Peripheral fundus findings in X-linked retinoschisis von Fahim, Abigail T, Ali, Naser, Blachley, Taylor, Michaelides, Michel

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Acute Panretinal Structural and Functional Abnormalities After Intravitreous Ocriplasmin Injection von Fahim, Abigail T, Khan, Naheed W, Johnson, Mark W

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Real-world outcomes of voretigene neparvovec treatment in pediatric patients with RPE65-associated Leber congenital amaurosis von Deng, Callie, Zhao, Peter Y., Branham, Kari, Schlegel, Dana, Fahim, Abigail T., Jayasundera, Thiran K., Khan, Naheed, Besirli, Cagri G.

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Selective nanosecond laser removal of retinal pigment epithelium for cell therapy von Nguyen, Van Phuc, Karoukis, Athanasios J., Hu, Justin, Wei, Zhuying, Yang, Dongshan, Fahim, Abigail T., Wang, Xueding, Paulus, Yannis M.

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Oxidative stress differentially impacts apical and basolateral secretion of angiogenic factors from human iPSC-derived retinal pigment epithelium cells von Chen, Lisheng, Perera, N. Dayanthi, Karoukis, Athanasios J., Feathers, Kecia L., Ali, Robin R., Thompson, Debra A., Fahim, Abigail T.

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Retinitis pigmentosa: recent advances and future directions in diagnosis and management von Fahim, Abigail

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Association of No-Cost Genetic Testing Program Implementation and Patient Characteristics With Access to Genetic Testing for Inherited Retinal Degenerations von Zhao, Peter Y, Branham, Kari, Schlegel, Dana, Fahim, Abigail T, Jayasundera, K. Thiran

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Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations von Fahim, Abigail T, Bowne, Sara J, Sullivan, Lori S, Webb, Kaylie D, Williams, Jessica T, Wheaton, Dianna K, Birch, David G, Daiger, Stephen P

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Multimodal Imaging-Guided Stem Cell Ocular Treatment von Nguyen, Van Phuc, Karoukis, Athanasios J., Qian, Wei, Chen, Lisheng, Perera, Nirosha D., Yang, Dongshan, Zhang, Qitao, Zhe, Josh, Henry, Jessica, Liu, Bing, Zhang, Wei, Fahim, Abigail T., Wang, Xueding, Paulus, Yannis M.

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A dual-Ca2+-sensor model for neurotransmitter release in a central synapse von Sun, Jianyuan, Pang, Zhiping P, Qin, Dengkui, Fahim, Abigail T, Adachi, Roberto, Südhof, Thomas C

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The Michigan Retinal Degeneration Questionnaire: A Patient-Reported Outcome Instrument for Inherited Retinal Degenerations von Lacy, Gabrielle D., Abalem, Maria Fernanda, Andrews, Chris A., Popova, Lilia T., Santos, Erin P., Yu, Gina, Rakine, Hanan Y., Baig, Natasha, Ehrlich, Joshua R., Fahim, Abigail T., Branham, Kari H., Stelmack, Joan A., Swenor, Bonnielin K., Dagnelie, Gislin, Musch, David C., Jayasundera, K. Thiran

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Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration von Fahim, Abigail T, Bouzia, Zaina, Branham, Kari H, Kumaran, Neruban, Vargas, Mauricio E, Feathers, Kecia L, Perera, N Dayanthi, Young, Kelly, Khan, Naheed W, Heckenlively, John R, Webster, Andrew R, Pennesi, Mark E, Ali, Robin R, Thompson, Debra A, Michaelides, Michel

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Baseline Microperimetry and OCT in the RUSH2A Study: Structure−Function Association and Correlation With Disease Severity von Lad, Eleonora M., Duncan, Jacque L., Liang, Wendi, Maguire, Maureen G., Ayala, Allison R., Audo, Isabelle, Birch, David G., Carroll, Joseph, Cheetham, Janet K., Durham, Todd A., Fahim, Abigail T., Loo, Jessica, Deng, Zengtian, Mukherjee, Dibyendu, Heon, Elise, Hufnagel, Robert B., Guan, Bin, Iannaccone, Alessandro, Jaffe, Glenn J., Kay, Christine N., Michaelides, Michel, Pennesi, Mark E., Vincent, Ajoy, Weng, Christina Y., Farsiu, Sina

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Racial Disparities in Genetic Detection Rates for Inherited Retinal Diseases von Abuzaitoun, Rebhi O, Branham, Kari H, Lacy, Gabrielle D, Hufnagel, Robert B, Kumar, Meenakshi M, Koskenvuo, Juha W, Tuupanen, Sari, Durham, Todd, Zhao, Peter Y, Abalem, Maria Fernanda, Andrews, Chris A, Schlegel, Dana, Khan, Naheed W, Fahim, Abigail T, Heckenlively, John R, Musch, David C, Jayasundera, K. Thiran

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Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years von Duncan, Jacque L., Cheng, Peiyao, Maguire, Maureen G., Ayala, Allison A., Birch, David G., Cheetham, Janet K., Durham, Todd A., Fahim, Abigail T., Hoyng, Carel B., Ishikawa, Hiroshi, Michaelides, Michel, Pennesi, Mark E., Sahel, José-Alain, Stingl, Katarina, Weng, Christina Y.

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Bullous X linked retinoschisis: clinical features and prognosis von Hinds, Anne-Marie, Fahim, Abigail, Moore, Anthony T, Wong, Sui Chien, Michaelides, Michel

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Development of a Gene Therapy Vector for RDH12 -Associated Retinal Dystrophy von Feathers, Kecia L, Jia, Lin, Perera, Nirosha Dayanthi, Chen, Adrienne, Presswalla, Feriel K, Khan, Naheed W, Fahim, Abigail T, Smith, Alexander J, Ali, Robin R, Thompson, Debra A

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Autoimmune retinopathy associated with monoclonal gammopathy of undetermined significance: a case report von Eton, Emily A., Abrams, Gary, Khan, Naheed W., Fahim, Abigail T.

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The Michigan Vision-Related Anxiety Questionnaire: A Psychosocial Outcomes Measure for Inherited Retinal Degenerations von Lacy, Gabrielle D., Abalem, Maria Fernanda, Andrews, Chris A., Abuzaitoun, Rebhi, Popova, Lilia T., Santos, Erin P., Yu, Gina, Rakine, Hanan Y., Baig, Natasha, Ehrlich, Joshua R., Fahim, Abigail T., Branham, Kari H., Swenor, Bonnielin K., Lichter, Paul R., Dagnelie, Gislin, Stelmack, Joan A., Musch, David C., Jayasundera, K. Thiran

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Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome von da Palma, Mariana Matioli, Igelman, Austin D., Ku, Cristy, Burr, Amanda, You, Jia Yue, Place, Emily M., Wang, Nan-Kai, Oh, Jin Kyun, Branham, Kari E., Zhang, Xinxin, Ahn, Jeeyun, Gorin, Michael B., Lam, Byron L., Ronquillo, Cecinio C., Bernstein, Paul S., Nagiel, Aaron, Huckfeldt, Rachel, Cabrera, Michelle T., Kelly, John P., Bakall, Benjamin, Iannaccone, Alessandro, Hufnagel, Robert B., Zein, Wadih M., Koenekoop, Robert K., Birch, David G., Yang, Paul, Fahim, Abigail T., Pennesi, Mark E.

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