Stephanie M. Fullerton
- Genetics top 0.5%
- BRCA gene mutations in cancer 48
- Genomics and Rare Diseases 29
- Race, Genetics, and Society 25
- Genetic Associations and Epidemiology 15
- Forensic and Genetic Research 10
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- Ethics in Clinical Research 62
- Health Informatics top 2%
- Physiology top 2%
- Biomedical Ethics and Regulation 14
- General Health Professions top 2%
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- Health Systems, Economic Evaluations, Quality of Life 10
- Co-authors
- Kenneth M. WeissWylie BurkeGail P. JarvikSusan Brown TrinidadAndrew G. ClarkRosalind M. HardingEric B. LarsonJ. B. Clegg
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Stephanie M. Fullerton
131 papers receiving 4.3k citations
Hit Papers
Peers
Comparison fields: 5 of 167
- Genetics 2.1k
- Public Health, Environmental and Occupational Health 1.5k
- Health Informatics 52
- Physiology 801
- General Health Professions 469
Countries citing papers authored by Stephanie M. Fullerton
This map shows the geographic impact of Stephanie M. Fullerton'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 Stephanie M. Fullerton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie M. Fullerton more than expected).
Fields of papers citing papers by Stephanie M. Fullerton
This network shows the impact of papers produced by Stephanie M. Fullerton. 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 Stephanie M. Fullerton. The network helps show where Stephanie M. Fullerton may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Stephanie M. Fullerton, 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 | 2025 | 2 | |
| 2 | 2025 | 1 | |
| 3 | 2024 | 2 | |
| 4 | 2024 | 1 | |
| 5 | 2024 | 2 | |
| 6 | 2022 | 6 | |
| 7 | 2022 | 2 | |
| 8 | 2022 | 18 | |
| 9 | 2021 | 25 | |
| 10 | 2020 | 4 | |
| 11 | 2017 | 6 | |
| 12 | 2014 | 30 | |
| 13 | It's not about the alert: Informing genetically-guided decision support with human-centered design. | 2013 | 1 |
| 14 | 2013 | 1 | |
| 15 | 2012 | 5 | |
| 16 | 2012 | 45 | |
| 17 | 2012 | 42 | |
| 18 | 2008 | 38 | |
| 19 | 2002 | 90 | |
| 20 | 1998 | 38 |
About Stephanie M. Fullerton
Stephanie M. Fullerton is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Transplantation, having authored 133 papers that have together received 4.4k indexed citations. Recurring topics across this work include Ethics in Clinical Research (62 papers), BRCA gene mutations in cancer (48 papers), Genomics and Rare Diseases (29 papers), Race, Genetics, and Society (25 papers), Genetic Associations and Epidemiology (15 papers), Biomedical Ethics and Regulation (14 papers), Forensic and Genetic Research (10 papers) and Health Systems, Economic Evaluations, Quality of Life (10 papers). The work is most often cited by research in Genetics (2.1k citations), Public Health, Environmental and Occupational Health (1.5k citations) and Health Informatics (52 citations). Stephanie M. Fullerton has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Kenneth M. Weiss, Wylie Burke, Gail P. Jarvik, Susan Brown Trinidad, Andrew G. Clark, Rosalind M. Harding, Eric B. Larson, J. B. Clegg, Eric Boerwinkle and Veikko Salomaa. Their work appears in journals such as Science, New England Journal of Medicine and Cell.
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.