Dong S. Lee

Seoul, 110744, Republic of Korea

Last Updated: 09/26/2026

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Found 14 publications

Author Correction: Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.

Author Correction: Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.

Journal: Scientific reports

Published: December 13, 2022

The importance of critically short telomere in myelodysplastic syndrome.

The importance of critically short telomere in myelodysplastic syndrome.

Journal: Biomarker research

Published: October 13, 2022

Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in Korea.

Analysis of clinical and genomic profiles of therapy-related myeloid neoplasm in Korea.

Journal: Human genomics

Published: August 08, 2022

Increased Apoptotic Activity in Low-Risk Myelodysplastic Syndrome.

Increased Apoptotic Activity in Low-Risk Myelodysplastic Syndrome.

Journal: Journal of clinical medicine

Published: July 08, 2022

Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.

Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.

Journal: Scientific reports

Published: June 16, 2021

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.

Journal: Orphanet journal of rare diseases

Published: December 01, 2018

Replicative senescence of hematopoietic cells in patients with idiopathic cytopenia of undetermined significance.

Replicative senescence of hematopoietic cells in patients with idiopathic cytopenia of undetermined significance.

Journal: Leukemia research

Published: October 17, 2018

ASXL1 is a molecular predictor in idiopathic cytopenia of undetermined significance.

ASXL1 is a molecular predictor in idiopathic cytopenia of undetermined significance.

Journal: Leukemia & lymphoma

Published: October 11, 2018

Mutation of ten-eleven translocation-2 is associated with increased risk of autoimmune disease in patients with myelodysplastic syndrome.

Mutation of ten-eleven translocation-2 is associated with increased risk of autoimmune disease in patients with myelodysplastic syndrome.

Journal: The Korean journal of internal medicine

Published: July 05, 2018

WHIM Syndrome With a Novel CXCR4 Variant in a Korean Child.

WHIM Syndrome With a Novel CXCR4 Variant in a Korean Child.

Journal: Annals of laboratory medicine

Published: November 03, 2016

Dysregulation of Telomere Lengths and Telomerase Activity in Myelodysplastic Syndrome.

Dysregulation of Telomere Lengths and Telomerase Activity in Myelodysplastic Syndrome.

Journal: Annals of laboratory medicine

Published: August 11, 2016

Short telomere length and its correlation with gene mutations in myelodysplastic syndrome.

Short telomere length and its correlation with gene mutations in myelodysplastic syndrome.

Journal: Journal of hematology & oncology

Published: May 27, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026