BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 24941903)

  • 1. New testing guidelines for hearing loss support next-generation sequencing: testing method may help determine genetic causes of hearing loss among patients whose phenotypes are not easily distinguished clinically.
    Levenson D
    Am J Med Genet A; 2014 Jul; 164A(7):vii-viii. PubMed ID: 24941903
    [No Abstract]   [Full Text] [Related]  

  • 2. [Application of next generation sequencing in gene identification and genetic diagnosis of hereditary hearing loss].
    Huijun Y; Yu L
    Yi Chuan; 2014 Nov; 36(11):1112-20. PubMed ID: 25567869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Navigating genetic diagnostics in patients with hearing loss.
    Sloan-Heggen CM; Smith RJ
    Curr Opin Pediatr; 2016 Dec; 28(6):705-712. PubMed ID: 27552069
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Development and Validation of a Next-Generation Sequencing Panel for Syndromic and Nonsyndromic Hearing Loss.
    Butz M; McDonald A; Lundquist PA; Meyer M; Harrington S; Kester S; Stein MI; Mistry NA; Zimmerman Zuckerman E; Niu Z; Schimmenti L; Hasadsri L; Boczek NJ
    J Appl Lab Med; 2020 May; 5(3):467-479. PubMed ID: 32445360
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Advances in genetic diagnostics for hereditary hearing loss.
    Idan N; Brownstein Z; Shivatzki S; Avraham KB
    J Basic Clin Physiol Pharmacol; 2013; 24(3):165-70. PubMed ID: 24006325
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-exome sequencing and its impact in hereditary hearing loss.
    Atik T; Bademci G; Diaz-Horta O; Blanton SH; Tekin M
    Genet Res (Camb); 2015 Mar; 97():e4. PubMed ID: 25825321
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Next-generation sequence testing expands research into causes of hearing loss: scientists examine role of multiple mutations in individual cases.
    Am J Med Genet A; 2014 Sep; 164A(9):vii-viii. PubMed ID: 25125343
    [No Abstract]   [Full Text] [Related]  

  • 8. Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing-based diagnostic testing and interpretation.
    Abou Tayoun AN; Al Turki SH; Oza AM; Bowser MJ; Hernandez AL; Funke BH; Rehm HL; Amr SS
    Genet Med; 2016 Jun; 18(6):545-53. PubMed ID: 26562227
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype phenotype correlations for hearing impairment: approaches to management.
    Hoefsloot LH; Feenstra I; Kunst HP; Kremer H
    Clin Genet; 2014 Jun; 85(6):514-23. PubMed ID: 24547994
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Massively Parallel Sequencing for Genetic Diagnosis of Hearing Loss: The New Standard of Care.
    Shearer AE; Smith RJ
    Otolaryngol Head Neck Surg; 2015 Aug; 153(2):175-82. PubMed ID: 26084827
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular diagnostics for hereditary hearing loss in children.
    Sommen M; Wuyts W; Van Camp G
    Expert Rev Mol Diagn; 2017 Aug; 17(8):751-760. PubMed ID: 28593790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic diagnostics of early childhood hearing loss: better testing with next-generation DNA sequencing.
    Sommen M; Van Camp G
    B-ENT; 2013; Suppl 21():51-6. PubMed ID: 24383223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic testing as part of the early hearing detection and intervention (EHDI) process.
    Schimmenti LA; Martinez A; Fox M; Crandall B; Shapiro N; Telatar M; Sininger Y; Grody WW; Palmer CG
    Genet Med; 2004; 6(6):521-5. PubMed ID: 15545749
    [No Abstract]   [Full Text] [Related]  

  • 14. Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform.
    Sun Y; Yuan J; Wu L; Li M; Cui X; Yan C; Du L; Mao L; Man J; Li W; Kristiansen K; Wu X; Pan W; Yang Y
    Medicine (Baltimore); 2019 Mar; 98(12):e14860. PubMed ID: 30896630
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.
    Sloan-Heggen CM; Bierer AO; Shearer AE; Kolbe DL; Nishimura CJ; Frees KL; Ephraim SS; Shibata SB; Booth KT; Campbell CA; Ranum PT; Weaver AE; Black-Ziegelbein EA; Wang D; Azaiez H; Smith RJH
    Hum Genet; 2016 Apr; 135(4):441-450. PubMed ID: 26969326
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing.
    Soares de Lima Y; Chiabai M; Shen J; Córdoba MS; Versiani BR; Benício ROA; Pogue R; Mingroni-Netto RC; Lezirovitz K; Pic-Taylor A; Mazzeu JF; Oliveira SF
    Hear Res; 2018 Dec; 370():181-188. PubMed ID: 30390570
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The role of next generation sequencing in predicting hearing loss.
    Skarżyński H
    Expert Rev Mol Diagn; 2021 Apr; 21(4):347-348. PubMed ID: 33706655
    [No Abstract]   [Full Text] [Related]  

  • 18. Next-generation sequencing in genetic hearing loss.
    Yan D; Tekin M; Blanton SH; Liu XZ
    Genet Test Mol Biomarkers; 2013 Aug; 17(8):581-7. PubMed ID: 23738631
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
    Wang R; Han S; Khan A; Zhang X
    Genet Test Mol Biomarkers; 2017 May; 21(5):316-321. PubMed ID: 28281779
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital hearing impairment.
    Robson CD
    Pediatr Radiol; 2006 Apr; 36(4):309-24. PubMed ID: 16465539
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.