Chai Y - Search Results

1

Impact of inner ear malformation and cochlear nerve deficiency on the development of auditory-language network in children with profound sensorineural hearing loss.

Wang Y, Jiang M, Zhu Y, Xue L, Shu W, Li X, Chen H, Li Y, Chen Y, Chai Y, Zhang Y, Chu Y, Song Y, Tao X, Wang Z, Wu H. Wang Y, et al. Among authors: chai y. Elife. 2023 Sep 12;12:e85983. doi: 10.7554/eLife.85983. Elife. 2023. PMID: 37697742 Free PMC article.

2

Genotype-phenotype correlation of two prevalent GJB2 mutations in Chinese newborn infants ascertained from the Universal Newborn Hearing Screening Program.

Ma Y, Yang T, Li Y, Tao Z, Huang Z, Li X, Chai Y, Ouyang Z, Shen X, Wu H. Ma Y, et al. Among authors: chai y. Am J Med Genet A. 2010 Nov;152A(11):2912-5. doi: 10.1002/ajmg.a.33698. Am J Med Genet A. 2010. PMID: 20954238 No abstract available.

3

Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening.

Lü J, Huang Z, Yang T, Li Y, Mei L, Xiang M, Chai Y, Li X, Li L, Yao G, Wang Y, Shen X, Wu H. Lü J, et al. Among authors: chai y. Int J Pediatr Otorhinolaryngol. 2011 Aug;75(8):1045-9. doi: 10.1016/j.ijporl.2011.05.022. Epub 2011 Jun 25. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21705096

4

Novel mutations in ATP6V0A4 are associated with atypical progressive sensorineural hearing loss in a Chinese patient with distal renal tubular acidosis.

Li X, Chai Y, Tao Z, Li L, Huang Z, Li Y, Wu H, Yang T. Li X, et al. Among authors: chai y. Int J Pediatr Otorhinolaryngol. 2012 Jan;76(1):152-4. doi: 10.1016/j.ijporl.2011.10.017. Epub 2011 Nov 16. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22093743

5

Double heterozygous mutations of MITF and PAX3 result in Waardenburg syndrome with increased penetrance in pigmentary defects.

Yang T, Li X, Huang Q, Li L, Chai Y, Sun L, Wang X, Zhu Y, Wang Z, Huang Z, Li Y, Wu H. Yang T, et al. Among authors: chai y. Clin Genet. 2013 Jan;83(1):78-82. doi: 10.1111/j.1399-0004.2012.01853.x. Epub 2012 Mar 5. Clin Genet. 2013. PMID: 22320238

6

The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

Li L, Lu J, Tao Z, Huang Q, Chai Y, Li X, Huang Z, Li Y, Xiang M, Yang J, Yao G, Wang Y, Yang T, Wu H. Li L, et al. Among authors: chai y. PLoS One. 2012;7(5):e36621. doi: 10.1371/journal.pone.0036621. Epub 2012 May 4. PLoS One. 2012. PMID: 22574200 Free PMC article.

7

[Prenatal screening and diagnosis of genetic deafness by microarray].

Sun LH, Li L, Wang XW, Zhu YZ, Chai YC, Li XH, Wu H, Yang T. Sun LH, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Dec;47(12):991-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23328038 Chinese.

8

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.

Yang T, Wei X, Chai Y, Li L, Wu H. Yang T, et al. Among authors: chai y. Orphanet J Rare Dis. 2013 Jun 14;8:85. doi: 10.1186/1750-1172-8-85. Orphanet J Rare Dis. 2013. PMID: 23767834 Free PMC article.

9

Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China.

Chai Y, Huang Z, Tao Z, Li X, Li L, Li Y, Wu H, Yang T. Chai Y, et al. Am J Med Genet A. 2013 Sep;161A(9):2226-33. doi: 10.1002/ajmg.a.36068. Epub 2013 Aug 5. Am J Med Genet A. 2013. PMID: 23918157

10

Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family.

Chen DY, Chai YC, Yang T, Wu H. Chen DY, et al. Int J Pediatr Otorhinolaryngol. 2013 Oct;77(10):1711-5. doi: 10.1016/j.ijporl.2013.07.031. Epub 2013 Aug 9. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23993205

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