Manami Akasaka

763 total citations
41 papers, 341 citations indexed

About

Manami Akasaka is a scholar working on Pediatrics, Perinatology and Child Health, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Manami Akasaka has authored 41 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Pediatrics, Perinatology and Child Health, 7 papers in Infectious Diseases and 7 papers in Molecular Biology. Recurrent topics in Manami Akasaka's work include Metabolism and Genetic Disorders (5 papers), Infectious Encephalopathies and Encephalitis (5 papers) and Neonatal and fetal brain pathology (4 papers). Manami Akasaka is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Infectious Encephalopathies and Encephalitis (5 papers) and Neonatal and fetal brain pathology (4 papers). Manami Akasaka collaborates with scholars based in Japan and United States. Manami Akasaka's co-authors include Atsushi Kamei, Shinji Saitoh, Jun Tohyama, Kiyoshi Hayasaka, Mitsuhiro Kato, Yuki Ueda, Hideaki Shiraishi, Noriyuki Akasaka, Shoichi Chida and Makoto Sasaki and has published in prestigious journals such as The American Journal of Human Genetics, The Journal of Pediatrics and Epilepsy Research.

In The Last Decade

Manami Akasaka

36 papers receiving 338 citations

Peers

Manami Akasaka

GENET

PPCH

PMH

Cha Gon Lee South Korea

Maya Thomas India

Ryuki Matsuura Japan

Kiyokuni Miura Japan

Yukiko Mogami Japan

Mahesh Kamate India

Keitaro Yamada Japan

Masami Togawa Japan

Ji Yoon Han South Korea

Megumi Tsuji Japan

Cha Gon Lee South Korea

Manami Akasaka

117 ×1.1

126 ×1.2

GENET

72 ×0.9

PPCH

72 ×0.9

PMH

32 ×0.7

Citations per year, relative to Manami Akasaka Manami Akasaka (= 1×) peers Cha Gon Lee

Countries citing papers authored by Manami Akasaka

Since Specialization

Citations

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

Fields of papers citing papers by Manami Akasaka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manami Akasaka

This figure shows the co-authorship network connecting the top 25 collaborators of Manami Akasaka. A scholar is included among the top collaborators of Manami Akasaka 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 Manami Akasaka. Manami Akasaka is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Mayanagi, Taira, Hideki Ohmomo, Manami Akasaka, et al.. (2026). Inter-individual differentially methylated region-targeted EWAS reveals epigenetic signatures of early childhood adversity. Epigenomics. 18(1). 89–100.

Hiraumi, Harukazu, et al.. (2024). Childhood fever and hearing loss associated with CAPOS syndrome. Auris Nasus Larynx. 51(4). 724–727. 1 indexed citations

Takahashi, Takuya, Seiko Kuwata, Satoshi Nakano, et al.. (2024). Electrical storm induced by premature ventricular beat with extremely short coupling interval in a patient with long QT syndrome type 3. Journal of Electrocardiology. 88. 153833–153833.

Ishikawa, Ken, et al.. (2024). Chronic kidney disease associated with extremely premature birth and extremely low birth weight may progress through the burden of growth. CEN Case Reports. 14(2). 224–229. 1 indexed citations

Takahashi, Takuya, Hirofumi Saiki, Seiko Kuwata, et al.. (2023). Significance of End-Diastolic Forward Flow in Patients With Repaired Tetralogy of Fallot　― Its Interaction With the Left Ventricular Property and End Organ Damage ―. Circulation Journal. 88(1). 73–80.

Kakisaka, Keisuke, Ai Ito, Hiroaki Abe, et al.. (2022). Lactulose: A treatment for hyperammonemia in a lysinuric protein–intolerant patient with dynamic blood amino acid concentrations. Molecular Genetics and Metabolism Reports. 32. 100898–100898. 1 indexed citations

Moriya, Kunihiko, et al.. (2022). Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis. Frontiers in Pediatrics. 10. 1051623–1051623. 2 indexed citations

Kurahashi, Hirokazu, Atsushi Sato, Masaya Kubota, et al.. (2021). Acute encephalopathy in children with tuberous sclerosis complex. Orphanet Journal of Rare Diseases. 16(1). 5–5. 3 indexed citations

Nakajima, Yuichi, Manami Akasaka, Kazuyuki Maeda, et al.. (2020). Impact of nitrogen metabolism-associated culture pH changes on regulation of Fusarium trichothecene biosynthesis: revision of roles of polyamine agmatine and transcription factor AreA. Current Genetics. 66(6). 1179–1190. 5 indexed citations

10.

Akasaka, Manami, Atsushi Kamei, Jun Ito, et al.. (2020). GNAO1 mutation-related severe involuntary movements treated with gabapentin. Brain and Development. 43(4). 576–579. 7 indexed citations

11.

Nakajima, Yuichi, Kazuyuki Maeda, Manami Akasaka, et al.. (2018). Identification of amino acids negatively affecting Fusarium trichothecene biosynthesis. Antonie van Leeuwenhoek. 112(3). 471–478. 10 indexed citations

12.

Nishimura, Takafumi, Yuji Inaba, Yozo Nakazawa, et al.. (2015). Reduction in peripheral regulatory T cell population in childhood ocular type myasthenia gravis. Brain and Development. 37(8). 808–816. 10 indexed citations

13.

Kamei, Atsushi, et al.. (2014). Hypofibrinogenemia caused by adrenocorticotropic hormone for infantile spasms: A case report. Brain and Development. 37(1). 137–139. 2 indexed citations

14.

Saitoh, Makiko, Atsushi Ishii, Shinichi Hirose, et al.. (2014). Clinical and genetic features of acute encephalopathy in children taking theophylline. Brain and Development. 37(5). 463–470. 16 indexed citations

15.

Akasaka, Manami, et al.. (2013). A Case of Severe Aplastic Anemia due to Ethosuximide Therapy for Epilepsy with Myoclonic Astatic Seizures. Journal of the Japan Epilepsy Society. 30(3). 504–510.

16.

Omama, Shinichi, Yuki Yoshida, Shunrou Fujiwara, et al.. (2012). Use of magnetic resonance imaging to identify the edge of a dural tear in an infant with growing skull fracture: a case study. Child s Nervous System. 28(11). 1951–1954. 9 indexed citations

17.

Akasaka, Manami, Atsushi Kamei, Makoto Sasaki, et al.. (2011). Hypofibrinogenemia Due to Combined Therapy with Valproic Acid and ACTH. Journal of the Japan Epilepsy Society. 28(3). 416–421. 1 indexed citations

18.

Kubo, Yoshitaka, Hiroshi Kashimura, Yasunari Otawara, et al.. (2011). Hemorrhagic infarction at 33 days after birth in a healthy full-term neonate. Vascular Health and Risk Management. 7. 667–667. 1 indexed citations

19.

Uematsu, Mitsugu, Kazuhiro Haginoya, Noriko Togashi, et al.. (2010). Unique discrepancy between cerebral blood flow and glucose metabolism in hemimegalencephaly. Epilepsy Research. 92(2-3). 201–208. 10 indexed citations

20.

Mimaki, Masakazu, Hideyuki Hatakeyama, Takashi Ichiyama, et al.. (2009). Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders. Mitochondrion. 9(2). 115–122. 24 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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