| 2009 | BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia. | CANCER GENETICS AND CYTOGENETICS |
| 2008 | Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion | PEDIATRIC NEUROLOGY |
| 2020 | Beneficial Chromosomal Integration of the Genes for CTX-M Extended-Spectrum β-Lactamase in Klebsiella pneumoniae for Stable Propagation
| MSYSTEMS |
| 2009 | Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21 | CANCER GENETICS AND CYTOGENETICS |
| 2016 | Bone marrow chimerism detection using next generation sequencing based on single nucleotide polymorphisms following liver transplantation: comparison with short tandem repeat-PCR
| ANNALS OF LABORATORY MEDICINE |
| 2014 | Bone marrow hypoplasia, isochromosome 8q and deletion of chromosome 6q preceding B-cell lymphoma
| BLOOD RESEARCH |
| 2012 | BRAFV600E mutation testing in fine needle aspirates of thyroid nodules: potential value of real-time PCR | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2015 | Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.
| JOURNAL OF MEDICAL GENETICS |
| 2009 | CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia | CANCER GENETICS AND CYTOGENETICS |
| 2012 | CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations
| ANNALS OF LABORATORY MEDICINE |
| 2009 | Changes in expression of fibulin-5 and lysyl oxidase-like 1 associated with pelvic organ prolapse. | EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY |
| 2021 | Chimerism Assay Using Single Nucleotide Polymorphisms Adjacent and in Linkage-Disequilibrium Enables Sensitive Disease Relapse Monitoring after Hematopoietic Stem-Cell Transplantation | CLINICAL CHEMISTRY |
| 2009 | Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2023 | Circulating Tumor DNA Analysis on Metastatic Prostate Cancer with Disease Progression
| CANCERS |
| 2024 | Circulating Tumor DNA Reflects Histologic and Clinical Characteristics of Various Lymphoma Subtypes
| CANCER RESEARCH AND TREATMENT |
| 2021 | Clinical characteristics of KCNQ2 encephalopathy | BRAIN & DEVELOPMENT |
| 2019 | Clinical Evaluation of Massively Parallel RNA Sequencing for Detecting Recurrent Gene Fusions in Hematologic Malignancies | JOURNAL OF MOLECULAR DIAGNOSTICS |
| 2006 | Clinical evaluation of micro-scale chip-based PCR system for rapid detection of hepatitis B virus | BIOSENSORS & BIOELECTRONICS |
| 2019 | Clinical features and treatment efficacy in cdkl5 mutation-related epileptic encephalopathy in the infant
| Annals of Child Neurology |
| 2020 | Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development | PEDIATRIC NEUROLOGY |
| 2015 | Clinical Implication of Highly Sensitive Detection of the BRAFV600E Mutation in Fine-Needle Aspirations According to the Thyroid Bethesda System in Patients With Conventional Papillary Thyroid Carcinoma | ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY |
| 2023 | Clinical relevance of clonal hematopoiesis and its interference in cell-free DNA profiling of patients with gastric cancer | CLINICAL CHEMISTRY AND LABORATORY MEDICINE |
| 2019 | Clinical utility of targeted NGS panel with comprehensive bioinformatics analysis for patients with acute lymphoblastic leukemia | LEUKEMIA & LYMPHOMA |
| 2004 | CMV 질환의 면역치료법 개발에 대한 최신지견 | Konkuk Journal of Medical Sciences (건국의과학학술지) |
| 2023 | Comparative Analysis of the Molecular Characteristics of Group B Streptococcus Isolates Collected from Pregnant Korean Women Using Whole-genome Sequencing
| ANNALS OF LABORATORY MEDICINE |
| 2012 | Comparison study of the rates of manual peripheral blood smear review from 3 automated hematology analyzers, Unicel DxH 800, ADVIA 2120i, and XE 2100, using international consensus group guidelines | ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE |
| 2010 | Comparisons of three automated systems for genomic DNA extraction in a clinical diagnostic laboratory
| YONSEI MEDICAL JOURNAL |
| 2014 | Complete Genome Sequence of the Siphoviral Bacteriophage YMC/09/04/R1988 MRSA BP: A lytic phage from a methicillin-resistant Staphylococcus aureus isolate.
