Jaewoo Song

Department of Laboratory Medicine, Yonsei University

Affiliated withYonsei University Yonsei University

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2016

Other Publications

Article	Year
t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma. Cancer genetics and cytogenetics\| PubMed ID: 17854675	2007
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia. Cancer genetics and cytogenetics\| PubMed ID: 18036400	2007
[Evaluation of the Abbott Cell-Dyn Sapphire hematology analyzer]. The Korean journal of laboratory medicine\| PubMed ID: 18094570	2007
Investigation of von Willebrand factor gene mutations in Korean von Willebrand disease patients. The Korean journal of laboratory medicine\| PubMed ID: 18094571	2007
8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eo... Cancer genetics and cytogenetics\| PubMed ID: 18295660	2008
A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer. Cancer genetics and cytogenetics\| PubMed ID: 18406877	2008
Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis. Cancer genetics and cytogenetics\| PubMed ID: 18474302	2008
Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature. Cancer genetics and cytogenetics\| PubMed ID: 18656695	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\| PubMed ID: 18722881	2008
Tetrasomy 8 in a patient with acute monoblastic leukemia. The Korean journal of laboratory medicine\| PubMed ID: 18728374	2008
Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine. Cancer genetics and cytogenetics\| PubMed ID: 18786444	2008
Rare translocations involving chromosome band 8p11 in myeloid neoplasms. Cancer genetics and cytogenetics\| PubMed ID: 18940479	2008
[Evaluation of multiplex PCR assay using dual priming oligonucleotide system for detection mutation in the Duchenne muscular dystrophy gene]. The Korean journal of laboratory medicine\| PubMed ID: 18971620	2008
Linear relationship between ADAMTS13 activity and platelet dynamics even before severe thrombocytopenia. Annals of clinical and laboratory science\| PubMed ID: 18988930	2008
MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of... Cancer genetics and cytogenetics\| PubMed ID: 18992643	2008
Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality. Cancer genetics and cytogenetics\| PubMed ID: 18992645	2008
Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript. Cancer genetics and cytogenetics\| PubMed ID: 19027486	2008
Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts. Cancer genetics and cytogenetics\| PubMed ID: 19061780	2009
Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer. Cancer genetics and cytogenetics\| PubMed ID: 19100506	2009
Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time pol... Cancer genetics and cytogenetics\| PubMed ID: 19100514	2009
Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21. Cancer genetics and cytogenetics\| PubMed ID: 19100520	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\| PubMed ID: 19155067	2009
JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature. Cancer genetics and cytogenetics\| PubMed ID: 19167611	2009
Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia. Leukemia research\| PubMed ID: 19195699	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\| PubMed ID: 19215788	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\| PubMed ID: 19215795	2009
BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia. Cancer genetics and cytogenetics\| PubMed ID: 19215796	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\| PubMed ID: 19264234	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\| PubMed ID: 19345416	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\| PubMed ID: 19389510	2009
Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia. Cancer genetics and cytogenetics\| PubMed ID: 19389511	2009
Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation. Annals of clinical and laboratory science\| PubMed ID: 19429805	2009
A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets. Annals of clinical and laboratory science\| PubMed ID: 19429806	2009
Two case reports of 1q triplication in myeloproliferative neoplasms. Cancer genetics and cytogenetics\| PubMed ID: 19446749	2009
Association between acute promyelocytic leukemia and ring chromosome 6. Cancer genetics and cytogenetics\| PubMed ID: 19480938	2009
Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality. Annals of clinical and laboratory science\| PubMed ID: 19667417	2009
A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome. Annals of hematology\| PubMed ID: 19697027	2010
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\| PubMed ID: 19781443	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 : an international journal in haemostasis and thrombosis\| PubMed ID: 19786944	2009
CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia. Cancer genetics and cytogenetics\| PubMed ID: 19837277	2009
Therapy-related myelodysplastic syndrome/acute myeloid leukemia after treatment with temozolomide in a patient with glioblastoma multiforme. Annals of clinical and laboratory science\| PubMed ID: 19880768	2009
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\| PubMed ID: 20113834	2010
Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia. Cancer genetics and cytogenetics\| PubMed ID: 20193844	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 quanti... The American journal of tropical medicine and hygiene\| PubMed ID: 20207865	2010
Constitutional pericentric inversion 9 in Korean patients with chronic myelogenous leukemia. The Korean journal of laboratory medicine\| PubMed ID: 20603579	2010
Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia. Cancer genetics and cytogenetics\| PubMed ID: 20682390	2010
Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years. Annals of clinical and laboratory science\| PubMed ID: 20689141	2010
An SRY-deleted XXY female resulting from a paternally inherited t(Y;22). Annals of clinical and laboratory science\| PubMed ID: 20689145	2010
Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21). Cancer genetics and cytogenetics\| PubMed ID: 20875878	2010
[Parvovirus B19-induced pure red cell aplasia in a liver transplant recipient]. The Korean journal of laboratory medicine\| PubMed ID: 21157144	2010
Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications. The Korean journal of hematology\| PubMed ID: 21253428	2010
Elevated levels of activated and inactivated thrombin-activatable fibrinolysis inhibitor in patients with sepsis. The Korean journal of hematology\| PubMed ID: 21253429	2010
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\| PubMed ID: 21325262	2011
Acute promyelocytic leukemia with trisomy 8 and del(9)(q22) after treatment of cervical cancer with concurrent chemoradiotherapy: a case report. Onkologie\| PubMed ID: 21734427	2011
Delta neutrophil index: a promising diagnostic and prognostic marker for sepsis. Shock (Augusta, Ga.)\| PubMed ID: 22258230	2012
CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations. Annals of laboratory medicine\| PubMed ID: 22259787	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\| PubMed ID: 22371917	2012
Fibrinogen residue γAla341 is necessary for calcium binding and 'A-a' interactions. Thrombosis and haemostasis\| PubMed ID: 22437918	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 gui... Archives of pathology & laboratory medicine\| PubMed ID: 23106587	2012
An engineered fibrinogen variant AαQ328,366P does not polymerise normally, but retains the ability to form α cross-links. Thrombosis and haemostasis\| PubMed ID: 23224113	2013
Immature platelet fraction in diabetes mellitus and metabolic syndrome. Thrombosis research\| PubMed ID: 24140451	2013
Comparison of prothrombin time derived from CoaguChek XS and laboratory test according to fibrinogen level. Journal of clinical laboratory analysis\| PubMed ID: 24687901	2015
The instability of commercial control materials in quality control of mean corpuscular volume. Clinica chimica acta; international journal of clinical chemistry\| PubMed ID: 24769249	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\| PubMed ID: 25117092	2014
Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure. Pflügers Archiv : European journal of physiology\| PubMed ID: 25630304	2015
Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering. Biosensors & bioelectronics\| PubMed ID: 26176206	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\| PubMed ID: 26244499	2015
Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures. Annals of laboratory medicine\| PubMed ID: 26709268	2016
Automated CH50 liposome-based immunoassay: consideration in dilution and validation of reference interval. Clinical chemistry and laboratory medicine\| PubMed ID: 27016150	2016
Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens. Journal of microbiological methods\| PubMed ID: 27030641	2016
Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity. PloS one\| PubMed ID: 27584569	2016