Chloe E. Mighton
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Health Informatics top 5%
- Artificial Intelligence in Healthcare and Education
Papers in
- Genetics 54
- Genomics and Rare Diseases 33
- BRCA gene mutations in cancer 23
- Genetic Associations and Epidemiology 4
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- Ethics in Clinical Research 7
- Medical and Health Sciences Research 5
- Co-authors
- Yvonne Bombard (24 shared papers)Salma Shickh (14 shared papers)Elizabeth M. Uleryk (3 shared papers)Petros Pechlivanoglou (2 shared papers)Jordan P. Lerner‐Ellis (16 shared papers)Marc Clausen (14 shared papers)George S. Charames (3 shared papers)Kasmintan A. Schrader (6 shared papers)
- Journals
- Genetics in Medicine (14 papers)European Journal of Human Genetics (9 papers)Human Genetics (6 papers)BMJ Open (5 papers)Journal of Medical Genetics (5 papers)
- Partner nations
- CanadaUnited StatesAustralia
In The Last Decade
Chloe E. Mighton
63 papers receiving 845 citations
Peers
Comparison fields: 5 of 69
- Genetics 592
- Health Informatics 38
- Public Health, Environmental and Occupational Health 154
- Health Information Management 39
- Pediatrics, Perinatology and Child Health 49
Countries citing papers authored by Chloe E. Mighton
This map shows the geographic impact of Chloe E. Mighton'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 Chloe E. Mighton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chloe E. Mighton more than expected).
Fields of papers citing papers by Chloe E. Mighton
This network shows the impact of papers produced by Chloe E. Mighton. 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 Chloe E. Mighton. The network helps show where Chloe E. Mighton may publish in the future.
Co-authors
The 25 scholars most cited alongside Chloe E. Mighton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 73 | |
| 2 | 2023 | 60 | |
| 3 | 2020 | 57 | |
| 4 | 2019 | 54 | |
| 5 | 2018 | 49 | |
| 6 | 2019 | 48 | |
| 7 | 2021 | 35 | |
| 8 | 2022 | 31 | |
| 9 | 2021 | 26 | |
| 10 | 2023 | 24 | |
| 11 | 2019 | 23 | |
| 12 | 2020 | 23 | |
| 13 | 2018 | 21 | |
| 14 | 2020 | 21 | |
| 15 | 2021 | 19 | |
| 16 | 2022 | 19 | |
| 17 | 2015 | 17 | |
| 18 | 2020 | 17 | |
| 19 | 2018 | 16 | |
| 20 | 2020 | 16 |
About Chloe E. Mighton
Chloe E. Mighton is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Health Informatics, General Health Professions and Infectious Diseases, having authored 67 papers that have together received 865 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (33 papers), BRCA gene mutations in cancer (23 papers), Ethics in Clinical Research (7 papers), Patient-Provider Communication in Healthcare (7 papers), Medical and Health Sciences Research (5 papers), Artificial Intelligence in Healthcare and Education (4 papers), Genetic Associations and Epidemiology (4 papers) and Health Systems, Economic Evaluations, Quality of Life (3 papers). The work is most often cited by research in Genetics (592 citations), Health Informatics (38 citations), Public Health, Environmental and Occupational Health (154 citations), Health Information Management (39 citations) and Pediatrics, Perinatology and Child Health (49 citations). Chloe E. Mighton has collaborated with scholars based in Canada, United States and Australia. Frequent co-authors include Yvonne Bombard, Salma Shickh, Elizabeth M. Uleryk, Petros Pechlivanoglou, Jordan P. Lerner‐Ellis, Marc Clausen, George S. Charames, Kasmintan A. Schrader, Matthew S. Lebo and Selina Casalino. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, Human Genetics, BMJ Open 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.