Satoshi Akamine

570 total citations
26 papers, 253 citations indexed

About

Satoshi Akamine is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Satoshi Akamine has authored 26 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Neurology. Recurrent topics in Satoshi Akamine's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (3 papers) and Infectious Encephalopathies and Encephalitis (3 papers). Satoshi Akamine is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (3 papers) and Infectious Encephalopathies and Encephalitis (3 papers). Satoshi Akamine collaborates with scholars based in Japan, United States and South Korea. Satoshi Akamine's co-authors include Masafumi Sanefuji, Yasunari Sakai, Hiroyuki Torisu, Toshiro Hara, Yoshito Ishizaki, Yuki Matsushita, Kenji Ihara, Marco Sardiello, Hirosuke Inoue and Michiko Torio and has published in prestigious journals such as Scientific Reports, BMJ Open and Genes to Cells.

In The Last Decade

Satoshi Akamine

24 papers receiving 250 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Satoshi Akamine Japan 8 95 94 94 54 51 26 253
Shakti Agrawal United Kingdom 11 143 1.5× 73 0.8× 47 0.5× 67 1.2× 91 1.8× 16 305
Bahadır Konuşkan Türkiye 10 129 1.4× 44 0.5× 26 0.3× 65 1.2× 30 0.6× 52 337
Pin Fee Chong Japan 9 35 0.4× 55 0.6× 29 0.3× 47 0.9× 20 0.4× 33 202
Sandra P. Toelle Switzerland 11 45 0.5× 106 1.1× 19 0.2× 88 1.6× 12 0.2× 27 360
Jinhee Kim South Korea 10 40 0.4× 86 0.9× 45 0.5× 23 0.4× 37 0.7× 24 305
Veena Rajaram United States 5 37 0.4× 71 0.8× 40 0.4× 28 0.5× 87 1.7× 7 443
Jurģis Strautmanis Latvia 7 121 1.3× 53 0.6× 35 0.4× 26 0.5× 57 1.1× 15 240
Po‐Cheng Hung Taiwan 12 192 2.0× 39 0.4× 21 0.2× 47 0.9× 136 2.7× 38 414
Bart K. Chwalisz United States 12 264 2.8× 78 0.8× 73 0.8× 10 0.2× 27 0.5× 61 456
Weihong Lin China 10 130 1.4× 29 0.3× 54 0.6× 20 0.4× 47 0.9× 30 285

Countries citing papers authored by Satoshi Akamine

Since Specialization
Citations

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

Fields of papers citing papers by Satoshi Akamine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoshi Akamine

