I. Hatada
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
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- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- Cancer-related gene regulation
Papers in
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- Epigenetics and DNA Methylation 5
- Genomics and Chromatin Dynamics 2
- Genetics 6
- Genetic Syndromes and Imprinting 5
- Virus-based gene therapy research 1
- Co-authors
- Shinji Hirotsune (3 shared papers)Yoshihide Hayashizaki (2 shared papers)H. Komatsubara (2 shared papers)T Mukai (1 shared paper)Laura P. O’Neill (1 shared paper)Bryan M. Turner (1 shared paper)Sanjeev Khosla (1 shared paper)Robert Feil (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (2 papers)The Journal of Biochemistry (1 paper)Human Genetics (1 paper)Human Molecular Genetics (1 paper)Molecular and Cellular Biology (1 paper)
- Partner nations
- JapanUnited KingdomAustria
In The Last Decade
I. Hatada
10 papers receiving 682 citations
Peers
Comparison fields: 5 of 63
- Genetics 353
- Molecular Biology 578
- Pediatrics, Perinatology and Child Health 133
- Cancer Research 90
- Oncology 53
Countries citing papers authored by I. Hatada
This map shows the geographic impact of I. Hatada'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 I. Hatada with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I. Hatada more than expected).
Fields of papers citing papers by I. Hatada
This network shows the impact of papers produced by I. Hatada. 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 I. Hatada. The network helps show where I. Hatada may publish in the future.
Co-authors
The 25 scholars most cited alongside I. Hatada, 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 | 1991 | 265 | |
| 2 | 1996 | 117 | |
| 3 | 2001 | 111 | |
| 4 | 2001 | 69 | |
| 5 | 1997 | 66 | |
| 6 | 1986 | 50 | |
| 7 | Genomic analysis of human hepatocellular carcinomas using Restriction Landmark Genomic Scanning. | 1993 | 15 |
| 8 | 2000 | 5 | |
| 9 | The lca as an onco-fetal gene: its expression in human fetal liver. | 1988 | 2 |
| 10 | [Restriction landmark genomic scanning (RLGS) method and its application]. | 1993 | 1 |
About I. Hatada
I. Hatada is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cancer Research and Surgery, having authored 10 papers that have together received 701 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (3 papers), Cancer Genomics and Diagnostics (2 papers), Genomics and Chromatin Dynamics (2 papers), Pancreatic function and diabetes (1 paper), Liver physiology and pathology (1 paper) and Virus-based gene therapy research (1 paper). The work is most often cited by research in Genetics (353 citations), Molecular Biology (578 citations), Pediatrics, Perinatology and Child Health (133 citations), Cancer Research (90 citations) and Oncology (53 citations). I. Hatada has collaborated with scholars based in Japan, United Kingdom and Austria. Frequent co-authors include Shinji Hirotsune, Yoshihide Hayashizaki, H. Komatsubara, T Mukai, Laura P. O’Neill, Bryan M. Turner, Sanjeev Khosla, Robert Feil, Richard I. Gregory and Colin A. Johnson. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Journal of Biochemistry, Human Genetics, Human Molecular Genetics and Molecular and Cellular Biology.
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.