| 2015 | Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure | PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY |
| 2015 | Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering | BIOSENSORS & BIOELECTRONICS |
| 2015 | Quantitative Influence of ABO Blood Groups on Factor VIII and Its Ratio to von Willebrand Factor, Novel Observations from an ARIC Study of 11,673 Subjects
| PLOS ONE |
| 2015 | Comparison of prothrombin time derived from CoaguChek XS and laboratory test according to fibrinogen level | JOURNAL OF CLINICAL LABORATORY ANALYSIS |
| 2014 | Monoclonal and polyclonal gammopathy measured by serum free light chain and immunofixation subdivide the clinical outcomes of diffuse large B-cell lymphoma according to molecular classification | ANNALS OF HEMATOLOGY |
| 2014 | Analytical and Clinical Performance of a New Point of Care LABGEOIB D-Dimer Test for Diagnosis of Venous Thromboembolism | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2014 | The instability of commercial control materials in quality control of mean corpuscular volume | CLINICA CHIMICA ACTA |
| 2013 | Immature platelet fraction in diabetes mellitus and metabolic syndrome | THROMBOSIS RESEARCH |
| 2013 | Image analysis of peripheral compression artefacts of ThinPrep® liquid-based cytology preparations | CYTOTECHNOLOGY |
| 2012 | Fibrinogen residue γAla341 is necessary for calcium binding and 'A-a' interactions | THROMBOSIS AND HAEMOSTASIS |
| 2012 | Delta neutrophil index: a promising diagnostic and prognostic marker for sepsis | SHOCK |
| 2012 | Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect. | CLINICAL GENETICS |
| 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 |
| 2012 | CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations
| ANNALS OF LABORATORY MEDICINE |
| 2012 | A Gly1609Arg missense mutation in the vWF gene in a Korean patient with von Willebrand disease type 2A | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2011 | Acute promyelocytic leukemia with trisomy 8 and del(9)(q22) after treatment of cervical cancer with concurrent chemoradiotherapy: a case report. | ONKOLOGIE |
| 2011 | Rapid identification of thrombocytopenia-associated multiple organ failure using red blood cell parameters and a volume/hemoglobin concentration cytogram
| YONSEI MEDICAL JOURNAL |
| 2011 | A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency. | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2010 | Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications
| Korean Journal of Hematology |
| 2010 | Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia. | CANCER GENETICS AND CYTOGENETICS |
| 2010 | Comparison of effects of two different formulations of clopidogrel bisulfate tablets on platelet aggregation and bleeding time in healthy Korean volunteers: A single-dose, randomized, open-label, 1-week, two-period, phase IV crossover study. | CLINICAL THERAPEUTICS |
| 2010 | Constitutional pericentric inversion 9 in Korean patients with chronic myelogenous leukemia
| KOREAN JOURNAL OF LABORATORY MEDICINE |
| 2010 | Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2010 | Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21). | CANCER GENETICS AND CYTOGENETICS |
| 2010 | Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia. | CANCER GENETICS AND CYTOGENETICS |
| 2010 | An SRY-deleted XXY female resulting from a paternally inherited t(Y;22) | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2010 | Agranular platelets as a cardinal feature of ARC syndrome | JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY |
| 2010 | Automated detection of malaria-associated pseudoeosinophilia and abnormal WBC scattergram by the Sysmex XE-2100 hematology analyzer: a clinical study with 1,801 patients and real-time quantitative PCR analysis in vivax malaria-endemic area
| AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE |
| 2010 | A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome | ANNALS OF HEMATOLOGY |
| 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 |
| 2009 | Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia. | CANCER GENETICS AND CYTOGENETICS |
| 2009 | Association between acute promyelocytic leukemia and ring chromosome 6 | 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 | CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia | CANCER GENETICS AND CYTOGENETICS |
| 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 |
| 2009 | Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2009 | BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia. | CANCER GENETICS AND CYTOGENETICS |
| 2009 | A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature | CANCER GENETICS AND CYTOGENETICS |
| 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 |
| 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 |
| 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 |
| 2009 | Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia. | LEUKEMIA RESEARCH |
| 2009 | Two case reports of 1q triplication in myeloproliferative neoplasms. | CANCER GENETICS AND CYTOGENETICS |
| 2009 | A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets. | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2009 | Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 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/acute myeloid leukemia after treatment with temozolomide in a patient with glioblastoma multiforme. | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2009 | A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family | BLOOD COAGULATION & FIBRINOLYSIS |
| 2009 | Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA). | THROMBOSIS RESEARCH |
| 2009 | JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature | CANCER GENETICS AND CYTOGENETICS |
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