Genetic etiology of hearing loss in Iran-Reference-Cited by-同舟云学术

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Genetic etiology of hearing loss in Iran

Published:2022-01-20 Issue:3-4 Volume:141 Page:623-631
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Babanejad Mojgan,Beheshtian Maryam,Jamshidi Fereshteh,Mohseni Marzieh,Booth Kevin T.,Kahrizi Kimia,Najmabadi Hossein

Funder

iran's national elites foundation

university of social welfare and rehabilitation sciences

nih/nigms

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s00439-021-02421-w.pdf

Reference49 articles.

1. Azaiez H, Chamberlin GP, Fischer SM, Welp CL, Prasad SD, Taggart RT, del Castillo I, Van Camp G, Smith RJ (2004) GJB2: the spectrum of deafness-causing allele variants and their phenotype. Hum Mutat 24:305–311. https://doi.org/10.1002/humu.20084

2. Azaiez H, Booth KT, Ephraim SS, Crone B, Black-Ziegelbein EA, Marini RJ, Shearer AE, Sloan-Heggen CM, Kolbe D, Casavant T, Schnieders MJ, Nishimura C, Braun T, Smith RJH (2018) Genomic landscape and mutational signatures of deafness-associated genes. Am J Hum Genet 103:484–497. https://doi.org/10.1016/j.ajhg.2018.08.006

3. Babanejad M, Fattahi Z, Bazazzadegan N, Nishimura C, Meyer N, Nikzat N, Sohrabi E, Najmabadi A, Jamali P, Habibi F (2012) A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. Am J Med Genet A 158:2485–2492

4. Bademci G, Foster J, Mahdieh N, Bonyadi M, Duygu Duman F, Cengiz B, Menendez I, Diaz-Horta O, Shirkavand A, Zeinali S (2016) Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. Genet Med 18:364–371

5. Bademci G, Abad C, Incesulu A, Rad A, Alper O, Kolb SM, Cengiz FB, Diaz-Horta O, Silan F, Mihci E (2018) MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss. Hum Genet 137:479–486

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1. Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis;Clinical Genetics;2024-08-06

2. Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing;Molecular Biology Reports;2024-05-20

3. Case report of a novel mutation in the TNC gene in Chinese patients with nonsyndromic hearing loss;Medicine;2024-04-19

4. The Cost Effectiveness of Newborn Hearing Screening Program: New Approach of Iran Ministry of Health and Medical Education in 2022;Iranian Journal of Pediatrics;2024-03-18

5. In silico Analysis of Two Novel Variants in the Pyruvate Carboxylase (PC) Gene Associated with the Severe Form of PC Deficiency;IRAN BIOMED J;2023

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