Author

Morad Khayat

Emek Medical CenterORCID 0000-0002-4817-7492Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Stavit Allon ShaleviD· 3 shared Karen B. AvrahamiD· 2 shared Nada Danial‐FarraniD· 2 shared Shahar TaiberiD· 2 shared Amal Abu RayyaniD· 1 shared Amihood Singer· 1 shared Amir PelegiD· 1 shared Asgeir Orn ArnthorssoniD· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Stavit Allon ShalevORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Human GeneticsPeer-reviewedNov 5, 2024

The distribution of regions of homozygosity (ROH) among consanguineous populations - implications for a routine genetic counseling service

Chen Gafni‐Amsalem, Nasim Warwar, Morad Khayat…·Stavit Allon Shalev

The paper analyzes ROH distribution in consanguineous populations and suggests pre-pregnancy genetic counseling to assess recessive disorder risks.

1 citation

humanstatistical model

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GeneticsEuropean Journal of Human GeneticsPeer-reviewedSep 16, 2020

Homozygote loss-of-function variants in the human COCH gene underlie hearing loss

Nada Danial‐Farran, Elena Chervinsky, Prathamesh T. Nadar‐Ponniah…·Stavit Allon Shalev

This study investigates a homozygous frameshift variant in the COCH gene, showing it causes loss-of-function through reduced cochlin translation, impacting genetic counseling for carriers.

13 citations

humanexperimental assay

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GeneticsClinical GeneticsPeer-reviewedJul 20, 2020

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Zippora Brownstein, Süleyman Gülsüner, Tom Walsh…·Karen B. Avraham

The paper identifies genetic causes of inherited hearing loss in the Israeli Jewish population, finding a novel deafness gene ATOH1 and demonstrating the effectiveness of targeted genomic sequencing.

31 citations

humanwhole-exome sequencing

𝕏 PostBluesky