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Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia

Scientific reports, 2020-08, Vol.10 (1), p.14297-14297, Article 14297

2020

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Low CtBP2 expression is associated with a stem cell-like signature and adverse clinical outcome in childhood B-cell lymphoblastic leukemia

Leukemia, 2021-09, Vol.35 (9), p.2684-2687

2021

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Diagnostic Approach for Double-Hit and Triple-Hit Lymphoma Based on Immunophenotypic and Cytogenetic Characteristics of Bone Marrow Specimens

Annals of Laboratory Medicine, 2020, 40(5), , pp.361-369

2020

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Impact of COVID-19 Pandemic Restrictions on Respiratory Virus Patterns: Insights from RSV Surveillance in Gwangju, South Korea

Viruses, 2024-05, Vol.16 (6), p.850

2024

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Accuracy of diagnostic methods and surveillance sensitivity for human enterovirus, South Korea, 1999-2011

Emerging infectious diseases, 2013-08, Vol.19 (8), p.1268-1275

2013

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Ethnicity-specific impact of HLA I/II genotypes on the risk of inhibitor development: data from Korean patients with severe hemophilia A

Annals of hematology, 2018-09, Vol.97 (9), p.1695-1700

2018

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Lymphoma-associated hemophagocytic syndrome: clinical features and treatment outcome

Annals of hematology, 2007-07, Vol.86 (7), p.493-498, Article 493

2007

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Patient-Specific Embryonic Stem Cells Derived from Human SCNT Blastocysts

Science (American Association for the Advancement of Science), 2005-06, Vol.308 (5729), p.1777-1783

2005

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Novel and recurrent mutations of ITGA2B and ITGB3 genes in Korean patients with Glanzmann thrombasthenia

Pediatric blood & cancer, 2012-08, Vol.59 (2), p.335-338

2012

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Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array

Haematologica (Roma), 2012-02, Vol.97 (2), p.304-309

2012

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Factors associated with the time to next attack in neuromyelitis optica: accelerated failure time models with random effects

PloS one, 2013-12, Vol.8 (12), p.e82325

2013

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Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses

Annals of Laboratory Medicine, 2019, 39(6), , pp.545-551

2019

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Immature platelet fraction: establishment of a reference interval and diagnostic measure for thrombocytopenia

Annals of laboratory medicine, 2010-10, Vol.30 (5), p.451-459

2010

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Gene mutation profiles and prognostic implications in Korean patients with T-lymphoblastic leukemia

Annals of hematology, 2013-05, Vol.92 (5), p.635-644

2013

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Neutropenia in parvovirus B19-associated pure red cell aplasia

Annals of hematology, 2011-08, Vol.90 (8), p.975-978

2011

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No association between interleukin 23 receptor gene polymorphisms and systemic lupus erythematosus

Rheumatology international, 2009-11, Vol.30 (1), p.33-38

2009

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Diagnostic utility of a multiplex RT-PCR assay in detecting fusion transcripts from recurrent genetic abnormalities of acute leukemia by WHO 2008 classification

Diagnostic molecular pathology, 2012-03, Vol.21 (1), p.40-44

2012

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Analysis of acute myeloid leukemia in Korean patients with sole trisomy 6

Annals of Laboratory Medicine, 2014, 34(5), , pp.402-404

2014

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Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea

Blood coagulation & fibrinolysis, 2011-03, Vol.22 (2), p.102-105

2011

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Therapy-related myeloid neoplasms in 39 Korean patients: a single institution experience

Annals of Laboratory Medicine, 2013, 33(2), , pp.97-104

2013

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Frequent CD7 antigen loss in aggressive natural killer-cell leukemia: a useful diagnostic marker

Annals of laboratory medicine, 2009-12, Vol.29 (6), p.491-496

2009

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Screening of subtelomeric rearrangements in 100 Korean Pediatric patients with unexplained mental retardation and anomalies using subtelomeric FISH (fluorescence in situ hybridization)

Journal of Korean Medical Science, 2008, 23(4), , pp.573-578

2008

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Increased frequencies of glutathione S-transferase(GSTM1 and GSTT1) gene deletions in Korean patients with acquired aplastic anemia

Blood, 2001-12, Vol.98 (12), p.3483-3485

2001

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Arthroscopic synovectomy in haemophilic arthropathy of the knee

International orthopaedics, 2005-10, Vol.29 (5), p.296-300

2005

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Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

Clinical genetics, 2004-10, Vol.66 (4), p.368-372

2004

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Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia

Low CtBP2 expression is associated with a stem cell-like signature and adverse clinical outcome in childhood B-cell lymphoblastic leukemia

Diagnostic Approach for Double-Hit and Triple-Hit Lymphoma Based on Immunophenotypic and Cytogenetic Characteristics of Bone Marrow Specimens

Impact of COVID-19 Pandemic Restrictions on Respiratory Virus Patterns: Insights from RSV Surveillance in Gwangju, South Korea

Accuracy of diagnostic methods and surveillance sensitivity for human enterovirus, South Korea, 1999-2011

Ethnicity-specific impact of HLA I/II genotypes on the risk of inhibitor development: data from Korean patients with severe hemophilia A

Lymphoma-associated hemophagocytic syndrome: clinical features and treatment outcome

Patient-Specific Embryonic Stem Cells Derived from Human SCNT Blastocysts

Novel and recurrent mutations of ITGA2B and ITGB3 genes in Korean patients with Glanzmann thrombasthenia

Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array

Factors associated with the time to next attack in neuromyelitis optica: accelerated failure time models with random effects

Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses

Immature platelet fraction: establishment of a reference interval and diagnostic measure for thrombocytopenia

Gene mutation profiles and prognostic implications in Korean patients with T-lymphoblastic leukemia

Neutropenia in parvovirus B19-associated pure red cell aplasia

No association between interleukin 23 receptor gene polymorphisms and systemic lupus erythematosus

Diagnostic utility of a multiplex RT-PCR assay in detecting fusion transcripts from recurrent genetic abnormalities of acute leukemia by WHO 2008 classification

Analysis of acute myeloid leukemia in Korean patients with sole trisomy 6

Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea

Therapy-related myeloid neoplasms in 39 Korean patients: a single institution experience

Frequent CD7 antigen loss in aggressive natural killer-cell leukemia: a useful diagnostic marker

Screening of subtelomeric rearrangements in 100 Korean Pediatric patients with unexplained mental retardation and anomalies using subtelomeric FISH (fluorescence in situ hybridization)

Increased frequencies of glutathione S-transferase(GSTM1 and GSTT1) gene deletions in Korean patients with acquired aplastic anemia

Arthroscopic synovectomy in haemophilic arthropathy of the knee

Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

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