Park HJ - Search Results

1

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.

Woo HM, Park HJ, Park MH, Kim BY, Shin JW, Yoo WG, Koo SK. Woo HM, et al. Among authors: park mh, park hj. BMC Med Genet. 2014 Apr 28;15:46. doi: 10.1186/1471-2350-15-46. BMC Med Genet. 2014. PMID: 24767429 Free PMC article.

2

Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss.

Bae JW, Lee KY, Choi SY, Lee SH, Park HJ, Kim UK. Bae JW, et al. Among authors: park hj. Int J Mol Med. 2008 Aug;22(2):175-80. Int J Mol Med. 2008. PMID: 18636170

3

Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population.

Han SH, Park HJ, Kang EJ, Ryu JS, Lee A, Yang YH, Lee KR. Han SH, et al. Among authors: park hj. J Hum Genet. 2008;53(11-12):1022-1028. doi: 10.1007/s10038-008-0342-7. Epub 2008 Dec 2. J Hum Genet. 2008. PMID: 19043807

4

Evidence for a founder mutation causing DFNA5 hearing loss in East Asians.

Park HJ, Cho HJ, Baek JI, Ben-Yosef T, Kwon TJ, Griffith AJ, Kim UK. Park HJ, et al. J Hum Genet. 2010 Jan;55(1):59-62. doi: 10.1038/jhg.2009.114. Epub 2009 Nov 13. J Hum Genet. 2010. PMID: 19911014 Free PMC article.

5

Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage.

Park MH, Park HJ, Kim KJ, Woo HM, Kim HJ, Lee JY, Park HY, Koo SK. Park MH, et al. Among authors: park hy, park hj. Genes Genet Syst. 2011;86(2):117-21. doi: 10.1266/ggs.86.117. Genes Genet Syst. 2011. PMID: 21670551 Free article.

6

Genetic Screening of GJB2 and SLC26A4 in Korean Cochlear Implantees: Experience of Soree Ear Clinic.

Shin JW, Lee SC, Lee HK, Park HJ. Shin JW, et al. Among authors: park hj. Clin Exp Otorhinolaryngol. 2012 Apr;5 Suppl 1(Suppl 1):S10-3. doi: 10.3342/ceo.2012.5.S1.S10. Epub 2012 Apr 30. Clin Exp Otorhinolaryngol. 2012. PMID: 22701767 Free PMC article.

7

Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.

Bae JW, Kim DB, Choi JY, Park HJ, Lee JD, Hur DG, Bae SH, Jung DJ, Lee SH, Kim UK, Lee KY. Bae JW, et al. Among authors: park hj. PLoS One. 2012;7(8):e42463. doi: 10.1371/journal.pone.0042463. Epub 2012 Aug 6. PLoS One. 2012. PMID: 22879993 Free PMC article.

8

A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing loss.

Kim Y, Kim HR, Kim J, Shin JW, Park HJ, Choi JY, Kim UK, Lee KA. Kim Y, et al. Among authors: park hj. Biochem Biophys Res Commun. 2013 Jan 18;430(3):1147-50. doi: 10.1016/j.bbrc.2012.12.022. Epub 2012 Dec 14. Biochem Biophys Res Commun. 2013. PMID: 23246836

9

Limitations of hearing screening in newborns with PDS mutations.

Kim BG, Shin JW, Park HJ, Kim JM, Kim UK, Choi JY. Kim BG, et al. Among authors: park hj. Int J Pediatr Otorhinolaryngol. 2013 May;77(5):833-7. doi: 10.1016/j.ijporl.2013.02.023. Epub 2013 Mar 21. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23523376

10

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.

Woo HM, Park HJ, Baek JI, Park MH, Kim UK, Sagong B, Koo SK. Woo HM, et al. Among authors: park mh, park hj. BMC Med Genet. 2013 Jul 17;14:72. doi: 10.1186/1471-2350-14-72. BMC Med Genet. 2013. PMID: 23865914 Free PMC article.

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