PubMed for id: 355180

Year	Number of Results
1998	1
2003	1
2004	4
2005	3
2008	1
2009	4
2010	2
2011	4
2012	3
2013	2
2014	1
2015	3
2016	3
2017	1
2019	1
2020	1
2021	6
2022	6
2023	0

1

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

Greinwald JH Jr, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ. Greinwald JH Jr, et al. Am J Med Genet. 1998 Jun 30;78(2):107-13. Am J Med Genet. 1998. PMID: 9674898

2

Genomic organization and expression analysis of the murine Fam3c gene.

Pilipenko VV, Reece A, Choo DI, Greinwald JH Jr. Pilipenko VV, et al. Gene. 2004 Jun 23;335:159-68. doi: 10.1016/j.gene.2004.03.026. Gene. 2004. PMID: 15194199

3

Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts.

Nakano A, Arimoto Y, Mutai H, Nara K, Inoue S, Matsunaga T. Nakano A, et al. Int J Pediatr Otorhinolaryngol. 2022 Jan;152:110975. doi: 10.1016/j.ijporl.2021.110975. Epub 2021 Nov 14. Int J Pediatr Otorhinolaryngol. 2022. PMID: 34801268

4

Crystallographic modeling of the PNPT1:c.1453A>G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical features.

Hosseini Bereshneh A, Rezaei Z, Jafarinia E, Rajabi F, Ashrafi MR, Tavasoli AR, Garshasbi M. Hosseini Bereshneh A, et al. Mitochondrion. 2021 Jul;59:1-7. doi: 10.1016/j.mito.2021.03.012. Epub 2021 Apr 1. Mitochondrion. 2021. PMID: 33812062

5

Spectrum of MYO7A Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous Mutations.

Kabahuma RI, Schubert WD, Labuschagne C, Yan D, Blanton SH, Pepper MS, Liu XZ. Kabahuma RI, et al. Genes (Basel). 2021 Feb 15;12(2):274. doi: 10.3390/genes12020274. Genes (Basel). 2021. PMID: 33671976 Free PMC article.

6

Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families.

Liu Y, Wen J, Sang S, Mei L, He C, Jiang L, Huang S, Feng Y. Liu Y, et al. Eur Arch Otorhinolaryngol. 2020 Dec;277(12):3331-3339. doi: 10.1007/s00405-020-06050-3. Epub 2020 May 23. Eur Arch Otorhinolaryngol. 2020. PMID: 32447495

7

Advances in genetic hearing loss: CIB2 gene.

Jacoszek A, Pollak A, Płoski R, Ołdak M. Jacoszek A, et al. Eur Arch Otorhinolaryngol. 2017 Apr;274(4):1791-1795. doi: 10.1007/s00405-016-4330-9. Epub 2016 Oct 22. Eur Arch Otorhinolaryngol. 2017. PMID: 27771768 Free PMC article. Review.

8

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.

Nayak G, Varga L, Trincot C, Shahzad M, Friedman PL, Klimes I, Greinwald JH Jr, Riazuddin SA, Masindova I, Profant M, Khan SN, Friedman TB, Ahmed ZM, Gasperikova D, Riazuddin S, Riazuddin S. Nayak G, et al. Hum Genet. 2015 Apr;134(4):423-37. doi: 10.1007/s00439-015-1532-y. Epub 2015 Feb 10. Hum Genet. 2015. PMID: 25666562 Free PMC article.

9

[The clinical application of gene chips combined with CT examination in the diagnosis of large vestibular aqueduct syndrome patients].

Zhou F, Lin Y, Luo Q, Chen X, Huang L, Liang Z, Wang H, Yu F. Zhou F, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Oct;27(19):1073-5. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24417166 Chinese.

10

Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.

Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C. Delmaghani S, et al. Hum Mol Genet. 2012 Sep 1;21(17):3835-44. doi: 10.1093/hmg/dds212. Epub 2012 Jun 7. Hum Mol Genet. 2012. PMID: 22678063

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