Mai Sato

1.3k total citations
81 papers, 686 citations indexed

About

Mai Sato is a scholar working on Nephrology, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Mai Sato has authored 81 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Nephrology, 21 papers in Pediatrics, Perinatology and Child Health and 14 papers in Molecular Biology. Recurrent topics in Mai Sato's work include Renal Diseases and Glomerulopathies (28 papers), Pediatric Urology and Nephrology Studies (13 papers) and Autoimmune Bullous Skin Diseases (8 papers). Mai Sato is often cited by papers focused on Renal Diseases and Glomerulopathies (28 papers), Pediatric Urology and Nephrology Studies (13 papers) and Autoimmune Bullous Skin Diseases (8 papers). Mai Sato collaborates with scholars based in Japan, United States and Australia. Mai Sato's co-authors include Koichi Kamei, Masao Ogura, Shuichi Ito, Kenji Ishikura, Kazumoto Iijima, Takuya Fujimaru, Tomoaki Ishikawa, Shuichi Ito, Mayumi Sako and Ken Saida and has published in prestigious journals such as Molecular Cell, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Mai Sato

74 papers receiving 670 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mai Sato Japan 16 361 145 130 130 116 81 686
Sophie Taque France 14 191 0.5× 160 1.1× 201 1.5× 86 0.7× 57 0.5× 36 929
Delbert R. Wigfall United States 11 239 0.7× 63 0.4× 83 0.6× 296 2.3× 228 2.0× 16 671
Hugh J. McCarthy Australia 14 466 1.3× 98 0.7× 307 2.4× 83 0.6× 26 0.2× 40 776
Helena Valta Finland 19 121 0.3× 97 0.7× 206 1.6× 26 0.2× 65 0.6× 41 919
A.M. Hernández Spain 14 60 0.2× 408 2.8× 181 1.4× 205 1.6× 50 0.4× 77 1.1k
Thomas Kiss Canada 19 66 0.2× 134 0.9× 133 1.0× 275 2.1× 756 6.5× 76 1.3k
Saling Huang United States 10 112 0.3× 52 0.4× 83 0.6× 32 0.2× 66 0.6× 14 580
Christophe Charasse France 8 382 1.1× 130 0.9× 312 2.4× 22 0.2× 15 0.1× 15 779
Cécile Brachet Belgium 14 63 0.2× 28 0.2× 362 2.8× 129 1.0× 95 0.8× 36 845
B. Boudailliez France 8 246 0.7× 32 0.2× 67 0.5× 48 0.4× 125 1.1× 16 513

Countries citing papers authored by Mai Sato

Since Specialization
Citations

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

Fields of papers citing papers by Mai Sato

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mai Sato

This figure shows the co-authorship network connecting the top 25 collaborators of Mai Sato. A scholar is included among the top collaborators of Mai Sato 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 Mai Sato. Mai Sato 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.
2.
Sato, Mai, et al.. (2024). The bioconversion of dietary α-linolenic acid to eicosapentaenoic acid in Bombyx mori. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 274. 111007–111007.
3.
Kamei, Koichi, Shuichiro Fujinaga, Riku Hamada, et al.. (2024). Efficacy of rituximab and risk factors for poor prognosis in patients with childhood-onset steroid-resistant nephrotic syndrome: a multicenter study. Pediatric Nephrology. 39(10). 2979–2988. 2 indexed citations
4.
Kaneda, Tomoya, et al.. (2023). Complications and prognosis of patients diagnosed with autosomal recessive polycystic kidney disease in neonatal period. CEN Case Reports. 13(3). 181–187. 1 indexed citations
5.
Habib, Ali A., et al.. (2023). Impact of social determinants of health on individuals living with generalized myasthenia gravis and implications for patient support programs. Frontiers in Public Health. 11. 1147489–1147489. 4 indexed citations
6.
Uchida, Hajime, Seisuke Sakamoto, Toshimasa Nakao, et al.. (2022). Preemptive liver transplant in two patients with primary hyperoxaluria type 1: Clinical significance of nephrolithiasis and nephrocalcinosis. Pediatric Transplantation. 26(8). e14380–e14380.
7.
Ogura, Masao, et al.. (2022). Glucocorticoid discontinuation in pediatric-onset systemic lupus erythematosus: a single-center experience. Pediatric Nephrology. 37(9). 2131–2139. 6 indexed citations
8.
Ishimori, Shingo, Tomoko Horinouchi, Junya Fujimura, et al.. (2022). Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective study. Pediatric Nephrology. 38(7). 2107–2116. 1 indexed citations
9.
10.
Suzuki, Ryutaro, et al.. (2021). Unilateral motor weakness with kidney failure: Answers. Pediatric Nephrology. 36(12). 4131–4134.
11.
Sato, Mai, et al.. (2020). Two cases of idiopathic steroid-resistant nephrotic syndrome complicated with thrombotic microangiopathy. BMC Nephrology. 21(1). 323–323. 3 indexed citations
12.
Kamei, Koichi, Mai Sato, Masao Ogura, et al.. (2020). Prophylactic rituximab administration in children with complicated nephrotic syndrome. Pediatric Nephrology. 36(3). 611–619. 5 indexed citations
13.
Kamei, Koichi, Shinsuke Shibata, Ichiro Takeuchi, et al.. (2020). A girl with MIRAGE syndrome who developed steroid-resistant nephrotic syndrome: a case report. BMC Nephrology. 21(1). 340–340. 7 indexed citations
14.
Ishimori, Shingo, Koichi Kamei, Takashi Ando, et al.. (2020). Influenza virus vaccination in children with nephrotic syndrome: insignificant risk of relapse. Clinical and Experimental Nephrology. 24(11). 1069–1076. 9 indexed citations
15.
Kamei, Koichi, Riku Hamada, Hiroshi Hataya, et al.. (2019). Detailed clinical manifestations at onset and prognosis of neonatal-onset Denys–Drash syndrome and congenital nephrotic syndrome of the Finnish type. Clinical and Experimental Nephrology. 23(8). 1058–1065. 15 indexed citations
16.
Sato, Mai, Tetsuji Kaneko, Masao Ogura, et al.. (2018). Favorable Kidney Function in Pediatric Liver Transplant Recipients: Results of a Single-center Cohort Study. Transplantation. 103(8). 1655–1662. 3 indexed citations
17.
Ishikura, Kenji, Mai Sato, Yuko Hamasaki, et al.. (2016). High incidence of idiopathic nephrotic syndrome in East Asian children: a nationwide survey in Japan (JP-SHINE study). Clinical and Experimental Nephrology. 21(4). 651–657. 36 indexed citations
18.
Sato, Mai, Shuichi Ito, Masao Ogura, & Koichi Kamei. (2014). Impact of rituximab on height and weight in children with refractory steroid-dependent nephrotic syndrome. Pediatric Nephrology. 29(8). 1373–1379. 16 indexed citations
19.
Peterson, Shaun, et al.. (2013). The MRN-CtIP Pathway Is Required for Metaphase Chromosome Alignment. Molecular Cell. 49(6). 1097–1107. 16 indexed citations
20.
Yamada, Takashi, Taketo Inoue, Atsushi Sato, Kiyoshi Yamagishi, & Mai Sato. (1995). Effects of short-term administration of .ALPHA.-chlorohydrin on reproductive toxicity parameters in male Sprague-Dawley rats.. The Journal of Toxicological Sciences. 20(3). 195–205. 13 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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