Belinda Rahman
- Genetics top 5%
- Oncology
- Public Health, Environmental and Occupational Health
- Pediatrics, Perinatology and Child Health top 10%
- Molecular Biology
- Co-authors
- Lucy SideAnne LanceleyLindsay FraserSue GesslerSaskia C. SandersonJo WallerMadeleine FreemanKatie E. J. Hann
- Topics
- BRCA gene mutations in cancer (19 papers)Prenatal Screening and Diagnostics (8 papers)Ovarian cancer diagnosis and treatment (6 papers)
- Journals
- BMC Public HealthBJOG An International Journal of Obstetrics & GynaecologyJournal of Medical Genetics
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Belinda Rahman
26 papers receiving 613 citations
Peers
Comparison fields: 5 of 78
- Genetics 434
- Oncology 158
- Public Health, Environmental and Occupational Health 128
- Pediatrics, Perinatology and Child Health 115
- Molecular Biology 101
Countries citing papers authored by Belinda Rahman
This map shows the geographic impact of Belinda Rahman'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 Belinda Rahman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Belinda Rahman more than expected).
Fields of papers citing papers by Belinda Rahman
This network shows the impact of papers produced by Belinda Rahman. 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 Belinda Rahman. The network helps show where Belinda Rahman may publish in the future.
Co-authorship network of co-authors of Belinda Rahman
This figure shows the co-authorship network connecting the top 25 collaborators of Belinda Rahman. A scholar is included among the top collaborators of Belinda Rahman 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 Belinda Rahman. Belinda Rahman 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 | 1 | |
| 3 | 14 | |
| 4 | 12 | |
| 5 | 220 | |
| 6 | 9 | |
| 7 | 26 | |
| 8 | 11 | |
| 9 | 29 | |
| 10 | 27 | |
| 11 | 51 | |
| 12 | 12 | |
| 13 | 1 | |
| 14 | 12 | |
| 15 | 5 | |
| 16 | 20 | |
| 17 | 9 | |
| 18 | 21 | |
| 19 | 24 | |
| 20 | 38 |
About Belinda Rahman
Belinda Rahman is a scholar working on Genetics, Reproductive Medicine and Cancer Research, having authored 27 papers that have together received 633 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (19 papers), Prenatal Screening and Diagnostics (8 papers) and Ovarian cancer diagnosis and treatment (6 papers). The work is most often cited by research in Genetics (434 citations), Reproductive Medicine (52 citations) and Pediatrics, Perinatology and Child Health (115 citations). Belinda Rahman has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Lucy Side, Anne Lanceley, Lindsay Fraser, Sue Gessler, Saskia C. Sanderson, Jo Waller, Madeleine Freeman, Katie E. J. Hann, Bettina Meiser and Jane Wardle. Their work appears in journals such as BMC Public Health, BJOG An International Journal of Obstetrics & Gynaecology and Journal of Medical 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.