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All papers authored by Rinki Ratnapriya

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2020 Tobias Strunz, Christina Kiel

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, Felix Grassmann

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, Rinki Ratnapriya

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, Madeline Kwicklis, Marcus Karlstetter

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, Sascha Fauser, Nicole Arend

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, Anand Swaroop

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, Thomas Langmann

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, Bernhard H. F. Weber

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A mega-analysis of expression quantitative trait loci in retinal tissue

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Rinki Ratnapriya

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, David Zipprer, Beverly Yashar, Anneke I. den Hollander, Anand Swaroop

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, İlhan E. Acar, Maartje J. Geerlings, Kari Branham, Alan Kwong, Nicole T. M. Saksens, Marc Pauper, Jordi Corominas

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, Madeline Kwicklis, Mohammad Othman, Goncalo R. Abecasis and 5 other authors

Family-based exome sequencing identifies rare coding variants in age-related macular degeneration

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2019 Felix Grassmann

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, Sebastian Harsch, Caroline Brandl, Christina Kiel

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, Peter Nürnberg, Mohammad R. Toliat, Monika Fleckenstein, Maximilian Pfau, Steffen Schmitz-Valckenberg, Frank G. Holz, Emily Y. Chew, Anand Swaroop, Rinki Ratnapriya

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, Michael L. Klein, Zufar Mulyukov and 2 other authors

Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration

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Freekje van Asten

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, Chi-Yang Chiu, Elvira Agrón, Traci E. Clemons, Rinki Ratnapriya

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, Anand Swaroop

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, Michael L. Klein, Ruzong Fan

ORCID

, Emily Y. Chew

ORCID

No CFH or ARMS2 Interaction with Omega-3 Fatty Acids, Low versus High Zinc, or β-Carotene versus Lutein and Zeaxanthin on Progression of Age-Related Macular Degeneration in the Age-Related Eye Disease Study 2

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Rinki Ratnapriya

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, Ashley Walton, Olukayode A. Sosina, Anand Swaroop

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, Madeline Kwicklis, Rebecca J. Kapphahn, Lars G. Fritsche

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, Marios Arvanitis, Linn Gieser, Alexandra Pietraszkiewicz, Margaret R. Starostik

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, Sandra R. Montezuma, Emily Y. Chew, Alexis Battle

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, Gonçalo R. Abecasis and 2 other authors

Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration

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Rinki Ratnapriya

ORCID

Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent.

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Rinki Ratnapriya

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Applications of Genomic Technologies in Retinal Degenerative Diseases

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2018 Tiarnan D. Keenan

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, Elvira Agrón, Amitha Domalpally, Traci E. Clemons, Freekje van Asten

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, Wai T. Wong, Ronald G. Danis, SriniVas Sadda, Philip J. Rosenfeld, Michael L. Klein, Rinki Ratnapriya

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, Anand Swaroop

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, Frederick L. Ferris

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, Emily Y. Chew

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, John Paul SanGiovanni and 987 other authors

Progression of Geographic Atrophy in Age-related Macular Degeneration

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Freekje van Asten

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, Michael Simmons

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, Ayush Singhal, Tiarnan D. Keenan, Rinki Ratnapriya

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, Elvira Agrón, Traci E. Clemons, Anand Swaroop

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, Zhiyong Lu, Emily Y. Chew

A Deep Phenotype Association Study Reveals Specific Phenotype Associations with Genetic Variants in Age-related Macular Degeneration

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Alexandra Pietraszkiewicz

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, Freekje van Asten

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, Alan Kwong, Rinki Ratnapriya

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, Goncalo Abecasis, Anand Swaroop

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, Emily Y. Chew

Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration

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Qi Yan, Tao Sun, Lai Wei, Anand Swaroop, Daniel E. Weeks, Ying Ding, Yi Liu, Lars G. Fritsche, Traci Clemons, Michael L. Klein, Richard J. Cook, Yu Liu, Ruzong Fan, Rinki Ratnapriya

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, Gonçalo R. Abecasis and 2 other authors

Genome-wide analysis of disease progression in age-related macular degeneration.

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2017 Akina Hoshino, Rinki Ratnapriya

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, Matthew J. Brooks, Vijender Chaitankar, Matthew S. Wilken, Chi Zhang, Margaret R. Starostik

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, Linn Gieser, Anna La Torre, Mario Nishio, Olivia Bates, Ashley Walton, Olivia Bermingham-Mcdonogh, Ian A. Glass, Rachel O. L. Wong and 2 other authors

Molecular Anatomy of the Developing Human Retina

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David McGuigan, Elise Heon, Artur Cideciyan, Rinki Ratnapriya

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, Monica Lu, Alexander Sumaroka, Alejandro Roman, Vaishnavi Batmanabane, Alexandra Garafalo, Edwin Stone, Anand Swaroop

ORCID

, Samuel Jacobson

EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression

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Laurence H. M. Pierrache, Adva Kimchi, Rinki Ratnapriya

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, Lisa Roberts, Galuh D. N. Astuti, Alexey Obolensky, Avigail Beryozkin, Martha J. H. Tjon-Fo-Sang, Jose Schuil, Caroline C. W. Klaver, Ernie M. H. F. Bongers, Lonneke Haer-Wigman

ORCID

, Nicoline Schalij, Martijn H. Breuning, Gratia M. Fischer and 6 other authors

Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma

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Veronika Grassmann, Me Zimmermann, Cindy Wen, Donald Zack, Bh Weber, Xiaowei Zhan, Brendan J. Vote, Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, Sebanti Sengupta, Felix Grassmann

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, Jennifer L. Bragg Gresham, Kathryn P. Burdon, Scott J. Hebbring and 37 other authors

Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.

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Ying Ding, Qi Yan, Anand Swaroop, Daniel E. Weeks, Yi Liu, Lars G. Fritsche, Richard J. Cook, Traci Clemons, Michael L. Klein, Gonçalo R. Abecasis, Rinki Ratnapriya

ORCID

, Emily Y. Chew, Wei Chen

Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk Scores.

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Shobi Veleri, Jacob Nellissery, Bibhudatta Mishra, Souparnika H. Manjunath, Matthew J. Brooks, Lijin Dong, Kunio Nagashima, Haohua Qian, Chun Gao, Yuri V. Sergeev, Xiu-Feng Huang, Jia Qu, Fan Lu, Artur V. Cideciyan, Tiansen Li and 5 other authors

REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival

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2016 Lisa Roberts, Rinki Ratnapriya

ORCID

, Morné du Plessis, Vijender Chaitankar, Raj S. Ramesar, Anand Swaroop

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

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Vijender Chaitankar, Gökhan Karakülah

ORCID

, Rinki Ratnapriya

ORCID

, Felipe O. Giuste, Matthew J. Brooks, Anand Swaroop

ORCID

Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research

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Prasanthi Namburi, Anand Swaroop, Dror Sharon, Samer Khateb, Csilla H. Lazar, Yael Kinarty, Alexey Obolensky, Inbar Erdinest, Devorah Marks-Ohana, Rinki Ratnapriya

ORCID

, Eran Pras, Tamar Ben-Yosef, Hadas Newman, Menachem Gross, Eyal Banin

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss

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