Koo SK - 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: koo sk. 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

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: koo sk. BMC Med Genet. 2014 Apr 28;15:46. doi: 10.1186/1471-2350-15-46. BMC Med Genet. 2014. PMID: 24767429 Free PMC article.

3

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

4

Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data.

Kim BY, Park JH, Jo HY, Koo SK, Park MH. Kim BY, et al. Among authors: koo sk. PLoS One. 2017 Aug 9;12(8):e0182272. doi: 10.1371/journal.pone.0182272. eCollection 2017. PLoS One. 2017. PMID: 28792971 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: koo sk. Genes Genet Syst. 2011;86(2):117-21. doi: 10.1266/ggs.86.117. Genes Genet Syst. 2011. PMID: 21670551 Free article.

6

KMD: Korean Mutation Database for genes related to diseases.

Park MH, Koo SK, Lee JS, Yoo HW, Kim JW, Cheong HI, Park HY. Park MH, et al. Among authors: koo sk. Hum Mutat. 2012 Apr;33(4):E2332-40. doi: 10.1002/humu.22039. Hum Mutat. 2012. PMID: 22323337

7

Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing.

Park MH, Rhee H, Park JH, Woo HM, Choi BO, Kim BY, Chung KW, Cho YB, Kim HJ, Jung JW, Koo SK. Park MH, et al. Among authors: koo sk. PLoS One. 2014 Jan 29;9(1):e86664. doi: 10.1371/journal.pone.0086664. eCollection 2014. PLoS One. 2014. PMID: 24489763 Free PMC article.

8

Patterns of gene expression associated with Pten deficiency in the developing inner ear.

Kim HJ, Ryu J, Woo HM, Cho SS, Sung MK, Kim SC, Park MH, Park T, Koo SK. Kim HJ, et al. Among authors: koo sk. PLoS One. 2014 Jun 3;9(6):e97544. doi: 10.1371/journal.pone.0097544. eCollection 2014. PLoS One. 2014. PMID: 24893171 Free PMC article.

9

Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing.

Kim BY, Park MH, Woo HM, Jo HY, Kim JH, Choi HJ, Koo SK. Kim BY, et al. Among authors: koo sk. BMC Med Genet. 2017 Oct 2;18(1):106. doi: 10.1186/s12881-017-0465-9. BMC Med Genet. 2017. PMID: 28969599 Free PMC article.

10

Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation.

Kim BY, Ko JM, Park MH, Koo SK. Kim BY, et al. Among authors: koo sk. Stem Cell Res. 2019 Dec;41:101622. doi: 10.1016/j.scr.2019.101622. Epub 2019 Oct 25. Stem Cell Res. 2019. PMID: 31715426 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

95 results

Search Page

Filters