Ryuichi Ono
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
-
- Prenatal Screening and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 8
- RNA modifications and cancer 7
- CRISPR and Genetic Engineering 4
- Extracellular vesicles in disease 3
- Genetics 13
- Genetic Syndromes and Imprinting 12
- Co-authors
- Fumitoshi Ishino (17 shared papers)Tomoko Kaneko‐Ishino (14 shared papers)Takashi Kohda (10 shared papers)Atsuo Ogura (4 shared papers)Narumi Ogonuki (2 shared papers)Kimiko Inoue (2 shared papers)Hirotaka Wagatsuma (3 shared papers)Kenji Nakamura (3 shared papers)
- Journals
- Development (3 papers)Genomics (2 papers)PLoS Genetics (2 papers)Nature Genetics (2 papers)Cancers (2 papers)
- Partner nations
- JapanAustraliaUnited States
In The Last Decade
Ryuichi Ono
27 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 98
- Genetics 1.1k
- Pediatrics, Perinatology and Child Health 585
- Molecular Biology 1.6k
- Cancer Research 144
- Plant Science 384
Countries citing papers authored by Ryuichi Ono
This map shows the geographic impact of Ryuichi Ono'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 Ryuichi Ono with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryuichi Ono more than expected).
Fields of papers citing papers by Ryuichi Ono
This network shows the impact of papers produced by Ryuichi Ono. 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 Ryuichi Ono. The network helps show where Ryuichi Ono may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryuichi Ono, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 359 | |
| 2 | 2002 | 354 | |
| 3 | 2008 | 270 | |
| 4 | 2001 | 215 | |
| 5 | 2007 | 173 | |
| 6 | 2020 | 122 | |
| 7 | 2003 | 120 | |
| 8 | 2000 | 101 | |
| 9 | 2014 | 57 | |
| 10 | 2019 | 49 | |
| 11 | 2013 | 42 | |
| 12 | 2015 | 35 | |
| 13 | 2015 | 33 | |
| 14 | 2021 | 28 | |
| 15 | 2002 | 27 | |
| 16 | 2006 | 24 | |
| 17 | 2020 | 21 | |
| 18 | 2011 | 18 | |
| 19 | 2020 | 13 | |
| 20 | 2013 | 12 |
About Ryuichi Ono
Ryuichi Ono is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Cancer Research, having authored 30 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (9 papers), Epigenetics and DNA Methylation (8 papers), RNA modifications and cancer (7 papers), Chromosomal and Genetic Variations (6 papers), MicroRNA in disease regulation (4 papers), CRISPR and Genetic Engineering (4 papers) and Extracellular vesicles in disease (3 papers). The work is most often cited by research in Genetics (1.1k citations), Pediatrics, Perinatology and Child Health (585 citations), Molecular Biology (1.6k citations), Cancer Research (144 citations) and Plant Science (384 citations). Ryuichi Ono has collaborated with scholars based in Japan, Australia and United States. Frequent co-authors include Fumitoshi Ishino, Tomoko Kaneko‐Ishino, Takashi Kohda, Atsuo Ogura, Narumi Ogonuki, Kimiko Inoue, Hirotaka Wagatsuma, Kenji Nakamura, Minesuke Yokoyama and Toshiaki Hino. Their work appears in journals such as Development, Genomics, PLoS Genetics, Nature Genetics and Cancers.
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.