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Morad Khayat

Emek Medical Center

38

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398

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An Update on the Cutaneous Manifestations of Darier Disease

2021 Journal of Cutaneous Medicine and Surgery
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175 Concomitant LZTR1 and NF1 mutations contribute to the diversity of the Neurofibromatosis 1 phenotypic spectrum

2021 Journal of Investigative Dermatology
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Author response for "The landscape of autosomal recessive variants in an isolated community: Implications for population screening for reproductive purposes"

2021
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Acral peeling in Nagashima type palmo-plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion.

2021 Experimental Dermatology
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Long-Term Outcome of Patients with TPO Mutations.

2021 Journal of Clinical Medicine
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Homozygote loss-of-function variants in the human COCH gene underlie hearing loss.

2020 European Journal of Human Genetics
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Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally.

2020 Archives of Gynecology and Obstetrics
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Homozygote loss-of-function variants in the human COCH gene underlie hearing loss

2020 bioRxiv
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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

2020 Clinical Genetics
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The role of Desmoglein 1 in gap junction turnover revealed through the study of SAM syndrome

2019 Journal of Investigative Dermatology
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