Ofer Sarig
17PUBLICATIONS
55CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (17)
Sort by Publication Date:
|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
|Jul 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes.Janan Mohamad, Ofer Sarig, Paula Beattie
|Jul 13, 2022
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy.Kiril Malovitski, Odile Meijers, Eran Cohen-Barak
|May 24, 2022
Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence.Mor Pavlovsky, Alon Peled, Ofer Sarig
Pageof 3
Frequent Collaborators
11 joint publications
Eli Sprecher
9 joint publications
Liat Samuelov
6 joint publications
Janan Mohamad
4 joint publications
Mor Pavlovsky
4 joint publications
Alon Peled
4 joint publications
Kiril Malovitski
4 joint publications
Sari Assaf
3 joint publications
Natalya Malchin
3 joint publications
Noam Shomron
2 joint publications
Arti Nanda
