Yuichi Mushimoto

622 total citations
30 papers, 425 citations indexed

About

Yuichi Mushimoto is a scholar working on Molecular Biology, Clinical Biochemistry and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Yuichi Mushimoto has authored 30 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 18 papers in Clinical Biochemistry and 9 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Yuichi Mushimoto's work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (11 papers) and Neonatal Health and Biochemistry (4 papers). Yuichi Mushimoto is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (11 papers) and Neonatal Health and Biochemistry (4 papers). Yuichi Mushimoto collaborates with scholars based in Japan, China and United States. Yuichi Mushimoto's co-authors include Hironori Kobayashi, Seiji Fukuda, Seiji Yamaguchi, Yuki Hasegawa, Takeshi Taketani, Jamiyan Purevsuren, Hong Li, Kazumichi Onigata, Takashi Hamajima and Toshiyuki Fukao and has published in prestigious journals such as SHILAP Revista de lepidopterología, Archives of Disease in Childhood and European Journal of Endocrinology.

In The Last Decade

Yuichi Mushimoto

26 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuichi Mushimoto Japan 12 262 222 126 75 45 30 425
Kerry‐Ann da Costa United States 7 108 0.4× 123 0.6× 41 0.3× 249 3.3× 121 2.7× 12 434
Mahoko Furujo Japan 10 99 0.4× 59 0.3× 71 0.6× 76 1.0× 48 1.1× 27 319
B. Leiendecker Germany 11 162 0.6× 280 1.3× 122 1.0× 48 0.6× 13 0.3× 17 650
Persephone Augoustides‐Savvopoulou Greece 10 233 0.9× 227 1.0× 13 0.1× 123 1.6× 38 0.8× 17 430
Mohamed A. Nada United States 11 424 1.6× 409 1.8× 37 0.3× 31 0.4× 60 1.3× 30 636
Rulai Yang China 12 128 0.5× 141 0.6× 55 0.4× 50 0.7× 99 2.2× 31 336
Monique B. Perry United States 6 448 1.7× 655 3.0× 47 0.4× 53 0.7× 46 1.0× 9 821
Roland Posset Germany 10 238 0.9× 386 1.7× 24 0.2× 89 1.2× 117 2.6× 18 468
M. E. J. den Boer Netherlands 6 346 1.3× 419 1.9× 36 0.3× 55 0.7× 150 3.3× 7 564
A. Kimberly Iafolla United States 9 298 1.1× 367 1.7× 46 0.4× 47 0.6× 139 3.1× 13 517

Countries citing papers authored by Yuichi Mushimoto

Since Specialization
Citations

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

Fields of papers citing papers by Yuichi Mushimoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuichi Mushimoto

