Rachel Stapleton
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
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- Metabolism and Genetic Disorders
Papers in
- Genetics 9
- Genomics and Rare Diseases 5
- Diabetes and associated disorders 2
- Hemoglobinopathies and Related Disorders 2
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- Blood groups and transfusion 4
- Co-authors
- C. Christopher Bowley (2 shared papers)Douglas Voak (2 shared papers)Zornitza Stark (3 shared papers)Dean Phelan (2 shared papers)Susan M. White (2 shared papers)Belinda Chong (2 shared papers)Sebastian Lunke (3 shared papers)Patrick Yap (2 shared papers)
- Journals
- Vox Sanguinis (6 papers)Genetics in Medicine (2 papers)Human Genetics (1 paper)Pediatric Pulmonology (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- AustraliaNigeriaNew Zealand
In The Last Decade
Rachel Stapleton
15 papers receiving 371 citations
Peers
Comparison fields: 5 of 58
- Genetics 252
- Clinical Biochemistry 27
- Hematology 33
- Genetics 25
- Pediatrics, Perinatology and Child Health 38
Countries citing papers authored by Rachel Stapleton
This map shows the geographic impact of Rachel Stapleton'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 Rachel Stapleton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rachel Stapleton more than expected).
Fields of papers citing papers by Rachel Stapleton
This network shows the impact of papers produced by Rachel Stapleton. 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 Rachel Stapleton. The network helps show where Rachel Stapleton may publish in the future.
Co-authors
The 25 scholars most cited alongside Rachel Stapleton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 140 | |
| 2 | 2020 | 66 | |
| 3 | 2017 | 48 | |
| 4 | 2017 | 29 | |
| 5 | 2020 | 29 | |
| 6 | 1970 | 22 | |
| 7 | 1968 | 19 | |
| 8 | 2021 | 19 | |
| 9 | 2021 | 5 | |
| 10 | 1959 | 4 | |
| 11 | 2018 | 4 | |
| 12 | 1951 | 3 | |
| 13 | 1970 | 2 | |
| 14 | 2020 | 1 | |
| 15 | 1968 | 1 | |
| 16 | 1959 | 1 |
About Rachel Stapleton
Rachel Stapleton is a scholar working on Genetics, Hematology, Clinical Biochemistry, Genetics and Physiology, having authored 16 papers that have together received 393 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Blood groups and transfusion (4 papers), Erythrocyte Function and Pathophysiology (3 papers), Diabetes and associated disorders (2 papers), Metabolism and Genetic Disorders (2 papers), Hemoglobinopathies and Related Disorders (2 papers), Cancer Genomics and Diagnostics (1 paper) and Congenital Diaphragmatic Hernia Studies (1 paper). The work is most often cited by research in Genetics (252 citations), Clinical Biochemistry (27 citations), Hematology (33 citations), Genetics (25 citations) and Pediatrics, Perinatology and Child Health (38 citations). Rachel Stapleton has collaborated with scholars based in Australia, Nigeria and New Zealand. Frequent co-authors include C. Christopher Bowley, Douglas Voak, Zornitza Stark, Dean Phelan, Susan M. White, Belinda Chong, Sebastian Lunke, Patrick Yap, Martin B. Delatycki and Chloe Stutterd. Their work appears in journals such as Vox Sanguinis, Genetics in Medicine, Human Genetics, Pediatric Pulmonology 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.