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Maryam Taghdiri | Researchclopedia

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Maryam Taghdiri

19

Works

489

Citations

8

h-index

7

i10-index

Research Topics

Hearing, Cochlea, Tinnitus, Genetics Skin and Cellular Biology Research Vestibular and auditory disorders

Affiliations

Shiraz University2015–2015

Shiraz University of Medical Sciences2017–2020

Iranian Legal Medicine Organization2008–2019

Genetic Resources Center2017–2019

Islamic Azad University Kazeron2020–2022

Top Works

Genetics of intellectual disability in consanguineous families

Hao Hu,Kimia Kahrizi,et al.

2018210 citations

Hearing Loss and Rehabilitation

Mitochondrial Function and Pathology

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

Christina Sloan-Heggen,Mojgan Babanejad,et al.

2015118 citations

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

Niloofar Bazazzadegan,Nooshin Nikzat,et al.

201241 citations

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

Kimia Kahrizi,Marzieh Mohseni,et al.

200837 citations

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Maryam Taghdiri,Hassan Dastsooz,et al.

201720 citations

Auditory Evaluation of High Risk Newborns by Automated Auditory Brain Stem Response

Maryam Taghdiri,Fatemeh Eghbalian,et al.

200818 citations

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

Maryam Taghdiri,Atie Kashef,et al.

201914 citations

Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population

Atie Kashef,Nooshin Nikzat,et al.

20149 citations

Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population

Ali Khanbazi,Maryam Beheshtian,et al.

20246 citations