Niloofar Bazazzadegan

Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants

A. Eliot Shearer, Robert W. Eppsteiner, Kevin T. Booth et al. · The American Journal of Human Genetics · 2014 · 151 citations · Full text

Allelic Variant, Variant Interpretation, Ethnic-specific Differences +9

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

Christina Sloan-Heggen, Mojgan Babanejad, Maryam Beheshtian et al. · Journal of Medical Genetics · 2015 · 118 citations · Full text

<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

A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran

Mojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan et al. · American Journal of Medical Genetics Part A · 2012 · 66 citations

Screening for <i>MYO15A</i> gene mutations in autosomal recessive nonsyndromic, <i>GJB2</i> negative Iranian deaf population

Zohreh Fattahi, A. Eliot Shearer, Mojgan Babanejad et al. · American Journal of Medical Genetics Part A · 2012 · 58 citations · Full text

Genetic Diseases, Iranian Families, Developmental Biology +13