Lista de obras - Seung-Tae Lee - Dominio Público Uruguay

A Child With Lymphangioma Due to Somatic Mutation in PIK3CA Successfully Treated With Everolimus

artículo científico publicado en 2018

A case of CD5-positive mature B-cell neoplasm with t(10;14)(q24;q11.2) and trisomy 12

artículo científico publicado en 2014

A cryptic ETV6/ABL1 rearrangement represents a unique fluorescence in situ hybridization signal pattern in a patient with B acute lymphoblastic leukemia

artículo científico publicado en 2014

A novel COL3A1 gene mutation in patient with aortic dissected aneurysm and cervical artery dissections

article

A patient with B-cell acute lymphoblastic leukemia with PAX5-ETV6 rearrangement with dic(9;12)(p13;p13) identified by chromosomal microarray

scientific article published on 08 March 2018

A subset of CD45+/CD19 - cells in bone marrow may be associated with clinical outcomes of patients with mantle cell lymphoma.

artículo científico publicado en 2015

A unique case of dendritic cell neoplasm from monocyte-derived myeloid origin with distinct immunophenotype and cytomorphology.

artículo científico publicado en 2013

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

artículo científico publicado en 2014

Antigen Expression Patterns of Plasma Cell Myeloma: An Association of Cytogenetic Abnormality and International Staging System (ISS) for Myeloma.

artículo científico publicado en 2014

Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population

artículo científico publicado en 2018

Associations of single nucleotide polymorphisms related to insulin resistance with polycystic ovary syndrome

artículo científico publicado en 2014

BRAF V600E and MAP2K1 mutations in hairy cell leukemia and splenic marginal zone lymphoma cases

artículo científico publicado en 2015

Bone marrow flow cytometry in staging of patients with B-cell non-Hodgkin lymphoma

artículo científico publicado en 2015

Challenges in assessing pathogenicity based on frequency of variants in mismatch repair genes: an extreme case of a MSH2 variant and a meta-analysis.

artículo científico publicado en 2014

Chronic Myeloid Leukemia With Rare Variant b2a3 (e13a3) BCR-ABL1 Fusion.

artículo científico publicado en 2016

Clinical Significance of Revised Banff Criteria in the Diagnosis of Antibody-Mediated Rejection

artículo científico publicado en 2019

Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis

artículo científico publicado en 2009

Clinical and genetic analysis of a Korean family with hereditary spastic paraplegia type 3.

artículo científico publicado en 2010

Clinical application of catalytically cleavable fluorescence probe technology for multiplexing quantification of BCR-ABL1 fusion transcripts

artículo científico publicado en 2013

Comparison of Clinical Outcomes of BRCA1/2 Pathologic Mutation, Variants of Unknown Significance, or Wild Type Epithelial Ovarian Cancer Patients

artículo científico publicado en 2016

Defining an Optimal Number of Immunophenotypic Markers for Lineage Assignment of Acute Leukemias Based on the EGIL Scoring System

scientific article published on 01 December 2006

Detection of MYD88 L265P in patients with lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia and other B-cell non-Hodgkin lymphomas.

artículo científico publicado en 2016

Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next-generation sequencing approaches

artículo científico publicado en 2020

Diagnostic application of clinical exome sequencing in Leber congenital amaurosis

artículo científico publicado en 2017

Difference in Risk of Breast and Ovarian Cancer According to Putative Functional Domain Regions in Korean BRCA1/2 Mutation Carriers

scientific article published on 20 February 2018

Discrepancy in genotyping of apolipoprotein E between allele-specific PCR and fluorescence resonance energy transfer or sequencing.

artículo científico publicado en 2010

Epigenetic remodeling in B-cell acute lymphoblastic leukemia occurs in two tracks and employs embryonic stem cell-like signatures.

artículo científico publicado en 2015

Evaluation of an amplicon-based next-generation sequencing panel for detection of BRCA1 and BRCA2 genetic variants.

