Jamie M. Ellingford
- Ophthalmology top 5%
- Retinal Diseases and Treatments 4
- Genetics top 5%
- Genomics and Rare Diseases 13
- Genomic variations and chromosomal abnormalities 11
- BRCA gene mutations in cancer 6
- Genetics and Neurodevelopmental Disorders 4
- Genetic and Kidney Cyst Diseases 4
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- Retinal Development and Disorders 10
- RNA modifications and cancer 4
- Co-authors
- Graeme C. BlackPanagiotis I. SergouniotisSimon RamsdenStephanie BartonSanjeev S. BhaskarWilliam G. NewmanGeorgina HallJanine A. Lamb
- Journals
- The Lancet (1 paper)SHILAP Revista de lepidopterología (2 papers)Scientific Reports (1 paper)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Jamie M. Ellingford
38 papers receiving 1.0k citations
Hit Papers
Peers
Comparison fields: 5 of 88
- Ophthalmology 174
- Genetics 500
- Molecular Biology 683
- Cancer Research 113
- Sensory Systems 25
Countries citing papers authored by Jamie M. Ellingford
This map shows the geographic impact of Jamie M. Ellingford'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 Jamie M. Ellingford with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jamie M. Ellingford more than expected).
Fields of papers citing papers by Jamie M. Ellingford
This network shows the impact of papers produced by Jamie M. Ellingford. 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 Jamie M. Ellingford. The network helps show where Jamie M. Ellingford may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Jamie M. Ellingford, 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 | 2023 | 3 | |
| 2 | 2022 | 11 | |
| 3 | 2022 | 2 | |
| 4 | 2021 | 3 | |
| 5 | 2021 | 5 | |
| 6 | 2021 | 1 | |
| 7 | 2021 | 9 | |
| 8 | 2021 | 4 | |
| 9 | 2021 | 3 | |
| 10 | 2020 | 15 | |
| 11 | 2020 | 12 | |
| 12 | 2019 | 30 | |
| 13 | 2019 | 35 | |
| 14 | 2019 | 40 | |
| 15 | 2018 | 57 | |
| 16 | 2017 | 24 | |
| 17 | 2017 | 46 | |
| 18 | 2016 | 22 | |
| 19 | 2016 | 93 | |
| 20 | 2015 | 21 |
About Jamie M. Ellingford
Jamie M. Ellingford is a scholar working on Genetics, Ophthalmology and Molecular Biology, having authored 39 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (11 papers), Retinal Development and Disorders (10 papers), BRCA gene mutations in cancer (6 papers), Retinal Diseases and Treatments (4 papers), RNA modifications and cancer (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). The work is most often cited by research in Ophthalmology (174 citations), Genetics (500 citations) and Molecular Biology (683 citations). Jamie M. Ellingford has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Graeme C. Black, Panagiotis I. Sergouniotis, Simon Ramsden, Stephanie Barton, Sanjeev S. Bhaskar, William G. Newman, Georgina Hall, Janine A. Lamb, Rachel L. Taylor and Simon G. Williams. Their work appears in journals such as The Lancet, SHILAP Revista de lepidopterología and Scientific Reports.
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.