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Methods in Molecular Biology (Clifton, N.J.)|September 6, 2024
In Vivo Imaging of Rodent Retina in Retinal DiseaseAvigail Beryozkin, Leah C Byrne
Advances in Experimental Medicine and Biology|July 13, 2023
Morphological and Functional Comparison of Mice Models for Retinitis PigmentosaPrakadeeswari Gopalakrishnan, Avigail Beryozkin, Eyal Banin, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Factors Affecting Readthrough of Natural Versus Premature Termination CodonsAvigail Beryozkin, Kerstin Nagel-Wolfum, Eyal Banin, et al.
Ophthalmology Science|November 24, 2022
Retinal Structure and Function in a Knock-in Mouse Model for the FAM161A-p.Arg523∗ Human Nonsense Pathogenic VariantChen Matsevich, Prakadeeswari Gopalakrishnan, Alexey Obolensky, et al.
Translational Vision Science & Technology|February 16, 2023
An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline DystrophyMor Hanany, Richard Rui Yang, Chun Man Lam, et al.
International Journal of Molecular Sciences|April 12, 2022
Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in FAM161AAvigail Beryozkin, Ananya Samanta, Prakadeeswari Gopalakrishnan, et al.
Scientific Reports|January 22, 2021
A new mouse model for retinal degeneration due to Fam161a deficiencyAvigail Beryozkin, Chen Matsevich, Alexey Obolensky, et al.
Case Reports in Ophthalmology|June 19, 2025
Exclusively Macular Phenotype of Non-Syndromic MFSD8-Related Disease: A Case ReportSean Ghiam, Ryan Zukerman, Morgan Brzozowski, et al.
Progress in Retinal and Eye Research|November 28, 2021
Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalitiesNina Schneider, Yogapriya Sundaresan, Prakadeeswari Gopalakrishnan, et al.
Investigative Ophthalmology & Visual Science|March 2, 2013
Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populationsAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
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