Matti A. Rookus
- Genetics top 1%
- Oncology top 2%
- Cancer Research top 2%
- Reproductive Medicine top 1%
- Pathology and Forensic Medicine top 2%
- Co-authors
- Flora E. van LeeuwenLaura J. van’t VeerRichard M. BrohetJanneke VerloopChristi J. van AsperenK van der KooyHans F. A. VasenDorien W. Voskuil
- Topics
- BRCA gene mutations in cancer (35 papers)Cancer Risks and Factors (18 papers)Ovarian cancer diagnosis and treatment (14 papers)
- Partner nations
- NetherlandsUnited StatesUnited Kingdom
In The Last Decade
Matti A. Rookus
60 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 113
- Genetics 1.5k
- Oncology 1.0k
- Cancer Research 729
- Reproductive Medicine 550
- Pathology and Forensic Medicine 500
Countries citing papers authored by Matti A. Rookus
This map shows the geographic impact of Matti A. Rookus'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 Matti A. Rookus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matti A. Rookus more than expected).
Fields of papers citing papers by Matti A. Rookus
This network shows the impact of papers produced by Matti A. Rookus. 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 Matti A. Rookus. The network helps show where Matti A. Rookus may publish in the future.
Co-authorship network of co-authors of Matti A. Rookus
This figure shows the co-authorship network connecting the top 25 collaborators of Matti A. Rookus. A scholar is included among the top collaborators of Matti A. Rookus 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 Matti A. Rookus. Matti A. Rookus is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 14 | |
| 3 | 7 | |
| 4 | 0 | |
| 5 | 42 | |
| 6 | 34 | |
| 7 | 7 | |
| 8 | 6 | |
| 9 | 5 | |
| 10 | 5 | |
| 11 | 133 | |
| 12 | BRCA1/2 mutation carriers do not have earlier natural menopause compared to proven non-carriers: report from the Dutch hereditary breast and ovarian cancer study group (HEBON) | 1 |
| 13 | 130 | |
| 14 | 62 | |
| 15 | 6 | |
| 16 | 43 | |
| 17 | 104 | |
| 18 | 92 | |
| 19 | 165 | |
| 20 | 45 |
About Matti A. Rookus
Matti A. Rookus is a scholar working on Reproductive Medicine, Genetics and Oncology, having authored 65 papers that have together received 2.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (35 papers), Cancer Risks and Factors (18 papers) and Ovarian cancer diagnosis and treatment (14 papers). The work is most often cited by research in Reproductive Medicine (550 citations), Genetics (1.5k citations) and Cancer Research (729 citations). Matti A. Rookus has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Flora E. van Leeuwen, Laura J. van’t Veer, Richard M. Brohet, Janneke Verloop, Christi J. van Asperen, K van der Kooy, Hans F. A. Vasen, Dorien W. Voskuil, Margreet G.E.M. Ausems and Emiel J. Rutgers. Their work appears in journals such as JAMA, Journal of Clinical Oncology and Gastroenterology.
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.