Hadas Newman

6 Weizmann Street
Tel Aviv, TA 64239, Israel

Last Updated: 09/26/2026

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Found 34 publications

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.

Journal: Genes

Published: May 25, 2025

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy.

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 27, 2024

Genetic and Clinical Analyses of the KIZ-c.226C>T Variant Resulting in a Dual Mutational Mechanism.

Genetic and Clinical Analyses of the KIZ-c.226C>T Variant Resulting in a Dual Mutational Mechanism.

Journal: Genes

Published: May 25, 2024

Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population.

Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population.

Journal: JAMA ophthalmology

Published: May 16, 2024

Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population.

Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population.

Journal: Investigative ophthalmology & visual science

Published: February 27, 2024

Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry.

Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry.

Journal: Molecular vision

Published: June 22, 2022

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Journal: Retina (Philadelphia, Pa.)

Published: May 21, 2022

THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus.

THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus.

Journal: Retina (Philadelphia, Pa.)

Published: March 07, 2022

UVEITIS AFTER THE BNT162b2 mRNA VACCINATION AGAINST SARS-CoV-2 INFECTION: A Possible Association.

UVEITIS AFTER THE BNT162b2 mRNA VACCINATION AGAINST SARS-CoV-2 INFECTION: A Possible Association.

Journal: Retina (Philadelphia, Pa.)

Published: August 09, 2021

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations.

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

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 26, 2019

Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental Approach.

Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental Approach.

Journal: Biomolecules

Published: October 05, 2019

Showing 1-12 of 34

Last Updated: 09/26/2026