울산대학교 의과대학원 의학박사 (2016)
울산대학교 의과대학원 의학석사 (2007)
울산대학교 의학사 (2005)
GC녹십자의료재단 진단검사의학본부 전문의 (2020~)
서울아산병원 전임의 (2016~2020)
서울아산병원 전공의 (2012~2016)
 
 
                     
                    
                        
                                - 
                                    Regions of Homozygosity Identified with a Chromosomal Microarray in a Korean Population: Distribution, Frequency, and Clinical Interpretation
                                    2025Annals of Laboratory Medicine설창안 
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                                    Novel causative RYR2 indel variant with exon and intron involvement inducing exon 13 skipping in a family exhibiting catecholaminergic polymorphic ventricular tachycardia
                                    2025Frontiers in Genetics설창안 
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                                    Recurrent Hemorrhagic Stroke and Microcephaly in a Newborn with Aicardi-Goutières Syndrome Caused by a Homozygous Intronic RNASEH2B Variant
                                    2025 Annals of Clinical & Laboratory Science설창안 
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                                    Genetic epidemiology of epithelial-stromal TGFBI dystrophies in a large Korean population
                                    2025Scientific Reports설창안 
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                                    Genetic counseling in prenatal chromosome test and CMA
                                    2025대한진단유전학회 제20차 학술대회설창안 
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                                    유전질환 NGS 검사에서의 CNV 분석
                                    20242024 제7회 유전의학융합회 정기 학술대회설창안 
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                                    Clinical utility of CytoScan Optima for prenatal diagnosis
                                    20242024 제7회 유전의학융합회 정기 학술대회설창안 
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                                    Copy number variants of targeted next-generation sequencing panels
                                    20242024 제7회 유전의학융합회 정기 학술대회설창안 
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                                    Clinical Application of Chromosomal Microarray for Hematologic Malignancies
                                    2024Journal of Interdisciplinary Genomics설창안 
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                                    Copy number variants of targeted next-generation sequencing panels
                                    2024KSMGG & EAUHGS 2024설창안 
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                                    Genetic Diagnosis Utilizing xGen Exome and mtDNA Research Solution
                                    2024대한진단유전학회 2024년 제19차 학술대회설창안 
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                                    LSD에 대한 분자유전학적 진단
                                    2024대한진단유전학회 2024년 제19차 학술대회설창안 
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                                    Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience
                                    2024Annals of Pediatric Endocrinology & Metabolism설창안 
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                                    Clinical application of chromosomal microarray for germline disorders
                                    2023Journal of Interdisciplinary Genomics설창안 
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                                    CytoScan Optima의 산전진단에 대한 임상적 유용성
                                    2023대한진단유전학회 학술대회설창안 
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                                    Practical Guidelines for Chromosomal Microarray Analysis for Constitutional Abnormalities: Part II, Reporting and Interpretation
                                    2023Laboratory Medicine Online설창안 
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                                    Practical Guidelines for Chromosomal Microarray Analysis for Constitutional Abnormalities: Part I, General and Prenatal
                                    2023Laboratory Medicine Online설창안 
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                                    혈액암에서의 CMA 적용
                                    2023대한진단유전학회 학술대회설창안 
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                                    Diagnostic Utility of CytoScan Xon Array
                                    2023대한진단유전학회 학술대회설창안 
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                                    Clinical application of prenatal chromosomal microarray
                                    2022Journal of Genetic Medicine설창안 
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                                    산전 이상의 염색체마이크로어레이의 검사지침
                                    2022대한진단유전학회 심포지엄설창안 
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                                    Microarray as a prenatal test
                                    2020대한진단유전학회설창안 
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                                    The first familial case of inherited intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA) with a novel FBXO11 variant
                                    2020Am J Med Genet A설창안 
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                                    First Case of Double T-Cell Receptor Alpha/Delta Rearrangements of t(11;14) and inv(14) and Subsequent JAK2 Rearrangement in a Patient With T-cell Acute Lymphoblastic Leukemia
                                    2020Ann Lab Med설창안 
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                                    POEMS Syndrome: Bone Marrow, Laboratory, and Clinical Findings in 24 Korean Patients
                                    2019Ann Lab Med설창안