Manar Salameh
Hebrew University of Jerusalem(IL)Hadassah Medical Center(IL)
Publications by Year
Research Areas
Retinal Development and Disorders, RNA regulation and disease, CRISPR and Genetic Engineering, Retinal Diseases and Treatments, Photoreceptor and optogenetics research
Most-Cited Works
- → Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics(2020)140 cited
- → Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction(2023)27 cited
- → Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa(2023)8 cited
- → ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease(2022)6 cited
- → Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice(2023)5 cited
- A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients.(2021)
- → Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes(2024)3 cited
- → Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics(2019)3 cited
- → Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration(2025)2 cited
- → Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss(2024)2 cited