artículo científico publicado en 2016

Frequency and Clinical Characteristics of Intrachromosomal Amplification of Chromosome 21 in Korean Childhood B-lineage Acute Lymphoblastic Leukemia

scientific article published on September 2016

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

artículo científico publicado en 2009

Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV.

artículo científico publicado en 2007

Genome-wide CpG island methylation and intergenic demethylation propensities vary among different tumor sites

artículo científico publicado en 2015

Genotyping of Mycobacterium intracellulare isolates and clinical characteristics of lung disease.

artículo científico publicado en 2013

Guidelines for Laboratory Diagnosis of Coronavirus Disease 2019 (COVID-19) in Korea

scientific article published on 31 March 2020

Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in the Korean population

artículo científico publicado en 2010

Identification of Mixed Lineage Leukemia Gene (MLL)/MLLT10 Fusion Transcripts by Reverse Transcription-PCR and Sequencing in a Case of AML With a FISH-Negative Cryptic MLL Rearrangement

artículo científico publicado en 2015

Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations

artículo científico publicado en 2007

Interaction of allergy history and antibodies to specific varicella-zoster virus proteins on glioma risk

artículo científico publicado en 2013

Internal Tandem Duplication in Patients With Acute Myeloid Leukemia Is Readily Detectable in a Single Next-Generation Sequencing Assay Using the Pindel Algorithm

artículo científico publicado en 2019

Isolated 9p Duplication With der(Y)t(Y;9)(q12;p13.2) in a Male Patient With Cardiac Defect and Mental Retardation Confirmed by Chromosomal Microarray.

artículo científico publicado en 2016

Korean Society for Genetic Diagnostics Guidelines for Validation of Next-Generation Sequencing-Based Somatic Variant Detection in Hematologic Malignancies

scientific article published on 01 November 2019

Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome

artículo científico publicado en 2019

Molecular characterization and clinical course of MLL-ACTN4 rearrangement in therapy-related hematologic malignancies

artículo científico publicado en 2014

Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement.

artículo científico publicado en 2014

Molecular characterization of near-complete trisomy 17p syndrome from inverted duplication in association with cryptic deletion of 17pter.

artículo científico publicado en 2014

Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster

artículo científico publicado en 2009

Mutant Enrichment with 3'-Modified Oligonucleotides (MEMO)-Quantitative PCR for Detection of NPM1 Mutations in Acute Myeloid Leukemia.

artículo científico publicado en 2014

Mutant Thr95Ile Transthyretin-Related Cardiac Amyloidosis With Polyneuropathy

scientific article published on 26 June 2019

Mutation profiling of 19 candidate genes in acute myeloid leukemia suggests significance of DNMT3A mutations

artículo científico publicado en 2016

NOTCH2 missplicing can occur in relation to apoptosis.

artículo científico publicado en 2015

Newborn hereditary elliptocytosis confirmed by familial genetic testing

scientific article published on 09 July 2019

Next-generation sequencing with comprehensive bioinformatics analysis facilitates somatic mosaic APC gene mutation detection in patients with familial adenomatous polyposis

artículo científico publicado en 2019

PTPRG inhibition by DNA methylation and cooperation with RAS gene activation in childhood acute lymphoblastic leukemia

artículo científico publicado en 2014

Performance evaluation of the new hematology analyzer Sysmex XN-series.

artículo científico

Report of the Korean Association of External Quality Assessment Service on Next-Generation Sequencing Analysis for Somatic Variants (2018–2020)

artículo científico publicado en 2021

SNP-based next-generation sequencing reveals low-level mixed chimerism after allogeneic hematopoietic stem cell transplantation

artículo científico publicado en 2018

Simultaneous occurrence of angioimmunoblastic T-cell lymphoma and plasma cell leukemia

artículo científico publicado en 2014

Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy

scientific article published on 26 June 2019

Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neoplasms

artículo científico publicado en 2019

Telomere length in alcohol dependence: A role for impulsive choice and childhood maltreatment.

