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RINKI RATNA PRIYA

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Ophthalmology
Address6501 Fannin St
Houston, TX 77030
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    Other Positions
    TitleAssistant Professor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Biochemistry and Molecular Pharmacology
    DivisionBiochemistry & Mol Pharmacology


    Collapse Biography 
    Collapse education and training
    National Eye Institute, NIH, Bethesda, MDPostdoctoral training05/2018Ophthalmic Genomics

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Ratnapriya R. The Role of Gene Expression Regulation on Genetic Risk of Age-Related Macular Degeneration. Adv Exp Med Biol. 2023; 1415:61-66. PMID: 37440015.
      Citations:    Fields:    Translation:Humans
    2. Ratnapriya R, Sosina OA, Starostik MR, Kwicklis M, Kapphahn RJ, Fritsche LG, Walton A, Arvanitis M, Gieser L, Pietraszkiewicz A, Montezuma SR, Chew EY, Battle A, Ferrington DA, Chatterjee N, Swaroop A, Abecasis GR. Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. Nat Genet. 2019 04; 51(4):606-610. PMID: 30742112; PMCID: PMC6441365.
      Citations: 72     Fields:    Translation:HumansCells
    3. Ratnapriya R. Applications of Genomic Technologies in Retinal Degenerative Diseases. Adv Exp Med Biol. 2019; 1185:281-285. PMID: 31884625.
      Citations:    Fields:    Translation:Humans
    4. Hoshino A, Ratnapriya R, Brooks MJ, Chaitankar V, Wilken MS, Zhang C, Starostik MR, Gieser L, La Torre A, Nishio M, Bates O, Walton A, Bermingham-McDonogh O, Glass IA, Wong ROL, Swaroop A, Reh TA. Molecular Anatomy of the Developing Human Retina. Dev Cell. 2017 12 18; 43(6):763-779.e4. PMID: 29233477; PMCID: PMC5776731.
      Citations: 91     Fields:    Translation:HumansAnimalsCells
    5. Roberts L, Ratnapriya R, Chaitankar V, Ramesar RS, Swaroop A, du Plessis M. Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing. Invest Ophthalmol Vis Sci. 2016 11 01; 57(14):6374-6381. PMID: 27898983; PMCID: PMC5132076.
      Citations: 10     Fields:    Translation:Humans
    6. Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D. Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. Am J Hum Genet. 2016 09 01; 99(3):777-784. PMID: 27588452; PMCID: PMC5011076.
      Citations: 15     Fields:    Translation:HumansCells
    7. Yang HJ, Ratnapriya R, Cogliati T, Kim JW, Swaroop A. Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease. Prog Retin Eye Res. 2015 May; 46:1-30. PMID: 25668385; PMCID: PMC4402139.
      Citations: 30     Fields:    Translation:Humans
    8. Ratnapriya R, Zhan X, Fariss RN, Branham KE, Zipprer D, Chakarova CF, Sergeev YV, Campos MM, Othman M, Friedman JS, Maminishkis A, Waseem NH, Brooks M, Rajasimha HK, Edwards AO, Lotery A, Klein BE, Truitt BJ, Li B, Schaumberg DA, Morgan DJ, Morrison MA, Tsironi EE, Grassmann F, Fishman GA, Silvestri G, Scholl HP, Kim IK, Ramke J, Tuo J, Merriam JE, Merriam JC, Park KH, Olson LM, Farrer LA, Johnson MP, Peachey NS, Baron RV, Igo RP, Klein R, Hagstrom SA, Martin TM, Jiang Y, Conley Y, Zack DJ, Chan CC, Pericak-Vance MA, Jacobson SG, Gorin MB, Klein ML, Allikmets R, Iyengar SK, Weber BH, Haines JL, Deangelis MM, Stambolian D, Weeks DE, Bhattacharya SS, Chew EY, Heckenlively JR, Swaroop A, Souied E, Lathrop M, Kamatani Y, Sahel JA, L?veillard T, Abecasis GR. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Hum Mol Genet. 2014 Nov 01; 23(21):5827-37. PMID: 24899048; PMCID: PMC4189898.
