Yoshiro Wada

2.7k total citations
141 papers, 2.0k citations indexed

About

Yoshiro Wada is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, Yoshiro Wada has authored 141 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 39 papers in Clinical Biochemistry and 36 papers in Neurology. Recurrent topics in Yoshiro Wada's work include Metabolism and Genetic Disorders (39 papers), Vestibular and auditory disorders (34 papers) and Biochemical and Molecular Research (22 papers). Yoshiro Wada is often cited by papers focused on Metabolism and Genetic Disorders (39 papers), Vestibular and auditory disorders (34 papers) and Biochemical and Molecular Research (22 papers). Yoshiro Wada collaborates with scholars based in Japan, United States and Netherlands. Yoshiro Wada's co-authors include Masanori Kobayashi, Hajime Togari, Kiyoshi Kidouchi, Naruji Sugiyama, Tsuneo Arakawa, Shinji Fujimoto, Satoshi Sumi, André B. P. Kuilenburg, Tetsuya Ito and Toshiaki Yamanaka and has published in prestigious journals such as The Lancet, Annals of Neurology and Brain Research.

In The Last Decade

Yoshiro Wada

135 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshiro Wada Japan 24 904 479 345 329 228 141 2.0k
Karen M. Weidenheim United States 25 965 1.1× 101 0.2× 251 0.7× 319 1.0× 556 2.4× 78 2.7k
D. N. Landon United Kingdom 31 1.2k 1.3× 391 0.8× 73 0.2× 163 0.5× 201 0.9× 53 2.9k
S. M. Chou United States 33 852 0.9× 124 0.3× 112 0.3× 582 1.8× 297 1.3× 101 2.9k
John T. Sladky United States 31 1.5k 1.6× 181 0.4× 123 0.4× 159 0.5× 176 0.8× 59 3.0k
Sabina Gallati Switzerland 26 893 1.0× 96 0.2× 127 0.4× 191 0.6× 108 0.5× 86 2.2k
Mohammad R. Toliat Germany 30 1.1k 1.2× 126 0.3× 132 0.4× 454 1.4× 58 0.3× 70 2.7k
Y Tanabe Japan 18 697 0.8× 220 0.5× 223 0.6× 86 0.3× 32 0.1× 30 1.3k
Glenn Anderson United Kingdom 21 567 0.6× 148 0.3× 145 0.4× 198 0.6× 75 0.3× 41 1.6k
Atchayaram Nalini India 30 989 1.1× 90 0.2× 139 0.4× 198 0.6× 259 1.1× 239 2.9k
Hiroshi Sakuma Japan 22 371 0.4× 54 0.1× 396 1.1× 118 0.4× 224 1.0× 146 1.8k

Countries citing papers authored by Yoshiro Wada

Since Specialization
Citations

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

Fields of papers citing papers by Yoshiro Wada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshiro Wada

