Jung J - Search Results

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. Among authors: jung j. J Clin Med. 2024 Mar 29;13(7):2001. doi: 10.3390/jcm13072001. J Clin Med. 2024. PMID: 38610765 Free PMC article.

2

A Fast Center of Pupil Detection Algorithm for VOG-Based Eye Movement Tracking.

Kim S, Cho J, Jung J, Kim S, Lim J, Nam T, Kim J. Kim S, et al. Among authors: jung j. Conf Proc IEEE Eng Med Biol Soc. 2005;2005:3188-91. doi: 10.1109/IEMBS.2005.1617153. Conf Proc IEEE Eng Med Biol Soc. 2005. PMID: 17282922

3

Cost-effectiveness analysis of 5 years of postoperative adjuvant tamoxifen therapy for Korean women with breast cancer: retrospective cohort study of the Korean breast cancer society database.

Yang JJ, Park SK, Cho LY, Han W, Park B, Kim H, Lee KS, Hahn SK, Cho SI, Ahn SH, Noh DY; Korean Breast Cancer Society. Yang JJ, et al. Clin Ther. 2010 Jun;32(6):1122-38. doi: 10.1016/j.clinthera.2010.05.013. Clin Ther. 2010. PMID: 20637966

4

Correlation between genotype and phenotype in patients with bi-allelic SLC26A4 mutations.

Lee HJ, Jung J, Shin JW, Song MH, Kim SH, Lee JH, Lee KA, Shin S, Kim UK, Bok J, Lee KY, Choi JY, Park HJ. Lee HJ, et al. Among authors: jung j. Clin Genet. 2014 Sep;86(3):270-5. doi: 10.1111/cge.12273. Epub 2013 Oct 3. Clin Genet. 2014. PMID: 24007330

5

Resistance to hypertension and high Cl^- excretion in humans with SLC26A4 mutations.

Kim BG, Yoo TH, Yoo JE, Seo YJ, Jung J, Choi JY. Kim BG, et al. Among authors: jung j. Clin Genet. 2017 Mar;91(3):448-452. doi: 10.1111/cge.12789. Epub 2016 May 20. Clin Genet. 2017. PMID: 27090054

6

Vibrant Soundbridge can improve the most comfortable listening level in sensorineural hearing loss: Our experience with 61 patients.

Jung J, Kim JW, Moon IS, Kim SH, Choi JY. Jung J, et al. Clin Otolaryngol. 2018 Feb;43(1):369-373. doi: 10.1111/coa.12958. Epub 2017 Sep 4. Clin Otolaryngol. 2018. PMID: 28834277 No abstract available.

7

Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report.

Choi HJ, Lee JS, Yu S, Cha DH, Gee HY, Choi JY, Lee JD, Jung J. Choi HJ, et al. Among authors: jung j. BMC Med Genet. 2017 Dec 19;18(1):151. doi: 10.1186/s12881-017-0511-7. BMC Med Genet. 2017. PMID: 29258540 Free PMC article.

8

Effects of self-reported hearing or vision impairment on depressive symptoms: a population-based longitudinal study.

Han JH, Lee HJ, Jung J, Park EC. Han JH, et al. Among authors: jung j. Epidemiol Psychiatr Sci. 2019 Jun;28(3):343-355. doi: 10.1017/S2045796018000045. Epub 2018 Feb 8. Epidemiol Psychiatr Sci. 2019. PMID: 29415786 Free PMC article.

9

Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency.

Rim JH, Lee JS, Jung J, Lee JH, Lee ST, Choi JR, Choi JY, Lee MG, Gee HY. Rim JH, et al. Among authors: jung j. Sci Rep. 2019 Mar 14;9(1):4583. doi: 10.1038/s41598-019-41068-6. Sci Rep. 2019. PMID: 30872718 Free PMC article.

10

The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report.

Nam GS, Rim JH, Choi JY, Gee HY, Choi JR, Lee ST, Jung J. Nam GS, et al. Among authors: jung j. BMC Med Genet. 2019 Apr 1;20(1):57. doi: 10.1186/s12881-019-0775-1. BMC Med Genet. 2019. PMID: 30935366 Free PMC article.

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