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Jongrak Choi
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Name Jongrak Choi
Department
Major Cell Molecular Genetic
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Research

  • A case of Klinefelter syndrome with retroperitoneal teratoma
    YONSEI MEDICAL JOURNAL 41/ :136-139,2000
  • Tissue plasminogen activator and plasminogen activator inhibitor-1 in human choledochal bile
    YONSEI MEDICAL JOURNAL 41/ :119-122,2000
  • A Case of del(13)(q22) with Multiple Major Congenital Anomalies, Imperforate Anus and Penoscrotal Transposition.
    YONSEI MEDICAL JOURNAL 42/0 :558-562,2001
  • Presence of 844ins68 in the cystathionine beta-synthase gene in Asians (Koreans)
    THROMBOSIS AND HAEMOSTASIS 86/ :1130-1130,2001
  • Homozygous VN (677C to T) and d/D (2756G to A) variants in the methylenetetrahydrofolate and methionine synthase genes in a case of hyperhomocysteinemia with stroke at young age.
    EXPERIMENTAL AND MOLECULAR MEDICINE 33/2 :106-109,2001
  • A novel silent substitution (C8516T) in exon 9 of the human PROC gene
    YONSEI MEDICAL JOURNAL 42/ :364-366,2001
  • Evaluation of HER2/neu status by real-time quantitative PCR in breast cancer
    YONSEI MEDICAL JOURNAL 43/ :335-340,2002
  • Detection of an ala601Thr mutation of plasminogen gene in 3 out of 36 Korean patients with deep vein thrombosis
    JOURNAL OF KOREAN MEDICAL SCIENCE 18/ :167-170,2003
  • Adoptive immunotherapy for Cytomegalovirus (CMV) disease in immunocompromised patients
    YONSEI MEDICAL JOURNAL 45/ :18-22,2004
  • CMV 질환의 면역치료법 개발에 대한 최신지견
    건국의과학학술지(The Konkuk Journal. Of Medical Sciences) 13/2 :-,2004
  • Rifampin 내성 결핵의 진단에서 INNO-LiPA 검사법의 임상적 의미
    결핵 및 호흡기질환(Tuberculosis And Respiratory Diseases) 55/4 :-,2004
  • Epidemiological characteristics and molecular basis of fluoroquinolone-resistant Neisseria gonorrhoeae strains isolated in Korea and nearby countries
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY 54/ :451-455,2004
  • Effectiveness of real-time quantitative PCR compare to repeat PCR for the diagnosis of Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies
    YONSEI MEDICAL JOURNAL 46/3 :347-352,2005
  • Homozygous type I protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene [4]
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS 3/ :593-595,2005
  • A novel fibrinogen variant (fibrinogen Seoul II; A alpha Gln328Pro) characterized by impaired fibrin alpha-chain cross-linking
    BLOOD 108/6 :1919-1924,2006
  • Plasma factor XIII activity in patients with disseminated intravascular coagulation
    YONSEI MEDICAL JOURNAL 47/2 :196-200,2006
  • GnRH (Gonadotropin-Releasing Hormone)에 의한 자궁내막암 유래 세포주의 세포 증식 억제 기전에 있어서 Integrin, FAK (FocalAdhesion Kinase) 및 ERK (Extracellular Signal Regulated Kinase)의 역할
    대한불임학회지(Korean Journal Of Fertility And Sterility) 33/ :115-117,2006
  • Plasma level of IL-6 and its relationship to procoagulant and fibrinolytic markers in acute ischemic stroke
    YONSEI MEDICAL JOURNAL 47/2 :201-206,2006
  • Clinical evaluation of micro-scale chip-based PCR system for rapid detection of hepatitis B virus
    BIOSENSORS & BIOELECTRONICS 21/ :2161-2169,2006
  • Fibrinogen Seoul (FGG Ala341Asp): A novel mutation associated with hypodysfibrinogenemia
    CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS 12/3 :338-343,2006
  • t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma
    CANCER GENETICS AND CYTOGENETICS 177/2 :158-160,2007
  • 자동혈구분석기 Cell-Dyn Sapphire의 평가
    대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :162-168,2007
  • 한국 von Willebrand병 환자의 von Willebrand 인자 유전자 돌연변이 조사
    대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :169-176,2007
  • A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia
    CANCER GENETICS AND CYTOGENETICS 179/2 :132-135,2007
  • 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 185/ :51-54,2008
  • A novel de novo mutation in the serine-threonine kinase STKII gene in a Korean patient with Peutz-Jeghers syndrome
    Bmc Medical Genetics 9/ :-,2008
  • Complex t(8;1.9;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia
    Cancer Genetics And Cytogenetics 185/ :109-112,2008
  • Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine
    Cancer Genetics And Cytogenetics 186/ :58-60,2008
  • Linear Relationship between ADAMTS13 Activity and Platelet Dynamics Even Before Severe Thrombocytopenia
    Annals Of Clinical And Laboratory Science 38/ :368-375,2008
  • Rare translocations involving chromosome band 8p11 in myeloid neoplasms
