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Viral RNA Load in Mildly Symptomatic and Asymptomatic Children with COVID-19, Seoul, South Korea

Emerging infectious diseases, 2020-10, Vol.26 (10), p.2497-2499

2020

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Evidence of Severe Acute Respiratory Syndrome Coronavirus 2 Reinfection After Recovery from Mild Coronavirus Disease 2019

Clinical infectious diseases, 2020-11, Vol.73 (9), p.e3002-e3008

2020

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

Orphanet journal of rare diseases, 2022-03, Vol.17 (1), p.111-111, Article 111

2022

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Longitudinal proteomic profiling provides insights into host response and proteome dynamics in COVID‐19 progression

Proteomics (Weinheim), 2021-06, Vol.21 (11-12), p.e2000278-n/a

2021

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ITDetect: a method to detect internal tandem duplication of FMS-like tyrosine kinase (FLT3) from next-generation sequencing data with high sensitivity and clinical application

BMC bioinformatics, 2023-02, Vol.24 (1), p.62-62, Article 62

2023

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Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation

International journal of molecular sciences, 2024-02, Vol.25 (5), p.2811

2024

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Viral RNA in Blood as Indicator of Severe Outcome in Middle East Respiratory Syndrome Coronavirus Infection

Emerging infectious diseases, 2016-10, Vol.22 (10), p.1813-1816

2016

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Molecular basis and diagnosis of thalassemia

Blood Research, 2021, 56(0), , pp.39-43

2021

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Noninvasive prenatal test of single-gene disorders by linked-read direct haplotyping: application in various diseases

European journal of human genetics : EJHG, 2021-03, Vol.29 (3), p.463-470

2021

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Comparative genomics of Mycoplasma pneumoniae isolated from children with pneumonia: South Korea, 2010-2016

BMC genomics, 2019-11, Vol.20 (1), p.910-910, Article 910

2019

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

Clinical chemistry (Baltimore, Md.), 2021-04, Vol.67 (4), p.691-693

2021

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Replication‐Based Rearrangements Are a Common Mechanism for SNCA Duplication in Parkinson's Disease

Movement disorders, 2020-05, Vol.35 (5), p.868-876

2020

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Direct Haplotyping-Based Noninvasive Prenatal Test for Myotonic Dystrophy Type 1 with Large CTG Expansion

Clinical chemistry (Baltimore, Md.), 2020-04, Vol.66 (4), p.614-615

2020

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

Virulence, 2022-12, Vol.13 (1), p.1242-1251

2022

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Clinical and genetic characteristics of Korean occult macular dystrophy patients

Investigative ophthalmology & visual science, 2013-07, Vol.54 (7), p.4856-4863

2013

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Accuracy and Performance Evaluation of Triplet Repeat Primed PCR as an Alternative to Conventional Diagnostic Methods for Fragile X Syndrome

Annals of Laboratory Medicine, 2021, 41(4), , pp.394-400

2021

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Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015

Emerging infectious diseases, 2016-02, Vol.22 (2), p.327-330

2016

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Strabismus in chronic progressive external ophthalmoplegia

Acta ophthalmologica (Oxford, England), 2021-03, Vol.99 (2), p.e274-e280

2021

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Leukemic stem cell phenotype is associated with mutational profile in acute myeloid leukemia

The Korean Journal of Internal Medicine, 2021, 36(2), , pp.401-412

2021

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Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome

Annals of Laboratory Medicine, 2022, 42(1), , pp.79-88

2022

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Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma

Endocrinology and Metabolism, 2020, 35(4), , pp.909-917

2020

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Evaluation of Two Hepatitis C Virus Genotyping Assays Based on the 5′ Untranslated Region (UTR): the Limitations of 5′ UTR-Based Assays and the Need for a Supplementary Sequencing-Based Approach

Journal of Clinical Microbiology, 2012-11, Vol.50 (11), p.3741-3743

2012

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Performance of two commercially available BCR-ABL1 quantification assays that use an international reporting scale

Clinical chemistry and laboratory medicine, 2016-07, Vol.54 (7), p.1157

2016

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Revisit of multiple epiphyseal dysplasia: Ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes

American journal of medical genetics. Part A, 2011-11, Vol.155A (11), p.2669-2680

2011

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Sequential Analysis of Viral Load in a Neonate and Her Mother Infected With Severe Acute Respiratory Syndrome Coronavirus 2

Clinical infectious diseases, 2020-11, Vol.71 (16), p.2236-2239

2020

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Viral RNA Load in Mildly Symptomatic and Asymptomatic Children with COVID-19, Seoul, South Korea

Evidence of Severe Acute Respiratory Syndrome Coronavirus 2 Reinfection After Recovery from Mild Coronavirus Disease 2019

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

Longitudinal proteomic profiling provides insights into host response and proteome dynamics in COVID‐19 progression

ITDetect: a method to detect internal tandem duplication of FMS-like tyrosine kinase (FLT3) from next-generation sequencing data with high sensitivity and clinical application

Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation

Viral RNA in Blood as Indicator of Severe Outcome in Middle East Respiratory Syndrome Coronavirus Infection

Molecular basis and diagnosis of thalassemia

Noninvasive prenatal test of single-gene disorders by linked-read direct haplotyping: application in various diseases

Comparative genomics of Mycoplasma pneumoniae isolated from children with pneumonia: South Korea, 2010-2016

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

Replication‐Based Rearrangements Are a Common Mechanism for SNCA Duplication in Parkinson's Disease

Direct Haplotyping-Based Noninvasive Prenatal Test for Myotonic Dystrophy Type 1 with Large CTG Expansion

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

Clinical and genetic characteristics of Korean occult macular dystrophy patients

Accuracy and Performance Evaluation of Triplet Repeat Primed PCR as an Alternative to Conventional Diagnostic Methods for Fragile X Syndrome

Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015

Strabismus in chronic progressive external ophthalmoplegia

Leukemic stem cell phenotype is associated with mutational profile in acute myeloid leukemia

Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome

Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma

Evaluation of Two Hepatitis C Virus Genotyping Assays Based on the 5′ Untranslated Region (UTR): the Limitations of 5′ UTR-Based Assays and the Need for a Supplementary Sequencing-Based Approach

Performance of two commercially available BCR-ABL1 quantification assays that use an international reporting scale

Revisit of multiple epiphyseal dysplasia: Ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes

Sequential Analysis of Viral Load in a Neonate and Her Mother Infected With Severe Acute Respiratory Syndrome Coronavirus 2

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