PubMed for id: 350931

Year	Number of Results
1998	1
2000	1
2003	3
2004	1
2007	1
2009	1
2010	2
2011	2
2013	3
2014	5
2015	5
2016	4
2017	7
2018	2
2019	2
2020	1
2021	3
2022	2
2023	3
2024	0

1

Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness.

Mustapha M, Salem N, Weil D, el-Zir E, Loiselet J, Petit C. Mustapha M, et al. Eur J Hum Genet. 1998 Nov-Dec;6(6):548-51. doi: 10.1038/sj.ejhg.5200261. Eur J Hum Genet. 1998. PMID: 9887371

2

The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).

Pshennikova VG, Teryutin FM, Cherdonova AM, Borisova TV, Solovyev AV, Romanov GP, Morozov IV, Bondar AA, Posukh OL, Fedorova SA, Barashkov NA. Pshennikova VG, et al. Genes (Basel). 2023 Apr 28;14(5):1001. doi: 10.3390/genes14051001. Genes (Basel). 2023. PMID: 37239361 Free PMC article.

3

Monogenic Causes of Low-Frequency Non-Syndromic Hearing Loss.

Gan NS, Oziębło D, Skarżyński H, Ołdak M. Gan NS, et al. Audiol Neurootol. 2023;28(5):327-337. doi: 10.1159/000529464. Epub 2023 Apr 28. Audiol Neurootol. 2023. PMID: 37121227 Free article. Review.

4

WFS1 autosomal dominant variants linked with hearing loss: update on structural analysis and cochlear implant outcome.

Lim HD, Lee SM, Yun YJ, Lee DH, Lee JH, Oh SH, Lee SY. Lim HD, et al. BMC Med Genomics. 2023 Apr 11;16(1):79. doi: 10.1186/s12920-023-01506-x. BMC Med Genomics. 2023. PMID: 37041640 Free PMC article.

5

Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene.

Riza AL, Alkhzouz C, Farcaș M, Pîrvu A, Miclea D, Mihuț G, Pleșea RM, Ștefan D, Drodar M, Lazăr C, On Behalf Of The Hint Study, On Behalf Of The Fuse Study, Ioana M, Popp R. Riza AL, et al. Genes (Basel). 2022 Dec 26;14(1):69. doi: 10.3390/genes14010069. Genes (Basel). 2022. PMID: 36672810 Free PMC article.

6

Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss.

Xiang Y, Xu C, Xu Y, Zhou L, Tang S, Xu X. Xiang Y, et al. J Clin Lab Anal. 2022 Nov;36(11):e24708. doi: 10.1002/jcla.24708. Epub 2022 Sep 26. J Clin Lab Anal. 2022. PMID: 36164746 Free PMC article.

7

Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population.

Al-Janabi AM, Ahmmed HS, Al-Khafaji SM. Al-Janabi AM, et al. J Med Life. 2021 Nov-Dec;14(6):841-846. doi: 10.25122/jml-2021-0152. J Med Life. 2021. PMID: 35126756 Free PMC article.

8

Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.

Van Heurck R, Carminho-Rodrigues MT, Ranza E, Stafuzza C, Quteineh L, Gehrig C, Hammar E, Guipponi M, Abramowicz M, Senn P, Guinand N, Cao-Van H, Paoloni-Giacobino A. Van Heurck R, et al. Genes (Basel). 2021 Aug 20;12(8):1277. doi: 10.3390/genes12081277. Genes (Basel). 2021. PMID: 34440452 Free PMC article.

9

[Application value of high-throughput gene copy number variation detection in the diagnosis of enlarged vestibular aqueduct].

Liu YL, Wang LL, Wen J, Mei LY, He CF, Jiang L, Feng Y. Liu YL, et al. Zhonghua Yi Xue Za Zhi. 2021 Jan 12;101(2):103-107. doi: 10.3760/cma.j.cn112137-20201010-02794. Zhonghua Yi Xue Za Zhi. 2021. PMID: 33455124 Chinese.

10

[Analysis of MYO15A variation in children with DFNB3].

Ren SM, Wu QH, Jiao ZH, Chen YB, Chen C, Kong XD, Qin ZB. Ren SM, et al. Zhonghua Er Ke Za Zhi. 2020 Oct 2;58(10):818-823. doi: 10.3760/cma.j.cn112140-20200220-00115. Zhonghua Er Ke Za Zhi. 2020. PMID: 32987461 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

45 results

Results by year