F. Boardman-Pretty
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Forensic and Genetic Research
- Genetic Associations and Epidemiology
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 7
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 2
- Forensic and Genetic Research 1
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- Cancer Genomics and Diagnostics 2
F. Boardman-Pretty
10 papers receiving 345 citations
F. Boardman-Pretty's Hit Papers
Peers
Comparison fields: 5 of 48
- Genetics 142
- Cancer Research 56
- Molecular Biology 152
- Hepatology 15
- Obstetrics and Gynecology 15
Countries citing papers authored by F. Boardman-Pretty
This map shows the geographic impact of F. Boardman-Pretty'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 F. Boardman-Pretty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Boardman-Pretty more than expected).
Fields of papers citing papers by F. Boardman-Pretty
This network shows the impact of papers produced by F. Boardman-Pretty. 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 F. Boardman-Pretty. The network helps show where F. Boardman-Pretty may publish in the future.
No co-authors to show.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 83 | |
| 2 | Origins and impact of extrachromosomal DNA Hit paper breakdown → | 2024 | 82 |
| 3 | 2020 | 81 | |
| 4 | 2022 | 30 | |
| 5 | 2022 | 30 | |
| 6 | 2022 | 15 | |
| 7 | 2023 | 12 | |
| 8 | 2023 | 6 | |
| 9 | 2022 | 5 | |
| 10 | 2023 | 5 |
About F. Boardman-Pretty
F. Boardman-Pretty is a scholar working on Genetics, Cancer Research, Hepatology, Obstetrics and Gynecology and Cellular and Molecular Neuroscience, having authored 10 papers that have together received 349 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (2 papers), Cancer Genomics and Diagnostics (2 papers), Pregnancy and preeclampsia studies (1 paper), Mitochondrial Function and Pathology (1 paper), Forensic and Genetic Research (1 paper), Hereditary Neurological Disorders (1 paper) and Liver Diseases and Immunity (1 paper). The work is most often cited by research in Genetics (142 citations), Cancer Research (56 citations), Molecular Biology (152 citations), Hepatology (15 citations) and Obstetrics and Gynecology (15 citations). F. Boardman-Pretty has collaborated with scholars based in United Kingdom, United States and Germany. Their work appears in journals such as Nature Communications, Genetics in Medicine, Nature, Journal of Cardiovascular Translational Research and European Journal of Human 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.