Ofer Sarig

6, Weizmann Street
Tel Aviv, TA 64239, Israel

Last Updated: 09/26/2026

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Found 105 publications

An ITGB4 variant modifies the severity of ITGA3-associated interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa (ILNEB).

An ITGB4 variant modifies the severity of ITGA3-associated interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa (ILNEB).

Journal: The Journal of investigative dermatology
Published: March 05, 2026

Interleukin 4-driven loss of stromal LIF signaling affects immune responses and cell-cell adhesion in atopic dermatitis.

Interleukin 4-driven loss of stromal LIF signaling affects immune responses and cell-cell adhesion in atopic dermatitis.

Journal: iScience
Published: January 12, 2026

Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibition.

Targeting ST18-mediated pathomechanism in pemphigus vulgaris through voltage-dependent anion channel inhibition.

Journal: Skin health and disease
Published: October 30, 2025

Defective Function of Inhibitor of κB Kinase Subunit Beta Associated With Multiple Immune-Mediated Disorders.

Defective Function of Inhibitor of κB Kinase Subunit Beta Associated With Multiple Immune-Mediated Disorders.

Journal: Experimental dermatology
Published: August 16, 2025

Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.

Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.

Journal: The Journal of investigative dermatology
Published: July 31, 2025

Expanding the Phenotypic Spectrum of PIK3CA-Related Disorders.

Expanding the Phenotypic Spectrum of PIK3CA-Related Disorders.

Journal: International journal of dermatology
Published: June 04, 2025

Loss-of-function variants in DUSP1 encoding dual specificity phosphatase 1 cause palmoplantar keratoderma.

Loss-of-function variants in DUSP1 encoding dual specificity phosphatase 1 cause palmoplantar keratoderma.

Journal: The British journal of dermatology
Published: March 28, 2025

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients.

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients.

Journal: Pediatric dermatology
Published: October 28, 2024

HMCN1 variants aggravate epidermolysis bullosa simplex phenotype.

HMCN1 variants aggravate epidermolysis bullosa simplex phenotype.

Journal: The Journal of experimental medicine
Published: May 11, 2024

Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.

Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.

Journal: Pediatric dermatology
Published: June 30, 2023

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Journal: American journal of medical genetics. Part A
Published: June 02, 2023

MicroRNA-200b-mediated reversion of a spectrum of epithelial-to-mesenchymal transition states in recessive dystrophic epidermolysis bullosa squamous cell carcinomas.

MicroRNA-200b-mediated reversion of a spectrum of epithelial-to-mesenchymal transition states in recessive dystrophic epidermolysis bullosa squamous cell carcinomas.

Journal: The British journal of dermatology
Published: March 21, 2023
Showing 1-12 of 105

Last Updated: 09/26/2026