Oh DY - Search Results

1

Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation.

Lee SY, Joo K, Oh J, Han JH, Park HR, Lee S, Oh DY, Woo SJ, Choi BY. Lee SY, et al. Among authors: oh j, oh dy. Clin Exp Otorhinolaryngol. 2020 May;13(2):113-122. doi: 10.21053/ceo.2019.00990. Epub 2019 Nov 2. Clin Exp Otorhinolaryngol. 2020. PMID: 31674169 Free PMC article.

2

Identification of a Potential Founder Effect of a Novel PDZD7 Variant Involved in Moderate-to-Severe Sensorineural Hearing Loss in Koreans.

Lee SY, Han JH, Kim BJ, Oh SH, Lee S, Oh DY, Choi BY. Lee SY, et al. Among authors: oh sh, oh dy. Int J Mol Sci. 2019 Aug 26;20(17):4174. doi: 10.3390/ijms20174174. Int J Mol Sci. 2019. PMID: 31454969 Free PMC article.

3

Genetic Information and Precision Medicine in Hearing Loss.

Oh DY, Choi BY. Oh DY, et al. Clin Exp Otorhinolaryngol. 2020 Nov;13(4):315-317. doi: 10.21053/ceo.2020.01606. Epub 2020 Nov 1. Clin Exp Otorhinolaryngol. 2020. PMID: 33176397 Free PMC article. No abstract available.

4

Otological aspects of NLRP3-related autoinflammatory disorder focusing on the responsiveness to anakinra.

Kim BJ, Kim YH, Lee S, Han JH, Lee SY, Seong J, Lee DH, Kim B, Park HR, Carandang M, Oh D, Oh SH, Kim JG, Lee S, Choi BY. Kim BJ, et al. Rheumatology (Oxford). 2021 Mar 2;60(3):1523-1532. doi: 10.1093/rheumatology/keaa511. Rheumatology (Oxford). 2021. PMID: 33020839

5

Discovery of MYH14 as an important and unique deafness gene causing prelingually severe autosomal dominant nonsyndromic hearing loss.

Kim BJ, Kim AR, Han JH, Lee C, Oh DY, Choi BY. Kim BJ, et al. Among authors: oh dy. J Gene Med. 2017 Apr;19(4). doi: 10.1002/jgm.2950. J Gene Med. 2017. PMID: 28221712

6

Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness.

Chang MY, Lee C, Han JH, Kim MY, Park HR, Kim N, Park WY, Oh DY, Choi BY. Chang MY, et al. Among authors: oh dy. BMC Med Genet. 2018 Feb 27;19(1):29. doi: 10.1186/s12881-018-0541-9. BMC Med Genet. 2018. PMID: 29482514 Free PMC article.

7

A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study.

Kim BJ, Han JH, Park HR, Kim MY, Kim AR, Oh SH, Park WY, Oh DY, Lee S, Choi BY. Kim BJ, et al. Among authors: oh sh, oh dy. J Gene Med. 2018 Jun;20(6):e3019. doi: 10.1002/jgm.3019. Epub 2018 Apr 30. J Gene Med. 2018. PMID: 29607572

8

Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics.

Kim BJ, Jang JH, Han JH, Park HR, Oh DY, Lee S, Kim MY, Kim AR, Lee C, Kim NKD, Park WY, Choung YH, Choi BY. Kim BJ, et al. Among authors: oh dy. J Transl Med. 2018 Nov 27;16(1):330. doi: 10.1186/s12967-018-1708-z. J Transl Med. 2018. PMID: 30482216 Free PMC article.

9

Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness.

Kim BJ, Kim DK, Han JH, Oh J, Kim AR, Lee C, Kim NK, Park HR, Kim MY, Lee S, Lee S, Oh DY, Park WY, Park S, Choi BY. Kim BJ, et al. Among authors: oh j, oh dy. Hum Mutat. 2019 May;40(5):525-531. doi: 10.1002/humu.23719. Epub 2019 Feb 28. Hum Mutat. 2019. PMID: 30740825 Free PMC article.

10

Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human DIAPH1-related cytoskeletopathy.

Kim BJ, Ueyama T, Miyoshi T, Lee S, Han JH, Park HR, Kim AR, Oh J, Kim MY, Kang YS, Oh DY, Yun J, Hwang SM, Kim NKD, Park WY, Kitajiri SI, Choi BY. Kim BJ, et al. Among authors: oh j, oh dy. J Med Genet. 2019 Dec;56(12):818-827. doi: 10.1136/jmedgenet-2019-106282. Epub 2019 Aug 31. J Med Genet. 2019. PMID: 31473629

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