    Cancer Genetics And Cytogenetics 186/ :127-129,2008
  • Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality
    Cancer Genetics And Cytogenetics 187/ :57-58,2008
  • 듀센형근이영양증 유전자의 결실 돌연변이 검출을 위한 Dual Priming Oligonucleotide 다중 PCR법의 평가
    Korean Journal Of Laboratory Medicine 28/5 :386-391,2008
  • 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 187/2 :61-73,2008
  • A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer
    Cancer Genetics And Cytogenetics 182/2 :136-139,2008
  • Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion
    Pediatric Neurology 39/2 :129-132,2008
  • 8번 염색체 사체성을 보인 급성단구성백혈병 1예
    Korean Journal Of Laboratory Medicine 28/4 :262-266,2008
  • 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 183/1 :72-76,2008
  • 8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality
    Cancer Genetics And Cytogenetics 181/ :93-99,2008
  • 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 rare MLL-related chromosome abnormalities
    Cancer Genetics And Cytogenetics 187/ :50-53,2008
  • Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer
    Cancer Genetics and Cytogenetics 188/ :61-64,2009
  • 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 polymerase chain reaction analysis
    Cancer Genetics and Cytogenetics 188/ :103-107,2009
  • Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21
    Cancer Genetics and Cytogenetics 188/ :129-131,2009
  • Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts
    Cancer Genetics and Cytogenetics 188/ :48-51,2009
  • The Relationship Between COL3A1 Exon 31 Polymorphism and Pelvic Organ Prolapse
    JOURNAL OF UROLOGY 181/ :1213-1216,2009
  • JAK2 V617F/C618R mutation in a patient with polycythemia vera: A case study and review of the literature
    Cancer Genetics and Cytogenetics 189/ :43-47,2009
  • Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA)
    Thrombosis Research 123/5 :793-795,2009
  • 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 20/ :150-156,2009
  • Therapy-Related Myelodysplastic Syndrome/Acute Myeloid Leukemia after Treatment with Temozolomide in a Patient with Glioblastoma Multiforme
    Annals Of Clinical And Laboratory Science 39/4 :392-398,2009
  • Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2): a case study and review of the literature
    Cancer Genetics and Cytogenetics 191/ :51-54,2009
  • Concomitant Isochromosome 17q and Trisomy 14 in a Patient with Myelodysplastic Syndrome in Leukemic Transformation
    Annals Of Clinical And Laboratory Science 39/2 :176-181,2009
  • A Novel PHEX Mutation in a Korean Patient with Sporadic Hypophosphatemic Rickets
    Annals Of Clinical And Laboratory Science 39/2 :182-187,2009
  • The clopidogrel resistance can be attenuated with triple antiplatelet therapy in patients undergoing drug-eluting stents implantation
    International Journal Of Cardiology 134/3 :351-355,2009
  • Two case reports of 1q triplication in myeloproliferative neoplasms
    Cancer Genetics and Cytogenetics 191/2 :111-112,2009
  • Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia
    Leukemia Research 33/ :e114-e115,2009
  • 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 33/8 :128-131,2009
  • Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia
    Cancer Genetics and Cytogenetics 190/ :46-48,2009
  • 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 189/2 :87-92,2009
  • A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature
    Cancer Genetics and Cytogenetics 189/ :127-131,2009
  • BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia
    Cancer Genetics and Cytogenetics 189/ :132-137,2009
  • Changes in expression of fibulin-5 and lysyl oxidase-like 1 associated with pelvic organ prolapse
    European Journal Of Obstetrics Gynecology And Reproductive Biology 145/ :117-122,2009
  • The First Korean Case of Camurati-Engelmann Disease (Progressive Diaphyseal Dysplasia) Confirmed by TGFB1 Gene Mutation Analysis
    Journal Of Korean Medical Science 24/ :737-740,2009
  • Chronic Myelomonocytic Leukemia with der(9)t(1;9)(q11;q34) as a Sole Abnormality
    Annals Of Clinical And Laboratory Science 39/3 :307-312,2009
  • Polymorphism of a COLIA1 Gene Sp1 Binding Site in Korean Women with Pelvic Organ Prolapse
    Yonsei Medical Journal 50/4 :564-568,2009
  • Oxidative Status in Iron-Deficiency Anemia
    Journal Of Clinical Laboratory Analysis 23/5 :319-323,2009
  • 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 194/2 :111-118,2009
  • De novo interstitial direct duplication 8 (p21.3p23.1) with Pierre Robin sequence
