Segev Meyer

Postnatal Outcomes of Fetuses with Prenatal Diagnosis of 6–9.9 mm Pyelectasis

S. Arnon, H. Gluska, O. Markovitch, 2023, Children.

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

D. Sharon, S. Lieberman, Samer Khateb, 2016, Journal of Medical Genetics.

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

A. Swaroop, D. Sharon, E. Banin, 2016, Investigative ophthalmology & visual science.

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

O. Schueler‐Furman, A. Swaroop, D. Sharon, 2020, Molecular vision.