Akira Sudo

1.4k total citations
35 papers, 685 citations indexed

About

Akira Sudo is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Akira Sudo has authored 35 papers receiving a total of 685 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Akira Sudo's work include Mitochondrial Function and Pathology (8 papers), ATP Synthase and ATPases Research (6 papers) and Metabolism and Genetic Disorders (5 papers). Akira Sudo is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), ATP Synthase and ATPases Research (6 papers) and Metabolism and Genetic Disorders (5 papers). Akira Sudo collaborates with scholars based in Japan and United States. Akira Sudo's co-authors include Shinji Saitoh, Yu‐ichi Goto, Ikuya Nonaka, Tohru Okanishi, A. James Barkovich, Jun‐ichi Takanashi, Hayato Tada, S. Fujimoto, Hiroshi Oba and Mitsuhiro Kato and has published in prestigious journals such as SHILAP Revista de lepidopterología, NeuroImage and Neurology.

In The Last Decade

Akira Sudo

34 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Akira Sudo Japan 14 307 200 122 108 95 35 685
Tommy Stödberg Sweden 14 169 0.6× 118 0.6× 174 1.4× 45 0.4× 59 0.6× 22 625
Hirokazu Kurahashi Japan 14 230 0.7× 263 1.3× 292 2.4× 122 1.1× 42 0.4× 67 838
Christopher Troedson Australia 13 147 0.5× 85 0.4× 97 0.8× 47 0.4× 19 0.2× 29 524
Yoshiteru Azuma Japan 13 168 0.5× 56 0.3× 74 0.6× 20 0.2× 18 0.2× 34 464
Faruk İncecik Türkiye 14 89 0.3× 66 0.3× 184 1.5× 19 0.2× 71 0.7× 86 587
Aithala Gururaj United Arab Emirates 15 254 0.8× 42 0.2× 170 1.4× 35 0.3× 27 0.3× 36 736
Reinier A. Mullaart Netherlands 14 201 0.7× 31 0.2× 44 0.4× 21 0.2× 54 0.6× 30 662
Michael J. Bresnan United States 16 168 0.5× 39 0.2× 34 0.3× 40 0.4× 32 0.3× 34 722
Daisaku Toyoshima Japan 12 58 0.2× 107 0.5× 96 0.8× 43 0.4× 14 0.1× 37 326
Ignacio Málaga Spain 13 137 0.4× 95 0.5× 83 0.7× 15 0.1× 38 0.4× 47 950

Countries citing papers authored by Akira Sudo

Since Specialization
Citations

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

Fields of papers citing papers by Akira Sudo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Akira Sudo

This figure shows the co-authorship network connecting the top 25 collaborators of Akira Sudo. A scholar is included among the top collaborators of Akira Sudo 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 Sudo. Akira Sudo 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.
Kawamura, Eriko, Jiro Abe, Akira Sudo, et al.. (2020). Validation of Gene Therapy for Mutant Mitochondria by Delivering Mitochondrial RNA Using a MITO-Porter. Molecular Therapy — Nucleic Acids. 20. 687–698. 64 indexed citations
2.
Tamura, Takuya, et al.. (2020). Successful recovery from severe hypertension in a patient with Leigh syndrome. Molecular Genetics and Metabolism Reports. 25. 100684–100684. 2 indexed citations
3.
Sudo, Akira & Yoshiki Kuroda. (2015). Media exposure, interactive health literacy, and adolescents’ susceptibility to future smoking. International Journal of Adolescent Medicine and Health. 29(2). 13 indexed citations
4.
Sudo, Akira & Yoshiki Kuroda. (2013). The Impact of Centralization of Obstetric Care Resources in Japan on the Perinatal Mortality Rate. SHILAP Revista de lepidopterología. 2013. 1–5. 5 indexed citations
5.
Tsurusaki, Yoshinori, Shinji Saitoh, Kazuhiro Tomizawa, et al.. (2012). A DYNC1H1 mutation causes a dominant spinal muscular atrophy with lower extremity predominance. Neurogenetics. 13(4). 327–332. 49 indexed citations
6.
Takeda, Atsuhito, Akira Sudo, Masafumi Yamada, et al.. (2011). Eponym. European Journal of Pediatrics. 170(11). 1365–1367. 15 indexed citations
7.
Sudo, Akira, et al.. (2011). Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition. The Journal of Laryngology & Otology. 125(12). 1282–1285. 13 indexed citations
8.
Sano, Hitomi, et al.. (2011). A 17-month-old boy with cerebral infarction following mild respiratory symptoms. Journal of Clinical Virology. 52(3). 160–163. 1 indexed citations
9.
Okumura, Akihisa, Mitsugu Uematsu, George Imataka, et al.. (2011). Acute encephalopathy in children with Dravet syndrome. Epilepsia. 53(1). 79–86. 47 indexed citations
10.
Nakamura, Masakazu, Ichiro Yabe, Akira Sudo, et al.. (2010). MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes. Journal of Medical Genetics. 47(10). 659–664. 17 indexed citations
11.
Matsumine, Akihiko, Rui Niimi, M Maeda, et al.. (2010). Diffuse gliomas in an adolescent with multiple enchondromatosis (Ollier’s disease). Oncology Letters. 1(4). 595–597. 9 indexed citations
12.
Egawa, Kiyoshi, Naoko Asahina, Hideaki Shiraishi, et al.. (2007). Aberrant somatosensory-evoked responses imply GABAergic dysfunction in Angelman syndrome. NeuroImage. 39(2). 593–599. 24 indexed citations
13.
Asahina, Naoko, Takayuki Okamoto, Akira Sudo, et al.. (2005). An infantile–juvenile form of Alexander disease caused by a R79H mutation in GFAP. Brain and Development. 28(2). 131–133. 9 indexed citations
14.
Yamasoba, Tatsuya, Yu‐ichi Goto, Hirofumi Komaki, et al.. (2005). Cochlear damage due to germanium-induced mitochondrial dysfunction in guinea pigs. Neuroscience Letters. 395(1). 18–22. 17 indexed citations
15.
Saitoh, Shinji, et al.. (2005). Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome. Brain and Development. 27(5). 389–391. 9 indexed citations
16.
Shiraishi, Hideaki, Steven M. Stufflebeam, Susanne Knake, et al.. (2005). Dynamic Statistical Parametric Mapping for Analyzing the Magnetoencephalographic Epileptiform Activity in Patients With Epilepsy. Journal of Child Neurology. 20(4). 363–369. 17 indexed citations
17.
Sudo, Akira, et al.. (2004). Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in Japan. Journal of Human Genetics. 49(2). 92–96. 61 indexed citations
18.
Takano, Kyoko, et al.. (2003). Cerebellar and brainstem involvement in familial juvenile nephronophthisis type I. Pediatric Neurology. 28(2). 142–144. 11 indexed citations
19.
Nagasawa, Tetsuro, Akira Sudo, Michio Fukumizu, et al.. (2003). Congenital monomelic neurogenic disorder with calf muscle hypertrophy. Brain and Development. 25(8). 571–573. 5 indexed citations
20.
Takahashi, Maki, Ayaka Yamamoto, Kyoko Takano, et al.. (2002). Germline mosaicism of a novel mutation in lysosome‐associated membrane protein‐2 deficiency (Danon disease). Annals of Neurology. 52(1). 122–125. 25 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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