Rinki Ratnapriya
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments 29
- Glaucoma and retinal disorders 5
-
- Retinal Imaging and Analysis 16
- Molecular Biology top 10%
- Retinal Development and Disorders 19
- Genetics top 10%
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 4
- Genetic Associations and Epidemiology 3
-
- Epilepsy research and treatment 5
- Co-authors
- Anand SwaroopEmily Y. ChewGonçalo R. AbecasisLars G. FritscheVijender ChaitankarMargaret R. StarostikAnuranjan AnandMatthew J. Brooks
- Journals
- Journal of Clinical Investigation (1 paper)Nature Communications (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesIndiaIsrael
In The Last Decade
Rinki Ratnapriya
44 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 91
- Ophthalmology 748
- Radiology, Nuclear Medicine and Imaging 443
- Molecular Biology 890
- Cellular and Molecular Neuroscience 171
- Genetics 243
Countries citing papers authored by Rinki Ratnapriya
This map shows the geographic impact of Rinki Ratnapriya'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 Rinki Ratnapriya with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rinki Ratnapriya more than expected).
Fields of papers citing papers by Rinki Ratnapriya
This network shows the impact of papers produced by Rinki Ratnapriya. 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 Rinki Ratnapriya. The network helps show where Rinki Ratnapriya may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Rinki Ratnapriya, 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 | 1 | |
| 2 | 2025 | 1 | |
| 3 | 2025 | 0 | |
| 4 | 2024 | 14 | |
| 5 | 2023 | 1 | |
| 6 | 2020 | 21 | |
| 7 | 2020 | 24 | |
| 8 | 2019 | 175 | |
| 9 | 2017 | 169 | |
| 10 | 2017 | 29 | |
| 11 | 2017 | 27 | |
| 12 | 2017 | 10 | |
| 13 | Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients | 2016 | 1 |
| 14 | 2016 | 23 | |
| 15 | 2014 | 62 | |
| 16 | 2013 | 27 | |
| 17 | 2010 | 11 | |
| 18 | 2009 | 23 | |
| 19 | 2009 | 24 | |
| 20 | 2008 | 54 |
About Rinki Ratnapriya
Rinki Ratnapriya is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Genetics, having authored 46 papers that have together received 1.5k indexed citations. Recurring topics across this work include Retinal Diseases and Treatments (29 papers), Retinal Development and Disorders (19 papers), Retinal Imaging and Analysis (16 papers), Glaucoma and retinal disorders (5 papers), Epilepsy research and treatment (5 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genetic Associations and Epidemiology (3 papers). The work is most often cited by research in Ophthalmology (748 citations), Radiology, Nuclear Medicine and Imaging (443 citations) and Molecular Biology (890 citations). Rinki Ratnapriya has collaborated with scholars based in United States, India and Israel. Frequent co-authors include Anand Swaroop, Emily Y. Chew, Gonçalo R. Abecasis, Lars G. Fritsche, Vijender Chaitankar, Margaret R. Starostik, Anuranjan Anand, Matthew J. Brooks, Linn Gieser and Ashley Walton. Their work appears in journals such as Journal of Clinical Investigation, Nature Communications and Nature 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.