Browsing by Yonsei Author : Kim, Yoon Jung

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Name:
Kim, Yoon Jung [김윤정]
orcid http://orcid.org/0000-0002-4370-4265
Department :
College of Medicine (의과대학) - Dept. of Laboratory Medicine (진단검사의학교실)

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Issue DateTitleJournal Title
2024Identification of Potential Genomic Alterations Using Pan-Cancer Cell-Free DNA Next-Generation Sequencing in Patients With Gastric Cancer ANNALS OF LABORATORY MEDICINE
2024Evaluation of diagnostic performance of SARS-CoV-2 infection using digital droplet polymerase chain reaction in individuals with or without COVID-19 symptomsCLINICA CHIMICA ACTA
2023Cost-Effectiveness Analysis of Three Diagnostic Strategies for the Detection of EGFR Mutation in Advanced Non-Small Cell Lung Cancer ANNALS OF LABORATORY MEDICINE
2023Associations of Perioperative Red Blood Cell Transfusion With Outcomes of Kidney Transplantation in Korea Over a 16-Year Period JOURNAL OF KOREAN MEDICAL SCIENCE
2023Comparison of Homologous Recombination Repair Gene Next-Generation Sequencing Analysis in Patients With Metastatic Castration-Resistant Prostate Cancer Between Local and Central Laboratories in Korea ANNALS OF LABORATORY MEDICINE
2023Cost-Effectiveness Analysis of Germline and Somatic BRCA Testing in Patients With Advanced Ovarian Cancer ANNALS OF LABORATORY MEDICINE
2022Caspase-10 affects the pathogenesis of primary biliary cholangitis by regulating inflammatory cell death JOURNAL OF AUTOIMMUNITY
2022유전성 암 유전자에서 검출된 염기 변이의 해석을 위한 기능 연구 근거의 적용 Laboratory Medicine Online
2022Primary endocrine resistance of ER+ breast cancer with ESR1 mutations interrogated by droplet digital PCR NPJ BREAST CANCER
2022Clinical Practice Guidelines for Pre-Analytical Procedures of Plasma Epidermal Growth Factor Receptor Variant Testing ANNALS OF LABORATORY MEDICINE
2022Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer CANCER CELL INTERNATIONAL
2022Association between TP53 mutation and high 21-gene recurrence score in estrogen receptor-positive/HER2-negative breast cancer NPJ BREAST CANCER
2021Evaluation of a hybridization capture-based hereditary cancer panel for the ion semiconductor-based next-generation sequencing systemCLINICA CHIMICA ACTA
2021De Novo Cancer Incidence after Kidney Transplantation in South Korea from 2002 to 2017 JOURNAL OF CLINICAL MEDICINE
2021팬더시스템을 이용한 Aptima HBV 및 HCV 바이러스 검사의 진단 성능 평가 Laboratory Medicine Online
2021한국인 췌장암 환자에서 발견한 UGT1A1*37 대립유전자 1예 보고 Laboratory Medicine Online
2021Hereditary cancer syndrome-associated pathogenic variants are common in patients with hematologic malignancies subsequent to primary solid cancer JOURNAL OF CANCER
2021Detection of EGFR-SEPT14 fusion in cell-free DNA of a patient with advanced gastric cancer: A case report WORLD JOURNAL OF CLINICAL CASES
2021Prediction of urine culture results by automated urinalysis with digital flow morphology analysis SCIENTIFIC REPORTS
2021Effect of sarcomere and mitochondria-related mutations on myocardial fibrosis in patients with hypertrophic cardiomyopathy JOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE
2021Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy CANCER CELL INTERNATIONAL
2021Contribution of sarcomere gene mutations to left atrial function in patients with hypertrophic cardiomyopathy CARDIOVASCULAR ULTRASOUND
2020Burden of premature ventricular contractions beyond nonsustained ventricular tachycardia is related to the myocardial extracellular space expansion in patients with hypertrophic-cardiomyopathy CLINICAL CARDIOLOGY
