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Human Mutation|December 23, 2018
Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous familiesLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 16, 2017
Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathyHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
The Journal of Investigative Dermatology|March 11, 2022
Recalcitrant Cutaneous Warts in a Family with Inherited ICOS DeficiencyLeila Youssefian, Amir Hossein Saeidian, Ali Reza Tavasoli, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|May 18, 2021
Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutationHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Experimental Dermatology|January 25, 2018
Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosaHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 20, 2019
Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin LymphomaLeila Youssefian, Hassan Vahidnezhad, Mehdi Yousefi, et al.
Clinical Chemistry|May 10, 2021
Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of ConsanguinityLeila Youssefian, Amir Hossein Saeidian, Fahimeh Palizban, et al.
DNA Repair|February 29, 2024
DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinityAmir Hozhabrpour, Marzieh Mojbafan, Fahimeh Palizban, et al.
Scientific Reports|December 11, 2020
Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragilityHassan Vahidnezhad, Leila Youssefian, Masoomeh Faghankhani, et al.
Nature Genetics|August 8, 2017
Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritabilityErna V Ivarsdottir, Valgerdur Steinthorsdottir, Maryam S Daneshpour, et al.
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