Hamideh Bagherian

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications

Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian et al. · Journal of Investigative Dermatology · 2017 · 43 citations · Full text

Molecular Diagnostic Techniques, Unknown Subtype, Medicine +12

Impact of Consanguineous Marriages in <i>GJB2</i> -Related Hearing Loss in the Iranian Population: A Report of a Novel Variant

Nejat Mahdieh, Bahareh Rabbani, Atefeh Shirkavand et al. · Genetic Testing and Molecular Biomarkers · 2011 · 32 citations

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect

Elham Davoudi-Dehaghani, Sirous Zeinali, Nejat Mahdieh et al. · International Journal of Pediatric Otorhinolaryngology · 2013 · 28 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene

Nejat Mahdieh, Hamideh Bagherian, Atefeh Shirkavand et al. · International Journal of Pediatric Otorhinolaryngology · 2010 · 27 citations

Mendelian Disorder, Lur Family, Genetic Disorder +12

Th‐1 cytokines gene polymorphism in human brucellosis

S. Davoudi, Aliakbar Amirzargar, Mahboubeh Hajiabdolbaghi et al. · International Journal of Immunogenetics · 2006 · 21 citations