      Citations: 24     Fields:    Translation:HumansCells
    9. Ratnapriya R, Swaroop A. Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing. Genome Med. 2013; 5(10):84. PMID: 24112618; PMCID: PMC4066589.
      Citations: 17     Fields:    
    10. Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Sim X, Weeks DE, Guymer RH, Merriam JE, Francis PJ, Hannum G, Agarwal A, Armbrecht AM, Audo I, Aung T, Barile GR, Benchaboune M, Bird AC, Bishop PN, Branham KE, Brooks M, Brucker AJ, Cade WH, Cain MS, Campochiaro PA, Chan CC, Cheng CY, Chew EY, Chin KA, Chowers I, Clayton DG, Cojocaru R, Conley YP, Cornes BK, Daly MJ, Dhillon B, Edwards AO, Evangelou E, Fagerness J, Ferreyra HA, Friedman JS, Geirsdottir A, George RJ, Gieger C, Gupta N, Hagstrom SA, Harding SP, Haritoglou C, Heckenlively JR, Holz FG, Hughes G, Ioannidis JP, Ishibashi T, Joseph P, Jun G, Kamatani Y, Katsanis N, N Keilhauer C, Khan JC, Kim IK, Kiyohara Y, Klein BE, Klein R, Kovach JL, Kozak I, Lee CJ, Lee KE, Lichtner P, Lotery AJ, Meitinger T, Mitchell P, Moore AT, Morgan DJ, Morrison MA, Myers CE, Naj AC, Nakamura Y, Okada Y, Orlin A, Ortube MC, Othman MI, Pappas C, Park KH, Pauer GJ, Peachey NS, Poch O, Priya RR, Reynolds R, Richardson AJ, Ripp R, Rudolph G, Ryu E, Schaumberg DA, Scholl HP, Schwartz SG, Scott WK, Shahid H, Sigurdsson H, Silvestri G, Sivakumaran TA, Smith RT, Sobrin L, Souied EH, Stambolian DE, Stefansson H, Sturgill-Short GM, Takahashi A, Tosakulwong N, Truitt BJ, Tsironi EE, van Duijn CM, Vijaya L, Vingerling JR, Vithana EN, Webster AR, Wichmann HE, Winkler TW, Wong TY, Wright AF, Zelenika D, Zhang M, Zhao L, Zhang K, Klein ML, Hageman GS, Lathrop GM, Stefansson K, Allikmets R, Baird PN, Gorin MB, Wang JJ, Klaver CC, Seddon JM, Pericak-Vance MA, Iyengar SK, Yates JR, Swaroop A, Weber BH, Kubo M, Deangelis MM, Thorsteinsdottir U, Haines JL, Farrer LA, Heid IM, AMD Gene Consortium, Buitendijk GH, Mohand-Sa?d S, Sahel JA, Uitterlinden AG, L?veillard T, Abecasis GR. Seven new loci associated with age-related macular degeneration. Nat Genet. 2013 Apr; 45(4):433-9, 439e1-2. PMID: 23455636; PMCID: PMC3739472.
      Citations: 370     Fields:    Translation:Humans
    11. Priya RR, Chew EY, Swaroop A. Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management. Ophthalmology. 2012 Dec; 119(12):2526-36. PMID: 23009893; PMCID: PMC3514599.
      Citations: 35     Fields:    Translation:Humans
    12. Ratnapriya R, Vijai J, Kadandale JS, Iyer RS, Radhakrishnan K, Anand A. A locus for juvenile myoclonic epilepsy maps to 2q33-q36. Hum Genet. 2010 Aug; 128(2):123-30. PMID: 20467754.
      Citations: 8     Fields:    Translation:Humans
    13. Ratnapriya R, Satishchandra P, Dilip S, Gadre G, Anand A. Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28. Hum Genet. 2009 Nov; 126(5):677-83. PMID: 19597845.
      Citations: 7     Fields:    Translation:HumansCells
    14. Ratnapriya R, Satishchandra P, Kumar SD, Gadre G, Reddy R, Anand A. A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3. Hum Genet. 2009 Jun; 125(5-6):541-9. PMID: 19266219.
      Citations: 11     Fields:    Translation:HumansCells
    15. Kapoor A, Satishchandra P, Ratnapriya R, Reddy R, Kadandale J, Shankar SK, Anand A. An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene. Ann Neurol. 2008 Aug; 64(2):158-67. PMID: 18756473.
      Citations: 27     Fields:    Translation:HumansCells
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