Kiril Malovitski

6PUBLICATIONS
49CO-AUTHORS
NeurogeneticsAutoimmunityEpigenetics (incl. genome methylation and epigenomics)Genetic immunologyCatalysis and mechanisms of reactions
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Publications (6)

|Sep 11, 2026
A Germline Missense Variant in the NSDHL Gene Underlies Inflammatory Linear Verrucous Epidermal Nevus.

|Jan 14, 2026
Defective Function of Inhibitor of κB Kinase Subunit Beta Associated With Multiple Immune-Mediated Disorders.

Kiril Malovitski, Noy Keller Rosenthal, Lubna Khair

|Feb 20, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotype.

Shir Bergson, Ofer Sarig, Moshe Giladi

|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

|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

4 joint publications

Janan Mohamad

4 joint publications

Ofer Sarig

3 joint publications

Liat Samuelov