Kim AR - Search Results

1

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.

Kim BJ, Kim AR, Lee C, Kim SY, Kim NK, Chang MY, Rhee J, Park MH, Koo SK, Kim MY, Han JH, Oh SH, Park WY, Choi BY. Kim BJ, et al. Among authors: kim ar, kim sy, kim my, kim nk. PLoS One. 2016 Oct 28;11(10):e0165680. doi: 10.1371/journal.pone.0165680. eCollection 2016. PLoS One. 2016. PMID: 27792758 Free PMC article.

2

Destabilization and mislocalization of POU3F4 by C-terminal frameshift truncation and extension mutation.

Choi BY, Kim DH, Chung T, Chang M, Kim EH, Kim AR, Seok J, Chang SO, Bok J, Kim D, Oh SH, Park WY. Choi BY, et al. Among authors: kim ar, kim eh, kim dh, kim d. Hum Mutat. 2013 Feb;34(2):309-16. doi: 10.1002/humu.22232. Epub 2012 Oct 17. Hum Mutat. 2013. PMID: 23076972

3

Audiological and surgical evidence for the presence of a third window effect for the conductive hearing loss in DFNX2 deafness irrespective of types of mutations.

Choi BY, An YH, Park JH, Jang JH, Chung HC, Kim AR, Lee JH, Kim CS, Oh SH, Chang SO. Choi BY, et al. Among authors: kim cs, kim ar. Eur Arch Otorhinolaryngol. 2013 Nov;270(12):3057-62. doi: 10.1007/s00405-013-2386-3. Epub 2013 Feb 12. Eur Arch Otorhinolaryngol. 2013. PMID: 23400403

4

Clinical characteristics of patients with narrow bony cochlear nerve canal: is the bilateral case just a duplicate of the unilateral case?

Cho SW, Kang SI, Park SJ, Kim AR, Koo JW, Kim CS, Lee JH, Chang SO, Oh SH, Choi BY. Cho SW, et al. Among authors: kim cs, kim ar. Laryngoscope. 2013 Aug;123(8):1996-2000. doi: 10.1002/lary.23998. Epub 2013 Feb 16. Laryngoscope. 2013. PMID: 23417507

5

Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family.

Park G, Gim J, Kim AR, Han KH, Kim HS, Oh SH, Park T, Park WY, Choi BY. Park G, et al. Among authors: kim ar, kim hs. BMC Genomics. 2013 Mar 18;14:191. doi: 10.1186/1471-2164-14-191. BMC Genomics. 2013. PMID: 23506231 Free PMC article.

6

Prevalence of p.V37I variant of GJB2 in mild or moderate hearing loss in a pediatric population and the interpretation of its pathogenicity.

Kim SY, Park G, Han KH, Kim A, Koo JW, Chang SO, Oh SH, Park WY, Choi BY. Kim SY, et al. PLoS One. 2013 Apr 25;8(4):e61592. doi: 10.1371/journal.pone.0061592. Print 2013. PLoS One. 2013. PMID: 23637863 Free PMC article.

7

Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss.

Choi BY, Park G, Gim J, Kim AR, Kim BJ, Kim HS, Park JH, Park T, Oh SH, Han KH, Park WY. Choi BY, et al. Among authors: kim ar, kim bj, kim hs. PLoS One. 2013 Aug 22;8(8):e68692. doi: 10.1371/journal.pone.0068692. eCollection 2013. PLoS One. 2013. PMID: 23990876 Free PMC article.

8

A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation.

Chung J, Park SM, Chang SO, Chung T, Lee KY, Kim AR, Park JH, Kim V, Park WY, Oh SH, Kim D, Park WJ, Choi BY. Chung J, et al. Among authors: kim v, kim ar, kim d. J Mol Med (Berl). 2014 Jun;92(6):651-63. doi: 10.1007/s00109-014-1128-3. Epub 2014 Feb 15. J Mol Med (Berl). 2014. PMID: 24526180

9

De novo large genomic deletions involving POU3F4 in incomplete partition type III inner ear anomaly in East Asian populations and implications for genetic counseling.

Choi JW, Min B, Kim A, Koo JW, Kim CS, Park WY, Chung J, Kim V, Ryu YJ, Kim SH, Chang SO, Oh SH, Choi BY. Choi JW, et al. Otol Neurotol. 2015 Jan;36(1):184-90. doi: 10.1097/MAO.0000000000000343. Otol Neurotol. 2015. PMID: 24608376

10

Identification of a novel splice site variant of OTOF in the Korean nonsyndromic hearing loss population with low prevalence of the OTOF mutations.

Jin YJ, Park J, Kim AR, Rah YC, Choi BY. Jin YJ, et al. Among authors: kim ar. Int J Pediatr Otorhinolaryngol. 2014 Jul;78(7):1030-5. doi: 10.1016/j.ijporl.2014.03.033. Epub 2014 Apr 24. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24814232

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