PubMed for id: 377905

Year	Number of Results
1976	1
1981	1
1987	2
1989	1
1992	1
1995	1
1997	3
1998	1
1999	1
2000	2
2001	2
2002	2
2003	2
2004	1
2005	1
2007	1
2008	2
2009	2
2010	3
2012	4
2013	3
2014	1
2016	1
2017	5
2018	2
2019	1
2020	3
2022	1
2024	0

1

A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred.

Häfner FM, Salam AA, Linder TE, Balmer D, Baumer A, Schinzel AA, Spillmann T, Leal SM. Häfner FM, et al. Am J Hum Genet. 2000 Apr;66(4):1437-42. doi: 10.1086/302865. Epub 2000 Mar 17. Am J Hum Genet. 2000. PMID: 10739769 Free PMC article.

2

MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family.

Zeraatpisheh Z, Sichani AS, Kamal N, Khamirani HJ, Zoghi S, Ehsani E, Mohammadi S, Tabei SS, Dastgheib SA, Bagher Tabei SM, Dianatpour M. Zeraatpisheh Z, et al. J Genet. 2022;101:24. J Genet. 2022. PMID: 35652205 Free article.

3

Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families.

Bai X, Zhang F, Xiao Y, Jin Y, Zheng Q, Wang H, Xu L. Bai X, et al. J Cell Mol Med. 2020 Jun;24(12):6978-6987. doi: 10.1111/jcmm.15359. Epub 2020 May 11. J Cell Mol Med. 2020. PMID: 32390314 Free PMC article.

4

A Novel PAX3 Mutation in a Chinese Family with Waardenburg Syndrome Type 1.

Li S, Guo M, Ruan B, Liu Y, Cui X, Han W, Li R. Li S, et al. Genet Test Mol Biomarkers. 2020 May;24(5):249-255. doi: 10.1089/gtmb.2019.0231. Epub 2020 Apr 3. Genet Test Mol Biomarkers. 2020. PMID: 32250160

5

First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding Cochlin.

Basu A, Boczek NJ, Robertson NG, Nasr SH, Jethanamest D, McPhail ED, Kurtin PJ, Dasari S, Butz M, Morton CC, Highsmith WE, Zhou F. Basu A, et al. Head Neck Pathol. 2020 Sep;14(3):808-816. doi: 10.1007/s12105-019-01073-7. Epub 2019 Sep 6. Head Neck Pathol. 2020. PMID: 31493294 Free PMC article.

6

Clinical presentation of rapidly progressive familial Danish dementia.

Zhou Z, Ainger TJ, Han DY. Zhou Z, et al. Neurocase. 2018 Oct-Dec;24(5-6):287-289. doi: 10.1080/13554794.2019.1590603. Epub 2019 Mar 7. Neurocase. 2018. PMID: 30843473

7

[Autosomal dominant hearing loss resulting from mutation in the GJB2 gene:nonsyndromic presentation in a Chinese family].

Dai X, Li J, Hu XJ, Tong J, Cai WQ. Dai X, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Dec;30(24):1939-1941;1945. doi: 10.13201/j.issn.1001-1781.2016.24.009. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016. PMID: 29798269 Chinese.

8

MYH9: Structure, functions and role of non-muscle myosin IIA in human disease.

Pecci A, Ma X, Savoia A, Adelstein RS. Pecci A, et al. Gene. 2018 Jul 20;664:152-167. doi: 10.1016/j.gene.2018.04.048. Epub 2018 Apr 19. Gene. 2018. PMID: 29679756 Free PMC article. Review.

9

The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese population.

Huang S, Huang B, Wang G, Kang DY, Zhang X, Meng X, Dai P. Huang S, et al. Int J Pediatr Otorhinolaryngol. 2017 Nov;102:67-70. doi: 10.1016/j.ijporl.2017.09.001. Epub 2017 Sep 7. Int J Pediatr Otorhinolaryngol. 2017. PMID: 29106878

10

STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic.

Plevova P, Paprskarova M, Tvrda P, Turska P, Slavkovsky R, Mrazkova E. Plevova P, et al. Otol Neurotol. 2017 Dec;38(10):e393-e400. doi: 10.1097/MAO.0000000000001571. Otol Neurotol. 2017. PMID: 28984810

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