artículo científico publicado en 2017

Thalidomide, cyclophosphamide and dexamethasone induction therapy: feasibility for myeloma patients destined for autologous stem cell transplantation

artículo científico publicado en 2014

The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report

artículo científico publicado en 2019

The effect of trauma and PTSD on telomere length: An exploratory study in people exposed to combat trauma

artículo científico publicado en 2017

The first Korean case of childhood acute myeloid leukemia with inv(11)(p15q22)/NUP98-DDX10 rearrangement: a rare but recurrent genetic abnormality

artículo científico publicado en 2014

Trends in contralateral prophylactic mastectomy rate according to clinicopathologic and socioeconomic status

scientific article published on 29 August 2019

Two cases of acute lymphoblastic leukemia with an e1a3 BCR-ABL1 fusion transcript

artículo científico publicado en 2014

Usefulness of Flow Cytometric Analysis for Detecting Leptomeningeal Diseases in Non-Hodgkin Lymphoma

artículo científico publicado en 2016

Validation and optimization of the Ion Torrent S5 XL sequencer and Oncomine workflow for BRCA1 and BRCA2 genetic testing

artículo científico publicado en 2017

Whole-genome fingerprint of the DNA methylome during human B cell differentiation

artículo científico publicado en 2015

Lista de obras de Seung-Tae Lee

A Child With Lymphangioma Due to Somatic Mutation in PIK3CA Successfully Treated With Everolimus

A case of CD5-positive mature B-cell neoplasm with t(10;14)(q24;q11.2) and trisomy 12

A cryptic ETV6/ABL1 rearrangement represents a unique fluorescence in situ hybridization signal pattern in a patient with B acute lymphoblastic leukemia

A novel COL3A1 gene mutation in patient with aortic dissected aneurysm and cervical artery dissections

A patient with B-cell acute lymphoblastic leukemia with PAX5-ETV6 rearrangement with dic(9;12)(p13;p13) identified by chromosomal microarray

A subset of CD45+/CD19 - cells in bone marrow may be associated with clinical outcomes of patients with mantle cell lymphoma.

A unique case of dendritic cell neoplasm from monocyte-derived myeloid origin with distinct immunophenotype and cytomorphology.

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

Antigen Expression Patterns of Plasma Cell Myeloma: An Association of Cytogenetic Abnormality and International Staging System (ISS) for Myeloma.

Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population

Associations of single nucleotide polymorphisms related to insulin resistance with polycystic ovary syndrome

BRAF V600E and MAP2K1 mutations in hairy cell leukemia and splenic marginal zone lymphoma cases

Bone marrow flow cytometry in staging of patients with B-cell non-Hodgkin lymphoma

Challenges in assessing pathogenicity based on frequency of variants in mismatch repair genes: an extreme case of a MSH2 variant and a meta-analysis.

Chronic Myeloid Leukemia With Rare Variant b2a3 (e13a3) BCR-ABL1 Fusion.

Clinical Significance of Revised Banff Criteria in the Diagnosis of Antibody-Mediated Rejection

Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis

Clinical and genetic analysis of a Korean family with hereditary spastic paraplegia type 3.

Clinical application of catalytically cleavable fluorescence probe technology for multiplexing quantification of BCR-ABL1 fusion transcripts

Comparison of Clinical Outcomes of BRCA1/2 Pathologic Mutation, Variants of Unknown Significance, or Wild Type Epithelial Ovarian Cancer Patients

Defining an Optimal Number of Immunophenotypic Markers for Lineage Assignment of Acute Leukemias Based on the EGIL Scoring System

Detection of MYD88 L265P in patients with lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia and other B-cell non-Hodgkin lymphomas.

Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next-generation sequencing approaches

Diagnostic application of clinical exome sequencing in Leber congenital amaurosis

Difference in Risk of Breast and Ovarian Cancer According to Putative Functional Domain Regions in Korean BRCA1/2 Mutation Carriers

Discrepancy in genotyping of apolipoprotein E between allele-specific PCR and fluorescence resonance energy transfer or sequencing.

Epigenetic remodeling in B-cell acute lymphoblastic leukemia occurs in two tracks and employs embryonic stem cell-like signatures.

