Wataru Satake

4.6k total citations
45 papers, 721 citations indexed

About

Wataru Satake is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Wataru Satake has authored 45 papers receiving a total of 721 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Neurology and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Wataru Satake's work include Parkinson's Disease Mechanisms and Treatments (12 papers), Astro and Planetary Science (7 papers) and Nuclear Receptors and Signaling (7 papers). Wataru Satake is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (12 papers), Astro and Planetary Science (7 papers) and Nuclear Receptors and Signaling (7 papers). Wataru Satake collaborates with scholars based in Japan, United States and China. Wataru Satake's co-authors include Tatsushi Toda, Nobutaka Hattori, Miho Murata, Ikuko Mizuta, Mitsutoshi Yamamoto, Chiyomi Ito, Satoko Suzuki, Daisuke Okuzaki, Shigeo Murayama and Aiko Hirata and has published in prestigious journals such as Circulation, PLoS ONE and Neurology.

In The Last Decade

Wataru Satake

39 papers receiving 710 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wataru Satake Japan 15 364 303 236 109 99 45 721
Diane Doummar France 16 181 0.5× 269 0.9× 109 0.5× 128 1.2× 145 1.5× 49 699
Gonzalo S. Nido Norway 12 268 0.7× 437 1.4× 170 0.7× 114 1.0× 59 0.6× 25 743
Fabián Bernal Spain 12 190 0.5× 194 0.6× 261 1.1× 94 0.9× 47 0.5× 15 588
Regina H. Reynolds United Kingdom 12 184 0.5× 341 1.1× 88 0.4× 137 1.3× 62 0.6× 26 741
Luis M. Guisasola Spain 13 278 0.8× 264 0.9× 146 0.6× 192 1.8× 42 0.4× 17 623
Bavo Heeman Belgium 9 193 0.5× 262 0.9× 118 0.5× 145 1.3× 38 0.4× 10 492
Petar Podlesniy Spain 17 131 0.4× 520 1.7× 292 1.2× 290 2.7× 56 0.6× 29 922
Michael Kurnellas United States 16 127 0.3× 473 1.6× 157 0.7× 190 1.7× 45 0.5× 30 819
Erika B. Villanueva Canada 15 187 0.5× 636 2.1× 489 2.1× 59 0.5× 44 0.4× 20 944
Maohong Cao China 14 164 0.5× 326 1.1× 117 0.5× 126 1.2× 37 0.4× 49 631

Countries citing papers authored by Wataru Satake

Since Specialization
Citations

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

Fields of papers citing papers by Wataru Satake

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wataru Satake

This figure shows the co-authorship network connecting the top 25 collaborators of Wataru Satake. A scholar is included among the top collaborators of Wataru Satake 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 Wataru Satake. Wataru Satake 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.
Nakano, Hiroko, Pei-Chieng Cha, Yukio Ando, et al.. (2025). Regulation of MCCC1 expression by a Parkinson’s disease-associated intronic variant: implications for pathogenesis. Journal of Human Genetics. 70(7). 371–374. 1 indexed citations
2.
Matsukawa, Takashi, et al.. (2025). A subgroup of multiple system atrophy with rapid decline in vital capacity. Journal of the Neurological Sciences. 469. 123391–123391.
3.
Iseki, Chifumi, Jun Miki, Hikaru Nagasawa, et al.. (2024). A novel TBK1 loss-of-function variant associated with ALS and parkinsonism phenotypes. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(7-8). 791–794. 1 indexed citations
4.
Ishiura, Hiroyuki, Atsushi Sudo, Kayoko Esaki, et al.. (2024). Genetic and functional analyses of SPTLC1 in juvenile amyotrophic lateral sclerosis. Journal of Neurology. 272(1). 36–36.
5.
Maeda, Meiko Hashimoto, Hiroyuki Ishiura, Yuichiro Shirota, et al.. (2024). Subacute Upper Motor Neuron Dysfunction Possibly Associated with the Anti-GM1 Autoantibody. Internal Medicine. 64(12). 1900–1905. 2 indexed citations
6.
Hirano, Makito, Wataru Satake, Nobuko Moriyama, et al.. (2020). Bardet–Biedl syndrome and related disorders in Japan. Journal of Human Genetics. 65(10). 847–853. 10 indexed citations
7.
Mori, Sotaro, Takuji Kurimoto, Kaori Ueda, et al.. (2020). A case of neurosarcoidosis presenting with multiple cranial neuropathies. American Journal of Ophthalmology Case Reports. 19. 100796–100796. 1 indexed citations
8.
Niimi, Yoshiki, Shinji Ito, Yasuaki Mizutani, et al.. (2018). Altered regulation of serum lysosomal acid hydrolase activities in Parkinson's disease: A potential peripheral biomarker?. Parkinsonism & Related Disorders. 61. 132–137. 15 indexed citations
9.
Endo, Hironobu, Takeshi Uenaka, Wataru Satake, et al.. (2017). Japanese WDR45 de novo mutation diagnosed by exome analysis: A case report. Neurology and Clinical Neuroscience. 5(4). 131–133. 1 indexed citations
10.
Oda, Tetsuya, Hui Xiong, Kazuhiro Kobayashi, et al.. (2015). A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy. Human Genome Variation. 2(1). 15022–15022. 5 indexed citations
11.
Hirano, Makito, Wataru Satake, Kenji Ihara, et al.. (2015). The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan. PLoS ONE. 10(9). e0136317–e0136317. 17 indexed citations
12.
Shigemizu, Daichi, Takeshi Aiba, Hidewaki Nakagawa, et al.. (2015). Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. PLoS ONE. 10(7). e0130329–e0130329. 23 indexed citations
13.
Aiba, Takeshi, Kohei Ishibashi, Mitsuru Wada, et al.. (2014). Abstract 13817: Clinical Significance of Whole Exome Analysis Using Next Generation Sequencing in the Genotype-negative Long-QT Syndrome. Circulation. 130. 1 indexed citations
14.
Frank, D., M. E. Zolensky, T. Mikouchi, et al.. (2011). A CAI in the Ivuna CI1 Chondrite. 2785. 4 indexed citations
15.
Sun, Hao, Wataru Satake, Chang-Jun Zhang, et al.. (2011). Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family. Journal of Human Genetics. 56(4). 330–334. 10 indexed citations
16.
Zolensky, M. E., T. Mikouchi, Wataru Satake, & Le Liu. (2010). The Valence State of Iron in CM2 Chondrite Serpentine. Meteoritics and Planetary Science Supplement. 73. 5160. 5 indexed citations
17.
Satake, Wataru, T. Mikouchi, & M. Miyamoto. (2010). Iron Micro-XANES Analysis of Achondritic Plagioclase: Implications for Their Redox States. M&PSA. 73. 5232.
18.
Miyamoto, M., et al.. (2010). The Cooling Rate of Several Olivine-Phyric Shergottites on the basis of Fe-Mg Zoning in Olivine. LPI. 1554. 1 indexed citations
19.
Mikouchi, T., M. E. Zolensky, H. Takeda, et al.. (2010). Mineralogy of Pyroxene and Olivine in the Almahata Sitta Ureilite. Lunar and Planetary Science Conference. 2344. 1 indexed citations
20.
Satake, Wataru, Ikuko Mizuta, Michiaki Kubo, et al.. (2010). Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Neuroscience Research. 68. e71–e71. 8 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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