This figure shows the co-authorship network connecting the top 25 collaborators of Satoshi Akamine. A scholar is included among the top collaborators of Satoshi Akamine 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 Satoshi Akamine. Satoshi Akamine 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.
Kajiwara, Kenta, Daiki Setoyama, Satoshi Akamine, et al.. (2025). Glutamate in cerebrospinal fluid as a diagnostic marker for acute encephalopathy in childhood. Brain and Development. 47(5). 104448–104448. 1 indexed citations
2.
Chong, Pin Fee, Kenta Kajiwara, Yuji Ueno, et al.. (2025). Altered lipidomic and metabolomic status in cerebrospinal fluid of children with myelin oligodendrocyte glycoprotein antibody-associated disorder. Biochemistry and Biophysics Reports. 44. 102233–102233.
3.
Yamashita, Fumiya, Satoshi Akamine, Pin Fee Chong, et al.. (2025). Methylmalonic acidemia with recurrent hemophagocytic lymphohistiocytosis: a case report and review of the literature. BMC Pediatrics. 25(1). 259–259.
4.
Akamine, Satoshi, Fumihiko Fujii, Hiroki Kato, et al.. (2024). Gnao1 is a molecular switch that regulates the Rho signaling pathway in differentiating neurons. Scientific Reports. 14(1). 17097–17097. 1 indexed citations
5.
Fujii, Fumihiko, Daiki Setoyama, Yohei Shinmyo, et al.. (2024). An N‐terminal and ankyrin repeat domain interactome of Shank3 identifies the protein complex with the splicing regulator Nono in mice. Genes to Cells. 29(9). 746–756. 1 indexed citations
6.
Fujii, Fumihiko, Yuki Matsushita, Daiki Setoyama, et al.. (2023). Shank3a/b isoforms regulate the susceptibility to seizures and thalamocortical development in the early postnatal period of mice. Neuroscience Research. 193. 13–19. 3 indexed citations
7.
Tetsuhara, Kenichi, Satoshi Akamine, Shunsuke Fujii, et al.. (2022). Severe encephalopathy associated with SARS-CoV-2 Omicron BA.1 variant infection in a neonate. Brain and Development. 44(10). 743–747. 15 indexed citations
8.
Akamine, Satoshi, Pin Fee Chong, Yoshitsugu Kaku, et al.. (2021). Infantile spasms and early-onset progressive polycystic renal lesions associated with TSC2/PKD1 contiguous gene deletion syndrome. Seizure. 86. 82–84. 2 indexed citations
9.
Chong, Pin Fee, Satoshi Akamine, Fumiya Yamashita, et al.. (2021). Case Report: Acute Fulminant Cerebral Edema With Perivascular Abnormalities Related to Kawasaki Disease. Frontiers in Pediatrics. 9. 732110–732110. 1 indexed citations
10.
Akamine, Satoshi, et al.. (2020). Isolated cranial neuritis of the oculomotor nerve: Expanding the MOG phenotype?. Multiple Sclerosis and Related Disorders. 41. 102040–102040. 5 indexed citations
11.
Sakai, Yasunari, Ryutaro Kira, Satoshi Akamine, et al.. (2019). Decision-making dilemmas of paediatricians: a qualitative study in Japan. BMJ Open. 9(8). e026579–e026579. 8 indexed citations
12.
Fukai, Ryoko, Noriko Miyake, Soo-Young Lee, et al.. (2018). An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome. Brain and Development. 41(4). 378–381. 3 indexed citations
13.
Akamine, Satoshi, Yoshito Ishizaki, Yasunari Sakai, et al.. (2018). A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia. European Journal of Medical Genetics. 61(8). 451–454. 5 indexed citations
14.
Sanefuji, Masafumi, Hiroshi Yamashita, Michiko Torio, et al.. (2018). A rightward saccade to an unexpected stimulus as a marker for lateralised visuospatial attention. Scientific Reports. 8(1). 7562–7562. 2 indexed citations
15.
Sakai, Yasunari, Fumiya Yamashita, Satoshi Akamine, et al.. (2017). Transient dysautonomia in an acute phase of encephalopathy with biphasic seizures and late reduced diffusion. Brain and Development. 39(7). 621–624. 7 indexed citations
16.
Torio, Michiko, Kentaro Nakashima, Shunsuke Kanno, et al.. (2017). A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia. Annals of Clinical Microbiology and Antimicrobials. 16(1). 61–61. 3 indexed citations
17.
Fukai, Ryoko, Yasunari Sakai, Michiko Torio, et al.. (2016). De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. BMC Neurology. 16(1). 174–174. 20 indexed citations
18.
Matsushita, Yuki, Yasunari Sakai, Hiroshi Shigeto, et al.. (2016). Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice. Scientific Reports. 6(1). 22991–22991. 22 indexed citations
19.
Ito, Naoko, Kenji Ihara, Tomohiro Kamoda, et al.. (2015). Autosomal dominant distal renal tubular acidosis caused by a mutation in the anion exchanger 1 gene in a Japanese family. CEN Case Reports. 4(2). 218–222. 7 indexed citations
20.
Sakai, Yasunari, Yuki Matsushita, Satoshi Akamine, et al.. (2013). Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamus. European Journal of Medical Genetics. 56(9). 475–483. 6 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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