Wada, et al.. (2000). Pontine Atrophy in Spinocerebellar Ataxia Type 6. European Neurology. 43(1). 17–22. 9 indexed citations
17.
Sugawara, Masashiro, Itaru Toyoshima, Kazuaki Kato, et al.. (1999). [Hereditary ataxias in Akita prefecture].. PubMed. 39(7). 763–6. 5 indexed citations
18.
Toyoshima, Itaru, Masashiro Sugawara, Chizu Wada, et al.. (1998). Kinesin and cytoplasmic dynein in spinal spheroids with motor neuron disease. Journal of the Neurological Sciences. 159(1). 38–44. 36 indexed citations
19.
Toyoshima, Itaru, et al.. (1998). Kinesin accumulation in chick spinal axonal swellings with β,β′-iminodipropionitrile (IDPN) intoxication. Neuroscience Letters. 249(2-3). 103–106. 17 indexed citations
20.
Wada, Chizu, et al.. (1998). [Muscle atrophy in isolated ACTH deficiency].. PubMed. 50(9). 841–8. 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.

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