Keiko Ichimoto

793 total citations
22 papers, 267 citations indexed

About

Keiko Ichimoto is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Keiko Ichimoto has authored 22 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 3 papers in Surgery. Recurrent topics in Keiko Ichimoto's work include Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (6 papers). Keiko Ichimoto is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (6 papers). Keiko Ichimoto collaborates with scholars based in Japan and Italy. Keiko Ichimoto's co-authors include Kei Murayama, Takuya Fushimi, Akira Ohtake, Masaru Shimura, Yasushi Okazaki, Yoshihito Kishita, Ayako Matsunaga, Makiko Tajika, Tomoko Tsuruoka and Masakazu Kohda and has published in prestigious journals such as Scientific Reports, Liver Transplantation and Archives of Disease in Childhood Fetal & Neonatal.

In The Last Decade

Keiko Ichimoto

21 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Keiko Ichimoto Japan 8 220 133 32 16 14 22 267
Takuya Fushimi Japan 9 259 1.2× 143 1.1× 30 0.9× 13 0.8× 14 1.0× 23 299
Tomoko Tsuruoka Japan 8 190 0.9× 131 1.0× 14 0.4× 13 0.8× 14 1.0× 18 241
Ayako Matsunaga Japan 8 200 0.9× 120 0.9× 15 0.5× 11 0.7× 15 1.1× 16 238
Makiko Tajika Japan 8 217 1.0× 144 1.1× 19 0.6× 39 2.4× 24 1.7× 15 283
Esmeralda Rodrigues Portugal 9 112 0.5× 102 0.8× 21 0.7× 29 1.8× 15 1.1× 26 199
Pilar Quijada‐Fraile Spain 10 177 0.8× 149 1.1× 32 1.0× 43 2.7× 35 2.5× 23 256
Mika Ishige Japan 8 148 0.7× 155 1.2× 28 0.9× 23 1.4× 29 2.1× 24 264
James R. Bonham United Kingdom 9 171 0.8× 180 1.4× 42 1.3× 44 2.8× 34 2.4× 20 302
Bijina Balakrishnan United States 8 108 0.5× 119 0.9× 27 0.8× 28 1.8× 30 2.1× 15 224
Helen Jiang United States 6 217 1.0× 44 0.3× 16 0.5× 26 1.6× 8 0.6× 9 319

Countries citing papers authored by Keiko Ichimoto

Since Specialization
Citations

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

Fields of papers citing papers by Keiko Ichimoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keiko Ichimoto

