Sagong B - Search Results

1

Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans.

Ryu N, Sagong B, Park HJ, Kim MA, Lee KY, Choi JY, Kim UK. Ryu N, et al. Among authors: sagong b. BMC Med Genet. 2016 Jan 22;17:6. doi: 10.1186/s12881-016-0269-3. BMC Med Genet. 2016. PMID: 26797701 Free PMC article.

2

Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

Sagong B, Park R, Kim YH, Lee KY, Baek JI, Cho HJ, Cho IJ, Kim UK, Lee SH. Sagong B, et al. Ann Clin Lab Sci. 2010 Fall;40(4):380-5. Ann Clin Lab Sci. 2010. PMID: 20947814

3

Identification and functional characterization of novel compound heterozygotic mutations in the TECTA gene.

Sagong B, Park HJ, Lee KY, Kim UK. Sagong B, et al. Gene. 2012 Jan 15;492(1):239-43. doi: 10.1016/j.gene.2011.10.022. Epub 2011 Oct 20. Gene. 2012. PMID: 22037481

4

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.

Sagong B, Seok JH, Kwon TJ, Kim UK, Lee SH, Lee KY. Sagong B, et al. Gene. 2012 Oct 15;508(1):135-9. doi: 10.1016/j.gene.2012.07.033. Epub 2012 Aug 4. Gene. 2012. PMID: 22884721

5

A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population.

Sagong B, Baek JI, Oh SK, Na KJ, Bae JW, Choi SY, Jeong JY, Choi JY, Lee SH, Lee KY, Kim UK. Sagong B, et al. PLoS One. 2013;8(3):e57237. doi: 10.1371/journal.pone.0057237. Epub 2013 Mar 1. PLoS One. 2013. PMID: 23469187 Free PMC article.

6

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: sagong b. BMC Med Genet. 2013 Jul 17;14:72. doi: 10.1186/1471-2350-14-72. BMC Med Genet. 2013. PMID: 23865914 Free PMC article.

7

Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss.

Kim MA, Kim YR, Sagong B, Cho HJ, Bae JW, Kim J, Lee J, Park HJ, Choi JY, Lee KY, Kim UK. Kim MA, et al. Among authors: sagong b. PLoS One. 2014 Apr 21;9(4):e95646. doi: 10.1371/journal.pone.0095646. eCollection 2014. PLoS One. 2014. PMID: 24752540 Free PMC article.

8

Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.

Kim YR, Kim MA, Sagong B, Bae SH, Lee HJ, Kim HJ, Choi JY, Lee KY, Kim UK. Kim YR, et al. Among authors: sagong b. PLoS One. 2015 Mar 17;10(3):e0119443. doi: 10.1371/journal.pone.0119443. eCollection 2015. PLoS One. 2015. PMID: 25781927 Free PMC article.

9

Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss.

Sagong B, Baek JI, Bok J, Lee KY, Kim UK. Sagong B, et al. Int J Pediatr Otorhinolaryngol. 2016 Jan;80:78-81. doi: 10.1016/j.ijporl.2015.11.018. Epub 2015 Nov 23. Int J Pediatr Otorhinolaryngol. 2016. PMID: 26746617

10

Genetic association of MYH genes with hereditary hearing loss in Korea.

Kim SJ, Lee S, Park HJ, Kang TH, Sagong B, Baek JI, Oh SK, Choi JY, Lee KY, Kim UK. Kim SJ, et al. Among authors: sagong b. Gene. 2016 Oct 10;591(1):177-182. doi: 10.1016/j.gene.2016.07.011. Epub 2016 Jul 5. Gene. 2016. PMID: 27393652

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