Nejat Mahdieh

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 158 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +11

Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Oscar Diaz‐Horta, Duygu Duman, Joseph Foster et al. · PLoS ONE · 2012 · 155 citations · Full text

Genetics, Pathology, Arnshl Genes +16

<i>GJB2</i> mutations: Passage through Iran

Hossein Najmabadi, Carla Nishimura, Kimia Kahrizi et al. · American Journal of Medical Genetics Part A · 2005 · 87 citations · Full text

Gjb2-related Deafness, Gjb2-related Deafness Reveal, Mendelian Disorder +15

An overview of mutation detection methods in genetic disorders.

Nejat Mahdieh, Bahareh Rabbani · PubMed · 2013 · 69 citations · Full text

Genetic Analysis, Genetic Diseases, Molecular Diagnostic Techniques +15

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

Güney Bademci, Filiz Başak Cengiz, Joseph Foster et al. · Scientific Reports · 2016 · 56 citations · Full text