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 *

359 related articles for article (PubMed ID: 26226137)

  • 1. 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]  

  • 2. Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.
    Diaz-Horta O; Duman D; Foster J; Sırmacı A; Gonzalez M; Mahdieh N; Fotouhi N; Bonyadi M; Cengiz FB; Menendez I; Ulloa RH; Edwards YJ; Züchner S; Blanton S; Tekin M
    PLoS One; 2012; 7(11):e50628. PubMed ID: 23226338
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey.
    Duman D; Sirmaci A; Cengiz FB; Ozdag H; Tekin M
    Genet Test Mol Biomarkers; 2011; 15(1-2):29-33. PubMed ID: 21117948
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of homozygous mutations for hearing loss.
    Dianatpour M; Smith E; Hashemi SB; Farazifard MA; Nezafat N; Razban V; Mani A
    Gene; 2021 Apr; 778():145464. PubMed ID: 33524517
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.
    Yang T; Wei X; Chai Y; Li L; Wu H
    Orphanet J Rare Dis; 2013 Jun; 8():85. PubMed ID: 23767834
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
    Riahi Z; Bonnet C; Zainine R; Louha M; Bouyacoub Y; Laroussi N; Chargui M; Kefi R; Jonard L; Dorboz I; Hardelin JP; Salah SB; Levilliers J; Weil D; McElreavey K; Boespflug OT; Besbes G; Abdelhak S; Petit C
    PLoS One; 2014; 9(6):e99797. PubMed ID: 24926664
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic causes of moderate to severe hearing loss point to modifiers.
    Naz S; Imtiaz A; Mujtaba G; Maqsood A; Bashir R; Bukhari I; Khan MR; Ramzan M; Fatima A; Rehman AU; Iqbal M; Chaudhry T; Lund M; Brewer CC; Morell RJ; Friedman TB
    Clin Genet; 2017 Apr; 91(4):589-598. PubMed ID: 27573290
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.
    Woo HM; Park HJ; Baek JI; Park MH; Kim UK; Sagong B; Koo SK
    BMC Med Genet; 2013 Jul; 14():72. PubMed ID: 23865914
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
    Trabelsi M; Bahri W; Habibi M; Zainine R; Maazoul F; Ghazi B; Chaabouni H; Mrad R
    Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive nonsyndromic deafness genes: a review.
    Duman D; Tekin M
    Front Biosci (Landmark Ed); 2012 Jun; 17(6):2213-36. PubMed ID: 22652773
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss.
    Pavlenkova Z; Varga L; Borecka S; Karhanek M; Huckova M; Skopkova M; Profant M; Gasperikova D
    Sci Rep; 2021 Nov; 11(1):22488. PubMed ID: 34795337
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.
    Xiang YB; Xu CY; Xu YZ; Li HZ; Zhou LL; Xu XQ; Chen ZH; Tang SH
    Mol Genet Genomic Med; 2020 Dec; 8(12):e1539. PubMed ID: 33095980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
    Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF
    Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families.
    Tlili A; Rebeh IB; Aifa-Hmani M; Dhouib H; Moalla J; Tlili-Chouchène J; Said MB; Lahmar I; Benzina Z; Charfedine I; Driss N; Ghorbel A; Ayadi H; Masmoudi S
    Audiol Neurootol; 2008; 13(4):213-8. PubMed ID: 18259073
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 18.