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 *

135 related articles for article (PubMed ID: 37473993)

  • 21. Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss.
    Kim SY; Kim BJ; Oh DY; Han JH; Yi N; Kim NJ; Park MK; Keum C; Seo GH; Choi BY
    Sci Rep; 2022 Jul; 12(1):12457. PubMed ID: 35864128
    [TBL] [Abstract][Full Text] [Related]  

  • 22. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss.
    Kitano T; Miyagawa M; Nishio SY; Moteki H; Oda K; Ohyama K; Miyazaki H; Hidaka H; Nakamura KI; Murata T; Matsuoka R; Ohta Y; Nishiyama N; Kumakawa K; Furutate S; Iwasaki S; Yamada T; Ohta Y; Uehara N; Noguchi Y; Usami SI
    PLoS One; 2017; 12(5):e0177636. PubMed ID: 28545070
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation.
    Elander J; Ullmark T; Ehrencrona H; Jonson T; Piccinelli P; Samuelsson S; Löwgren K; Falkenius-Schmidt K; Ehinger J; Stenfeldt K; Värendh M
    Int J Pediatr Otorhinolaryngol; 2022 Aug; 159():111218. PubMed ID: 35779349
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Association Between Expanded Genomic Sequencing Combined With Hearing Screening and Detection of Hearing Loss Among Newborns in a Neonatal Intensive Care Unit.
    Zhu Y; Hu L; Yang L; Wang L; Lu Y; Dong X; Xiao T; Xu Z; Wu B; Zhou W
    JAMA Netw Open; 2022 Jul; 5(7):e2220986. PubMed ID: 35816303
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Targeted Exome Sequencing of Deafness Genes After Failure of Auditory Phenotype-Driven Candidate Gene Screening.
    Kim BJ; Kim AR; Park G; Park WY; Chang SO; Oh SH; Choi BY
    Otol Neurotol; 2015 Jul; 36(6):1096-102. PubMed ID: 25830873
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Risk Factors Associated with Delays in Hearing Loss Identification in Pediatric Patients.
    Lindeborg MM; Khalsa IK; Liao EN; Stephans JR; Chan DK
    Otolaryngol Head Neck Surg; 2024 Mar; 170(3):896-904. PubMed ID: 37925623
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population.
    Kim NK; Kim AR; Park KT; Kim SY; Kim MY; Nam JY; Woo SJ; Oh SH; Park WY; Choi BY
    Genet Med; 2015 Nov; 17(11):901-11. PubMed ID: 25719458
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children.
    Xie L; Qiu Y; Jin Y; Xu K; Bai X; Liu XZ; Wang XH; Chen S; Sun Y
    Neural Plast; 2021; 2021():6151973. PubMed ID: 34335733
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.
    Likar T; Hasanhodžić M; Teran N; Maver A; Peterlin B; Writzl K
    PLoS One; 2018; 13(1):e0188578. PubMed ID: 29293505
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hearing outcomes in children with congenital cytomegalovirus infection: From management controversies to lack of parents' knowledge.
    Aldè M; Caputo E; Di Berardino F; Ambrosetti U; Barozzi S; Piatti G; Zanetti D; Pignataro L; Cantarella G
    Int J Pediatr Otorhinolaryngol; 2023 Jan; 164():111420. PubMed ID: 36563581
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.
    Kannan-Sundhari A; Yan D; Saeidi K; Sahebalzamani A; Blanton SH; Liu XZ
    Genet Test Mol Biomarkers; 2020 Oct; 24(10):674-680. PubMed ID: 32991204
    [No Abstract]   [Full Text] [Related]  

  • 32. Causes of hearing loss and implantation age in a cohort of Danish pediatric cochlear implant recipients.
    Friis IJ; Aaberg K; Edholm B
    Int J Pediatr Otorhinolaryngol; 2023 Aug; 171():111640. PubMed ID: 37441990
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation.
    Song MH; Jung J; Rim JH; Choi HJ; Lee HJ; Noh B; Lee JS; Gee HY; Choi JY
    Ear Hear; 2020; 41(1):114-124. PubMed ID: 31045651
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Targeted Next-Generation Sequencing in Children With Bilateral Sensorineural Hearing Loss: Diagnostic Yield and Predictors of a Genetic Cause.
    Boudewyns A; van den Ende J; Peeters N; Van Camp G; Hofkens-Van den Brandt A; Van Schil K; Wouters K; Wuyts W
    Otol Neurotol; 2023 Apr; 44(4):360-366. PubMed ID: 36804529
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China.
    Zhu QW; Li MT; Zhuang X; Chen K; Xu WQ; Jiang YH; Qin G
    JAMA Netw Open; 2021 Sep; 4(9):e2125544. PubMed ID: 34533568
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.
    Wang Q; Xiang J; Sun J; Yang Y; Guan J; Wang D; Song C; Guo L; Wang H; Chen Y; Leng J; Wang X; Zhang J; Han B; Zou J; Yan C; Zhao L; Luo H; Han Y; Yuan W; Zhang H; Wang W; Wang J; Yang H; Xu X; Yin Y; Morton CC; Zhao L; Zhu S; Shen J; Peng Z
    Genet Med; 2019 Oct; 21(10):2231-2238. PubMed ID: 30890784
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients.
    Usami SI; Nishio SY
    Hum Genet; 2022 Apr; 141(3-4):665-681. PubMed ID: 34599366
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Analysis of a cohort of children with sensory hearing loss using the SCALE systematic nomenclature.
    Sculerati N
    Laryngoscope; 2000 May; 110(5 Pt 1):787-98. PubMed ID: 10807358
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.