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Response to "Familial Intracranial Aneurysm Requires Not Only Whole-Exome Sequencing, But Also Mitochondrial DNA Sequencing"

Korean Journal of Radiology, 2022, 23(5), , pp.568-569

2022

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Clinical implications and genetic features of clonal cytopenia of undetermined significance compared to lower‐risk myelodysplastic syndrome

British journal of haematology, 2022-08, Vol.198 (4), p.703-712

2022

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Unique ethnic features of DDX41 mutations in patients with idiopathic cytopenia of undetermined significance, myelodysplastic syndrome, or acute myeloid leukemia

Haematologica (Roma), 2022-02, Vol.107 (2), p.510

2022

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Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm

Korean Journal of Radiology, 2022, 23(1), , pp.101-111

2022

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Emergence of a BCR::ABL1 rearrangement following a uniquely complex clonal evolution pattern in a patient undergoing Fms‐like tyrosine kinase 3 inhibitor therapy for acute myeloid leukemia

International journal of laboratory hematology, 2023-04, Vol.45 (2), p.e24-e27

2023

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Patient-derived multicellular tumor spheroids towards optimized treatment for patients with hepatocellular carcinoma

Journal of experimental & clinical cancer research, 2018-05, Vol.37 (1), p.109-109, Article 109

2018

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Association between ARID2 and RAS-MAPK pathway in intellectual disability and short stature

Journal of medical genetics, 2021-11, Vol.58 (11), p.767

2021

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The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research

PloS one, 2020-05, Vol.15 (5), p.e0233057-e0233057

2020

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Rare Neurovascular Diseases in Korea: Classification and Related Genetic Variants

Korean Journal of Radiology, 2021, 22(8), , pp.1379-1396

2021

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Comparison of clinical and laboratory characteristics of nonsecretory multiple myeloma and secretory multiple myeloma in a tertiary care hospital

International journal of laboratory hematology, 2022-06, Vol.44 (3), p.582-588

2022

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Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients

Scientific reports, 2020-11, Vol.10 (1), p.19540-19540, Article 19540

2020

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Pathological roles of the VEGF/SphK pathway in Niemann-Pick type C neurons

Nature communications, 2014-11, Vol.5 (1), p.5514-5514, Article 5514

2014

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Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing

PloS one, 2016-12, Vol.11 (12), p.e0167641-e0167641

2016

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Genetic Profile and Associated Characteristics of 150 Korean Patients with Retinitis Pigmentosa

Journal of ophthalmology, 2021-10, Vol.2021, p.5067271-15

2021

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Increased circulating plasma cells detected by flow cytometry predicts poor prognosis in patients with plasma cell myeloma

Cytometry. Part B, Clinical cytometry, 2018-05, Vol.94 (3), p.493-499

2018

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Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort

Genes, 2021-04, Vol.12 (5), p.675

2021

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Rare Case of Accelerated-Phase Chronic Myeloid Leukemia Diagnosed During Treatment for JAK2 V617F–Positive Primary Myelofibrosis

Laboratory medicine, 2022-11, Vol.53 (6), p.e140-e144

2022

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Mammalian Sterile 20―like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation

Cancer research (Chicago, Ill.), 2012-10, Vol.72 (20), p.5386-5395

2012

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Frequency and Clinicopathologic Features of RUNX1 Mutations in Patients With Acute Myeloid Leukemia Not Otherwise Specified

American journal of clinical pathology, 2017-07, Vol.148 (1), p.64-72

2017

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Bone Marrow Findings in Patients With Ewing Sarcoma/Primitive Neuroectodermal Tumor

Annals of Laboratory Medicine, 2021, 41(5), , pp.499-501

2021

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Clinical, Laboratory, and Bone Marrow Findings of 31 Patients With Waldenström Macroglobulinemia

Annals of Laboratory Medicine, 2020, 40(3), , pp.193-200

2020

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P404: IMMUNOGLOBULIN GENE REARRANGEMENT IN KOREAN PATIENTS WITH B‐LYMPHOBLASTIC LEUKEMIA – AN IMMUNOPHENOTYPE AND REPERTOIRE ANALYSIS

HemaSphere, 2023-08, Vol.7 (S3), p.e58008b2-n/a

2023

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Identification of the mechanism underlying a human chimera by SNP array analysis

American journal of medical genetics. Part A, 2012-09, Vol.158A (9), p.2119-2123

2012

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VLA-4 and CXCR4 expression levels show contrasting prognostic impact (favorable and unfavorable, respectively) in acute myeloid leukemia

Annals of hematology, 2015-10, Vol.94 (10), p.1631-1638

2015

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First Case of Double T-Cell Receptor Alpha/Delta Rearrangements of t(11;14) and inv(14) and Subsequent JAK2 Rearrangement in a Patient With T-cell Acute Lymphoblastic Leukemia

Annals of Laboratory Medicine, 2020, 40(1), , pp.76-79

2020

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Response to "Familial Intracranial Aneurysm Requires Not Only Whole-Exome Sequencing, But Also Mitochondrial DNA Sequencing"

Clinical implications and genetic features of clonal cytopenia of undetermined significance compared to lower‐risk myelodysplastic syndrome

Unique ethnic features of DDX41 mutations in patients with idiopathic cytopenia of undetermined significance, myelodysplastic syndrome, or acute myeloid leukemia

Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm

Emergence of a BCR::ABL1 rearrangement following a uniquely complex clonal evolution pattern in a patient undergoing Fms‐like tyrosine kinase 3 inhibitor therapy for acute myeloid leukemia

Patient-derived multicellular tumor spheroids towards optimized treatment for patients with hepatocellular carcinoma

Association between ARID2 and RAS-MAPK pathway in intellectual disability and short stature

The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research

Rare Neurovascular Diseases in Korea: Classification and Related Genetic Variants

Comparison of clinical and laboratory characteristics of nonsecretory multiple myeloma and secretory multiple myeloma in a tertiary care hospital

Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients

Pathological roles of the VEGF/SphK pathway in Niemann-Pick type C neurons

Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing

Genetic Profile and Associated Characteristics of 150 Korean Patients with Retinitis Pigmentosa

Increased circulating plasma cells detected by flow cytometry predicts poor prognosis in patients with plasma cell myeloma

Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort

Rare Case of Accelerated-Phase Chronic Myeloid Leukemia Diagnosed During Treatment for JAK2 V617F–Positive Primary Myelofibrosis

Mammalian Sterile 20―like Kinase 1 Suppresses Lymphoma Development by Promoting Faithful Chromosome Segregation

Frequency and Clinicopathologic Features of RUNX1 Mutations in Patients With Acute Myeloid Leukemia Not Otherwise Specified

Bone Marrow Findings in Patients With Ewing Sarcoma/Primitive Neuroectodermal Tumor

Clinical, Laboratory, and Bone Marrow Findings of 31 Patients With Waldenström Macroglobulinemia

P404: IMMUNOGLOBULIN GENE REARRANGEMENT IN KOREAN PATIENTS WITH B‐LYMPHOBLASTIC LEUKEMIA – AN IMMUNOPHENOTYPE AND REPERTOIRE ANALYSIS

Identification of the mechanism underlying a human chimera by SNP array analysis

VLA-4 and CXCR4 expression levels show contrasting prognostic impact (favorable and unfavorable, respectively) in acute myeloid leukemia

First Case of Double T-Cell Receptor Alpha/Delta Rearrangements of t(11;14) and inv(14) and Subsequent JAK2 Rearrangement in a Patient With T-cell Acute Lymphoblastic Leukemia

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