Michèle Ramsay
- Genetics top 0.5%
- Genetic Associations and Epidemiology 46
- Genomics and Rare Diseases 16
- Cell Biology top 1%
- melanin and skin pigmentation 18
- Dermatology top 1%
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- Birth, Development, and Health 11
- Sensory Systems top 2%
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- Biochemical Analysis and Sensing Techniques 14
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- Cystic Fibrosis Research Advances 13
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- Diabetes, Cardiovascular Risks, and Lipoproteins 13
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- Genetics, Bioinformatics, and Biomedical Research 12
- Co-authors
- T JenkinsFrancisco C. CeballosJames F. WilsonDavid W. ClarkPeter K. JoshiPhilip HaycockTrefor JenkinsWen‐Hsiung Li
- Cited by
- GeneticsCell BiologyDermatology
- Journals
- Nucleic Acids Research (12 papers)Frontiers in Genetics (11 papers)Human Genetics (9 papers)
- Partner nations
- South AfricaUnited StatesUnited Kingdom
In The Last Decade
Michèle Ramsay
227 papers receiving 5.2k citations
Hit Papers
Peers
Comparison fields: 5 of 166
- Genetics 2.0k
- Cell Biology 871
- Dermatology 339
- Pediatrics, Perinatology and Child Health 636
- Sensory Systems 157
Countries citing papers authored by Michèle Ramsay
This map shows the geographic impact of Michèle Ramsay'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 Michèle Ramsay with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michèle Ramsay more than expected).
Fields of papers citing papers by Michèle Ramsay
This network shows the impact of papers produced by Michèle Ramsay. 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 Michèle Ramsay. The network helps show where Michèle Ramsay may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Michèle Ramsay, 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 | 0 | |
| 2 | 2025 | 1 | |
| 3 | 2024 | 2 | |
| 4 | 2023 | 1 | |
| 5 | 2023 | 4 | |
| 6 | 2023 | 1 | |
| 7 | 2023 | 12 | |
| 8 | 2023 | 4 | |
| 9 | 2023 | 2 | |
| 10 | 2022 | 19 | |
| 11 | 2021 | 47 | |
| 12 | 2021 | 14 | |
| 13 | 2021 | 4 | |
| 14 | 2021 | 4 | |
| 15 | 2020 | 9 | |
| 16 | 2020 | 1 | |
| 17 | Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family. | 2018 | 19 |
| 18 | Myocilin mutations in black South Africans with POAG. | 2011 | 15 |
| 19 | 2001 | 100 | |
| 20 | Cystic fibrosis carrier frequencies in populations of African origin. | 1999 | 64 |
About Michèle Ramsay
Michèle Ramsay is a scholar working on Genetics, Cell Biology, Genetics, Ophthalmology and Nutrition and Dietetics, having authored 237 papers that have together received 5.4k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (46 papers), melanin and skin pigmentation (18 papers), Genomics and Rare Diseases (16 papers), Biochemical Analysis and Sensing Techniques (14 papers), Cystic Fibrosis Research Advances (13 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (13 papers), Genetics, Bioinformatics, and Biomedical Research (12 papers) and Birth, Development, and Health (11 papers). The work is most often cited by research in Genetics (2.0k citations), Cell Biology (871 citations), Dermatology (339 citations), Pediatrics, Perinatology and Child Health (636 citations) and Sensory Systems (157 citations). Michèle Ramsay has collaborated with scholars based in South Africa, United States and United Kingdom. Frequent co-authors include T Jenkins, Francisco C. Ceballos, James F. Wilson, David W. Clark, Peter K. Joshi, Philip Haycock, Trefor Jenkins, Wen‐Hsiung Li, Jaysen Knezovich and Scott Hazelhurst. Their work appears in journals such as Nucleic Acids Research, Frontiers in Genetics, Human Genetics, Human Molecular Genetics 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.