This figure shows the co-authorship network connecting the top 25 collaborators of Keiko Ichimoto. A scholar is included among the top collaborators of Keiko Ichimoto 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 Keiko Ichimoto. Keiko Ichimoto 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.
Akiyama, Tomoyuki, Takuo Kubota, Kei Murayama, et al.. (2025). Vitamin B6 Status in Hypophosphatasia: Association With Clinical Severity, Diagnostic Utility, and Effects on Vitamin B6 Metabolism by Supplementation and Enzyme Replacement Therapy. Journal of Inherited Metabolic Disease. 48(3). e70036–e70036.
2.
Ichimoto, Keiko, et al.. (2024). Increased ketone levels as a key magnetic resonance spectroscopic findings during acute exacerbation in ECHS1-related Leigh syndrome. Radiology Case Reports. 19(12). 6292–6296. 1 indexed citations
3.
Tanaka, Atsushi, Keiji Tsuji, Yasuyuki Komiyama, et al.. (2024). RECAM‐J 2023—Validation and development of the Japanese version of RECAM for the diagnosis of drug‐induced liver injury. Hepatology Research. 54(6). 503–512. 7 indexed citations
4.
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
5.
Hattori, Atsushi, Torayuki Okuyama, Motomichi Kosuga, et al.. (2022). Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndrome. Human Genome Variation. 9(1). 32–32. 1 indexed citations
6.
Tajika, Makiko, Tetsuro Matsuhashi, Masaru Shimura, et al.. (2022). A Japanese single-center experience of the efficacy and safety of asfotase alfa in pediatric-onset hypophosphatasia. Orphanet Journal of Rare Diseases. 17(1). 78–78. 6 indexed citations
7.
Tsuruoka, Tomoko, Masaru Shimura, Makiko Tajika, et al.. (2022). Severe spinal cord hypoplasia due to a novel ATAD3A compound heterozygous deletion. Molecular Genetics and Metabolism Reports. 33. 100912–100912. 4 indexed citations
8.
Nitta, Kazuhiro R., Yukiko Yatsuka, Ayumu Sugiura, et al.. (2022). Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single‐cell level in individuals with mitochondrial disease. Journal of Inherited Metabolic Disease. 45(6). 1143–1150. 1 indexed citations
9.
Shimura, Masaru, Taro Yamazaki, Hiroko Harashima, et al.. (2021). Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan. Scientific Reports. 11(1). 3531–3531. 1 indexed citations
10.
Shimura, Masaru, Tetsuro Matsuhashi, Takuya Fushimi, et al.. (2021). Development of Leigh syndrome with a high probability of cardiac manifestations in infantile-onset patients with m.14453G > A. Mitochondrion. 63. 1–8. 7 indexed citations
11.
Tsuruoka, Tomoko, Masaru Shimura, Makiko Tajika, et al.. (2021). Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis. Archives of Disease in Childhood Fetal & Neonatal. 107(3). 329–334. 10 indexed citations
12.
Kasahara, Mureo, Seisuke Sakamoto, Akinari Fukuda, et al.. (2021). Macroscopic Characteristics of the Native Liver in Children With MPV17‐Related Mitochondrial DNA Depletion Syndrome: An Indication for Performing Liver Transplantation?. Liver Transplantation. 28(3). 497–500. 2 indexed citations
13.
Shimura, Masaru, Minako Ogawa‐Tominaga, Tetsuro Matsuhashi, et al.. (2020). Therapeutic effect of N-carbamylglutamate in CPS1 deficiency. Molecular Genetics and Metabolism Reports. 24. 100622–100622. 11 indexed citations
14.
Ogawa, Erika, Hitoshi Osaka, Kei Murayama, et al.. (2020). Valine-restricted diet for patients with ECHS1 deficiency: Divergent clinical outcomes in two Japanese siblings. Brain and Development. 43(2). 308–313. 15 indexed citations
15.
Ichimoto, Keiko, Tomoo Fujisawa, Takuya Fushimi, et al.. (2020). Two cases of a non-progressive hepatic form of glycogen storage disease type IV with atypical liver pathology. Molecular Genetics and Metabolism Reports. 24. 100601–100601. 4 indexed citations
16.
Shimura, Masaru, Takuya Fushimi, Keiko Ichimoto, et al.. (2020). Efficacy of bezafibrate in two patients with mitochondrial trifunctional protein deficiency. Molecular Genetics and Metabolism Reports. 24. 100610–100610. 7 indexed citations
17.
Mori, Jun, Hideo Sasai, Keiko Ichimoto, et al.. (2020). Short-chain enoyl-CoA hydratase deficiency causes prominent ketoacidosis with normal plasma lactate levels: A case report. Molecular Genetics and Metabolism Reports. 25. 100672–100672. 5 indexed citations
18.
Borna, Nurun Nahar, Yoshihito Kishita, Masakazu Kohda, et al.. (2019). Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome. Neurogenetics. 20(1). 9–25. 44 indexed citations
19.
Shimura, Masaru, Minako Ogawa‐Tominaga, Takuya Fushimi, et al.. (2019). Effects of 5-aminolevulinic acid and sodium ferrous citrate on fibroblasts from individuals with mitochondrial diseases. Scientific Reports. 9(1). 10549–10549. 26 indexed citations
20.
Ogawa, Erika, Masaru Shimura, Takuya Fushimi, et al.. (2017). Clinical validity of biochemical and molecular analysis in diagnosing Leigh syndrome: a study of 106 Japanese patients. Journal of Inherited Metabolic Disease. 40(5). 685–693. 77 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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