186 related articles for article (PubMed ID: 35050400)
1. Genetic etiology of hearing loss in Iran.
Babanejad M; Beheshtian M; Jamshidi F; Mohseni M; Booth KT; Kahrizi K; Najmabadi H
Hum Genet; 2022 Apr; 141(3-4):623-631. PubMed ID: 35050400
[TBL] [Abstract][Full Text] [Related]
2. Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.
Aliazami F; Gilani S; Farhud D; Naraghi M; Afshari M; Eslami M
Int J Pediatr Otorhinolaryngol; 2023 May; 168():111512. PubMed ID: 37086676
[TBL] [Abstract][Full Text] [Related]
3. Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries.
Al Mutery A; Mahfood M; Chouchen J; Tlili A
Hum Genet; 2022 Apr; 141(3-4):595-605. PubMed ID: 34338889
[TBL] [Abstract][Full Text] [Related]
4. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
Sloan-Heggen CM; Babanejad M; Beheshtian M; Simpson AC; Booth KT; Ardalani F; Frees KL; Mohseni M; Mozafari R; Mehrjoo Z; Jamali L; Vaziri S; Akhtarkhavari T; Bazazzadegan N; Nikzat N; Arzhangi S; Sabbagh F; Otukesh H; Seifati SM; Khodaei H; Taghdiri M; Meyer NC; Daneshi A; Farhadi M; Kahrizi K; Smith RJ; Azaiez H; Najmabadi H
J Med Genet; 2015 Dec; 52(12):823-9. PubMed ID: 26445815
[TBL] [Abstract][Full Text] [Related]
5. Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.
Sadeghian L; Tabatabaiefar MA; Fattahi N; Pourreza MR; Tahmasebi P; Alavi Z; Hashemzadeh Chaleshtori M
Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():99-105. PubMed ID: 31176026
[TBL] [Abstract][Full Text] [Related]
6. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
Liang P; Chen F; Wang S; Li Q; Li W; Wang J; Chen J; Zha D
Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623
[TBL] [Abstract][Full Text] [Related]
7. Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
Beheshtian M; Babanejad M; Azaiez H; Bazazzadegan N; Kolbe D; Sloan-Heggen C; Arzhangi S; Booth K; Mohseni M; Frees K; Azizi MH; Daneshi A; Farhadi M; Kahrizi K; Smith RJ; Najmabadi H
Arch Iran Med; 2016 Oct; 19(10):720-728. PubMed ID: 27743438
[TBL] [Abstract][Full Text] [Related]
8. Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients.
Fu Y; Huang S; Gao X; Han M; Wang G; Kang D; Yuan Y; Dai P
BMC Med Genomics; 2022 Mar; 15(1):71. PubMed ID: 35346193
[TBL] [Abstract][Full Text] [Related]
9. An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population.
Ghasemnejad T; Shekari Khaniani M; Zarei F; Farbodnia M; Mansoori Derakhshan S
Int J Pediatr Otorhinolaryngol; 2017 Jun; 97():113-126. PubMed ID: 28483220
[TBL] [Abstract][Full Text] [Related]
10. Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
Doll J; Vona B; Schnapp L; Rüschendorf F; Khan I; Khan S; Muhammad N; Alam Khan S; Nawaz H; Khan A; Ahmad N; Kolb SM; Kühlewein L; Labonne JDJ; Layman LC; Hofrichter MAH; Röder T; Dittrich M; Müller T; Graves TD; Kong IK; Nanda I; Kim HG; Haaf T
Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33187236
[TBL] [Abstract][Full Text] [Related]
11. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.
Sarmadi A; Nasrniya S; Narrei S; Nouri Z; Abtahi H; Tabatabaiefar MA
Mol Biol Rep; 2020 Jul; 47(7):5355-5364. PubMed ID: 32623615
[TBL] [Abstract][Full Text] [Related]
12. Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
Khatami S; Askari M; Bahreini F; Hashemzadeh-Chaleshtori M; Hematian S; Asgharzade S
BMC Med Genet; 2020 Nov; 21(1):226. PubMed ID: 33208113
[TBL] [Abstract][Full Text] [Related]
13. Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades.
Shadab M; Abbasi AA; Ejaz A; Ben-Mahmoud A; Gupta V; Kim HG; Vona B
J Cell Mol Med; 2024 Apr; 28(8):e18119. PubMed ID: 38534090
[TBL] [Abstract][Full Text] [Related]
14. Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
Zarepour N; Koohiyan M; Taghipour-Sheshdeh A; Nemati-Zargaran F; Saki N; Mohammadi-Asl J; Tabatabaiefar MA; Hashemzadeh-Chaleshtori M
Audiol Neurootol; 2019; 24(1):25-31. PubMed ID: 30943474
[TBL] [Abstract][Full Text] [Related]
15. Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.
Shang H; Yan D; Tayebi N; Saeidi K; Sahebalzamani A; Feng Y; Blanton S; Liu X
Biomed Res Int; 2018; 2018():3103986. PubMed ID: 29568747
[TBL] [Abstract][Full Text] [Related]
16. Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.
Reiisi S; Tabatabaiefar MA; Sanati MH; Chaleshtori MH
Iran J Basic Med Sci; 2016 Jul; 19(7):772-8. PubMed ID: 27635202
[TBL] [Abstract][Full Text] [Related]
17. Identification of a founder mutation for Pendred syndrome in families from northwest Iran.
Mohseni M; Honarpour A; Mozafari R; Davarnia B; Najmabadi H; Kahrizi K
Int J Pediatr Otorhinolaryngol; 2014 Nov; 78(11):1828-32. PubMed ID: 25239229
[TBL] [Abstract][Full Text] [Related]
18. Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss.
Budde BS; Aly MA; Mohamed MR; Breß A; Altmüller J; Motameny S; Kawalia A; Thiele H; Konrad K; Becker C; Toliat MR; Nürnberg G; Sayed EAF; Mohamed ES; Pfister M; Nürnberg P
Clin Genet; 2020 Jul; 98(1):32-42. PubMed ID: 32279305
[TBL] [Abstract][Full Text] [Related]
19. A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss.
Azadegan-Dehkordi F; Ahmadi R; Bahrami T; Yazdanpanahi N; Farrokhi E; Tabatabaiefar MA; Hashemzadeh-Chaleshtori M
Am J Otolaryngol; 2018; 39(6):719-725. PubMed ID: 30077349
[TBL] [Abstract][Full Text] [Related]
20. Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the
Olsson KS; Wålinder O; Jansson U; Wilbe M; Bondeson ML; Stattin EL; Raha-Chowdhury R; Williams R
Hereditas; 2017; 154():16. PubMed ID: 29270100
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]