| 2008 | The role of a whole blood interferon-gamma assay for the detection of latent tuberculosis infection in Bacille Calmette-Guérin vaccinated children | DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE |
| 2009 | The role of BRAFV600E mutation and ultrasonography for the surgical management of a thyroid nodule suspicious for papillary thyroid carcinoma on cytology | ANNALS OF SURGICAL ONCOLOGY |
| 2013 | The role of failure modes and effects analysis in showing the benefits of automation in the blood bank | TRANSFUSION |
| 2021 | The Role of Ion Channel-Related Genes in Autism Spectrum Disorder: A Study Using Next-Generation Sequencing
| FRONTIERS IN GENETICS |
| 2022 | The role of Jagged1 as a dynamic switch of cancer cell plasticity in PDAC assembloids
| THERANOSTICS |
| 2021 | The significance of cytoplasmic antinuclear antibody patterns in autoimmune liver disease
| PLOS ONE |
| 2015 | The sul1 gene in Stenotrophomonas maltophilia with high-level resistance to trimethoprim/sulfamethoxazole
| ANNALS OF LABORATORY MEDICINE |
| 2019 | The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
| BMC MEDICAL GENETICS |
| 1999 | The validity of random urine specimen albumin measurement as a screening test for diabetic nephropathy
| YONSEI MEDICAL JOURNAL |
| 2016 | Therapeutic effects of late outgrowth endothelial progenitor cells or mesenchymal stem cells derived from human umbilical cord blood on infarct repair | INTERNATIONAL JOURNAL OF CARDIOLOGY |
| 2015 | Therapeutic plasma exchange using the Spectra Optia cell separator compared with the COBE Spectra
| ANNALS OF LABORATORY MEDICINE |
| 2022 | Therapy-related Acute Lymphoblastic Leukaemia has a Unique Genetic Profile Compared to De Novo Acute Lymphoblastic Leukaemia
| JOURNAL OF CANCER |
| 2009 | Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2):a case study and review of the literature | CANCER GENETICS AND CYTOGENETICS |
| 2009 | Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia | LEUKEMIA RESEARCH |
| 2009 | Therapy-related myelodysplastic syndrome/acute myeloid leukemia after treatment with temozolomide in a patient with glioblastoma multiforme. | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2011 | Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy.
| YONSEI MEDICAL JOURNAL |
| 2010 | Three Cases of Moraxella osloensis Meningitis: A Difficult Experience in Species Identification and Determination of Clinical Significance
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2009 | Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer | CANCER GENETICS AND CYTOGENETICS |
| 2009 | Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia. | CANCER GENETICS AND CYTOGENETICS |
| 2010 | Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23). | CANCER GENETICS AND CYTOGENETICS |
