PubMed for id: 341854

Year	Number of Results
2004	2
2005	1
2009	1
2012	1
2014	1
2015	1
2017	1
2021	1
2022	2
2023	2
2024	0

1

DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22.

Ansar M, Chahrour MH, Amin Ud Din M, Arshad M, Haque S, Pham TL, Yan K, Ahmad W, Leal SM. Ansar M, et al. Hum Hered. 2004;57(4):195-9. doi: 10.1159/000081446. Hum Hered. 2004. PMID: 15583425 Free PMC article.

2

Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions.

Achard S, Campion M, Parodi M, MacAskill M, Hochet B, Simon F, Rouillon I, Jonard L, Serey-Gaut M, Denoyelle F, Loundon N, Marlin S. Achard S, et al. Otol Neurotol. 2023 Apr 1;44(4):e241-e245. doi: 10.1097/MAO.0000000000003825. Epub 2023 Feb 10. Otol Neurotol. 2023. PMID: 36764706

3

[Correlation of temporal bone HRCT, SLC26A4 gene and hearing loss in enlarged vestibular aqueduct].

Zhao Z, Zhu Y, Fu Y, Jiang H. Zhao Z, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022 Oct;36(10):736-740. doi: 10.13201/j.issn.2096-7993.2022.10.002. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022. PMID: 36217650 Free PMC article. Chinese.

4

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.

5

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.

6

Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.

Olsson KS, Wålinder O, Jansson U, Wilbe M, Bondeson ML, Stattin EL, Raha-Chowdhury R, Williams R. Olsson KS, et al. Hereditas. 2017 Dec 19;154:16. doi: 10.1186/s41065-017-0052-2. eCollection 2017. Hereditas. 2017. PMID: 29270100 Free PMC article.

7

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Riazuddin S, Belyantseva IA, Giese AP, Lee K, Indzhykulian AA, Nandamuri SP, Yousaf R, Sinha GP, Lee S, Terrell D, Hegde RS, Ali RA, Anwar S, Andrade-Elizondo PB, Sirmaci A, Parise LV, Basit S, Wali A, Ayub M, Ansar M, Ahmad W, Khan SN, Akram J, Tekin M, Riazuddin S, Cook T, Buschbeck EK, Frolenkov GI, Leal SM, Friedman TB, Ahmed ZM. Riazuddin S, et al. Nat Genet. 2012 Nov;44(11):1265-71. doi: 10.1038/ng.2426. Epub 2012 Sep 30. Nat Genet. 2012. PMID: 23023331 Free PMC article.

8

Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients With Enlarged Vestibular Aqueduct or GJB2 Mutation.

Jahn KN, Morse-Fortier C, Griffin AM, Faller D, Cohen MS, Kenna MA, Doney E, Arenberg JG. Jahn KN, et al. Otol Neurotol. 2023 Jun 1;44(5):e273-e280. doi: 10.1097/MAO.0000000000003879. Otol Neurotol. 2023. PMID: 37167444

9

Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss.

Gao X, Huang SS, Yuan YY, Wang GJ, Xu JC, Ji YB, Han MY, Yu F, Kang DY, Lin X, Dai P. Gao X, et al. Am J Med Genet A. 2015 Oct;167A(10):2357-65. doi: 10.1002/ajmg.a.37206. Epub 2015 Jun 16. Am J Med Genet A. 2015. PMID: 26079994 Free PMC article.

10

Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.

Santos-Cortez RL, Lee K, Giese AP, Ansar M, Amin-Ud-Din M, Rehn K, Wang X, Aziz A, Chiu I, Hussain Ali R, Smith JD; University of Washington Center for Mendelian Genomics; Shendure J, Bamshad M, Nickerson DA, Ahmed ZM, Ahmad W, Riazuddin S, Leal SM. Santos-Cortez RL, et al. Hum Mol Genet. 2014 Jun 15;23(12):3289-98. doi: 10.1093/hmg/ddu042. Epub 2014 Jan 29. Hum Mol Genet. 2014. PMID: 24482543 Free PMC article.

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