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Dermatologic Therapy|November 2, 2020
Keratitis-ichthyosis-deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutationTina Asgari, Mahtab Naji, Parvin Mansouri, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|May 30, 2014
BMI1 and TWIST1 downregulated mRNA expression in basal cell carcinomaFatemeh Vand Rajabpour, Reza Raoofian, Leila Youssefian, et al.
European Journal of Human Genetics : EJHG|September 7, 2017
Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genesLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.
Experimental Dermatology|December 23, 2014
Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1Leila Youssefian, Hassan Vahidnezhad, Maryam Daneshpazhooh, et al.
Journal of Hepatology|April 8, 2019
Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutationsLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.
The Journal of Investigative Dermatology|December 1, 2016
Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous MarriagesHassan Vahidnezhad, Leila Youssefian, Sirous Zeinali, et al.
Genome Biology|July 10, 2026
Computational strategies for copy number variation detection, disease association, and beyondAmir Hossein Saeidian, Hani Sabaie, Mahdi Akbarzadeh, et al.
Plos Genetics|April 28, 2022
ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcificationDouglas Ralph, Yvonne Nitschke, Michael A Levine, et al.
American Journal of Medical Genetics. Part A|June 12, 2019
Widespread aplasia cutis congenita in sibs with PLEC1 and ITGB4 variantsAriana Kariminejad, Hassan Vahidnezhad, Siavash Ghaderi-Sohi, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|July 15, 2019
Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 "knock-out"Hassan Vahidnezhad, Leila Youssefian, Maryam Daneshpazhooh, et al.
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