Rinki Ratnapriya

4.7k total citations
46 papers, 1.5k citations indexed

About

Rinki Ratnapriya is a scholar working on Ophthalmology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Rinki Ratnapriya has authored 46 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Ophthalmology, 25 papers in Molecular Biology and 17 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Rinki Ratnapriya's work include Retinal Diseases and Treatments (29 papers), Retinal Development and Disorders (19 papers) and Retinal Imaging and Analysis (16 papers). Rinki Ratnapriya is often cited by papers focused on Retinal Diseases and Treatments (29 papers), Retinal Development and Disorders (19 papers) and Retinal Imaging and Analysis (16 papers). Rinki Ratnapriya collaborates with scholars based in United States, India and Israel. Rinki Ratnapriya's co-authors include Anand Swaroop, Emily Y. Chew, Gonçalo R. Abecasis, Lars G. Fritsche, Vijender Chaitankar, Anuranjan Anand, Margaret R. Starostik, Ashley Walton, Matthew J. Brooks and Linn Gieser and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Nature Genetics.

In The Last Decade

Rinki Ratnapriya

44 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rinki Ratnapriya United States 24 890 748 443 243 171 46 1.5k
Yoshitsugu Saishin Japan 22 749 0.8× 1.1k 1.4× 727 1.6× 115 0.5× 112 0.7× 56 1.8k
Itay Chowers Israel 20 862 1.0× 859 1.1× 398 0.9× 134 0.6× 98 0.6× 87 1.5k
Pete Humphries Ireland 26 1.3k 1.5× 553 0.7× 241 0.5× 249 1.0× 428 2.5× 55 1.7k
Shoji Notomi Japan 23 1.1k 1.3× 1.1k 1.4× 483 1.1× 50 0.2× 179 1.0× 62 1.8k
Manir Ali United Kingdom 24 654 0.7× 302 0.4× 356 0.8× 277 1.1× 53 0.3× 61 1.4k
Aimee V. Chappelow United States 11 685 0.8× 554 0.7× 248 0.6× 104 0.4× 199 1.2× 18 1.1k
Rosa Riveiro-Álvarez Spain 24 1.2k 1.4× 640 0.9× 160 0.4× 329 1.4× 166 1.0× 53 1.5k
J. L. Haines United States 18 590 0.7× 229 0.3× 149 0.3× 295 1.2× 121 0.7× 45 1.3k
Marko Hawlina Slovenia 24 1.4k 1.6× 1.6k 2.1× 729 1.6× 96 0.4× 306 1.8× 131 2.5k
Manuel Simonutti France 14 509 0.6× 530 0.7× 211 0.5× 45 0.2× 190 1.1× 17 1.0k

Countries citing papers authored by Rinki Ratnapriya

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Rinki Ratnapriya

This figure shows the co-authorship network connecting the top 25 collaborators of Rinki Ratnapriya. A scholar is included among the top collaborators of Rinki Ratnapriya based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rinki Ratnapriya. Rinki Ratnapriya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ratnapriya, Rinki, Rui Chen, Alex W. Hewitt, et al.. (2025). Functional genomics in age-related macular degeneration: From genetic associations to understanding disease mechanisms. Experimental Eye Research. 254. 110344–110344. 1 indexed citations
2.
3.
Rajendran, Naresh Kumar, Songhua Hu, Ajeet Singh, et al.. (2025). Generation of induced pluripotent stem cell lines (RFSCi003-A, RFSCi004-A) from monozygotic twins discordant for age-related macular degeneration. Stem Cell Research. 87. 103768–103768.
4.
Singh, Ajeet & Rinki Ratnapriya. (2025). Integration of multiomic data identifies core-module of inherited-retinal diseases. Human Molecular Genetics. 34(5). 454–465.
5.
Advani, Jayshree, Andrew R. Hamel, Christina Kiel, et al.. (2024). QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration. Nature Communications. 15(1). 1972–1972. 14 indexed citations
6.
Ratnapriya, Rinki. (2023). The Role of Gene Expression Regulation on Genetic Risk of Age-Related Macular Degeneration. Advances in experimental medicine and biology. 1415. 61–66. 1 indexed citations
7.
Alam, Jehan, Ghasem Yazdanpanah, Rinki Ratnapriya, et al.. (2022). IL-17 Producing Lymphocytes Cause Dry Eye and Corneal Disease With Aging in RXRα Mutant Mouse. Frontiers in Medicine. 9. 849990–849990. 24 indexed citations
8.
Ratnapriya, Rinki, Samuel G. Jacobson, Artur V. Cideciyan, et al.. (2021). A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration. Frontiers in Cell and Developmental Biology. 9. 720782–720782. 9 indexed citations
9.
Ratnapriya, Rinki, İlhan E. Acar, Maartje J. Geerlings, et al.. (2020). Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. Human Molecular Genetics. 29(12). 2022–2034. 24 indexed citations
10.
Strunz, Tobias, Christina Kiel, Felix Graßmann, et al.. (2020). A mega-analysis of expression quantitative trait loci in retinal tissue. PLoS Genetics. 16(9). e1008934–e1008934. 21 indexed citations
11.
Ratnapriya, Rinki, Olukayode Sosina, Margaret R. Starostik, et al.. (2019). Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. Nature Genetics. 51(4). 606–610. 175 indexed citations
12.
Ding, Ying, Yi Liu, Qi Yan, et al.. (2017). Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk Scores. Genetics. 206(1). 119–133. 44 indexed citations
13.
Hoshino, Akina, Rinki Ratnapriya, Matthew J. Brooks, et al.. (2017). Molecular Anatomy of the Developing Human Retina. Developmental Cell. 43(6). 763–779.e4. 169 indexed citations
14.
Pietraszkiewicz, Alexandra, Freekje van Asten, Alan Kwong, et al.. (2017). Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration. Ophthalmology. 125(3). 398–406. 10 indexed citations
15.
Sharon, Dror, Prasanthi Namburi, Rinki Ratnapriya, et al.. (2016). Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients. Investigative Ophthalmology & Visual Science. 57(12). 3153–3153. 1 indexed citations
16.
Liu, Chunqiao, Kathleen A. Williamson, Rinki Ratnapriya, et al.. (2016). A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma. Human Molecular Genetics. 25(7). 1382–1391. 32 indexed citations
17.
Namburi, Prasanthi, Rinki Ratnapriya, Samer Khateb, et al.. (2016). Bi-allelic Truncating Mutations in CEP78 , Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. The American Journal of Human Genetics. 99(3). 777–784. 23 indexed citations
18.
Ratnapriya, Rinki & Anand Swaroop. (2013). Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing. Genome Medicine. 5(9). 84–84. 27 indexed citations
19.
Ratnapriya, Rinki, et al.. (2010). A locus for juvenile myoclonic epilepsy maps to 2q33–q36. Human Genetics. 128(2). 123–130. 11 indexed citations
20.
Ratnapriya, Rinki, et al.. (2009). A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3. Human Genetics. 125(5-6). 541–549. 24 indexed citations

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.

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