Chloe Mighton
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 25
- Genomics and Rare Diseases 20
- BRCA gene mutations in cancer 18
- Genomic variations and chromosomal abnormalities 4
- Genetic Associations and Epidemiology 3
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- Genetic factors in colorectal cancer 10
- Co-authors
- Yvonne Bombard (22 shared papers)Salma Shickh (14 shared papers)Elizabeth Uleryk (3 shared papers)Petros Pechlivanoglou (2 shared papers)Jordan Lerner‐Ellis (16 shared papers)Marc Clausen (13 shared papers)George S. Charames (3 shared papers)Andrew Wong (4 shared papers)
- Journals
- Genetics in Medicine (6 papers)European Journal of Human Genetics (5 papers)Human Genetics (3 papers)Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Chloe Mighton
26 papers receiving 315 citations
Peers
Comparison fields: 5 of 51
- Genetics 252
- Cancer Research 49
- Pathology and Forensic Medicine 57
- Pediatrics, Perinatology and Child Health 36
- Public Health, Environmental and Occupational Health 49
Countries citing papers authored by Chloe Mighton
This map shows the geographic impact of Chloe 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 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 Mighton more than expected).
Fields of papers citing papers by Chloe Mighton
This network shows the impact of papers produced by Chloe 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 Mighton. The network helps show where Chloe Mighton may publish in the future.
Co-authors
The 25 scholars most cited alongside Chloe 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 54 | |
| 2 | 2019 | 44 | |
| 3 | 2020 | 39 | |
| 4 | 2018 | 36 | |
| 5 | 2022 | 24 | |
| 6 | 2020 | 17 | |
| 7 | 2020 | 12 | |
| 8 | 2022 | 12 | |
| 9 | 2021 | 11 | |
| 10 | 2020 | 11 | |
| 11 | 2022 | 9 | |
| 12 | 2020 | 7 | |
| 13 | 2019 | 7 | |
| 14 | 2021 | 7 | |
| 15 | 2021 | 7 | |
| 16 | 2021 | 4 | |
| 17 | 2024 | 3 | |
| 18 | 2024 | 2 | |
| 19 | 2022 | 2 | |
| 20 | 2022 | 2 |
About Chloe Mighton
Chloe Mighton is a scholar working on Genetics, Pathology and Forensic Medicine, Public Health, Environmental and Occupational Health, Economics and Econometrics and Cancer Research, having authored 30 papers that have together received 318 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (20 papers), BRCA gene mutations in cancer (18 papers), Genetic factors in colorectal cancer (10 papers), Cancer Genomics and Diagnostics (5 papers), Health Systems, Economic Evaluations, Quality of Life (5 papers), Ethics in Clinical Research (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Associations and Epidemiology (3 papers). The work is most often cited by research in Genetics (252 citations), Cancer Research (49 citations), Pathology and Forensic Medicine (57 citations), Pediatrics, Perinatology and Child Health (36 citations) and Public Health, Environmental and Occupational Health (49 citations). Chloe Mighton has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Yvonne Bombard, Salma Shickh, Elizabeth Uleryk, Petros Pechlivanoglou, Jordan Lerner‐Ellis, Marc Clausen, George S. Charames, Andrew Wong, Nicholas A. Watkins and Kasmintan A. Schrader. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, Human Genetics, Journal of Medical Genetics and The American 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.