| FEMS MICROBIOLOGY LETTERS |
| 2008 | Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia | CANCER GENETICS AND CYTOGENETICS |
| 2017 | Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia
| ANNALS OF LABORATORY MEDICINE |
| 2022 | Concomitant Diagnosis of Primary Bone Marrow B-Cell Non-Hodgkin Lymphoma and Essential Thrombocythemia: A Case Report
| ANNALS OF LABORATORY MEDICINE |
| 2009 | Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2009 | Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia | CANCER GENETICS AND CYTOGENETICS |
| 2010 | Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2010 | Constitutional pericentric inversion 9 in Korean patients with chronic myelogenous leukemia
| KOREAN JOURNAL OF LABORATORY MEDICINE |
| 2020 | Copy Number Variations and Multiallelic Variants in Korean Patients With Leber Congenital Amaurosis
| MOLECULAR VISION |
| 2023 | Copy-number analysis by base-level normalization: An intuitive visualization tool for evaluating copy number variations | CLINICAL GENETICS |
| 2014 | Cys482Trp Missense Mutation in the Coagulation Factor XI Gene (F11) in a Korean Patient with Factor XI Deficiency
| ANNALS OF LABORATORY MEDICINE |
| 2022 | Cytogenetic testing by fluorescence in situ hybridization is improved by plasma cell sorting in multiple myeloma
| SCIENTIFIC REPORTS |
| 2009 | De novo interstitial direct duplication 8 (p21.3p23.1) with Pierre Robin sequence
| Korean Journal of Pediatrics |
| 2018 | Deletion of 20p13 and Duplication of 20p13p12.3 in a Patient with Delayed Speech and Development.
| ANNALS OF LABORATORY MEDICINE |
| 2012 | Delta neutrophil index: a promising diagnostic and prognostic marker for sepsis | SHOCK |
| 2009 | der(1)t(1;19)(p13;p13.1) in two elderly patients with myeloid neoplasms: new case reports and review of the literature. | LEUKEMIA RESEARCH |
| 2022 | Derivation of YCMi005-A, a human-induced pluripotent stem cell line, from a patient with dilated cardiomyopathy carrying missense variant in TPM1 (p. Glu192Lys)
| STEM CELL RESEARCH |
| 2023 | Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders | JOURNAL OF MOLECULAR DIAGNOSTICS |
| 2009 | Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits | CANCER GENETICS AND CYTOGENETICS |
| 2003 | Detection of an Ala601Thr Mutation of Plasminogen Gene in 3 out of 36 Korean Patients with Deep Vein Thrombosis
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2009 | Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics. | CANCER GENETICS AND CYTOGENETICS |
| 2017 | Detection of Immunoglobulin Heavy Chain Gene Clonality by Next-Generation Sequencing for Minimal Residual Disease Monitoring in B-Lymphoblastic Leukemia
| ANNALS OF LABORATORY MEDICINE |
| 2020 | Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next-generation sequencing approaches | HEMATOLOGICAL ONCOLOGY |
| 2012 | Detection of SET-NUP214 rearrangement using multiplex reverse transcriptase-polymerase chain reaction (RT-PCR) in acute leukemias: a case report and literature review on a Korean case series | ANNALS OF HEMATOLOGY |
| 2010 | Detection of t(3;5) and NPM1/MLF1 rearrangement in an elderly patient with acute myeloid leukemia: clinical and laboratory study with review of the literature | CANCER GENETICS AND CYTOGENETICS |
| 2016 | Development and comparison of warfarin dosing algorithms for stroke patients
| YONSEI MEDICAL JOURNAL |
| 2023 | Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing
| CANCER CELL INTERNATIONAL |
| 2023 | Development of a Next-generation Sequencing-based Gene Panel Test to Detect Measurable Residual Disease in Acute Myeloid Leukemi
| ANNALS OF LABORATORY MEDICINE |
| 2017 | Diagnostic application of clinical exome sequencing in Leber congenital amaurosis
| MOLECULAR VISION |
| 1995 | Diagnostic efficacy of plasma urokinase-type plasminogen activator and plasminogen activator inhibitor-2 in differentiation of hepatocellular carcinoma from cirrhosis | THROMBOSIS AND HAEMOSTASIS |
| 2018 | Diagnostic exome sequencing을 통한 KBG 증후군의 조기 진단
| Journal of the Korean Child Neurology Society |
| 2011 | Diagnostic standardization of leukemia fusion gene detection system using multiplex reverse transcriptase-polymerase chain reaction in Korea
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2011 | Diagnostic value of BRAF(V600E) mutation analysis of thyroid nodules according to ultrasonographic features and the time of aspiration. | ANNALS OF SURGICAL ONCOLOGY |
