Yejin Yun

Seoul St. Mary's Hospital
Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 20 publications

Next-generation sequencing (NGS) analysis and age-based survival comparison among glioblastoma (GBM) patients: a two-center cohort study.

Next-generation sequencing (NGS) analysis and age-based survival comparison among glioblastoma (GBM) patients: a two-center cohort study.

Journal: Acta neurochirurgica
Published: February 23, 2026

Association of circulating proteasome activity with Alzheimer's pathology and cognitive functions in APOE ε4 carriers.

Association of circulating proteasome activity with Alzheimer's pathology and cognitive functions in APOE ε4 carriers.

Journal: Alzheimer's research & therapy
Published: December 08, 2025

Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approach.

Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approach.

Journal: Cell reports. Medicine
Published: December 09, 2024

Comparative study on structural and functional brain differences in mild cognitive impairment patients with tinnitus.

Comparative study on structural and functional brain differences in mild cognitive impairment patients with tinnitus.

Journal: Frontiers in aging neuroscience
Published: July 26, 2024

Updates on Genetic Hearing Loss: From Diagnosis to Targeted Therapies.

Updates on Genetic Hearing Loss: From Diagnosis to Targeted Therapies.

Journal: Journal of audiology & otology
Published: February 22, 2024

Full-cycle study on developing a novel structured micromixer and evaluating the nanoparticle products as mRNA delivery carriers.

Full-cycle study on developing a novel structured micromixer and evaluating the nanoparticle products as mRNA delivery carriers.

Journal: Journal of controlled release : official journal of the Controlled Release Society
Published: February 11, 2024

Discovery of novel disease-causing mutation in SSBP1 and its correction using adenine base editor to improve mitochondrial function.

Discovery of novel disease-causing mutation in SSBP1 and its correction using adenine base editor to improve mitochondrial function.

Journal: Molecular therapy. Nucleic acids
Published: January 17, 2024

CRISPR-based editing strategies to rectify EYA1 complex genomic rearrangement linked to haploinsufficiency.

CRISPR-based editing strategies to rectify EYA1 complex genomic rearrangement linked to haploinsufficiency.

Journal: Molecular therapy. Nucleic acids
Published: December 21, 2023

Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss.

Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss.

Journal: International journal of molecular sciences
Published: October 19, 2023

Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South Korea.

Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South Korea.

Journal: Scientific reports
Published: June 01, 2023

Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects.

Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects.

Journal: Scientific reports
Published: March 05, 2023

Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions.

Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions.

Journal: BMC medical genomics
Published: January 21, 2023
Showing 1-12 of 20

Last Updated: 09/26/2026