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Archives of Iranian Medicine|July 14, 2020
Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype SpectrumSara Taghizadeh, Raheleh Vazehan, Maryam Beheshtian, et al.
Archives of Iranian Medicine|October 8, 2015
Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with AtaxiaRoshanak Jazayeri, Hao Hu, Zohreh Fattahi, et al.
Plos One|August 27, 2015
The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri FamiliesBehzad Davarniya, Hao Hu, Kimia Kahrizi, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Did the GJB2 35delG mutation originate in Iran?Vahideh Norouzi, Hiva Azizi, Zohreh Fattahi, et al.
Biochemical Genetics|February 26, 2024
Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>AMasoumeh Heidari Feizabadi, Masoome Alerasool, Atieh Eslahi, et al.
International Journal of Pediatric Otorhinolaryngology|January 4, 2015
Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian populationAtie Kashef, Nooshin Nikzat, Niloofar Bazzazadegan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 20, 2018
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disabilitySomayeh Kazeminasab, Ibrahim Ihsan Taskiran, Zohreh Fattahi, et al.
Archives of Iranian Medicine|April 29, 2025
Haplogroup Structure and Genetic Variation Analyses of Mitochondrial Genome SNPs in the Iranian PopulationMasoumeh Ghasemi, Marzieh Mohseni, Zohreh Fattahi, et al.
Archives of Iranian Medicine|April 15, 2024
Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic GroupsSomayeh Alinaghi, Marzieh Mohseni, Zohreh Fattahi, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2011
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing lossBehzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, et al.
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