Evaluation of an amplicon-based next-generation sequencing panel for detection of BRCA1 and BRCA2 genetic variants.

Frequency and Clinical Characteristics of Intrachromosomal Amplification of Chromosome 21 in Korean Childhood B-lineage Acute Lymphoblastic Leukemia

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

Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV.

Genome-wide CpG island methylation and intergenic demethylation propensities vary among different tumor sites

Genotyping of Mycobacterium intracellulare isolates and clinical characteristics of lung disease.

Guidelines for Laboratory Diagnosis of Coronavirus Disease 2019 (COVID-19) in Korea

Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in the Korean population

Identification of Mixed Lineage Leukemia Gene (MLL)/MLLT10 Fusion Transcripts by Reverse Transcription-PCR and Sequencing in a Case of AML With a FISH-Negative Cryptic MLL Rearrangement

Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations

Interaction of allergy history and antibodies to specific varicella-zoster virus proteins on glioma risk

Internal Tandem Duplication in Patients With Acute Myeloid Leukemia Is Readily Detectable in a Single Next-Generation Sequencing Assay Using the Pindel Algorithm

Isolated 9p Duplication With der(Y)t(Y;9)(q12;p13.2) in a Male Patient With Cardiac Defect and Mental Retardation Confirmed by Chromosomal Microarray.

Korean Society for Genetic Diagnostics Guidelines for Validation of Next-Generation Sequencing-Based Somatic Variant Detection in Hematologic Malignancies

Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome

Molecular characterization and clinical course of MLL-ACTN4 rearrangement in therapy-related hematologic malignancies

Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement.

Molecular characterization of near-complete trisomy 17p syndrome from inverted duplication in association with cryptic deletion of 17pter.

Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster

Mutant Enrichment with 3'-Modified Oligonucleotides (MEMO)-Quantitative PCR for Detection of NPM1 Mutations in Acute Myeloid Leukemia.

Mutant Thr95Ile Transthyretin-Related Cardiac Amyloidosis With Polyneuropathy

Mutation profiling of 19 candidate genes in acute myeloid leukemia suggests significance of DNMT3A mutations

NOTCH2 missplicing can occur in relation to apoptosis.

Newborn hereditary elliptocytosis confirmed by familial genetic testing

Next-generation sequencing with comprehensive bioinformatics analysis facilitates somatic mosaic APC gene mutation detection in patients with familial adenomatous polyposis

PTPRG inhibition by DNA methylation and cooperation with RAS gene activation in childhood acute lymphoblastic leukemia

Performance evaluation of the new hematology analyzer Sysmex XN-series.

Report of the Korean Association of External Quality Assessment Service on Next-Generation Sequencing Analysis for Somatic Variants (2018–2020)

SNP-based next-generation sequencing reveals low-level mixed chimerism after allogeneic hematopoietic stem cell transplantation

Simultaneous occurrence of angioimmunoblastic T-cell lymphoma and plasma cell leukemia

Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy

Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neoplasms

Telomere length in alcohol dependence: A role for impulsive choice and childhood maltreatment.

Thalidomide, cyclophosphamide and dexamethasone induction therapy: feasibility for myeloma patients destined for autologous stem cell transplantation

The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report

The effect of trauma and PTSD on telomere length: An exploratory study in people exposed to combat trauma

The first Korean case of childhood acute myeloid leukemia with inv(11)(p15q22)/NUP98-DDX10 rearrangement: a rare but recurrent genetic abnormality

Trends in contralateral prophylactic mastectomy rate according to clinicopathologic and socioeconomic status

Two cases of acute lymphoblastic leukemia with an e1a3 BCR-ABL1 fusion transcript

Usefulness of Flow Cytometric Analysis for Detecting Leptomeningeal Diseases in Non-Hodgkin Lymphoma

Validation and optimization of the Ion Torrent S5 XL sequencer and Oncomine workflow for BRCA1 and BRCA2 genetic testing

Whole-genome fingerprint of the DNA methylome during human B cell differentiation