Joo Sun Y[au] - Search Results

Year	Number of Results
2007	2
2008	5
2009	2
2011	1
2014	1
2015	2
2016	3
2017	1
2018	2
2019	2
2020	1
2021	4
2022	7
2023	4
2024	5

1

Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.

Han JH, Bae SH, Joo SY, Kim JA, Kim SJ, Jang SH, Won D, Gee HY, Choi JY, Jung J, Kim SH. Han JH, et al. J Clin Med. 2024 Mar 29;13(7):2001. doi: 10.3390/jcm13072001. J Clin Med. 2024. PMID: 38610765 Free PMC article.

2

Overlooked KCNQ4 variants augment the risk of hearing loss.

Oh KS, Roh JW, Joo SY, Ryu K, Kim JA, Kim SJ, Jang SH, Koh YI, Kim DH, Kim HY, Choi M, Jung J, Namkung W, Nam JH, Choi JY, Gee HY. Oh KS, et al. Exp Mol Med. 2023 Apr;55(4):844-859. doi: 10.1038/s12276-023-00976-4. Epub 2023 Apr 3. Exp Mol Med. 2023. PMID: 37009795 Free PMC article.

3

OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin.

Koh YI, Oh KS, Kim JA, Noh B, Choi HJ, Joo SY, Rim JH, Kim HY, Kim DY, Yu S, Kim DH, Lee SG, Jung J, Choi JY, Gee HY. Koh YI, et al. Autophagy. 2022 Nov;18(11):2593-2614. doi: 10.1080/15548627.2022.2040891. Epub 2022 Mar 6. Autophagy. 2022. PMID: 35253614 Free PMC article.

4

Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.

Joo SY, Jang SH, Kim JA, Kim SJ, Kim B, Kim HY, Choi JY, Gee HY, Jung J. Joo SY, et al. J Korean Med Sci. 2023 Dec 11;38(48):e355. doi: 10.3346/jkms.2023.38.e355. J Korean Med Sci. 2023. PMID: 38084023 Free PMC article.

5

Trampoline-related fractures of the proximal tibia in children.

Jeong C, Lee SU, Kim HG, Joo SY. Jeong C, et al. J Orthop Surg Res. 2021 Sep 8;16(1):551. doi: 10.1186/s13018-021-02707-9. J Orthop Surg Res. 2021. PMID: 34496913 Free PMC article.

6

COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype study.

Oh KS, Walls D, Joo SY, Kim JA, Yoo JE, Koh YI, Kim DH, Rim JH, Choi HJ, Kim HY, Yu S, Smith RJ, Choi JY, Gee HY, Jung J. Oh KS, et al. Hum Genet. 2022 Apr;141(3-4):889-901. doi: 10.1007/s00439-021-02368-y. Epub 2021 Sep 16. Hum Genet. 2022. PMID: 34529116 Free PMC article.

7

Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss.

Kang M, Kim JA, Song MH, Joo SY, Kim SJ, Jang SH, Lee H, Seong JK, Choi JY, Gee HY, Jung J. Kang M, et al. Cells. 2023 Sep 21;12(18):2328. doi: 10.3390/cells12182328. Cells. 2023. PMID: 37759551 Free PMC article.

8

Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains.

Joo SY, Na G, Kim JA, Yoo JE, Kim DH, Kim SJ, Jang SH, Yu S, Kim HY, Choi JY, Gee HY, Jung J. Joo SY, et al. Biomedicines. 2022 Mar 29;10(4):798. doi: 10.3390/biomedicines10040798. Biomedicines. 2022. PMID: 35453549 Free PMC article.

9

Identification of highly potent and selective HTRA1 inhibitors.

Dennis DG, Joo Sun Y, Parsons DE, Mahajan VB, Smith M. Dennis DG, et al. Among authors: joo sun y. Bioorg Med Chem Lett. 2024 Sep 1;109:129814. doi: 10.1016/j.bmcl.2024.129814. Epub 2024 May 28. Bioorg Med Chem Lett. 2024. PMID: 38815872

10

Comprehensive Prediction Model, Including Genetic Testing, for the Outcomes of Cochlear Implantation.

Han JH, Kim SH, Moon IS, Joo SY, Kim JA, Gee HY, Jung J, Choi JY. Han JH, et al. Ear Hear. 2023 Jan-Feb 01;44(1):223-231. doi: 10.1097/AUD.0000000000001269. Epub 2022 Aug 15. Ear Hear. 2023. PMID: 35973050

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