Nooshin Nikzat

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 · 120 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 67 citations

Life Sciences, Genetics, Molecular Genetics +16

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

Life Sciences, Genetics, Molecular Genetics +17

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study

Niloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi et al. · International Journal of Pediatric Otorhinolaryngology · 2012 · 41 citations

Medicine, Genetics, Otolaryngology +13

Mutations in <i>TMC1</i> are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population

Michael S. Hildebrand, Kimia Kahrizi, Catherine Bromhead et al. · Annals of Otology Rhinology & Laryngology · 2010 · 31 citations · Full text

Life Sciences, Audiology, Genetics +16