Publications by authors named "Hadas Newman"

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Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy.
Miriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, Abigail R Moye, Riccardo Sangermano, Hadas Newman

Genet Med· June 2025

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Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis.
Sofia Kulyamzin, Rina Leibu, Hadas Newman, Miriam Ehrenberg, Nitza Goldenberg-Cohen

Genes (Basel)· June 2025

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Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population.
Sapir Shalom, Tamar Ben-Yosef, Ifat Sher, Amir Zag, Ygal Rotenstreich, Hadas Newman

JAMA Ophthalmol· July 2024

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Genetic and Clinical Analyses of the -c.226C>T Variant Resulting in a Dual Mutational Mechanism.
Yogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, Prakadeeswari Gopalakrishnan, Hanit Ohayon Hadad, Hadas Newman

Genes (Basel)· June 2024

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Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population.
Avigail Beryozkin, Ifat Sher, Miriam Ehrenberg, Dinah Zur, Hadas Newman

Invest Ophthalmol Vis Sci· February 2024

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Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry.
Tamar Ben Yosef, Eyal Banin, Elana Chervinsky, Stavit A Shalev, Rina Leibu, Hadas Newman

Mol Vis· June 2023

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Reply.
Hadas Newman, Ido Perlman, Eran Pras, Assaf Rozenberg, Tamar Ben-Yosef

Retina· October 2022

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THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus.
Hadas Newman, Ido Perlman, Eran Pras, Assaf Rozenberg, Tamar Ben-Yosef

Retina· July 2022

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UVEITIS AFTER THE BNT162b2 mRNA VACCINATION AGAINST SARS-CoV-2 INFECTION: A Possible Association.
Tamar Rabinovitch, Yael Ben-Arie-Weintrob, Tamar Hareuveni-Blum, Boaz Shaer, Vicktoria Vishnevskia-Dai, Hadas Newman

Retina· December 2021

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Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations.
Avigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, Muhammad Imran Khan, Frans P M Cremers, Hadas Newman

Sci Rep· September 2020

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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Mubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, Laura Whelan, Esmee H Runhart, Hadas Newman

Genet Med· July 2020

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Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case series.
Yair Rubinstein, Chen Weiner, Noa Chetrit, Hadas Newman, Idan Hecht

Graefes Arch Clin Exp Ophthalmol· March 2020

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A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC).
Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, Eran Pras, Libe Gradstein, Hadas Newman

Hum Mutat· January 2020

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Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental Approach.
Michal Lisnyansky Bar-El, Su Youn Lee, Ah Young Ki, Noa Kapelushnik, Anat Loewenstein, Hadas Newman

Biomolecules· October 2019

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Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy.
Daniel Ben Ner, Ifat Sher, Amit Hamburg, Mohamad O Mhajna, Ron Chibel, Hadas Newman

Clin Ophthalmol· March 2019

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[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES].
Dror Sharon, Tamar Ben-Yosef, Eran Pras, Nitza Goldenberg-Cohen, Libe Gradstein, Hadas Newman

Harefuah· February 2019

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Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population.
Mor Hanany, Gilad Allon, Adva Kimchi, Anat Blumenfeld, Hadas Newman

Eur J Hum Genet· August 2018

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Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.
Adva Kimchi, Samer Khateb, Rong Wen, Ziqiang Guan, Alexey Obolensky, Hadas Newman

Ophthalmology· May 2018

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Prevalence of choroidal nevus and retinal pigment epithelial alterations in vitiligo patients.
Efrat Fleissig, Mor Pavlovksy, Anat Loewenstein, Dinah Zur, Hadas Newman

Graefes Arch Clin Exp Ophthalmol· May 2018

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Home use of binocular dichoptic video content device for treatment of amblyopia: a pilot study.
Daphna Mezad-Koursh, Amir Rosenblatt, Hadas Newman, Chaim Stolovitch

J AAPOS· April 2018

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Overexpression and Purification of Human Cis-prenyltransferase in Escherichia coli.
Ilan Edri, Michal Goldenberg, Michal Lisnyansky, Roi Strulovich, Hadas Newman

J Vis Exp· August 2017

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Oculopharyngeal Muscular Dystrophy and Inherited Retinal Dystrophy in Bukhara Jews Due to Linked Mutations in the PABPN1 and NRL Genes.
Itzhak Braverman, Sergiu C Blumen, Hadas Newman, Leah Rizel, Morad Khayat

Genet Test Mol Biomarkers· July 2017

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Purification and characterization of human dehydrodolychil diphosphate synthase (DHDDS) overexpressed in E. coli.
Moshe Giladi, Ilan Edri, Michal Goldenberg, Hadas Newman, Roi Strulovich

Protein Expr Purif· April 2017

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Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, Csilla H Lazar, Yael Kinarty, Hadas Newman

Am J Hum Genet· November 2016

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Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone Syndrome.
Hadas Newman, Sergiu C Blumen, Itzhak Braverman, Rana Hanna, Beatrice Tiosano

Invest Ophthalmol Vis Sci· October 2016

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