2020A novel approach for tuberculosis diagnosis using exosomal DNA and droplet digital PCRCLINICAL MICROBIOLOGY AND INFECTION
2020Differential Contributions of Sarcomere and Mitochondria-Related Multigene Variants to the Endophenotype of Hypertrophic CardiomyopathyMITOCHONDRION
2020Genetic Spectrum of UGT1A1 in Korean Patients With Unconjugated Hyperbilirubinemia ANNALS OF LABORATORY MEDICINE
2020An optimized BRCA1/2 next-generation sequencing for different clinical sample types JOURNAL OF GYNECOLOGIC ONCOLOGY
2020Frequency and Clinical Characteristics of Unselected Korean Gastric Cancer Patients with a Germline CDH1 V832M Mutation JOURNAL OF CANCER
2019Genetic relevance and determinants of mitral leaflet size in hypertrophic cardiomyopathy CARDIOVASCULAR ULTRASOUND
2019진단상의 어려움: 전신성 자가면역 질환의 증상을 모방하는 원발성 골수 광범위큰B세포림프종 진단 Laboratory Medicine Online
2019Selecting short length nucleic acids localized in exosomes improves plasma EGFR mutation detection in NSCLC patients Cancer Cell International
2018DeviCNV: Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data BMC BIOINFORMATICS
2018Electrocardiography based prediction of hypertrophy pattern and fibrosis amount in hypertrophic cardiomyopathy: comparative study with cardiac magnetic resonance imagingINTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING
2018A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories BIOMED RESEARCH INTERNATIONAL
2017Assessment of real-time PCR method for detection of EGFR mutation using both supernatant and cell pellet of malignant pleural effusion samples from non-small-cell lung cancer patientsCLINICAL CHEMISTRY AND LABORATORY MEDICINE
2017Profiling cancer-associated genetic alterations and molecular classification of cancer in Korean gastric cancer patients ONCOTARGET
2017Validation and Optimization of the Ion Torrent S5 XL Sequencer and Oncomine Workflow for BRCA1 and BRCA2 Genetic Testing ONCOTARGET
2017Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia ANNALS OF LABORATORY MEDICINE
2015Analytical Performance of Multiplex Real-Time PCR for Six Sexually Transmitted PathogensCLINICAL LABORATORY
2015Breakpoint 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
2014Partial Gene Deletions of PMP22 Causing Hereditary Neuropathy with Liability to Pressure Palsies Case Reports in Genetics
2014Bone marrow hypoplasia, isochromosome 8q and deletion of chromosome 6q preceding B-cell lymphoma BLOOD RESEARCH
2014Prevalence of Sexually Transmitted Infections in Korean Healthy Women; Implications of Multiplex PCR pathogen detection on antibiotic therapyJOURNAL OF INFECTION AND CHEMOTHERAPY
2014Evaluation of Three Automated Nucleic Acid Extraction Systems for Identification of Respiratory Viruses in Clinical Specimens by Multiplex Real-time PCR BIOMED RESEARCH INTERNATIONAL
2014Ethnic Differences in Genetic Susceptibility to Gastric Cancer : Allele Flips of Interleukin Gene between Asians and Non-Asians WORLD JOURNAL OF GASTROENTEROLOGY
2014Differential association of RANTES-403 and IL-1B-1464 polymorphisms on histological subtypes in male Korean patients with gastric cancerTUMOR BIOLOGY
2013Analysis of mutations in the XPD gene in a patient with brittle hairANNALS OF CLINICAL AND LABORATORY SCIENCE
2013A novel F11 mutation in a Korean pediatric patient with recurrent epistaxisBLOOD COAGULATION & FIBRINOLYSIS
2013Spectrum of EGFR Gene Copy Number Changes and KRAS Gene Mutation Status in Korean Triple Negative Breast Cancer Patients PLOS ONE
2013A Case of Late-Onset Li-Fraumeni-like Syndrome with Unilateral Breast Cancer ANNALS OF LABORATORY MEDICINE
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