Sung S. Park

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 172 publications

Poor visual prognosis of Asian patients with 3460 mitochondrial DNA mutation in Leber's hereditary optic neuropathy.

Poor visual prognosis of Asian patients with 3460 mitochondrial DNA mutation in Leber's hereditary optic neuropathy.

Journal: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie

Published: November 16, 2023

The Korean Genetic Diagnosis Program for Rare Disease Phase II: outcomes of a 6-year national project.

The Korean Genetic Diagnosis Program for Rare Disease Phase II: outcomes of a 6-year national project.

Journal: European journal of human genetics : EJHG

Published: March 07, 2023

SARS-CoV-2 shedding dynamics and transmission in immunosuppressed patients.

SARS-CoV-2 shedding dynamics and transmission in immunosuppressed patients.

Journal: Virulence

Published: July 27, 2022

The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure.

The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure.

Journal: Orphanet journal of rare diseases

Published: May 26, 2022

Parallel Analysis of Pre- and Postoperative Circulating Tumor DNA and Matched Tumor Tissues in Resectable Pancreatic Ductal Adenocarcinoma: A Prospective Cohort Study.

Parallel Analysis of Pre- and Postoperative Circulating Tumor DNA and Matched Tumor Tissues in Resectable Pancreatic Ductal Adenocarcinoma: A Prospective Cohort Study.

Journal: Clinical chemistry

Published: April 28, 2022

Rapid Targeted Sequencing Using Dried Blood Spot Samples for Patients With Suspected Actionable Genetic Diseases.

Rapid Targeted Sequencing Using Dried Blood Spot Samples for Patients With Suspected Actionable Genetic Diseases.

Journal: Annals of laboratory medicine

Published: March 18, 2022

Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing.

Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing.

Journal: Scientific reports

Published: January 26, 2022

Consistent count region-copy number variation (CCR-CNV): an expandable and robust tool for clinical diagnosis of copy number variation at the exon level using next-generation sequencing data.

Consistent count region-copy number variation (CCR-CNV): an expandable and robust tool for clinical diagnosis of copy number variation at the exon level using next-generation sequencing data.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 29, 2021

Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene.

Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene.

Journal: Orphanet journal of rare diseases

Published: August 11, 2021

The First Korean Case of Griscelli Syndrome Type 2 With Hemophagocytic Lymphohistiocytosis and Partial Albinism.

The First Korean Case of Griscelli Syndrome Type 2 With Hemophagocytic Lymphohistiocytosis and Partial Albinism.

Journal: Annals of laboratory medicine

Published: July 28, 2021

Night-time gastric acid suppression by tegoprazan compared to vonoprazan or esomeprazole.

Night-time gastric acid suppression by tegoprazan compared to vonoprazan or esomeprazole.

Journal: British journal of clinical pharmacology

Published: July 01, 2021

FMS-like Tyrosine Kinase 3-Internal Tandem Duplication Allele Concentrations Should Be Determined in a Mutation-Type-Specific Manner.

FMS-like Tyrosine Kinase 3-Internal Tandem Duplication Allele Concentrations Should Be Determined in a Mutation-Type-Specific Manner.

Journal: Clinical chemistry

Published: March 09, 2021

Showing 1-12 of 172

Last Updated: 09/26/2026