    Korean Journal of Pediatrics 52/5 :603-606,2009
  • 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 16/11 :3125-3131,2009
  • CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia
    Cancer Genetics and Cytogenetics 195/1 :94-95,2009
  • 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 33/7 :1001-1004,2009
  • A novel three-way t(7;21;8)(q11.2;q22;q22) in a patient with acute myeloid leukemia
    Cancer Genetics and Cytogenetics 195/ :195-197,2009
  • Association of BRAFV600E mutation with poor clinical prognostic factors and US features in korean patients with papillary thyroid microcarcinoma
    Radiology 253/3 :854-860,2009
  • AML1-ETO 양성인 양표현형 급성 백혈병의 1예
    대한내과학회지 76/5 :617-621,2009
  • Association between acute promyelocytic leukemia and ring chromosome 6
    Cancer Genetics and Cytogenetics 192/1 :48-50,2009
  • Comparisons of Three Automated Systems for Genomic DNA Extraction in a Clinical Diagnostic Laboratory
    YONSEI MEDICAL JOURNAL 51/1 :104-110,2010
  • 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 197/1 :32-38,2010
  • Dual priming oligonucleotide-based multiplex PCR analysis for detection of BRAFV600E mutation in FNAB samples of thyroid nodules in BRAF V600E mutation-prevalent area
    HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK 32/4 :490-498,2010
  • A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome
    Annals of Hematology 89/ :513-516,2010
  • Short Report: 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
    American Journal of Tropical Medicine and Hygiene 82/3 :412-414,2010
  • Analysis of fluorescence in situ hybridization, mtDNA quantification, and mtDNA sequence for the detection of early bladder cancer
    Cancer Genetics and Cytogenetics 198/2 :107-117,2010
  • 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 199/ :101-109,2010
  • Two childhood cases of acute leukemia with t(16;21)(p11.2;q22): second case report of infantile acute lymphoblastic leukemia with unusual type of FUS-ERG chimeric transcript
    Cancer Genetics and Cytogenetics 200/2 :180-183,2010
  • An SRY-Deleted XXY Female Resulting from a Paternally Inherited t(Y;22)
    Annals of Clinical and Laboratory Science 40/3 :295-299,2010
  • Identification of Adenovirus, Influenza Virus, Parainfluenza Virus, and Respiratory Syncytial Virus by Two Kinds of Multiplex Polymerase Chain Reaction (PCR) and a Shell Vial Culture in Pediatric Patients with Viral Pneumonia
    YONSEI MEDICAL JOURNAL 51/5 :761-767,2010
  • Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia
    Cancer Genetics and Cytogenetics 201/2 :73-80,2010
  • Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21)
    Cancer Genetics and Cytogenetics 202/2 :141-143,2010
  • Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years
    Annals of Clinical and Laboratory Science 40/3 :273-277,2010
  • Constitutional Pericentric Inversion 9 in Korean Patients with Chronic Myelogenous Leukemia
    KOREAN JOURNAL OF LABORATORY MEDICINE 30/3 :218-223,2010
  • Ambras syndrome in a Korean patient with balanced pericentric inversion (8)(p11.2q24.2)
    Journal of Dermatological Science 59/3 :204-206,2010
  • A Case of Pseudoisodicentric Chromosome 18q Detected at Prenatal Diagnosis
    KOREAN JOURNAL OF LABORATORY MEDICINE 30/4 :440-443,2010
  • Leukemic transformation associated with massive hyperdiploidy in myelodysplastic syndrome (MDS) with der(1;7)(q10;p10): A novel case study
    Leukemia Research 34/8 :E208-E209,2010
  • Association between Survivor Motor Neuron 2 (SMN2) Gene Homozygous Deletion and Sporadic Lower Motor Neuron Disease in a Korean Population
    Annals of Clinical and Laboratory Science 40/4 :368-374,2010
  • Diagnostic Value of BRAF(V600E) Mutation Analysis of Thyroid Nodules According to Ultrasonographic Features and the Time of Aspiration
    ANNALS OF SURGICAL ONCOLOGY 18/ :792-799,2011
  • Alteration of Elastin Metabolism in Women With Pelvic Organ Prolapse
    JOURNAL OF UROLOGY 185/5 :1786-1792,2011
  • A Novel PTEN Mutation in a Korean Patient with Cowden Syndrome and Vascular Anomalies
    ACTA DERMATO-VENEREOLOGICA 91/1 :88-90,2011
  • Acute Promyelocytic Leukemia With Complex Translocation t(5;17;15)(q35;q21;q22): Case Report and Review of the Literature
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY 33/7 :326-329,2011
  • Case Report: 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 41/1 :89-92,2011
  • Letter to the Editor: Diagnostic Standardization of Leukemia Fusion Gene Detection System using Multiplex Reverse Transcriptase-polymerase Chain Reaction in Korea
