Maryam Taghdiri

Genetics of intellectual disability in consanguineous families

Hao Hu, Kimia Kahrizi, Luciana Musante et al. · Molecular Psychiatry · 2018 · 206 citations

Intellectual Impairment, Complex Trait Genetics, Genetic Disorder +5

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

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

Iranian Population, Genetic Disorder, Genetics +11

Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment

Kimia Kahrizi, Marzieh Mohseni, Carla Nishimura et al. · European Journal of Pediatrics · 2008 · 37 citations · Full text

Iranian Families, Hereditary Hearing Impairment, Mendelian Disorder +10

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Maryam Taghdiri, Hassan Dastsooz, Majid Fardaei et al. · Frontiers in Pediatrics · 2017 · 19 citations · Full text