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ARVO Annual Meeting Abstract June 2024

Cellular and molecular changes in retinal microglia contributes to neurodegeneration in AMD

Rinki Ratnapriya; Khang Ma; Arko Barman

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):403.

ARVO Annual Meeting Abstract June 2024

First report of RNA editing in human retina – a process central to photoreceptor health, and a risk factor for both AMD and rarer macular degeneration

Brendan Robert E Ansell; Roberto Bonelli; Simon N Thomas; Aravind Manda; Rinki Ratnapriya; Michele Pinelli; Anand Swaroop; Diego diBernardo; Sandro Banfi; Melanie Bahlo

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3314.

ARVO Annual Meeting Abstract June 2023

Machine learning approaches to identify genes related to Age-related Macular Degeneration

Rinki Ratnapriya; Khang Ma; Arko Barman

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):1855.

ARVO Annual Meeting Abstract June 2022

Single cell transcriptional profiling of murine conjunctival immune cells reveals distinct populations expressing homeostatic and regulatory genes.

Jahan Alam; Ghasem Yazdanpanah; Nicholas Borcherding; Rinki Ratnapriya; Cintia S De Paiva; De-Quan Li; Stephen C Pflugfelder

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):857.

ARVO Annual Meeting Abstract June 2022

Artificial neural network-based classification of Age-related Macular Degeneration using gene expression profiles.

Rinki Ratnapriya; Hosei Nakajima; Daniel Christl

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1175 – A0029.

ARVO Annual Meeting Abstract June 2022

Reduced RXRα signaling increases dry eye disease inducing γδT17 cells in the conjunctiva

Stephen C Pflugfelder; Jahan Alam; Ghasem Yazdanpanah; Rinki Ratnapriya; Nicholas Borcherding; Cintia S De Paiva; De-Quan Li; Rodrigo Guimaraes de Souza; Zhiyuan Yu

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2276.

ARVO Annual Meeting Abstract June 2021

Retinoid X receptor alpha (RXRa) mutant Pinkie and vitamin A deficient B6 mice develop similar spectrum of corneal inflammation

Jehan Alam; Zhiyuan Yu; Rinki Ratnapriya; Cintia S De Paiva; Stephen C Pflugfelder

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):912.

ARVO Annual Meeting Abstract July 2019

Beyond GWAS: Functional genomics of age-related macular degeneration

Anand Swaroop; Freekje Van Asten; Madeline Kwiklis; Kayode Sosina; Margaret Starostik; Nivedita Singh; Dena Hernandez; Emily Y Chew; Andrew Singleton; Alexis Battle; Deb A Ferrington; Nilanjan Chatterjee; Rinki Ratnapriya

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4246.

ARVO Annual Meeting Abstract July 2018

Epigenetic disease mechanisms associated with age-related macular degeneration

Freekje Van Asten; Ximena Corso Diaz; Vijender Chaitankar; Rinki Ratnapriya; Margaret Starostik; Emily Y. Chew; Deborah A. Ferrington; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):370.

ARVO Annual Meeting Abstract July 2018

Complement activation products, single nucleotide polymorphisms and age-related macular degeneration (AMD).

Baerbel Rohrer; ashley Frazer-Abel; Anthony Leonard; Rinki Ratnapriya; Tyson Ward; Alexandra Pietraszkiewicz; Elizabeth O’Quinn; Katherine Adams; Anand Swaroop; Bethany Wolf

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):792.

ARVO Annual Meeting Abstract July 2018

Geographic atrophy of age-related macular degeneration in the Age-Related Eye Disease Study 2 (AREDS2): incidence, clinical characteristics and factors influencing growth rate

Tiarnan D L Keenan; Elvira Agron; Amitha Domalpally; Traci E Clemons; Freekje Van Asten; Wai T Wong; Ronald P Danis; Michael L Klein; Rinki Ratnapriya; Anand Swaroop; Frederick L Ferris; Emily Y. Chew

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):6010.

ARVO Annual Meeting Abstract July 2018

Integrative functional genomics of age-related macular degeneration

Rinki Ratnapriya; Kayode Sosina; Margaret Starostik; Madeline Kwicklis; Rebecca J Kapphahn; Ashley Walton; Alexandra Pietraszkiewicz; Sandra Rocio Montezuma; Lars Fritsche; Emily Y. Chew; Goncalo R. Abecasis; Deborah A. Ferrington; Nilanjan Chatterjee; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):6025.

