187 related articles for article (PubMed ID: 35050400)
21. Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.
Yazdanpanahi N; Chaleshtori MH; Tabatabaiefar MA; Noormohammadi Z; Farrokhi E; Najmabadi H; Shahbazi S; Hosseinipour A
Int J Pediatr Otorhinolaryngol; 2012 Jun; 76(6):845-50. PubMed ID: 22444735
[TBL] [Abstract][Full Text] [Related]
22. Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
Mahdieh N; Rabbani B; Wiley S; Akbari MT; Zeinali S
J Hum Genet; 2010 Oct; 55(10):639-48. PubMed ID: 20739942
[TBL] [Abstract][Full Text] [Related]
23. A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.
Ghasemnejad T; Shekari Khaniani M; Nouri Nojadeh J; Mansoori Derakhshan S
BMC Med Genomics; 2022 Feb; 15(1):18. PubMed ID: 35101039
[TBL] [Abstract][Full Text] [Related]
24. Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss.
Zardadi S; Razmara E; Asgaritarghi G; Jafarinia E; Bitarafan F; Rayat S; Almadani N; Morovvati S; Garshasbi M
Mol Genet Genomic Med; 2020 Dec; 8(12):e1550. PubMed ID: 33205915
[TBL] [Abstract][Full Text] [Related]
25. Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review.
Koohiyan M
Int J Pediatr Otorhinolaryngol; 2020 Feb; 129():109756. PubMed ID: 31704577
[TBL] [Abstract][Full Text] [Related]
26. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
Mehregan H; Mohseni M; Jalalvand K; Arzhangi S; Nikzat N; Banihashemi S; Kahrizi K; Najmabadi H
Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():115-126. PubMed ID: 30579064
[TBL] [Abstract][Full Text] [Related]
27. Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.
Mohseni M; Babanejad M; Booth KT; Jamali P; Jalalvand K; Davarnia B; Ardalani F; Khoshaeen A; Arzhangi S; Ghodratpour F; Beheshtian M; Jahanshad F; Otukesh H; Bahrami F; Seifati SM; Bazazzadegan N; Habibi F; Behravan H; Mirzaei S; Keshavarzi F; Nikzat N; Mehrjoo Z; Thiele H; Nothnagel M; Azaiez H; Smith RJ; Kahrizi K; Najmabadi H
Clin Genet; 2021 Jul; 100(1):59-78. PubMed ID: 33713422
[TBL] [Abstract][Full Text] [Related]
28. The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness.
Yazdanpanahi N; Tabatabaiefar MA; Bagheri N; Azadegan Dehkordi F; Farrokhi E; Hashemzadeh Chaleshtori M
Int J Audiol; 2015 Feb; 54(2):124-30. PubMed ID: 25290043
[TBL] [Abstract][Full Text] [Related]
29. Molecular genetic landscape of hereditary hearing loss in Pakistan.
Naz S
Hum Genet; 2022 Apr; 141(3-4):633-648. PubMed ID: 34308486
[TBL] [Abstract][Full Text] [Related]
30. Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Bademci G; Foster J; Mahdieh N; Bonyadi M; Duman D; Cengiz FB; Menendez I; Diaz-Horta O; Shirkavand A; Zeinali S; Subasioglu A; Tokgoz-Yilmaz S; Huesca-Hernandez F; de la Luz Arenas-Sordo M; Dominguez-Aburto J; Hernandez-Zamora E; Montenegro P; Paredes R; Moreta G; Vinueza R; Villegas F; Mendoza-Benitez S; Guo S; Bozan N; Tos T; Incesulu A; Sennaroglu G; Blanton SH; Ozturkmen-Akay H; Yildirim-Baylan M; Tekin M
Genet Med; 2016 Apr; 18(4):364-71. PubMed ID: 26226137
[TBL] [Abstract][Full Text] [Related]
31. Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
Ben Said M; Dhouib H; BenZina Z; Ghorbel A; Moreno F; Masmoudi S; Ayadi H; Hmani-Aifa M
Int J Pediatr Otorhinolaryngol; 2012 Jun; 76(6):832-6. PubMed ID: 22429511
[TBL] [Abstract][Full Text] [Related]
32. Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing.
Bai X; Nian S; Feng L; Ruan Q; Luo X; Wu M; Yan Z
Mol Genet Genomic Med; 2019 Aug; 7(8):e808. PubMed ID: 31250571
[TBL] [Abstract][Full Text] [Related]
33. An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the
Mohseni M; Mohammadi Y; Zare Ashrafi F; Ghodratpour F; Jalalvand K; Arzhangi S; Babanejad M; Azizi MH; Kahrizi K; Najmabadi H
Arch Iran Med; 2023 Mar; 26(3):176-180. PubMed ID: 37543941
[TBL] [Abstract][Full Text] [Related]
34. Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.
Atik T; Onay H; Aykut A; Bademci G; Kirazli T; Tekin M; Ozkinay F
PLoS One; 2015; 10(11):e0142154. PubMed ID: 26561413
[TBL] [Abstract][Full Text] [Related]
35. Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population.
Vallian Broojeni J; Kazemi A; Rezaei H; Vallian S
PLoS One; 2023; 18(8):e0289247. PubMed ID: 37561809
[TBL] [Abstract][Full Text] [Related]
36. [Hereditary hearing loss].
Tropitzsch A; Schade-Mann T; Gamerdinger P
HNO; 2023 Feb; 71(2):131-142. PubMed ID: 36526931
[TBL] [Abstract][Full Text] [Related]
37. A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.
Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Noori-Daloii MR; Tabatabaiefar MA
Audiol Neurootol; 2020; 25(5):258-262. PubMed ID: 32485727
[TBL] [Abstract][Full Text] [Related]
38. Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.
Liu C; Huang Y; Zhang Y; Ding H; Yu L; Wang A; Wang Y; Zeng Y; Liu L; Liu Y; Qi Y; Li F; Wu J; Du L; Mai F; Zhang Q; Wang X; Yin A
Int J Pediatr Otorhinolaryngol; 2022 Oct; 161():111258. PubMed ID: 35939872
[TBL] [Abstract][Full Text] [Related]
39. Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing.
Bitarafan F; Seyedena SY; Mahmoudi M; Garshasbi M
J Clin Lab Anal; 2020 Dec; 34(12):e23544. PubMed ID: 32864763
[TBL] [Abstract][Full Text] [Related]
40. A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population.
Koohiyan M
Int J Pediatr Otorhinolaryngol; 2019 Oct; 125():1-5. PubMed ID: 31228605
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