    JOURNAL OF KOREAN MEDICAL SCIENCE 26/10 :1399-1400,2011
  • Rapid Identification of Thrombocytopenia-Associated Multiple Organ Failure Using Red Blood Cell Parameters and a Volume/Hemoglobin Concentration Cytogram
    YONSEI MEDICAL JOURNAL 52/5 :845-850,2011
  • Case Report: A Novel Mutation in the MECP2 Gene in a Korean Patient with Rett Syndrome
    ANNALS OF CLINICAL AND LABORATORY SCIENCE 41/1 :93-96,2011
  • Acute Promyelocytic Leukemia with Trisomy 8 and del(9)(q22) after Treatment of Cervical Cancer with Concurrent Chemoradiotherapy: A Case Report
    ONKOLOGIE 34/7 :388-390,2011
  • Pharmacokinetic Comparison of Sustained- and Immediate-Release Oral Formulations of Cilostazol in Healthy Korean Subjects: A Randomized, Open-Label, 3-Part, Sequential, 2-Period, Crossover, Single-Dose, Food-Effect, and Multiple-Dose Study
    CLINICAL THERAPEUTICS 33/12 :2038-2053,2011
  • Osteolytic mandible presenting as an initial manifestation of an adult acute lymphoblastic leukaemia
    INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY 40/12 :1438-1440,2011
  • DELTA NEUTROPHIL INDEX: A PROMISING DIAGNOSTIC AND PROGNOSTIC MARKER FOR SEPSIS
    SHOCK 37/ :242-246,2012
  • Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect
    CLINICAL GENETICS 82/2 :180-186,2012
  • CD5-negative Blastoid Variant Mantle Cell Lymphoma with Complex CCND1/IGH and MYC Aberrations
    ANNALS OF LABORATORY MEDICINE 32/1 :95-98,2012
  • 정상 산모들과 임신중독증 산모들의 혈청 중 네프린 발현 빈도의 차이: 예비결과 보고
    Korean Journal of Obstetrics and Gynecology 55/08 :546-551,2012
  • BRAFV600E mutation testing in fine needle aspirates of thyroid nodules: Potential value of real-time PCR
    ANNALS OF CLINICAL AND LABORATORY SCIENCE 42/3 :258-265,2012
  • Fibrinogen residue gamma Ala341 is necessary for calcium binding and 'A-a' interactions
    THROMBOSIS AND HAEMOSTASIS 107/5 :875-883,2012
  • A novel three-way variant t(4;17;5)(p16;q23;q31) in a case of secondary plasma cell leukemia
    LEUKEMIA RESEARCH 36/5 :101-102,2012
  • Submicroscopic Deletion of FGFR1 Gene Is Recurrently Detected in Myeloid and Lymphoid Neoplasms Associated with ZMYM2-FGFR1 Rearrangements: A Case Study
    ACTA HAEMATOLOGICA 127/2 :119-123,2012
  • 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 136/11 :1408-1413,2012
  • 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 91/7 :1135-1138,2012
  • A Gly1609Arg Missense Mutation in the vWF Gene in a Korean Patient with von Willebrand Disease Type 2A
    ANNALS OF CLINICAL AND LABORATORY SCIENCE 42/1 :98-102,2012
  • Proper Indication of BRAFV600E Mutation Testing in Fine-Needle Aspirates of Thyroid Nodules
    PLOS ONE 8/5 :e64505-e64505,2013
  • Application of BRAF, NRAS, KRAS mutations as markers for the detection of papillary thyroid cancer from FNAB specimens by pyrosequencing analysis
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE 51/8 :1673-1680,2013
  • Study of peripheral BRAFV600E mutation as a possible novel marker for papillary thyroid carcinomas
    HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK 35/11 :1630-1633,2013
  • A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis
    BLOOD COAGULATION & FIBRINOLYSIS 24/ :433-435,2013
  • The MLL recombinome of acute leukemias in 2013
    LEUKEMIA 27/11 :2165-2176,2013
  • A Comparative Study of the Diagnostic Performance of the GENEDIA Avellino Corneal Dystrophy Mutation Detection Kit and Screening Master Mix and a Direct Sequencing Method to Detect Mutations in the TGFB1 Gene
    Journal of Laboratory Medicine and Quality Assurance 35/- :115-121,2013
  • Cys482Trp Missense Mutation in the Coagulation Factor XI Gene (F11) in a Korean Patient with Factor XI Deficiency
    ANNALS OF LABORATORY MEDICINE 34/4 :332-335,2014
  • Bone marrow hypoplasia, isochromosome 8q and deletion of chromosome 6q preceding B-cell lymphoma
    Blood Research 49/3 :200-203,2014
  • Complete genome sequence of the bacteriophage YMC/09/04/R1988 MRSA BP: A lytic phage from a methicillin-resistant Staphylococcus aureus isolate
    FEMS MICROBIOLOGY LETTERS 359/2 :144-146,2014
  • MicroRNA-30d and microRNA-181a regulate HOXA11 expression in the uterosacral ligaments and are overexpressed in pelvic organ prolapse
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 19/2 :501-509,2015
  • 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 124/5 :392-399,2015
  • 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 52/10 :706-709,2015
  • Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.
