Rinki Ratnapriya, PhD
Rinki Ratnapriya, PhD
Assistant Professor, Baylor College of Medicine
Verified email at
Cited by
Cited by
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
Age‐related macular degeneration—clinical review and genetics update
R Ratnapriya, EY Chew
Clinical genetics 84 (2), 160-166, 2013
Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration
R Ratnapriya, OA Sosina, MR Starostik, M Kwicklis, RJ Kapphahn, ...
Nature genetics 51 (4), 606-610, 2019
Molecular anatomy of the developing human retina
A Hoshino, R Ratnapriya, MJ Brooks, V Chaitankar, MS Wilken, C Zhang, ...
Developmental cell 43 (6), 763-779. e4, 2017
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
X Zhan, DE Larson, C Wang, DC Koboldt, YV Sergeev, RS Fulton, ...
Nature genetics 45 (11), 1375-1379, 2013
Progression of geographic atrophy in age-related macular degeneration: AREDS2 report number 16
TD Keenan, E Agrón, A Domalpally, TE Clemons, F van Asten, WT Wong, ...
Ophthalmology 125 (12), 1913-1928, 2018
No clinically significant association between CFH and ARMS2 genotypes and response to nutritional supplements: AREDS report number 38
EY Chew, ML Klein, TE Clemons, E Agrón, R Ratnapriya, AO Edwards, ...
Ophthalmology 121 (11), 2173-2180, 2014
Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research
V Chaitankar, G Karakülah, R Ratnapriya, FO Giuste, MJ Brooks, ...
Progress in retinal and eye research 55, 1-31, 2016
Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management
RR Priya, EY Chew, A Swaroop
Ophthalmology 119 (12), 2526-2536, 2012
An idiopathic epilepsy syndrome linked to 3q13. 3‐q21 and missense mutations in the extracellular calcium sensing receptor gene
A Kapoor, P Satishchandra, R Ratnapriya, R Reddy, J Kadandale, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
Genome-wide analysis of disease progression in age-related macular degeneration
Q Yan, Y Ding, Y Liu, T Sun, LG Fritsche, T Clemons, R Ratnapriya, ...
Human molecular genetics 27 (5), 929-940, 2018
Increased retinal mtDNA damage in the CFH variant associated with age-related macular degeneration
DA Ferrington, RJ Kapphahn, MM Leary, SR Atilano, MR Terluk, ...
Experimental eye research 145, 269-277, 2016
Whole exome sequencing reveals mutations in known retinal disease genes in 33 out of 68 Israeli families with inherited retinopathies
A Beryozkin, E Shevah, A Kimchi, L Mizrahi-Meissonnier, S Khateb, ...
Scientific reports 5 (1), 13187, 2015
Clinical and genetic factors associated with progression of geographic atrophy lesions in age-related macular degeneration
F Grassmann, M Fleckenstein, EY Chew, T Strunz, ...
PLoS One 10 (5), e0126636, 2015
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
JE Roger, A Hiriyanna, N Gotoh, H Hao, DF Cheng, R Ratnapriya, ...
The Journal of clinical investigation 124 (2), 631-643, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
R Ratnapriya, X Zhan, RN Fariss, KE Branham, D Zipprer, CF Chakarova, ...
Human molecular genetics 23 (21), 5827-5837, 2014
Bivariate analysis of age-related macular degeneration progression using genetic risk scores
Y Ding, Y Liu, Q Yan, LG Fritsche, RJ Cook, T Clemons, R Ratnapriya, ...
Genetics 206 (1), 119-133, 2017
Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease
HJ Yang, R Ratnapriya, T Cogliati, JW Kim, A Swaroop
Progress in retinal and eye research 46, 1-30, 2015
A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21. 3-q22. 3
R Ratnapriya, P Satishchandra, SD Kumar, G Gadre, R Reddy, A Anand
Human genetics 125, 541-549, 2009
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