Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Terminat... von Beryozkin, Avigail, Samanta, Ananya, Gopalakrishnan, Prakadeeswari, Khateb, Samer, Banin, Eyal, Sharon, Dror, Nagel-Wolfrum, Kerstin

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Disease quiescence in endophthalmitis patients treated with anti-VEGF injections for retinal pathologies von Vofo, Brice Nguedia, Saada, Majd, Rivera, Antonio, Cohen, Sigalit, Jaouni, Tareq, Khateb, Samer

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Genome wide association study and genomic risk prediction of age related macular degeneration in Israel von Grunin, Michelle, Triffon, Daria, Beykin, Gala, Rahmani, Elior, Schweiger, Regev, Tiosano, Liran, Khateb, Samer, Hagbi-Levi, Shira, Rinsky, Batya, Munitz, Refael, Winkler, Thomas W., Heid, Iris M., Halperin, Eran, Carmi, Shai, Chowers, Itay

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Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations von Beryozkin, Avigail, Khateb, Samer, Idrobo-Robalino, Carlos Alberto, Khan, Muhammad Imran, Cremers, Frans P. M., Obolensky, Alexey, Hanany, Mor, Mezer, Eedy, Chowers, Itay, Newman, Hadas, Ben-Yosef, Tamar, Sharon, Dror, Banin, Eyal

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Postoperative Macular Proliferative Vitreoretinopathy: A Case Series and Literature Review von Khateb, Samer, Aweidah, Hamzah, Halpert, Michael, Jaouni, Tareq

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Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease von Yahalom, Claudia, Blumenfeld, Anat, Hendler, Karen, Wussuki-Lior, Orly, Macarov, Michal, Shohat, Mordechai, Khateb, Samer

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TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations von AlTalbishi, Alaa, Zelinger, Lina, Zeitz, Christina, Hendler, Karen, Namburi, Prasanthi, Audo, Isabelle, Sheffer, Ruth, Yahalom, Claudia, Khateb, Samer, Banin, Eyal, Sharon, Dror

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Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population von Kimchi, Adva, Khateb, Samer, Wen, Rong, Guan, Ziqiang, Obolensky, Alexey, Beryozkin, Avigail, Kurtzman, Shoshi, Blumenfeld, Anat, Pras, Eran, Jacobson, Samuel G., Ben-Yosef, Tamar, Newman, Hadas, Sharon, Dror, Banin, Eyal

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Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss von Khateb, Samer, Zelinger, Lina, Ben-Yosef, Tamar, Merin, Saul, Crystal-Shalit, Ornit, Gross, Menachem, Banin, Eyal, Sharon, Dror

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Docking interactions of the JNK scaffold protein WDR62 von Cohen-Katsenelson, Ksenya, Wasserman, Tanya, Khateb, Samer, Whitmarsh, Alan J, Aronheim, Ami

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Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 Patients von Beryozkin, Avigail, Aweidah, Hamzah, Carrero Valenzuela, Roque Daniel, Berman, Myriam, Iguzquiza, Oscar, Cremers, Frans P. M., Khan, Muhammad Imran, Swaroop, Anand, Amer, Radgonde, Khateb, Samer, Ben-Yosef, Tamar, Sharon, Dror, Banin, Eyal

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What Can We Learn From the Surprising Insight Into the Genetic Background of Age-Related Macular Degeneration and Central Serous Chorioretinopathy? von Khateb, Samer, Chowers, Itay, Grunin, Michelle

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Outcomes of primary rhegmatogenous retinal detachment repair among young adult patients von Safadi, Khaled, Chowers, Itay, Khateb, Samer

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The Effect of Glucagon-like-Peptide-1 Receptor Agonists on Diabetic Retinopathy Progression, Central Subfield Thickness, and Response to Intravitreal Injections von Michaeli, Tomer, Khateb, Samer, Levy, Jaime

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Homodimeric MyoD Preferentially Binds Tetraplex Structures of Regulatory Sequences of Muscle-specific Genes von Etzioni, Shulamit, Yafe, Anat, Khateb, Samer, Weisman-Shomer, Pnina, Bengal, Eyal, Fry, Michael

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Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular Degeneration von Rinsky, Batya, Beykin, Gala, Grunin, Michelle, Amer, Radgonde, Khateb, Samer, Tiosano, Liran, Almeida, Diego, Hagbi-Levi, Shira, Elbaz-Hayoun, Sarah, Chowers, Itay

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Prevalence and associated factors of cystoid macular edema in children with early onset inherited retinal dystrophies von Ben-Avi, Ravid, Rivera, Antonio, Hendler, Karen, Sharon, Dror, Banin, Eyal, Khateb, Samer, Yahalom, Claudia

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A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans von Khateb, Samer, Kowalewski, Björn, Bedoni, Nicola, Damme, Markus, Pollack, Netta, Saada, Ann, Obolensky, Alexey, Ben-Yosef, Tamar, Gross, Menachem, Dierks, Thomas, Banin, Eyal, Rivolta, Carlo, Sharon, Dror

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A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome von Khateb, Samer, Zelinger, Lina, Mizrahi-Meissonnier, Liliana, Ayuso, Carmen, Koenekoop, Robert K, Laxer, Uri, Gross, Menachem, Banin, Eyal, Sharon, Dror

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Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes von Abu Elasal, Maria, Mousa, Samira, Salameh, Manar, Blumenfeld, Anat, Khateb, Samer, Banin, Eyal, Sharon, Dror

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