Devon Bonner
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 14
- BRCA gene mutations in cancer 10
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 1
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- Cancer Genomics and Diagnostics 3
- Co-authors
- Tuya Pal (9 shared papers)Susan T. Vadaparampil (9 shared papers)Deborah Cragun (7 shared papers)Jongphil Kim (3 shared papers)Courtney Lewis (2 shared papers)Anne Weidner (1 shared paper)Steven A. Narod (5 shared papers)Mohammad R. Akbari (4 shared papers)
- Journals
- Journal of Clinical Oncology (2 papers)Cancer (2 papers)The Breast Journal (2 papers)Cancer Epidemiology Biomarkers & Prevention (1 paper)Genome Research (1 paper)
- Partner nations
- United StatesCanadaFrance
In The Last Decade
Devon Bonner
14 papers receiving 460 citations
Peers
Comparison fields: 5 of 39
- Genetics 354
- Cancer Research 88
- Oncology 88
- Pediatrics, Perinatology and Child Health 38
- Reproductive Medicine 16
Countries citing papers authored by Devon Bonner
This map shows the geographic impact of Devon Bonner'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 Devon Bonner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Devon Bonner more than expected).
Fields of papers citing papers by Devon Bonner
This network shows the impact of papers produced by Devon Bonner. 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 Devon Bonner. The network helps show where Devon Bonner may publish in the future.
Co-authors
The 25 scholars most cited alongside Devon Bonner, 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 | 2017 | 210 | |
| 2 | 2015 | 93 | |
| 3 | 2015 | 72 | |
| 4 | 2013 | 32 | |
| 5 | 2013 | 16 | |
| 6 | 2019 | 15 | |
| 7 | 2015 | 14 | |
| 8 | 2019 | 5 | |
| 9 | 2024 | 5 | |
| 10 | 2025 | 2 | |
| 11 | 2012 | 2 | |
| 12 | 2016 | 1 | |
| 13 | 2024 | 1 | |
| 14 | 2014 | 1 | |
| 15 | 2025 | 0 |
About Devon Bonner
Devon Bonner is a scholar working on Genetics, Cancer Research, Molecular Biology, Oncology and Pathology and Forensic Medicine, having authored 15 papers that have together received 469 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Phylogenetic Studies (2 papers), Global Cancer Incidence and Screening (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Ethics in Clinical Research (1 paper). The work is most often cited by research in Genetics (354 citations), Cancer Research (88 citations), Oncology (88 citations), Pediatrics, Perinatology and Child Health (38 citations) and Reproductive Medicine (16 citations). Devon Bonner has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Tuya Pal, Susan T. Vadaparampil, Deborah Cragun, Jongphil Kim, Courtney Lewis, Anne Weidner, Steven A. Narod, Mohammad R. Akbari, Álvaro N.A. Monteiro and Catherine Phelan. Their work appears in journals such as Journal of Clinical Oncology, Cancer, The Breast Journal, Cancer Epidemiology Biomarkers & Prevention and Genome Research.
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.