Dongju Y. Won

Seoul, Republic of Korea

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 58 publications

Response to the letter regarding "Genetic diagnosis of hereditary kidney disease in pediatric patients through whole-exome sequencing and mitochondrial DNA analysis".

Response to the letter regarding "Genetic diagnosis of hereditary kidney disease in pediatric patients through whole-exome sequencing and mitochondrial DNA analysis".

Journal: Kidney research and clinical practice
Published: June 17, 2026

Genetic diagnosis of hereditary kidney disease in pediatric patients through whole-exome sequencing and mitochondrial DNA analysis.

Genetic diagnosis of hereditary kidney disease in pediatric patients through whole-exome sequencing and mitochondrial DNA analysis.

Journal: Kidney research and clinical practice
Published: November 05, 2025

Impact of germline RAD51D mutations on breast cancer: Susceptibility to DNA-damaging agents.

Impact of germline RAD51D mutations on breast cancer: Susceptibility to DNA-damaging agents.

Journal: Molecular therapy. Oncology
Published: November 05, 2025

A novel PSEN1 (p.Gln223Leu) variant associated with spastic paraparesis and early-onset Alzheimer's disease.

A novel PSEN1 (p.Gln223Leu) variant associated with spastic paraparesis and early-onset Alzheimer's disease.

Journal: Journal of Alzheimer's disease reports
Published: September 15, 2025

Clinical Application of Circulating Tumor DNA in Surgically Treated Esophageal Squamous Cell Carcinoma.

Clinical Application of Circulating Tumor DNA in Surgically Treated Esophageal Squamous Cell Carcinoma.

Journal: Annals of laboratory medicine
Published: September 12, 2025

Germline Mutations Related to Complete Remission After Neoadjuvant Chemotherapy in Patients With Triple-negative Breast Cancer.

Germline Mutations Related to Complete Remission After Neoadjuvant Chemotherapy in Patients With Triple-negative Breast Cancer.

Journal: Journal of breast cancer
Published: July 23, 2025

Performance Evaluation of PacBio PureTarget for Multiple Short Tandem Repeat Expansion Detection.

Performance Evaluation of PacBio PureTarget for Multiple Short Tandem Repeat Expansion Detection.

Journal: Annals of laboratory medicine
Published: July 22, 2025

Auditory genotype-phenotype correlation of patients with variants in STRC.

Auditory genotype-phenotype correlation of patients with variants in STRC.

Journal: Scientific reports
Published: July 15, 2025

Utilization of cell-free DNA metagenomic analysis for early detection and microbial identification in prosthetic joint infections: a prospective cohort study in Korea.

Utilization of cell-free DNA metagenomic analysis for early detection and microbial identification in prosthetic joint infections: a prospective cohort study in Korea.

Journal: Frontiers in cellular and infection microbiology
Published: July 11, 2025

Evaluation of ACMG/AMP guidelines for classifying APC variants in Korean patients with suspected familial adenomatous polyposis.

Evaluation of ACMG/AMP guidelines for classifying APC variants in Korean patients with suspected familial adenomatous polyposis.

Journal: Cancer cell international
Published: June 27, 2025

Performance Evaluation of Whole-Genome Amplification Platforms for Clinical Next-Generation Sequencing with Minimal Nucleic Acid Input.

Performance Evaluation of Whole-Genome Amplification Platforms for Clinical Next-Generation Sequencing with Minimal Nucleic Acid Input.

Journal: Annals of laboratory medicine
Published: June 26, 2025

Prevalence of germline CHEK2 variants in East Asians and Koreans based on population genomic databases.

Prevalence of germline CHEK2 variants in East Asians and Koreans based on population genomic databases.

Journal: Breast cancer (Tokyo, Japan)
Published: June 26, 2025
Showing 1-12 of 58

Last Updated: 09/26/2026