Radha Ayyagari
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Explore the profile of Radha Ayyagari including associated specialties, affiliations and a list of published articles.
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105
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2094
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Recent Articles
1.
Woodard D, Ayyagari R
Adv Exp Med Biol
. 2025 Feb;
1468:75-79.
PMID: 39930176
The membrane-frizzled related protein (MFRP) is a retinal pigment epithelium (RPE) and ciliary epithelium-expressed gene of unknown function. Interest in MFRP stems from clinical manifestations that range from acute-angle closure...
2.
Biswas P, Woodard D, Hollingsworth T, Khan N, Lazaro D, Berry A, et al.
JCI Insight
. 2025 Feb;
10(3).
PMID: 39927462
The high-temperature requirement A1 (HTRA1), a serine protease, has been demonstrated to play a pivotal role in the extracellular matrix (ECM) and has been reported to be associated with the...
3.
Quinodoz M, Rodenburg K, Cvackova Z, Kaminska K, de Bruijn S, Iglesias-Romero A, et al.
medRxiv
. 2025 Jan;
PMID: 39830270
The U4 small nuclear RNA (snRNA) forms a duplex with the U6 snRNA and, together with U5 and ~30 proteins, is part of the U4/U6.U5 tri-snRNP complex, located at the...
4.
Yuan Y, Biswas P, Zemke N, Dang K, Wu Y, DAntonio M, et al.
bioRxiv
. 2025 Jan;
PMID: 39764062
Most genetic risk variants linked to ocular diseases are non-protein coding and presumably contribute to disease through dysregulation of gene expression, however, deeper understanding of their mechanisms of action has...
5.
Ayyagari R, Borooah S, Durham T, Gelfman C, Bowman A
Transl Vis Sci Technol
. 2024 Oct;
13(10):16.
PMID: 39382871
Purpose And Methods: A workshop of affected individuals and their families, clinicians, researchers, and industry representatives was convened in March 2023 to define the knowledge landscape of peripherin 2 (PRPH2)...
6.
Biswas P, Villanueva A, Krajacich B, Moreno J, Zhao J, Berry A, et al.
PLoS One
. 2024 Oct;
19(10):e0307266.
PMID: 39365799
Whole genome sequencing has been an effective tool in the discovery of variants that cause rare diseases. In this study, we determined the suitability of a novel avidity sequencing approach...
7.
Malka S, Biswas P, Berry A, Sangermano R, Ullah M, Lin S, et al.
Am J Hum Genet
. 2024 Aug;
111(9):2012-2030.
PMID: 39191256
Genome analysis of individuals affected by retinitis pigmentosa (RP) identified two rare nucleotide substitutions at the same genomic location on chromosome 11 (g.61392563 [GRCh38]), 69 base pairs upstream of the...
8.
Verma S, Gudiseva H, Chavali V, Salowe R, Bradford Y, Guare L, et al.
Cell
. 2024 Jan;
187(2):464-480.e10.
PMID: 38242088
Primary open-angle glaucoma (POAG), the leading cause of irreversible blindness worldwide, disproportionately affects individuals of African ancestry. We conducted a genome-wide association study (GWAS) for POAG in 11,275 individuals of...
9.
Garland D, Harnly J, Ayyagari R
Adv Exp Med Biol
. 2023 Jul;
1415:359-363.
PMID: 37440057
Age is a major risk factor for age-related macular degeneration (AMD), and age has a role in the disease phenotypes of heritable macular dystrophies. The proteomes of C57Bl6/J mouse choroids...
10.
Borooah S, Chekuri A, Pachauri S, Sahu B, Vorochikhina M, Suk J, et al.
Adv Exp Med Biol
. 2023 Jul;
1415:335-340.
PMID: 37440053
Late-onset retinal degeneration (L-ORD) is an autosomal dominant macular dystrophy resulting from mutations in the gene CTRP5/C1QTNF5. A mouse model (Ctrp5) for the most common S163R developed many features of...