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Pediatric Dermatology|February 8, 2021
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
Scientific Reports|April 9, 2022
Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expressionSari Assaf, Dan Vodo, Kiril Malovitski, et al.
The British Journal of Dermatology|July 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genesJanan Mohamad, Ofer Sarig, Paula Beattie, et al.
Skin Health and Disease|April 2, 2026
Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibitionSari Assaf, Ofer Sarig, Rawaa Ishtewy, et al.
Frontiers in Medicine|August 30, 2018
The Genetics of Pemphigus VulgarisDan Vodo, Ofer Sarig, Eli Sprecher
American Journal of Medical Genetics. Part A|August 3, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1Janan Mohamad, Liat Samuelov, Sari Assaf, et al.
The Journal of Investigative Dermatology|April 6, 2020
Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar KeratodermaJanan Mohamad, Ofer Sarig, Liron Malki, et al.
Experimental Dermatology|April 1, 2018
SAM syndrome is characterized by extensive phenotypic heterogeneityShahar Taiber, Liat Samuelov, Janan Mohamad, et al.
The British Journal of Dermatology|May 20, 2023
Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratodermaKiril Malovitski, Ofer Sarig, Yarden Feller, et al.
Pediatric Dermatology|January 20, 2021
Epidermolysis bullosa simplex due to bi-allelic DST mutations: Case series and review of the literatureDalit Ganani, Kiril Malovitski, Ofer Sarig, et al.
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