Segev Meyer

Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data

Samer Khateb, Mor Hanany, Ayat Khalaileh et al. · Journal of Medical Genetics · 2016 · 35 citations

Life Sciences, Genetics, Ophthalmology +16

Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual

Avigail Beryozkin, Gal Levy, Anat Blumenfeld et al. · Investigative Ophthalmology & Visual Science · 2016 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

A unique <i>PRDM13</i>-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique <i>CFH</i> variant.

Prasanthi Namburi, Samer Khateb, Segev Meyer et al. · PubMed · 2020 · 16 citations · Full text

Medicine, Genetics, Molecular Genetics +8