Janan Mohamad
6PUBLICATIONS
53CO-AUTHORS
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Publications (6)
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|Feb 20, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotype.Shir Bergson, Ofer Sarig, Moshe Giladi
|Sep 19, 2023
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.Alon Peled, Ofer Sarig, Janan Mohamad
|Aug 03, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.Janan Mohamad, Liat Samuelov, Sari Assaf
|Mar 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population.Janan Mohamad, Liat Samuelov, Natalia Malchin
|Feb 08, 2021
Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.Janan Mohamad, Liat Samuelov, Sari Assaf
|Jul 04, 2020
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.Janan Mohamad, Arti Nanda, Mor Pavlovsky
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Frequent Collaborators
6 joint publications
Eli Sprecher
6 joint publications
Ofer Sarig
4 joint publications
Kiril Malovitski
4 joint publications
Sari Assaf
3 joint publications
Natalya Malchin
3 joint publications
Noam Shomron
3 joint publications
Liat Samuelov
2 joint publications
Arti Nanda
2 joint publications
Mor Pavlovsky
2 joint publications
Alon Peled