ARVO Annual Meeting Abstract June 2017

Deep Phenotype Association Study in AREDS2 Suggests Pleiotropic Genetic Associations with Ocular and Systemic Disease

Tiarnan D Keenan; Michael Simmons; Freekje Van Asten; Ayush Singhal; Rinki Ratnapriya; Elvira Agron; Anand Swaroop; Zhiyong Lu; Emily Chew

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):177.

ARVO Annual Meeting Abstract June 2017

A Deep Phenotype Association Study (DeePAS) in AREDS2 reveals specific phenotype associations with AMD-related genetic variants

Freekje Van Asten; Michael Simmons; Ayush Singhal; Rinki Ratnapriya; Elvira Agron; Anand Swaroop; Zhiyong Lu; Emily Chew

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2984.

ARVO Annual Meeting Abstract June 2017

Reference Transcriptome Landscape of Adult Human Retina

Margaret Risa Starostik; Rinki Ratnapriya; Rebecca Kapphahn; Ashley Walton; Alexandra Pietraszkiewicz; Matthew Brooks; Sandra Rocio Montezuma; Lars Fritsche; Goncalo Abecasis; Deborah A Ferrington; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):567.

ARVO Annual Meeting Abstract June 2017

Rare Variant Pathway Analysis in the Age-Related Eye Disease Study 2

Alexandra Pietraszkiewicz; Freekje Van Asten; Alan Kwong; Rinki Ratnapriya; Goncalo Abecasis; Anand Swaroop; Emily Chew

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1833.

ARVO Annual Meeting Abstract June 2017

Transcriptome analysis of AMD retina reveals convergent molecular pathology

Rinki Ratnapriya; Margaret Risa Starostik; Rebecca Kapphahn; Ashley Walton; Alexandra Pietraszkiewicz; Matthew Brooks; Sandra Rocio Montezuma; Lars Fritsche; Goncalo Abecasis; Deborah A Ferrington; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4772.

Genetics November 2016

Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing

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Lisa Roberts; Rinki Ratnapriya; Morné du Plessis; Vijender Chaitankar; Raj S. Ramesar; Anand Swaroop
TAGS: cohort studies, exome, family, molecular diagnostic techniques, retinal diseases, whole exome sequencing, mutation
Invest. Ophthalmol. Vis. Sci.. 2016; 57(14):6374-6381. https://doi.org/10.1167/iovs.16-19785

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

Retinal transcriptome signatures associated with age-related macular degeneration

Rinki Ratnapriya; Ashley Walton; Margaret Starostik; Sandra Rocio Montezuma; Deborah A Ferrington; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12)

ARVO Annual Meeting Abstract September 2016

Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients

Dror Sharon; Prasanthi Namburi; Rinki Ratnapriya; Csilla Lazar; Alexey Obolensky; Tamar Ben-Yosef; Eran Pras; Menachem Gross; Eyal Banin; Anand Swaroop

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3153.

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Cellular and molecular changes in retinal microglia contributes to neurodegeneration in AMD

First report of RNA editing in human retina – a process central to photoreceptor health, and a risk factor for both AMD and rarer macular degeneration

Machine learning approaches to identify genes related to Age-related Macular Degeneration

Single cell transcriptional profiling of murine conjunctival immune cells reveals distinct populations expressing homeostatic and regulatory genes.

Artificial neural network-based classification of Age-related Macular Degeneration using gene expression profiles.

Reduced RXRα signaling increases dry eye disease inducing γδT17 cells in the conjunctiva

Retinoid X receptor alpha (RXRa) mutant Pinkie and vitamin A deficient B6 mice develop similar spectrum of corneal inflammation

Beyond GWAS: Functional genomics of age-related macular degeneration

Epigenetic disease mechanisms associated with age-related macular degeneration

Complement activation products, single nucleotide polymorphisms and age-related macular degeneration (AMD).

Geographic atrophy of age-related macular degeneration in the Age-Related Eye Disease Study 2 (AREDS2): incidence, clinical characteristics and factors influencing growth rate

Integrative functional genomics of age-related macular degeneration

Deep Phenotype Association Study in AREDS2 Suggests Pleiotropic Genetic Associations with Ocular and Systemic Disease

A Deep Phenotype Association Study (DeePAS) in AREDS2 reveals specific phenotype associations with AMD-related genetic variants

Reference Transcriptome Landscape of Adult Human Retina

Rare Variant Pathway Analysis in the Age-Related Eye Disease Study 2

Transcriptome analysis of AMD retina reveals convergent molecular pathology

Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing

Retinal transcriptome signatures associated with age-related macular degeneration

Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients

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