Aritoshi Iida
Impact in
- Genetics top 1%
- Genetic Associations and Epidemiology
- Inflammatory Bowel Disease
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Rheumatology top 2%
- Osteoarthritis Treatment and Mechanisms
Papers in
-
- Muscle Physiology and Disorders 7
- RNA modifications and cancer 7
- Genetics 32
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 6
- Co-authors
- Yusuke Nakamura (17 shared papers)Akihiro Sekine (19 shared papers)Susumu Saito (20 shared papers)A. Sekine (9 shared papers)Tatsuhiko Tsunoda (7 shared papers)Toshihiro Tanaka (9 shared papers)Kouichi Ozaki (8 shared papers)Shiro Ikegawa (31 shared papers)
- Journals
- Genes Chromosomes and Cancer (10 papers)Neuromuscular Disorders (9 papers)Journal of Human Genetics (38 papers)Human Genetics (3 papers)Human Molecular Genetics (3 papers)
- Partner nations
- JapanChinaUnited States
In The Last Decade
Aritoshi Iida
123 papers receiving 4.5k citations
Aritoshi Iida's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 1.3k
- Rheumatology 470
- Oncology 711
- Immunology 573
- Molecular Biology 1.8k
Countries citing papers authored by Aritoshi Iida
This map shows the geographic impact of Aritoshi Iida'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 Aritoshi Iida with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aritoshi Iida more than expected).
Fields of papers citing papers by Aritoshi Iida
This network shows the impact of papers produced by Aritoshi Iida. 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 Aritoshi Iida. The network helps show where Aritoshi Iida may publish in the future.
Co-authors
The 25 scholars most cited alongside Aritoshi Iida, 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 128 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction Hit paper breakdown → | 2002 | 698 |
| 2 | 2005 | 354 | |
| 3 | 2005 | 350 | |
| 4 | 2004 | 191 | |
| 5 | 2002 | 105 | |
| 6 | 2002 | 95 | |
| 7 | 2004 | 94 | |
| 8 | 2005 | 86 | |
| 9 | 1998 | 86 | |
| 10 | 2006 | 82 | |
| 11 | 2018 | 77 | |
| 12 | 2020 | 74 | |
| 13 | 2001 | 73 | |
| 14 | 2001 | 73 | |
| 15 | 2002 | 72 | |
| 16 | 2004 | 70 | |
| 17 | 1996 | 70 | |
| 18 | 2001 | 65 | |
| 19 | 2005 | 64 | |
| 20 | 1997 | 60 |
About Aritoshi Iida
Aritoshi Iida is a scholar working on Molecular Biology, Genetics, Rheumatology, Cancer Research and Oncology, having authored 128 papers that have together received 4.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Cardiomyopathy and Myosin Studies (8 papers), Genetic factors in colorectal cancer (8 papers), Muscle Physiology and Disorders (7 papers), Drug Transport and Resistance Mechanisms (7 papers), RNA modifications and cancer (7 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Genetics (1.3k citations), Rheumatology (470 citations), Oncology (711 citations), Immunology (573 citations) and Molecular Biology (1.8k citations). Aritoshi Iida has collaborated with scholars based in Japan, China and United States. Frequent co-authors include Yusuke Nakamura, Akihiro Sekine, Susumu Saito, A. Sekine, Tatsuhiko Tsunoda, Toshihiro Tanaka, Kouichi Ozaki, Shiro Ikegawa, Hiroshi Sato and Masatsugu Hori. Their work appears in journals such as Genes Chromosomes and Cancer, Neuromuscular Disorders, Journal of Human Genetics, Human Genetics and Human Molecular Genetics.
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.