Mor Hanany
Jerusalem, JM 91120, Israel
Last Updated: 09/26/2026
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Found 12 publications
Simultaneous Detection of Common Founder Mutations Using a Cost-Effective Deep Sequencing Panel.
Journal: Genes
Published: April 15, 2024
Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation Considerations.
Journal: Cold Spring Harbor perspectives in medicine
Published: July 17, 2023
An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy.
Journal: Translational vision science & technology
Published: February 16, 2023
Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 28, 2021
Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities.
Journal: Progress in retinal and eye research
Published: July 19, 2021
SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis.
Journal: Retina (Philadelphia, Pa.)
Published: January 29, 2021
Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children.
Journal: European journal of ophthalmology
Published: November 26, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations.
Journal: Scientific reports
Published: February 06, 2020
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: January 23, 2020
Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variants.
Journal: Journal of medical genetics
Published: December 25, 2018
Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population.
Journal: European journal of human genetics : EJHG
Published: January 16, 2018
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data.
Journal: Journal of medical genetics
Published: February 07, 2016
Showing 1-12 of 12
Last Updated: 09/26/2026