    ANNALS OF LABORATORY MEDICINE 35/5 :510-518,2015
  • NOTCH2 missplicing can occur in relation to apoptosis
    BLOOD 126/14 :1731-1732,2015
  • 천식 치료 중 우연히 발견된 Birt-Hogg-Dube 증후군 1예
    Allergy Asthma & Respiratory Disease 3/3 :232-235,2015
  • Isodicentric Chromosome 15 Syndrome in a Korean Patient With Caf?-au-lait Spots
    ANNALS OF LABORATORY MEDICINE 35/4 :474-476,2015
  • Survey of Clinical Laboratory Practices for 2015 Middle East Respiratory Syndrome Coronavirus Outbreak in the Republic of Korea
    ANNALS OF LABORATORY MEDICINE 36/2 :154-161,2016
  • 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 36/1 :82-84,2016
  • A multicenter phase II study of sorafenib in combination with erlotinib in patients with advanced non-small cell lung cancer (KCSG-0806)
    LUNG CANCER 93/0 :1-8,2016
  • Minor BCR-ABL1-Positive Acute Myeloid Leukemia Associated With the NPM1 Mutation and FLT3 Internal Tandem Duplication
    ANNALS OF LABORATORY MEDICINE 36/3 :263-265,2016
  • Development and comparison of warfarin dosing algorithms for stroke patients
    YONSEI MEDICAL JOURNAL 57/3 :635-640,2016
  • Guidelines for the Laboratory Diagnosis of Middle East Respiratory Syndrome Coronavirus in Korea
    Infection and Chemotherapy 48/1 :61-69,2016
  • Korean Society for Laboratory Medicine Practice Guidelines for the Molecular Diagnosis of Middle East Respiratory Syndrome During an Outbreak in Korea in 2015
    ANNALS OF LABORATORY MEDICINE 36/3 :203-208,2016
  • Frequency and Clinical Characteristics of Intrachromosomal Amplification of Chromosome 21 in Korean Childhood B-lineage Acute Lymphoblastic Leukemia
    ANNALS OF LABORATORY MEDICINE 36/5 :475-480,2016
  • Evaluation of an amplicon-based next-generation sequencing panel for detection of BRCA1 and BRCA2 genetic variants
    BREAST CANCER RESEARCH AND TREATMENT 158/3 :433-440,2016
  • t(12;17)(p13;q12)/TAF15-ZNF384 Rearrangement in Acute Lymphoblastic Leukemia
    ANNALS OF LABORATORY MEDICINE 36/4 :396-398,2016
  • Chronic Myeloid Leukemia With Rare Variant b2a3 (e13a3) BCR-ABL1 Fusion
    ANNALS OF LABORATORY MEDICINE 36/3 :287-289,2016
  • Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia
    ANNALS OF LABORATORY MEDICINE 37/2 :177-179,2017
  • Identification of cell morphology parameters from automatic hematology analyzers to predict peripheral blood CD34 positive cell count after mobilization
    PLOS ONE 12/3 :174,286-,2017
  • Panel strain of Klebsiella pneumoniae for beta-lactam antibiotic evaluation: their phenotypic and genotypic characterization
    PeerJ 5/ :e2896-,2017
  • First report of blaOXA-499 as a carbapenemase 1 gene from Acinetobacter pittii
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