Kevin Gregory-Evans
Impact in
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
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- Circadian rhythm and melatonin
Papers in
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- Retinal Diseases and Treatments 19
- Glaucoma and retinal disorders 4
- Retinal and Optic Conditions 4
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- Retinal Development and Disorders 28
- Connexins and lens biology 6
- Co-authors
- Cheryl Y. Gregory‐EvansAlan C. BirdDavid M. HuntStephanie HalfordMichael WilliamsRosemary E. KelsellAnthony T. MooreShomi S. Bhattacharya
- Journals
- Eye (4 papers)Journal of Medical Genetics (4 papers)Human Molecular Genetics (3 papers)Investigative Ophthalmology & Visual Science (3 papers)Human Genetics (3 papers)
- Partner nations
- United KingdomCanadaUnited States
In The Last Decade
Kevin Gregory-Evans
54 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 115
- Ophthalmology 682
- Endocrine and Autonomic Systems 262
- Molecular Biology 1.6k
- Cellular and Molecular Neuroscience 367
- Radiology, Nuclear Medicine and Imaging 356
Countries citing papers authored by Kevin Gregory-Evans
This map shows the geographic impact of Kevin Gregory-Evans'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 Kevin Gregory-Evans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kevin Gregory-Evans more than expected).
Fields of papers citing papers by Kevin Gregory-Evans
This network shows the impact of papers produced by Kevin Gregory-Evans. 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 Kevin Gregory-Evans. The network helps show where Kevin Gregory-Evans may publish in the future.
Co-authors
The 25 scholars most cited alongside Kevin Gregory-Evans, 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 | 2023 | 4 | |
| 3 | NIPAAm Based Cell Delivery Scaffolds for Posterior Segment Therapeutics | 2013 | 1 |
| 4 | 2012 | 41 | |
| 5 | 2007 | 255 | |
| 6 | 2007 | 30 | |
| 7 | 2005 | 10 | |
| 8 | 2004 | 3 | |
| 9 | 2004 | 7 | |
| 10 | 2004 | 167 | |
| 11 | 2002 | 8 | |
| 12 | 1999 | 22 | |
| 13 | 1999 | 12 | |
| 14 | 1998 | 16 | |
| 15 | 1997 | 39 | |
| 16 | The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16 (vol 5, pg 1055, 1996) | 1996 | 22 |
| 17 | 1996 | 32 | |
| 18 | 1996 | 25 | |
| 19 | 1995 | 38 | |
| 20 | 1994 | 93 |
About Kevin Gregory-Evans
Kevin Gregory-Evans is a scholar working on Ophthalmology, Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology and Endocrine and Autonomic Systems, having authored 55 papers that have together received 2.3k indexed citations. Recurring topics across this work include Retinal Development and Disorders (28 papers), Retinal Diseases and Treatments (19 papers), Photoreceptor and optogenetics research (6 papers), Connexins and lens biology (6 papers), Glaucoma and retinal disorders (4 papers), Neuroscience and Neural Engineering (4 papers), Ocular Disorders and Treatments (4 papers) and Retinal and Optic Conditions (4 papers). The work is most often cited by research in Ophthalmology (682 citations), Endocrine and Autonomic Systems (262 citations), Molecular Biology (1.6k citations), Cellular and Molecular Neuroscience (367 citations) and Radiology, Nuclear Medicine and Imaging (356 citations). Kevin Gregory-Evans has collaborated with scholars based in United Kingdom, Canada and United States. Frequent co-authors include Cheryl Y. Gregory‐Evans, Alan C. Bird, David M. Hunt, Stephanie Halford, Michael Williams, Rosemary E. Kelsell, Anthony T. Moore, Shomi S. Bhattacharya, Chris F. Inglehearn and F. Foster. Their work appears in journals such as Eye, Journal of Medical Genetics, Human Molecular Genetics, Investigative Ophthalmology & Visual Science and 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.