Morad Khayat

Afula, Z, Israel

Last Updated: 09/26/2026

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Found 54 publications

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

Journal: Journal of medical genetics

Published: April 29, 2026

Intermediate FMR1 cytosine‒guanine‒guanine repeats do not impair assisted reproductive technology outcomes in a large real-world cohort.

Intermediate FMR1 cytosine‒guanine‒guanine repeats do not impair assisted reproductive technology outcomes in a large real-world cohort.

Journal: Reproductive biomedicine online

Published: January 27, 2026

CARMIL2 deficiency disrupts activation-induced metabolic reprogramming in T cells and is partially rescued by glutamine supplementation.

CARMIL2 deficiency disrupts activation-induced metabolic reprogramming in T cells and is partially rescued by glutamine supplementation.

Journal: The Journal of allergy and clinical immunology

Published: February 20, 2025

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

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

Journal: Journal of human genetics

Published: August 15, 2024

Persistent Cutaneous Lesions of Darier Disease and Second-Hit Somatic Variants in ATP2A2 Gene.

Persistent Cutaneous Lesions of Darier Disease and Second-Hit Somatic Variants in ATP2A2 Gene.

Journal: JAMA dermatology

Published: March 27, 2024

Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality.

Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality.

Journal: Orphanet journal of rare diseases

Published: October 11, 2023

Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family.

Genetic variant in complement receptor 1 (CR1, CD35) is associated with a cluster of severe fatal COVID-19 in a family.

Journal: The Journal of infection

Published: March 11, 2023

Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population.

Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population.

Journal: Journal of community genetics

Published: February 28, 2023

Potential di-genic contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex.

Potential di-genic contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex.

Journal: Experimental dermatology

Published: May 10, 2022

A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia.

A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia.

Journal: Journal of medical genetics

Published: March 03, 2022

A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay.

A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay.

Journal: Frontiers in pediatrics

Published: January 20, 2022

Parental mosaic cutaneous-gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis-deafness syndrome.

Parental mosaic cutaneous-gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis-deafness syndrome.

Journal: The Journal of dermatology

Published: August 29, 2021

Showing 1-12 of 54

Last Updated: 09/26/2026