Feng Y - Search Results

1

The Advances in Hearing Rehabilitation and Cochlear Implants in China.

Li JN, Chen S, Zhai L, Han DY, Eshraghi AA, Feng Y, Yang SM, Liu XZ. Li JN, et al. Among authors: feng y. Ear Hear. 2017 Nov/Dec;38(6):647-652. doi: 10.1097/AUD.0000000000000441. Ear Hear. 2017. PMID: 28471842 Free PMC article. Review.

2

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

Wang H, Wang X, He C, Li H, Qing J, Grati M, Hu Z, Li J, Hu Y, Xia K, Mei L, Wang X, Yu J, Chen H, Jiang L, Liu Y, Men M, Zhang H, Guan L, Xiao J, Zhang J, Liu X, Feng Y. Wang H, et al. Among authors: feng y. J Hum Genet. 2015 Mar;60(3):119-126. doi: 10.1038/jhg.2014.114. Epub 2015 Jan 15. J Hum Genet. 2015. PMID: 25589040 Free PMC article.

3

A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes.

Tekin D, Yan D, Bademci G, Feng Y, Guo S, Foster J 2nd, Blanton S, Tekin M, Liu X. Tekin D, et al. Among authors: feng y. Hear Res. 2016 Mar;333:179-184. doi: 10.1016/j.heares.2016.01.018. Epub 2016 Feb 2. Hear Res. 2016. PMID: 26850479 Free PMC article.

4

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

Niu Z, Feng Y, Mei L, Sun J, Wang X, Wang J, Hu Z, Dong Y, Chen H, He C, Liu Y, Cai X, Liu X, Jiang L. Niu Z, et al. Among authors: feng y. PLoS One. 2017 May 25;12(5):e0178384. doi: 10.1371/journal.pone.0178384. eCollection 2017. PLoS One. 2017. PMID: 28542515 Free PMC article.

5

The genetic basis of deafness in populations of African descent.

Rudman JR, Kabahuma RI, Bressler SE, Feng Y, Blanton SH, Yan D, Liu XZ. Rudman JR, et al. Among authors: feng y. J Genet Genomics. 2017 Jun 20;44(6):285-294. doi: 10.1016/j.jgg.2017.03.008. Epub 2017 May 6. J Genet Genomics. 2017. PMID: 28642064 Review.

6

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.

Niu Z, Feng Y, Hu Z, Li J, Sun J, Chen H, He C, Wang X, Jiang L, Liu Y, Cai X, Wang L, Cai Y, Liu X, Mei L. Niu Z, et al. Among authors: feng y. Int J Pediatr Otorhinolaryngol. 2017 Sep;100:1-7. doi: 10.1016/j.ijporl.2017.06.008. Epub 2017 Jun 15. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28802351

7

A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss.

Niu Z, Yan D, Bressler S, Mei L, Feng Y, Liu X. Niu Z, et al. Among authors: feng y. Int J Pediatr Otorhinolaryngol. 2018 Jan;104:47-50. doi: 10.1016/j.ijporl.2017.10.040. Epub 2017 Nov 2. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29287879

8

Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.

Shang H, Yan D, Tayebi N, Saeidi K, Sahebalzamani A, Feng Y, Blanton S, Liu X. Shang H, et al. Among authors: feng y. Biomed Res Int. 2018 Jan 15;2018:3103986. doi: 10.1155/2018/3103986. eCollection 2018. Biomed Res Int. 2018. PMID: 29568747 Free PMC article.

9

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss.

Wang L, Feng Y, Yan D, Qin L, Grati M, Mittal R, Li T, Sundhari AK, Liu Y, Chapagain P, Blanton SH, Liao S, Liu X. Wang L, et al. Among authors: feng y. Hum Genet. 2018 Jul;137(6-7):437-446. doi: 10.1007/s00439-018-1895-y. Epub 2018 Jun 2. Hum Genet. 2018. PMID: 29860631 Free PMC article.

10

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review.

Li T, Feng Y, Liu Y, He C, Liu J, Chen H, Deng Y, Li M, Li W, Song J, Niu Z, Sang S, Wen J, Men M, Chen X, Li J, Liu X, Ling J. Li T, et al. Among authors: feng y. Gene. 2019 Jul 1;704:113-120. doi: 10.1016/j.gene.2019.04.008. Epub 2019 Apr 8. Gene. 2019. PMID: 30974196 Review.

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