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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2023
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic reviewSajjad Biglari, Atefeh Sohanforooshan Moghaddam, Mohammad Amin Tabatabaiefar, et al.
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.
Clinical Genetics|December 20, 2024
Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and In Silico AnalysisSajjad Biglari, Pooneh Nikuei, Atefeh Mir, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohortAmir Hossein Saeidian, Leila Youssefian, Jianhe Huang, 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.
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