Daisuke Ieda
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- PI3K/AKT/mTOR signaling in cancer
- Genomics and Chromatin Dynamics
Papers in
- Genetics 10
- Genetic Syndromes and Imprinting 6
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 2
- Neurogenetic and Muscular Disorders Research 1
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- Epigenetics and DNA Methylation 3
- RNA regulation and disease 2
- Co-authors
- Shinji Saitoh (16 shared papers)Ikumi Hori (13 shared papers)Ayako Hattori (14 shared papers)Yutaka Negishi (12 shared papers)Y. Nakamura (8 shared papers)Kei Ohashi (6 shared papers)Mitsuko Nakashima (2 shared papers)Hirotomo Saitsu (1 shared paper)
- Journals
- Brain and Development (7 papers)Epilepsia Open (1 paper)Journal of Medical Genetics (1 paper)Human Genetics and Genomics Advances (1 paper)Orphanet Journal of Rare Diseases (1 paper)
- Partner nations
- Japan
In The Last Decade
Daisuke Ieda
15 papers receiving 169 citations
Peers
Comparison fields: 5 of 35
- Genetics 92
- Molecular Biology 79
- Pediatrics, Perinatology and Child Health 16
- Clinical Biochemistry 6
- Psychiatry and Mental health 12
Countries citing papers authored by Daisuke Ieda
This map shows the geographic impact of Daisuke Ieda'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 Daisuke Ieda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daisuke Ieda more than expected).
Fields of papers citing papers by Daisuke Ieda
This network shows the impact of papers produced by Daisuke Ieda. 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 Daisuke Ieda. The network helps show where Daisuke Ieda may publish in the future.
Co-authors
The 25 scholars most cited alongside Daisuke Ieda, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 27 | |
| 2 | 2019 | 22 | |
| 3 | 2017 | 20 | |
| 4 | 2017 | 19 | |
| 5 | 2017 | 18 | |
| 6 | 2018 | 16 | |
| 7 | 2018 | 13 | |
| 8 | 2020 | 8 | |
| 9 | 2019 | 7 | |
| 10 | 2017 | 7 | |
| 11 | 2019 | 4 | |
| 12 | 2024 | 3 | |
| 13 | 2021 | 3 | |
| 14 | 2021 | 1 | |
| 15 | 2022 | 1 | |
| 16 | 2024 | 0 |
About Daisuke Ieda
Daisuke Ieda is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Cellular and Molecular Neuroscience, having authored 16 papers that have together received 169 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (3 papers), Epigenetics and DNA Methylation (3 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA regulation and disease (2 papers), Epilepsy research and treatment (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Genetics (92 citations), Molecular Biology (79 citations), Pediatrics, Perinatology and Child Health (16 citations), Clinical Biochemistry (6 citations) and Psychiatry and Mental health (12 citations). Daisuke Ieda has collaborated with scholars based in Japan. Frequent co-authors include Shinji Saitoh, Ikumi Hori, Ayako Hattori, Yutaka Negishi, Y. Nakamura, Kei Ohashi, Mitsuko Nakashima, Hirotomo Saitsu, Takuya Hiraide and Kazuhiko Nakabayashi. Their work appears in journals such as Brain and Development, Epilepsia Open, Journal of Medical Genetics, Human Genetics and Genomics Advances and Orphanet Journal of Rare Diseases.
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.