Hirohito Shima
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Congenital Ear and Nasal Anomalies
Papers in
- Genetics 15
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Congenital Ear and Nasal Anomalies 6
- Genomic variations and chromosomal abnormalities 4
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- Sexual Differentiation and Disorders 4
- Genomics and Chromatin Dynamics 2
- Co-authors
- Maki Fukami (17 shared papers)Satoshi Narumi (10 shared papers)Tsutomu Ogata (8 shared papers)Erina Suzuki (9 shared papers)Keiko Matsubara (4 shared papers)Saquib A. Lakhani (1 shared paper)Shuichi Yatsuga (4 shared papers)Weizhen Ji (1 shared paper)
- Journals
- Cytogenetic and Genome Research (4 papers)European Journal of Medical Genetics (1 paper)Blood Advances (1 paper)Journal of Medical Genetics (1 paper)European Journal of Endocrinology (1 paper)
- Partner nations
- JapanUnited StatesIran
In The Last Decade
Hirohito Shima
27 papers receiving 299 citations
Peers
Comparison fields: 5 of 43
- Genetics 140
- Reproductive Medicine 30
- Genetics 34
- Hematology 32
- Molecular Biology 149
Countries citing papers authored by Hirohito Shima
This map shows the geographic impact of Hirohito Shima'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 Hirohito Shima with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hirohito Shima more than expected).
Fields of papers citing papers by Hirohito Shima
This network shows the impact of papers produced by Hirohito Shima. 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 Hirohito Shima. The network helps show where Hirohito Shima may publish in the future.
Co-authors
The 25 scholars most cited alongside Hirohito Shima, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 48 | |
| 2 | 2017 | 40 | |
| 3 | 2018 | 28 | |
| 4 | 2017 | 26 | |
| 5 | Elastofibroma dorsi. Cytologic, histologic, immunohistochemical and ultrastructural studies. | 1992 | 19 |
| 6 | 2018 | 18 | |
| 7 | 2016 | 15 | |
| 8 | 2017 | 14 | |
| 9 | 2017 | 12 | |
| 10 | 2017 | 12 | |
| 11 | 2019 | 11 | |
| 12 | 2016 | 10 | |
| 13 | 2019 | 10 | |
| 14 | 2019 | 9 | |
| 15 | 1984 | 8 | |
| 16 | 2018 | 6 | |
| 17 | 2019 | 5 | |
| 18 | 2021 | 4 | |
| 19 | 2019 | 3 | |
| 20 | 1998 | 3 |
About Hirohito Shima
Hirohito Shima is a scholar working on Genetics, Molecular Biology, Genetics, Reproductive Medicine and Surgery, having authored 29 papers that have together received 313 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Congenital Ear and Nasal Anomalies (6 papers), Hypothalamic control of reproductive hormones (4 papers), Chromosomal and Genetic Variations (4 papers), Sexual Differentiation and Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (140 citations), Reproductive Medicine (30 citations), Genetics (34 citations), Hematology (32 citations) and Molecular Biology (149 citations). Hirohito Shima has collaborated with scholars based in Japan, United States and Iran. Frequent co-authors include Maki Fukami, Satoshi Narumi, Tsutomu Ogata, Erina Suzuki, Keiko Matsubara, Saquib A. Lakhani, Shuichi Yatsuga, Weizhen Ji, Katrin Koehler and Kazuhiko Sugimoto. Their work appears in journals such as Cytogenetic and Genome Research, European Journal of Medical Genetics, Blood Advances, Journal of Medical Genetics and European Journal of Endocrinology.
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.