PubMed (Bookshelf cited) for id: 400917

Year	Number of Results
1999	1
2005	1
2006	2
2007	2
2010	1
2013	3
2014	1
2015	3
2016	3
2017	5
2018	2
2019	2
2020	3
2021	6
2022	6
2025	0

1

Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4).

Yang T, Vidarsson H, Rodrigo-Blomqvist S, Rosengren SS, Enerback S, Smith RJ. Yang T, et al. Am J Hum Genet. 2007 Jun;80(6):1055-63. doi: 10.1086/518314. Epub 2007 Apr 23. Am J Hum Genet. 2007. PMID: 17503324 Free PMC article.

2

The children speak: an examination of the quality of life of pediatric cochlear implant users.

Loy B, Warner-Czyz AD, Tong L, Tobey EA, Roland PS. Loy B, et al. Otolaryngol Head Neck Surg. 2010 Feb;142(2):247-53. doi: 10.1016/j.otohns.2009.10.045. Otolaryngol Head Neck Surg. 2010. PMID: 20115983 Free PMC article.

3

Long term speech perception after cochlear implant in pediatric patients with GJB2 mutations.

Yoshida H, Takahashi H, Kanda Y, Usami S. Yoshida H, et al. Auris Nasus Larynx. 2013 Oct;40(5):435-9. doi: 10.1016/j.anl.2013.01.006. Epub 2013 Mar 9. Auris Nasus Larynx. 2013. PMID: 23477838

4

School performance and wellbeing of children with CI in different communicative-educational environments.

Langereis M, Vermeulen A. Langereis M, et al. Int J Pediatr Otorhinolaryngol. 2015 Jun;79(6):834-839. doi: 10.1016/j.ijporl.2015.03.014. Epub 2015 Mar 23. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25840945

5

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.

6

International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.

Liming BJ, Carter J, Cheng A, Choo D, Curotta J, Carvalho D, Germiller JA, Hone S, Kenna MA, Loundon N, Preciado D, Schilder A, Reilly BJ, Roman S, Strychowsky J, Triglia JM, Young N, Smith RJ. Liming BJ, et al. Int J Pediatr Otorhinolaryngol. 2016 Nov;90:251-258. doi: 10.1016/j.ijporl.2016.09.016. Epub 2016 Sep 15. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27729144 Review.

7

Genetic variants in the peripheral auditory system significantly affect adult cochlear implant performance.

Shearer AE, Eppsteiner RW, Frees K, Tejani V, Sloan-Heggen CM, Brown C, Abbas P, Dunn C, Hansen MR, Gantz BJ, Smith RJH. Shearer AE, et al. Hear Res. 2017 May;348:138-142. doi: 10.1016/j.heares.2017.02.008. Epub 2017 Feb 15. Hear Res. 2017. PMID: 28213135 Free PMC article.

8

Predictive Value of GJB2 Mutation Status for Hearing Outcomes of Pediatric Cochlear Implantation.

Abdurehim Y, Lehmann A, Zeitouni AG. Abdurehim Y, et al. Otolaryngol Head Neck Surg. 2017 Jul;157(1):16-24. doi: 10.1177/0194599817697054. Epub 2017 Mar 21. Otolaryngol Head Neck Surg. 2017. PMID: 28322114 Review.

9

The genetic basis of deafness in populations of African descent.

Rudman JR, Kabahuma RI, Bressler SE, Feng Y, Blanton SH, Yan D, Liu XZ. Rudman JR, et al. J Genet Genomics. 2017 Jun 20;44(6):285-294. doi: 10.1016/j.jgg.2017.03.008. Epub 2017 May 6. J Genet Genomics. 2017. PMID: 28642064 Review.

10

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, Smith RJ. Green GE, et al. JAMA. 1999 Jun 16;281(23):2211-6. doi: 10.1001/jama.281.23.2211. JAMA. 1999. PMID: 10376574

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PubMed (Bookshelf cited) for id: 400917

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