Keiko Shimojima
- Genetics top 1%
- Molecular Biology top 10%
- Pediatrics, Perinatology and Child Health top 5%
- Cellular and Molecular Neuroscience top 10%
- Cell Biology top 10%
- Co-authors
- Toshiyuki YamamotoNobuhiko OkamotoShino ShimadaKatsumi ImaiMidori SugawaraMakiko ŌsawaAkihisa OkumuraNoriko Sangu
- Topics
- Genomic variations and chromosomal abnormalities (62 papers)Genetics and Neurodevelopmental Disorders (32 papers)Genomics and Rare Diseases (21 papers)
- Partner nations
- JapanAustraliaUnited States
In The Last Decade
Keiko Shimojima
125 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 86
- Genetics 1.2k
- Molecular Biology 1.0k
- Pediatrics, Perinatology and Child Health 218
- Cellular and Molecular Neuroscience 190
- Cell Biology 190
Countries citing papers authored by Keiko Shimojima
This map shows the geographic impact of Keiko Shimojima'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 Keiko Shimojima with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Keiko Shimojima more than expected).
Fields of papers citing papers by Keiko Shimojima
This network shows the impact of papers produced by Keiko Shimojima. 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 Keiko Shimojima. The network helps show where Keiko Shimojima may publish in the future.
Co-authorship network of co-authors of Keiko Shimojima
This figure shows the co-authorship network connecting the top 25 collaborators of Keiko Shimojima. A scholar is included among the top collaborators of Keiko Shimojima based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Keiko Shimojima. Keiko Shimojima is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 7 | |
| 2 | 24 | |
| 3 | 13 | |
| 4 | 19 | |
| 5 | 10 | |
| 6 | 9 | |
| 7 | 13 | |
| 8 | 12 | |
| 9 | 38 | |
| 10 | 29 | |
| 11 | 25 | |
| 12 | 10 | |
| 13 | 16 | |
| 14 | 7 | |
| 15 | 58 | |
| 16 | 18 | |
| 17 | 79 | |
| 18 | 3 | |
| 19 | 11 | |
| 20 | 33 |
About Keiko Shimojima
Keiko Shimojima is a scholar working on Genetics, Molecular Biology and Genetics, having authored 125 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (62 papers), Genetics and Neurodevelopmental Disorders (32 papers) and Genomics and Rare Diseases (21 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (1.0k citations) and Developmental Neuroscience (49 citations). Keiko Shimojima has collaborated with scholars based in Japan, Australia and United States. Frequent co-authors include Toshiyuki Yamamoto, Nobuhiko Okamoto, Shino Shimada, Katsumi Imai, Midori Sugawara, Makiko Ōsawa, Akihisa Okumura, Noriko Sangu, Yumiko Ondo and Kousaku Ohno. Their work appears in journals such as Gene, Epilepsia and Journal of the Neurological Sciences.
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.