Hidefumi Tonoki
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Hereditary Neurological Disorders
Papers in
- Genetics 28
- Genomic variations and chromosomal abnormalities 16
- Genetic Syndromes and Imprinting 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Congenital Ear and Nasal Anomalies 3
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- Epigenetics and DNA Methylation 7
- Protein Tyrosine Phosphatases 3
- Co-authors
- Hiroshi Mitsubuchi (1 shared paper)Ichiro Matsuda (1 shared paper)Yasuhiro Indo (1 shared paper)Yutaka Awaya (1 shared paper)Tomoyasu Kawano (1 shared paper)Mohammad A. Karim (1 shared paper)Kohji Ohta (1 shared paper)Tetsuya Moriuchi (9 shared papers)
- Journals
- Human Genetics (3 papers)International Journal of Cancer (2 papers)American Journal of Medical Genetics (11 papers)Pediatric Research (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- JapanUnited StatesIndia
In The Last Decade
Hidefumi Tonoki
46 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 100
- Genetics 494
- Cellular and Molecular Neuroscience 292
- Sensory Systems 59
- Molecular Biology 670
- Pediatrics, Perinatology and Child Health 157
Countries citing papers authored by Hidefumi Tonoki
This map shows the geographic impact of Hidefumi Tonoki'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 Hidefumi Tonoki with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hidefumi Tonoki more than expected).
Fields of papers citing papers by Hidefumi Tonoki
This network shows the impact of papers produced by Hidefumi Tonoki. 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 Hidefumi Tonoki. The network helps show where Hidefumi Tonoki may publish in the future.
Co-authors
The 25 scholars most cited alongside Hidefumi Tonoki, 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 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 462 | |
| 2 | 2000 | 158 | |
| 3 | 1999 | 145 | |
| 4 | 1997 | 74 | |
| 5 | 1989 | 72 | |
| 6 | 1999 | 68 | |
| 7 | 1997 | 66 | |
| 8 | 1991 | 58 | |
| 9 | Dominant-negative mutations of the tumor suppressor p53 relating to early onset of glioblastoma multiforme. | 1999 | 52 |
| 10 | 2000 | 32 | |
| 11 | 2009 | 27 | |
| 12 | 2000 | 27 | |
| 13 | 1998 | 25 | |
| 14 | 2001 | 24 | |
| 15 | 1988 | 20 | |
| 16 | 1998 | 19 | |
| 17 | 2001 | 17 | |
| 18 | 1991 | 17 | |
| 19 | 2004 | 14 | |
| 20 | 2011 | 13 |
About Hidefumi Tonoki
Hidefumi Tonoki is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Oncology and Pathology and Forensic Medicine, having authored 48 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (13 papers), Epigenetics and DNA Methylation (7 papers), Cancer-related Molecular Pathways (7 papers), Genetic Syndromes and Imprinting (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Protein Tyrosine Phosphatases (3 papers) and Congenital Ear and Nasal Anomalies (3 papers). The work is most often cited by research in Genetics (494 citations), Cellular and Molecular Neuroscience (292 citations), Sensory Systems (59 citations), Molecular Biology (670 citations) and Pediatrics, Perinatology and Child Health (157 citations). Hidefumi Tonoki has collaborated with scholars based in Japan, United States and India. Frequent co-authors include Hiroshi Mitsubuchi, Ichiro Matsuda, Yasuhiro Indo, Yutaka Awaya, Tomoyasu Kawano, Mohammad A. Karim, Kohji Ohta, Tetsuya Moriuchi, Norio Niikawa and Keiko Wakui. Their work appears in journals such as Human Genetics, International Journal of Cancer, American Journal of Medical Genetics, Pediatric Research and Prenatal Diagnosis.
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.