Feng Y - Search Results

1

Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

Mittal R, Patel AP, Nguyen D, Pan DR, Jhaveri VM, Rudman JR, Dharmaraja A, Yan D, Feng Y, Chapagain P, Lee DJ, Blanton SH, Liu XZ. Mittal R, et al. Among authors: feng y. Gene. 2018 Mar 20;647:297-305. doi: 10.1016/j.gene.2018.01.027. Epub 2018 Jan 10. Gene. 2018. PMID: 29331482 Free PMC article. Review.

2

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.

3

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.

Yan D, Tekin D, Bademci G, Foster J 2nd, Cengiz FB, Kannan-Sundhari A, Guo S, Mittal R, Zou B, Grati M, Kabahuma RI, Kameswaran M, Lasisi TJ, Adedeji WA, Lasisi AO, Menendez I, Herrera M, Carranza C, Maroofian R, Crosby AH, Bensaid M, Masmoudi S, Behnam M, Mojarrad M, Feng Y, Duman D, Mawla AM, Nord AS, Blanton SH, Liu XZ, Tekin M. Yan D, et al. Among authors: feng y. Hum Genet. 2016 Aug;135(8):953-61. doi: 10.1007/s00439-016-1697-z. Epub 2016 Jun 25. Hum Genet. 2016. PMID: 27344577 Free PMC article.

4

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.

Cai XZ, Li Y, Xia L, Peng Y, He CF, Jiang L, Feng Y, Xia K, Liu XZ, Mei LY, Hu ZM. Cai XZ, et al. Among authors: feng y. J Hum Genet. 2017 Feb;62(2):317-320. doi: 10.1038/jhg.2016.102. Epub 2016 Aug 18. J Hum Genet. 2017. PMID: 27535032

5

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.

6

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.

7

Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I.

Niu Z, Li J, Tang F, Sun J, Wang X, Jiang L, Mei L, Chen H, Liu Y, Cai X, Feng Y, He C. Niu Z, et al. Among authors: feng y. Gene. 2018 Feb 5;642:362-366. doi: 10.1016/j.gene.2017.11.035. Epub 2017 Nov 20. Gene. 2018. PMID: 29158168

8

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

9

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.

10

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss.

Li W, Sun J, Ling J, Li J, He C, Liu Y, Chen H, Men M, Niu Z, Deng Y, Li M, Li T, Wen J, Sang S, Li H, Wan Z, Richard EM, Chapagain P, Yan D, Liu XZ, Mei L, Feng Y. Li W, et al. Among authors: feng y. Hum Genet. 2018 Apr;137(4):329-342. doi: 10.1007/s00439-018-1885-0. Epub 2018 Apr 30. Hum Genet. 2018. PMID: 29713870

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