This figure shows the co-authorship network connecting the top 25 collaborators of Yuichi Mushimoto. A scholar is included among the top collaborators of Yuichi Mushimoto 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 Yuichi Mushimoto. Yuichi Mushimoto 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.
Nakashima, Kentaro, Takashi Imai, Akira Shiraishi, et al.. (2024). The immunoreactive signature of monocyte-derived dendritic cells from patients with Down syndrome. Clinical & Experimental Immunology. 217(3). 291–299. 1 indexed citations
2.
Yoshimaru, Koichiro, et al.. (2022). Anesthesia management in living-donor liver transplantation in a patient with carbamoyl phosphate synthetase deficiency: a case report. JA Clinical Reports. 8(1). 71–71. 1 indexed citations
3.
Yamada, Kenji, Hironori Kobayashi, Yuichi Mushimoto, et al.. (2022). Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype. Molecular Genetics and Metabolism Reports. 33. 100940–100940. 2 indexed citations
4.
Nagasaki, Keisuke, Kanshi Minamitani, Akie Nakamura, et al.. (2022). Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision). Clinical Pediatric Endocrinology. 32(1). 26–51. 13 indexed citations
5.
6.
Torio, Michiko, Yuhki Koga, Fumiya Yamashita, et al.. (2021). Brain-sparing cord blood transplantation for the borderline stage of adrenoleukodystrophy. Molecular Genetics and Metabolism Reports. 28. 100778–100778.
7.
Kido, Jun, Shirou Matsumoto, Tetsuya Ito, et al.. (2021). Physical, cognitive, and social status of patients with urea cycle disorders in Japan. Molecular Genetics and Metabolism Reports. 27. 100724–100724. 12 indexed citations
8.
Yamada, Kenji, Hironori Kobayashi, Jamiyan Purevsuren, et al.. (2016). Efficacy of bezafibrate on fibroblasts of glutaric acidemia type II patients evaluated using an in vitro probe acylcarnitine assay. Brain and Development. 39(1). 48–57. 14 indexed citations
9.
Yamamoto, Kei, et al.. (2015). Acute Myositis Associated with Concurrent Infection of Rotavirus and Norovirus in a 2-Year-Old Girl. SHILAP Revista de lepidopterología. 7(3). 5873–5873. 3 indexed citations
10.
Taketani, Takeshi, Kazumichi Onigata, Hironori Kobayashi, et al.. (2013). Clinical and genetic aspects of hypophosphatasia in Japanese patients. Archives of Disease in Childhood. 99(3). 211–215. 68 indexed citations
11.
Yamaguchi, Seiji, Hong Li, Jamiyan Purevsuren, et al.. (2012). Bezafibrate can be a new treatment option for mitochondrial fatty acid oxidation disorders: Evaluation by in vitro probe acylcarnitine assay. Molecular Genetics and Metabolism. 107(1-2). 87–91. 40 indexed citations
12.
Purevsuren, Jamiyan, Yuki Hasegawa, Seiji Fukuda, et al.. (2012). Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency. Molecular Genetics and Metabolism. 107(1-2). 237–240. 9 indexed citations
13.
Fukuda, Seiji, et al.. (2011). Adenovirus serotype 31 infection in a newborn girl and review of the literature. Pediatrics International. 53(3). 408–411. 4 indexed citations
14.
Hasegawa, Yuki, Seiji Fukuda, Hironori Kobayashi, et al.. (2010). In vitro probe acylcarnitine profiling assay using cultured fibroblasts and electrospray ionization tandem mass spectrometry predicts severity of patients with glutaric aciduria type 2. Journal of Chromatography B. 878(20). 1673–1676. 6 indexed citations
15.
Mushimoto, Yuichi, Seiji Fukuda, Yuki Hasegawa, et al.. (2010). Clinical and molecular investigation of 19 Japanese cases of glutaric acidemia type 1. Molecular Genetics and Metabolism. 102(3). 343–348. 78 indexed citations
16.
Li, Hong, Seiji Fukuda, Yuki Hasegawa, et al.. (2010). Heat stress deteriorates mitochondrial β-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid β-oxidation disorders. Journal of Chromatography B. 878(20). 1669–1672. 11 indexed citations
17.
Mushimoto, Yuichi, Yuki Hasegawa, Hironori Kobayashi, et al.. (2009). Enzymatic evaluation of glutaric acidemia type 1 by an in vitro probe assay of acylcarnitine profiling using fibroblasts and electrospray ionization/tandem mass spectrometry (MS/MS). Journal of Chromatography B. 877(25). 2648–2651. 2 indexed citations
18.
19.
Purevsuren, Jamiyan, Toshiyuki Fukao, Yuki Hasegawa, et al.. (2009). Clinical and molecular aspects of Japanese patients with mitochondrial trifunctional protein deficiency. Molecular Genetics and Metabolism. 98(4). 372–377. 26 indexed citations
20.
Purevsuren, Jamiyan, Hironori Kobayashi, Yuki Hasegawa, et al.. (2008). A novel molecular aspect of Japanese patients with medium-chain acyl-CoA dehydrogenase deficiency (MCADD): c.449-452delCTGA is a common mutation in Japanese patients with MCADD. Molecular Genetics and Metabolism. 96(2). 77–79. 21 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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2026