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshiro Wada. A scholar is included among the top collaborators of Yoshiro 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 Yoshiro Wada. Yoshiro 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.
Wada, Yoshiro, et al.. (2023). Gravity perception disturbance in patients with unilateral Meniere disease. Laryngoscope Investigative Otolaryngology. 8(1). 212–219. 1 indexed citations
2.
Wada, Yoshiro, et al.. (2021). Changes in the Results of the Subjective Visual Vertical Test After Endolymphatic Sac Drainage for Intractable Meniere’s Disease. The Journal of International Advanced Otology. 17(2). 121–126. 2 indexed citations
3.
Sakagami, Masaharu, et al.. (2020). What diagnosis should we make for long-lasting vertiginous sensation after acute peripheral vertigo?. Acta Oto-Laryngologica. 140(12). 1001–1006. 3 indexed citations
4.
Kitahara, Tadashi, Masaharu Sakagami, Taeko Ito, et al.. (2018). Ménière’s disease with unremitting floating sensation is associated with canal paresis, gravity-sensitive dysfunction, mental illness, and bilaterality. Auris Nasus Larynx. 46(2). 186–192. 10 indexed citations
5.
6.
Ikeda, Sei, Yoshiro Wada, & Tomohiro Shibata. (2010). Construction of a Mixed Reality Environment for Evaluating an Illusory Sense of Linear Acceleration Based on Vergence Eye Movement. The Journal of The Institute of Image Information and Television Engineers. 64(2). 244–247. 1 indexed citations
7.
Yamashita, Masayuki, et al.. (2009). Active linear head motion improves dynamic visual acuity in pursuing a high-speed moving object. Experimental Brain Research. 194(4). 505–516. 5 indexed citations
8.
Claure, Nelson, et al.. (2008). Mechanisms of Hypoxemia Episodes in Spontaneously Breathing Preterm Infants after Mechanical Ventilation. Neonatology. 94(2). 100–104. 25 indexed citations
9.
Gennip, Albert H., Henk van Lenthe, Tetsuya Ito, et al.. (2002). HPLC/ESI Tandem-MS of Liquid Urine or Urine Soaked Filter-Paper Strips for the Detection of Thymine-Uraciluria and Dihydropyrimidinuria. Advances in experimental medicine and biology. 486. 377–382. 3 indexed citations
10.
Miyachi, Taishi, Kiyofumi Asai, Haruo Mizuno, et al.. (2001). Interleukin-1β induces the expression of lipocortin 1 mRNA in cultured rat cortical astrocytes. Neuroscience Research. 40(1). 53–60. 26 indexed citations
11.
Aoyama, Mineyoshi, Kiyofumi Asai, Tomotane Shishikura, et al.. (2001). Human neuroblastomas with unfavorable biologies express high levels of brain-derived neurotrophic factor mRNA and a variety of its variants. Cancer Letters. 164(1). 51–60. 67 indexed citations
12.
Hamajima, Naoki, P. Vreken, Satoshi Sumi, et al.. (1998). Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase Gene. The American Journal of Human Genetics. 63(3). 717–726. 53 indexed citations
13.
Ito, Tetsuya, Kiyoshi Kidouchi, Naruji Sugiyama, et al.. (1995). Liquid chromatographic-atmospheric pressure chemical ionization mass spectrometric analysis of glycine conjugates and urinary isovalerylglycine in isovaleric acidemia. Journal of Chromatography B Biomedical Sciences and Applications. 670(2). 317–322. 8 indexed citations
14.
15.
Sugiyama, Naruji, et al.. (1992). The urinary acylcarnitine profile in three cases of transient hyperammonemia of the newborn. Acta Paediatrica. 81(5). 436–438. 4 indexed citations
16.
Nagasawa, Hiroyuki, Seiji Yamaguchi, Yasuyuki Suzuki, et al.. (1992). Neuroradiological Findings in Glutaric Aciduria Type I: Report of Four Japanese Patients. Pediatrics International. 34(4). 409–415. 8 indexed citations
17.
Inagaki, Hiroshi, Yoshiro Wada, Keiko Nakanishi, et al.. (1992). Identification of immuno-reactive lipocortin 1-like molecules in serum and plasma by an enzyme immunoassay for lipocortin 1. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1119(3). 250–255. 16 indexed citations
18.
Kidouchi, Kiyoshi, Chié Nakamura, Toshiyuki Katoh, et al.. (1991). Automated Quantitative Analysis for Orotidine and Uridine/Thymine in Urine by High-Performance Liquid Chromatography with Column Switching. Advances in experimental medicine and biology. 309B. 31–34. 3 indexed citations
19.
Eimoto, Tadaaki, Hidemasa Kishimoto, Hideko Morishita, et al.. (1990). Glutaric Aciduria Type II: Autopsy Study of a Case with Electron-Transferring Flavoprotein Dehydrogenase Deficiency. Pediatric Pathology. 10(6). 1007–1019. 7 indexed citations
20.
Sugiyama, Naruji, Kiyoshi Kidouchi, Masanori Kobayashi, & Yoshiro Wada. (1990). Carnitine Deficiency in Inherited Organic Acid Disorders and Reye Syndrome. Pediatrics International. 32(4). 410–416. 11 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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