Yuya Aoto

781 total citations
29 papers, 324 citations indexed

About

Yuya Aoto is a scholar working on Molecular Biology, Immunology and Allergy and Genetics. According to data from OpenAlex, Yuya Aoto has authored 29 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 11 papers in Immunology and Allergy and 8 papers in Genetics. Recurrent topics in Yuya Aoto's work include Renal and related cancers (13 papers), Cell Adhesion Molecules Research (11 papers) and RNA Research and Splicing (6 papers). Yuya Aoto is often cited by papers focused on Renal and related cancers (13 papers), Cell Adhesion Molecules Research (11 papers) and RNA Research and Splicing (6 papers). Yuya Aoto collaborates with scholars based in Japan, Indonesia and United Kingdom. Yuya Aoto's co-authors include Tomohiko Yamamura, Kandai Nozu, Tomoko Horinouchi, Nana Sakakibara, Kazumoto Iijima, China Nagano, Shinya Ishiko, Hiroaki Nagase, Koichi Nakanishi and Yuko Shima and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Kidney International.

In The Last Decade

Yuya Aoto

27 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuya Aoto Japan 12 199 115 86 84 39 29 324
Rini Rossanti Japan 12 187 0.9× 99 0.9× 62 0.7× 82 1.0× 31 0.8× 24 285
Korbinian M. Riedhammer Germany 10 134 0.7× 32 0.3× 59 0.7× 47 0.6× 19 0.5× 26 231
Gemma Bullich Spain 4 165 0.8× 25 0.2× 314 3.7× 90 1.1× 64 1.6× 4 372
Yuko Kajiho Japan 10 135 0.7× 15 0.1× 87 1.0× 28 0.3× 14 0.4× 19 275
Liangzhong Sun China 9 131 0.7× 11 0.1× 62 0.7× 72 0.9× 43 1.1× 35 222
Emanuela Heller Germany 6 126 0.6× 25 0.2× 47 0.5× 44 0.5× 16 0.4× 6 302
Ron Krofft United States 8 213 1.1× 14 0.1× 371 4.3× 129 1.5× 23 0.6× 8 486
Juling Zhou United States 11 175 0.9× 9 0.1× 48 0.6× 131 1.6× 30 0.8× 14 381
Kevin D. Healy United States 7 226 1.1× 24 0.2× 38 0.4× 44 0.5× 88 2.3× 10 484
Veronica Moreno United States 7 132 0.7× 69 0.6× 14 0.2× 16 0.2× 19 0.5× 9 301

Countries citing papers authored by Yuya Aoto

Since Specialization
Citations

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

Fields of papers citing papers by Yuya Aoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuya Aoto

This figure shows the co-authorship network connecting the top 25 collaborators of Yuya Aoto. A scholar is included among the top collaborators of Yuya Aoto 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 Yuya Aoto. Yuya Aoto 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.
Aoto, Yuya, et al.. (2025). Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants. Kidney International Reports. 11(3). 103754–103754.
2.
Rossanti, Rini, Eri Okada, Ryota Suzuki, et al.. (2025). Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions. Kidney International Reports. 10(5). 1509–1517. 1 indexed citations
3.
Suzuki, Ryota, Nana Sakakibara, Yu Tanaka, et al.. (2024). Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome. Nephrology Dialysis Transplantation. 40(4). 688–695. 1 indexed citations
4.
Horinouchi, Tomoko, Yuka Kimura, Yu Tanaka, et al.. (2024). COL4A5 Intronic Variants at Third to Fifth Nucleotides Cause Alport Syndrome. Kidney International Reports. 10(2). 516–521.
5.
Horinouchi, Tomoko, Takeshi Ninchoji, Yu Tanaka, et al.. (2023). Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis. Pediatric Nephrology. 38(12). 4023–4031. 2 indexed citations
6.
Okada, Eri, Tomoko Horinouchi, Tomohiko Yamamura, et al.. (2023). All reported non-canonical splice site variants in GLA cause aberrant splicing. Clinical and Experimental Nephrology. 27(9). 737–746. 5 indexed citations
7.
Horinouchi, Tomoko, Takeshi Ninchoji, Atsushi Kondo, et al.. (2022). Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch–Schönlein purpura nephritis of moderate severity. Pediatric Nephrology. 37(8). 1845–1853. 2 indexed citations
8.
Horinouchi, Tomoko, Atsushi Kondo, Yuya Aoto, et al.. (2022). Clinical and pathological investigation of oligomeganephronia. Pediatric Nephrology. 38(3). 757–762. 1 indexed citations
9.
Okada, Eri, Yuya Aoto, Tomoko Horinouchi, et al.. (2022). Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene. Clinical and Experimental Nephrology. 27(3). 218–226. 7 indexed citations
10.
Yamamura, Tomohiko, Tomoko Horinouchi, Yuya Aoto, Rachel Lennon, & Kandai Nozu. (2022). The Contribution of COL4A5 Splicing Variants to the Pathogenesis of X-Linked Alport Syndrome. Frontiers in Medicine. 9. 841391–841391. 11 indexed citations
11.
Ishiko, Shinya, Naoya Morisada, Atsushi Kondo, et al.. (2021). Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes. Clinical and Experimental Nephrology. 26(2). 140–153. 7 indexed citations
12.
Aoto, Yuya, Tomoko Horinouchi, Tomohiko Yamamura, et al.. (2021). Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing. Kidney International Reports. 7(1). 108–116. 19 indexed citations
13.
Yamamura, Tomohiko, China Nagano, Tomoko Horinouchi, et al.. (2021). Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome. Kidney International Reports. 6(10). 2585–2593. 16 indexed citations
14.
Yamaguchi, Hiroshi, Kandai Nozu, Shinya Ishiko, et al.. (2021). Multivariate analysis of the impact of weather and air pollution on emergency department visits for unprovoked seizure among children: A retrospective clinical observational study. Epilepsy & Behavior. 125. 108434–108434. 5 indexed citations
15.
Kondo, Atsushi, China Nagano, Shinya Ishiko, et al.. (2021). Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases. Scientific Reports. 11(1). 16099–16099. 20 indexed citations
16.
Rossanti, Rini, Kandai Nozu, Atsushi Fukunaga, et al.. (2021). X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay. Clinical and Experimental Nephrology. 25(11). 1224–1230. 11 indexed citations
17.
Nagano, China, Yutaka Takaoka, Koichi Kamei, et al.. (2021). Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants. Kidney International Reports. 6(8). 2114–2121. 13 indexed citations
18.
Yamamura, Tomohiko, Tomoko Horinouchi, China Nagano, et al.. (2020). Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome. Kidney International. 98(6). 1605–1614. 63 indexed citations
19.
Nagano, China, Masafumi Matsuo, Tomohiko Yamamura, et al.. (2020). Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1. Clinical and Experimental Nephrology. 24(7). 606–612. 12 indexed citations
20.
Aoto, Yuya, Koichi Nakanishi, China Nagano, et al.. (2020). A case with somatic and germline mosaicism in COL4A5 detected by multiplex ligation-dependent probe amplification in X-linked Alport syndrome. CEN Case Reports. 9(4). 431–436. 2 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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