Chen Y - Search Results

1

A novel MPZL2 c.68delC variant is associated with progressive hearing loss in Chinese population and literature review.

Wang Z, Jiang M, Wu H, Li Y, Chen Y. Wang Z, et al. Among authors: chen y. Laryngoscope Investig Otolaryngol. 2022 May 27;7(3):870-876. doi: 10.1002/lio2.829. eCollection 2022 Jun. Laryngoscope Investig Otolaryngol. 2022. PMID: 35734045 Free PMC article.

2

[Individual management of Meniere's disease and evaluation of functional outcome].

Chen Y, Yang J, Wu H, Huang Q, Wang Z, Zhang Z. Chen Y, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 Aug;25(16):721-5. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 22070076 Chinese.

3

Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss.

Chai Y, Sun L, Pang X, Wang X, Chen D, Chen Y, Wu H, Yang T. Chai Y, et al. Among authors: chen d, chen y. Int J Pediatr Otorhinolaryngol. 2014 Apr;78(4):614-7. doi: 10.1016/j.ijporl.2014.01.011. Epub 2014 Jan 16. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24507663 Free article.

4

Newborn dried blood-spot screening of the p.V37I variant of GJB2 by high-resolution melting analysis.

Chen Y, Li L, Sun LH, Yang T, Wu H. Chen Y, et al. Int J Pediatr Otorhinolaryngol. 2014 Jul;78(7):1080-3. doi: 10.1016/j.ijporl.2014.04.009. Epub 2014 Apr 16. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24814571

5

Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hans.

Pang X, Chai Y, Sun L, Chen D, Chen Y, Zhang Z, Wu H, Yang T. Pang X, et al. Among authors: chen d, chen y. PLoS One. 2014 Jun 19;9(6):e100483. doi: 10.1371/journal.pone.0100483. eCollection 2014. PLoS One. 2014. PMID: 24945352 Free PMC article.

6

P14ARF deficiency and its correlation with overexpression of p53/MDM2 in sporadic vestibular schwannomas.

Chen Y, Wang ZY, Wu H. Chen Y, et al. Eur Arch Otorhinolaryngol. 2015 Sep;272(9):2227-34. doi: 10.1007/s00405-014-3135-y. Epub 2014 Jun 26. Eur Arch Otorhinolaryngol. 2015. PMID: 24964769

7

Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.

Wang ZT, Chen Y, Chen DY, Chai YC, Pang XH, Sun LH, Wang XW, Yang T, Wu H. Wang ZT, et al. Among authors: chen dy, chen y. Int J Pediatr Otorhinolaryngol. 2014 Sep;78(9):1513-6. doi: 10.1016/j.ijporl.2014.06.023. Epub 2014 Jun 23. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25015771

8

Molecular etiology of non-dominant, non-syndromic, mild-to-moderate childhood hearing impairment in Chinese Hans.

Chai Y, Pang X, Chen D, Li L, Chen Y, Sun L, Wang X, Wu H, Yang T. Chai Y, et al. Among authors: chen d, chen y. Am J Med Genet A. 2014 Dec;164A(12):3115-9. doi: 10.1002/ajmg.a.36785. Epub 2014 Sep 23. Am J Med Genet A. 2014. PMID: 25251670

9

Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss.

Chen Y, Wang Z, Wang Z, Chen D, Chai Y, Pang X, Sun L, Wang X, Yang T, Wu H. Chen Y, et al. Among authors: chen d. PLoS One. 2015 May 26;10(5):e0127879. doi: 10.1371/journal.pone.0127879. eCollection 2015. PLoS One. 2015. PMID: 26011067 Free PMC article.

10

Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss.

Chen DY, Zhu WD, Chai YC, Chen Y, Sun L, Yang T, Wu H. Chen DY, et al. Among authors: chen y. Int J Pediatr Otorhinolaryngol. 2015 Oct;79(10):1654-7. doi: 10.1016/j.ijporl.2015.07.008. Epub 2015 Jul 11. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26279247

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