Similar articles for PMID: 26084827

Year	Number of Results
2007	1
2008	1
2010	1
2011	2
2012	3
2013	9
2014	8
2015	17
2016	11
2017	4
2018	7
2019	10
2020	8
2021	8
2022	19
2023	8
2024	0

1

Massively Parallel Sequencing for Genetic Diagnosis of Hearing Loss: The New Standard of Care.

Shearer AE, Smith RJ. Shearer AE, et al. Otolaryngol Head Neck Surg. 2015 Aug;153(2):175-82. doi: 10.1177/0194599815591156. Epub 2015 Jun 17. Otolaryngol Head Neck Surg. 2015. PMID: 26084827 Free PMC article. Review.

2

Navigating genetic diagnostics in patients with hearing loss.

Sloan-Heggen CM, Smith RJ. Sloan-Heggen CM, et al. Curr Opin Pediatr. 2016 Dec;28(6):705-712. doi: 10.1097/MOP.0000000000000410. Curr Opin Pediatr. 2016. PMID: 27552069 Free PMC article. Review.

3

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. Sloan-Heggen CM, et al. Hum Genet. 2016 Apr;135(4):441-450. doi: 10.1007/s00439-016-1648-8. Epub 2016 Mar 11. Hum Genet. 2016. PMID: 26969326 Free PMC article.

4

Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.

Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T. Mutai H, et al. Orphanet J Rare Dis. 2013 Oct 28;8:172. doi: 10.1186/1750-1172-8-172. Orphanet J Rare Dis. 2013. PMID: 24164807 Free PMC article.

5

Genetic background in late-onset sensorineural hearing loss patients.

Uehara N, Fujita T, Yamashita D, Yokoi J, Katsunuma S, Kakigi A, Nishio SY, Nibu KI, Usami SI. Uehara N, et al. J Hum Genet. 2022 Apr;67(4):223-230. doi: 10.1038/s10038-021-00990-2. Epub 2021 Nov 26. J Hum Genet. 2022. PMID: 34824372 Free PMC article.

6

Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations.

Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li H. Gu X, et al. Clin Genet. 2015 Jun;87(6):588-93. doi: 10.1111/cge.12431. Epub 2014 Aug 7. Clin Genet. 2015. PMID: 24853665

7

Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?

Clabout T, Maes L, Acke F, Wuyts W, Van Schil K, Coucke P, Janssens S, De Leenheer E. Clabout T, et al. Genes (Basel). 2022 Dec 29;14(1):105. doi: 10.3390/genes14010105. Genes (Basel). 2022. PMID: 36672845 Free PMC article.

8

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. Liu C, et al. Int J Pediatr Otorhinolaryngol. 2022 Oct;161:111258. doi: 10.1016/j.ijporl.2022.111258. Epub 2022 Jul 31. Int J Pediatr Otorhinolaryngol. 2022. PMID: 35939872

9

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients.

Baux D, Vaché C, Blanchet C, Willems M, Baudoin C, Moclyn M, Faugère V, Touraine R, Isidor B, Dupin-Deguine D, Nizon M, Vincent M, Mercier S, Calais C, García-García G, Azher Z, Lambert L, Perdomo-Trujillo Y, Giuliano F, Claustres M, Koenig M, Mondain M, Roux AF. Baux D, et al. Sci Rep. 2017 Dec 1;7(1):16783. doi: 10.1038/s41598-017-16846-9. Sci Rep. 2017. PMID: 29196752 Free PMC article.

10

Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.

Wu CC, Tsai CY, Lin YH, Chen PY, Lin PH, Cheng YF, Wu CM, Lin YH, Lee CY, Erdenechuluun J, Liu TC, Chen PL, Hsu CJ. Wu CC, et al. Genes (Basel). 2019 Oct 1;10(10):772. doi: 10.3390/genes10100772. Genes (Basel). 2019. PMID: 31581539 Free PMC article.

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