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76 results

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Page 1
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, Bala E, Lee KE, Hunter DJ, Sardell RJ, Mitchell P, Merriam JE, Cipriani V, Hoffman JD, Schick T, Lechanteur YT, Guymer RH, Johnson MP, Jiang Y, Stanton CM, Buitendijk GH, Zhan X, Kwong AM, Boleda A, Brooks M, Gieser L, Ratnapriya R, Branham KE, Foerster JR, Heckenlively JR, Othman MI, Vote BJ, Liang HH, Souzeau E, McAllister IL, Isaacs T, Hall J, Lake S, Mackey DA, Constable IJ, Craig JE, Kitchner TE, Yang Z, Su Z, Luo H, Chen D, Ouyang H, Flagg K, Lin D, Mao G, Ferreyra H, Stark K, von Strachwitz CN, Wolf A, Brandl C, Rudolph G, Olden M, Morrison MA, Morgan DJ, Schu M, Ahn J, Silvestri G, Tsironi EE, Park KH, Farrer LA, Orlin A, Brucker A, Li M, Curcio CA, Mohand-Saïd S, Sahel JA, Audo I, Benchaboune M, Cree AJ, Rennie CA, Goverdhan SV, Grunin M, Hagbi-Levi S, Campochiaro P, Katsanis N, Holz FG, Blond F, Blanché H, Deleuze JF, Igo RP Jr, Truitt B, Peachey NS, Meuer SM, Myers CE, Moore EL, Klein R, Hauser MA, Postel EA, Courtenay MD, Schwartz SG, Kovach JL, Scott WK, Liew G, Tan AG, Gopinath B, Merriam JC, Smith RT, K… See abstract for full author list ➔ Fritsche LG, et al. Among authors: ferreyra h. Nat Genet. 2016 Feb;48(2):134-43. doi: 10.1038/ng.3448. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691988 Free PMC article.
Authors' Response.
Pellegrini F, Interlandi E, Pavesio C, Ferreyra HA. Pellegrini F, et al. Among authors: ferreyra ha. Surv Ophthalmol. 2018 May-Jun;63(3):451. doi: 10.1016/j.survophthal.2018.02.002. Epub 2018 Feb 13. Surv Ophthalmol. 2018. PMID: 29447838 No abstract available.
Acquired unilateral scotoma.
Marvasti AH, Chen KC, Ferreyra HA, Falardeau J. Marvasti AH, et al. Among authors: ferreyra ha. Surv Ophthalmol. 2019 Jan-Feb;64(1):117-122. doi: 10.1016/j.survophthal.2017.06.006. Epub 2017 Jul 4. Surv Ophthalmol. 2019. PMID: 28684101
Microperimetry Findings in Pentosan Polysulfate Maculopathy.
Most J, Kalaw FGP, Walker E, Arias JD, Charng J, Baxter SL, Nudleman E, Ferreyra H, Freeman WR, Chen FK, Borooah S. Most J, et al. Among authors: ferreyra h. Ophthalmol Retina. 2023 Nov;7(11):1022-1024. doi: 10.1016/j.oret.2023.08.009. Epub 2023 Aug 22. Ophthalmol Retina. 2023. PMID: 37619623 No abstract available.
Atypical choroidal neovascular membrane.
Rezaei K, Yassin SH, Ferreyra H, Borooah S. Rezaei K, et al. Among authors: ferreyra h. Am J Ophthalmol Case Rep. 2024 Oct 5;36:102191. doi: 10.1016/j.ajoc.2024.102191. eCollection 2024 Dec. Am J Ophthalmol Case Rep. 2024. PMID: 39435156 Free PMC article.
Myelinated Retinal Nerve Fiber Layer (RNFL): A Comprehensive Review.
Ramkumar HL, Verma R, Ferreyra HA, Robbins SL. Ramkumar HL, et al. Among authors: ferreyra ha. Int Ophthalmol Clin. 2018 Fall;58(4):147-156. doi: 10.1097/IIO.0000000000000239. Int Ophthalmol Clin. 2018. PMID: 30239369 Review. No abstract available.
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries.
Gorman BR, Voloudakis G, Igo RP Jr, Kinzy T, Halladay CW, Bigdeli TB, Zeng B, Venkatesh S, Cooke Bailey JN, Crawford DC, Markianos K, Dong F, Schreiner PA, Zhang W; VA Million Veteran Program; International AMD Genomics Consortium (IAMDGC); Hadi T, Anger MD, Stockwell A, Melles RB, Yin J, Choquet H, Kaye R, Patasova K, Patel PJ, Yaspan BL, Jorgenson E, Hysi PG, Lotery AJ, Gaziano JM, Tsao PS, Fliesler SJ, Sullivan JM, Greenberg PB, Wu WC, Assimes TL, Pyarajan S, Roussos P, Peachey NS, Iyengar SK. Gorman BR, et al. Nat Genet. 2024 Dec;56(12):2659-2671. doi: 10.1038/s41588-024-01764-0. Epub 2024 Dec 2. Nat Genet. 2024. PMID: 39623103
ELECTRONEGATIVE ELECTRORETINOGRAM IN ACHROMATOPSIA.
Schallhorn CS, Granet DB, Ferreyra HA. Schallhorn CS, et al. Among authors: ferreyra ha. Retin Cases Brief Rep. 2018 Spring;12(2):143-148. doi: 10.1097/ICB.0000000000000451. Retin Cases Brief Rep. 2018. PMID: 27820752
76 results