Publications by authors named "Shirli Israeli"

Claim this Profile
C
Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.
Shir Bergson, Daniel Daniely, David Bomze, Janan Mohamad, Kiril Malovitski, Shirli Israeli

Pediatr Dermatol· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
From biorepositories to data repositories: Open-access resources accelerate early R&D and validation of equitable diagnostic tools.
Roger Peck, Helen L Storey, Becky Barney, Shirli Israeli, Olivia Halas

PLOS Glob Public Health· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies.
Shirli Israeli, Allison Golden, Melissa Atalig, Najla Mekki, Afef Rais

J Clin Immunol· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population.
Janan Mohamad, Liat Samuelov, Natalia Malchin, Tom Rabinowitz, Sari Assaf, Shirli Israeli

Exp Dermatol· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular analysis of a series of Israeli families with Comèl-Netherton syndrome.
Shirli Israeli, Ofer Sarig, Ben Zion Garty, Margarita Indelman, Reuven Bergman

Dermatology· December 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A mutation in TP63 causing a mild ectodermal dysplasia phenotype.
Tomer Goldsmith, Ori Eytan, Lee Magal, Michal Solomon, Shirli Israeli

J Invest Dermatol· August 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Semidominant inheritance in epidermolytic ichthyosis.
Janna Nousbeck, Gilly Padalon-Brauch, Dana Fuchs-Telem, Shirli Israeli, Ofer Sarig

J Invest Dermatol· November 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12.
Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, Ofer Sarig, Gilly Padalon-Brauch

Exp Dermatol· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.
Ofer Sarig, Sagi Nahum, Debora Rapaport, Akemi Ishida-Yamamoto, Dana Fuchs-Telem, Shirli Israeli

Am J Hum Genet· August 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.
Ofer Sarig, Sivan Bercovici, Lilach Zoller, Ilan Goldberg, Margarita Indelman, Shirli Israeli

J Invest Dermatol· July 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial pityriasis rubra pilaris is caused by mutations in CARD14.
Dana Fuchs-Telem, Ofer Sarig, Maurice A M van Steensel, Ofer Isakov, Shirli Israeli

Am J Hum Genet· July 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inflammatory peeling skin syndrome caused a novel mutation in CDSN.
Dana Fuchs Telem, Shirli Israeli, Ofer Sarig, Eli Sprecher

Arch Dermatol Res· April 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosis.
Shirli Israeli, Ziyad Khamaysi, Dana Fuchs-Telem, Janna Nousbeck, Reuven Bergman

Am J Hum Genet· April 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.
Shirli Israeli, Hadas Zamir, Ofer Sarig, Reuven Bergman, Eli Sprecher

J Invest Dermatol· March 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis