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Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
Biological Psychiatry|December 6, 2021
Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau PathologiesGidon Karmon, Shlomo Sragovich, Gal Hacohen-Kleiman, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
Annals of Neurology|September 5, 2018
Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia SyndromeAlicia Guemez-Gamboa, Ahmet Okay Çağlayan, Valentina Stanley, et al.
Clinical Genetics|October 28, 2020
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, et al.
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