These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 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. Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis.
    Alerasool M; Eslahi A; Vona B; Kahaei MS; Mojaver NK; Rajati M; Pasdar A; Ghasemi MM; Saburi E; Ardehaie RM; Aval MH; Tale MR; Nourizadeh N; Afzalzadeh MR; Niknezhad HT; Mojarrad M
    Clin Genet; 2024 Dec; 106(6):693-701. PubMed ID: 39107234
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.