Akira Ohtake

6.0k total citations
138 papers, 2.7k citations indexed

About

Akira Ohtake is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Akira Ohtake has authored 138 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Molecular Biology, 77 papers in Clinical Biochemistry and 20 papers in Genetics. Recurrent topics in Akira Ohtake's work include Metabolism and Genetic Disorders (76 papers), Mitochondrial Function and Pathology (70 papers) and ATP Synthase and ATPases Research (29 papers). Akira Ohtake is often cited by papers focused on Metabolism and Genetic Disorders (76 papers), Mitochondrial Function and Pathology (70 papers) and ATP Synthase and ATPases Research (29 papers). Akira Ohtake collaborates with scholars based in Japan, Australia and United States. Akira Ohtake's co-authors include David R. Thorburn, Michael T. Ryan, Kei Murayama, Denise M. Kirby, Matthew McKenzie, Yasushi Okazaki, Michael Lazarou, Yoshihito Kishita, Masaru Shimura and Masaki Takayanagi and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Akira Ohtake

134 papers receiving 2.6k citations

Peers

Akira Ohtake

GENET

PHYSI

SURGE

Lambert van den Heuvel Netherlands

Janet Koster Netherlands

M. Brivet France

Hélène Ogier de Baulny France

Cary O. Harding United States

C. Charpentier France

Wenjuan Qiu China

J. G. M. Huijmans Netherlands

Yanling Yang China

Daniel Leclerc Canada

Lambert van den Heuvel Netherlands

Akira Ohtake

2.9k ×1.5

1.4k ×1.2

247 ×0.8

GENET

239 ×1.1

PHYSI

102 ×0.5

SURGE

Citations per year, relative to Akira Ohtake Akira Ohtake (= 1×) peers Lambert van den Heuvel

Countries citing papers authored by Akira Ohtake

Since Specialization

Citations

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

Fields of papers citing papers by Akira Ohtake

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Akira Ohtake

This figure shows the co-authorship network connecting the top 25 collaborators of Akira Ohtake. A scholar is included among the top collaborators of Akira Ohtake 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 Akira Ohtake. Akira Ohtake 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

Iijima, Hiroyuki, Ayumu Sugiura, Masaru Shimura, et al.. (2025). Role of BOLA3 in the mitochondrial Fe-S cluster clarified by metabolomic analysis. Molecular Genetics and Metabolism. 145(2). 109113–109113.

Kishita, Yoshihito, Ayumu Sugiura, Tetsuro Matsuhashi, et al.. (2023). Strategic validation of variants of uncertain significance in ECHS1 genetic testing. Journal of Medical Genetics. 60(10). 1006–1015. 2 indexed citations

Ittiwut, Chupong, Rungnapa Ittiwut, Tetsuro Matsuhashi, et al.. (2023). Genetic, metabolic and clinical delineation of an MRPS23-associated mitochondrial disorder. Scientific Reports. 13(1). 22005–22005. 2 indexed citations

Kishita, Yoshihito, Mina Nakama, Hideo Sasai, et al.. (2023). Novel ITPA variants identified by whole genome sequencing and RNA sequencing. Journal of Human Genetics. 68(9). 649–652. 2 indexed citations

Sharpe, Alice J., Shuai Nie, Mark Ziemann, et al.. (2022). Loss of mitochondrial fatty acid β‐oxidation protein short‐chain Enoyl‐CoA hydratase disrupts oxidative phosphorylation protein complex stability and function. FEBS Journal. 290(1). 225–246. 11 indexed citations

Nitta, Kazuhiro R., et al.. (2021). Clinical heterogeneity in patients with m.4412G > A MT-TM mutation and different heteroplasmy levels. Mitochondrion. 59. 214–215.

Borna, Nurun Nahar, Yoshihito Kishita, Norio Sakai, et al.. (2020). Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL. Genes. 11(11). 1325–1325. 8 indexed citations

Hirono, Keiichi, Fukiko Ichida, Minako Ogawa‐Tominaga, et al.. (2019). Mitochondrial complex deficiency by novel compound heterozygous TMEM 70 variants and correlation with developmental delay, undescended testicle, and left ventricular noncompaction in a Japanese patient: A case report. SHILAP Revista de lepidopterología. 7(3). 553–557. 13 indexed citations

Kishita, Yoshihito, Masakazu Kohda, Yosuke Mizuno, et al.. (2019). Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background. International Journal of Cardiology. 279. 115–121. 33 indexed citations

10.

Inaba, Yuji, Mitsuo Motobayashi, Yoshiro Amano, et al.. (2018). An infant case of diffuse cerebrospinal lesions and cardiomyopathy caused by a BOLA3 mutation. Brain and Development. 40(6). 484–488. 18 indexed citations

11.

Borna, Nurun Nahar, Yoshihito Kishita, Kaori Ishikawa, et al.. (2017). A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy. Journal of Human Genetics. 62(5). 539–547. 5 indexed citations

12.

Maegaki, Yoshihiro, Kei Murayama, Taro Yamazaki, et al.. (2014). Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological report. Brain and Development. 37(7). 719–724. 11 indexed citations

13.

Arakawa, Chikako, Ayumi Endo, Yukihiko Fujita, et al.. (2011). Liver-specific mitochondrial respiratory chain complex I deficiency in fatal influenza encephalopathy. Brain and Development. 34(2). 115–117. 3 indexed citations

14.

Murayama, Kei & Akira Ohtake. (2009). Mitochondrial respiratory chain disorder and liver disease in children. The Journal of Toxicological Sciences. 34. 1 indexed citations

15.

Yasuno, Tetsuhiko, H Kaneoka, Masaki Takayanagi, et al.. (2008). Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiency. Clinical Genetics. 73(5). 496–501. 21 indexed citations

16.

Kirby, Denise M., Renato Salemi, Canny Sugiana, et al.. (2004). NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency. Journal of Clinical Investigation. 114(6). 837–845. 14 indexed citations

17.

Thorburn, David R., Canny Sugiana, Renato Salemi, et al.. (2004). Biochemical and molecular diagnosis of mitochondrial respiratory chain disorders. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1659(2-3). 121–128. 86 indexed citations

18.

Kobayashi, Koji, Akiharu Kimura, Tomonori Minagawa, et al.. (2003). 94 AN INFANTILE CASE OF PERMANENT TYPE 1 DIABETES MELLITUS SHOWlNG POSITIVE ANTI-GAD ANTIB0DY 8 MONTHS AFTER ONSET. Clinical Pediatric Endocrinology. 12(2). 133. 1 indexed citations

19.

McFarland, Robert, Denise M. Kirby, Kerry J. Fowler, et al.. (2003). De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. Annals of Neurology. 55(1). 58–64. 145 indexed citations

20.

Okano, Yoshiyuki, Minoru Asada, Akie Fujimoto, et al.. (2001). A Genetic Factor for Age-Related Cataract: Identification and Characterization of a Novel Galactokinase Variant, “Osaka,” in Asians. The American Journal of Human Genetics. 68(4). 1036–1042. 60 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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