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Journal Articles

WHO2016 Vs. WHO2008 Criteria for the Diagnosis of Chronic Myelomonocytic Leukemia

Sung-Ran Cho, MD, Joon Seong Park, MD, Yeonsook Moon, MD, Mi Hyang Kim, MD, Jeong-Yeal Ahn, MD, Jungwon Huh, MD, Hye Ryoun Kim, MD PhD, Jae Ho Han, MD

Blood (2017) 130 (Supplement 1): 5314.

https://doi.org/10.1182/blood.V130.Suppl_1.5314.5314

Published: 2017

Journal Articles

Different Characteristics Identified by Single Nucleotide Polymorphism Array Analsysis in Leukemia Suggest the Need for Different Application Strategics Depending On Disease Category.

Jungwon Huh, MD, PhD, Chul Won Jung, Hyeoung-Joon Kim, MD, PhD, Yeo-Kyeoung Kim, MD, PhD, Joon Ho Moon, MD, PhD, Sang Kyun Sohn, MD, Hee-je Kim, Woo-Sung Min, MD, PhD, Dennis Dong Hwan Kim, MD, PhD

Blood (2012) 120 (21): 2490.

https://doi.org/10.1182/blood.V120.21.2490.2490

Published: 2012

Journal Articles

NPM1, IDH1/2 and DNAH11 Gene Mutations Can Improve a Prognostic Stratification of Acute Myeloid Leukemia Patients with Normal Karyotype but Not Harboring FLT3/ITD Mutation.

Yeo-Kyeoung Kim, MD, PhD, Il-Kwon Lee, PhD, Dennis Dong Hwan Kim, MD, PhD, Chul Won Jung, MD, PhD, Jun-Ho Jang, MD, PhD, Hee Je Kim, MD, PhD, Joon Ho Moon, MD, Sang Kyun Sohn, MD, Jong-Ho Won, MD, PhD, Sung-Hyun Kim, Jungwon Huh, MD, PhD, Namshin Kim, PhD, Yun Gyeong Lee, PhD, Sung-Hoon Jung, MD, Je-Jung Lee, MD, PhD, Hyeoung-Joon Kim, MD, PhD

Blood (2012) 120 (21): 2534.

https://doi.org/10.1182/blood.V120.21.2534.2534

Published: 2012

Journal Articles

Whole Exome Sequencing Analysis in AML with Normal Karyotype Not Harboring FLT3/ITD Mutation Reveals Novel Genetic Alterations.

Blood (2012) 120 (21): 2593.

https://doi.org/10.1182/blood.V120.21.2593.2593

Published: 2012

Journal Articles

Definition of Commonly Deleted Regions and Identification of Candidate Genes of Chromosome 20 in Myeloid Malignancies Using Genome-Wide Single Nucleotide Polymorphism (SNP) Array.

Jungwon Huh, MD, Ramon V. Tiu, MD, BS, Ying Jiang, MD, PhD, Lukasz P Gondek, MD, PhD, Christine O’Keefe, PhD, Karl S. Theil, MD, Jaroslaw P Maciejewski, MD, PhD

Blood (2008) 112 (11): 2056.

https://doi.org/10.1182/blood.V112.11.2056.2056

Published: 2008

Journal Articles

Using Combined High Density SNP/CNV Arrays as a Clinical Karyotyping Tool in Myeloid Malignancies.

Jungwon Huh, MD, Lukasz Gondek, Christine O’Keefe, PhD, Karl S. Theil, MD, Jaroslaw P. Maciejewski, MD, PhD

Blood (2008) 112 (11): 1504.

https://doi.org/10.1182/blood.V112.11.1504.1504

Published: 2008

Journal Articles

SNP-Array Based Karyotyping Complements Routine Cytogenetics in Diagnosis and Risk Stratification Schemes of MDS

Ramon V. Tiu, MD, BS, Lukasz P Gondek, MD, PhD, Jungwon Huh, MD, Christine O’Keefe, PhD, Mikkael A. Sekeres, MD, MS, Ghulam J Mufti, MBBS, DM, FRCP, FRCPath, Michael A McDevitt, MD, PhD, Jaroslaw Maciejewski, MD, PhD

Blood (2008) 112 (11): 639.

https://doi.org/10.1182/blood.V112.11.639.639

Published: 2008

Journal Articles

FISH and SNP-Array Karyotyping Improve the Detection of Recurrent Chromosomal Defects Including Del(5q), Monosomy 7, Del(7q), Trisomy 8, and Del(20q) in Myelodysplastic Syndromes.

Hideki Makishima, MD, PhD, Manjot Rataul, MD, Lukasz P. Gondek, MD, PhD, Jungwon Huh, MD, James R. Cook, MD, PhD, Karl S. Theil, MD, Mikkael A Sekeres, MD, MS, Elizabeth Kuczkowski, Jaroslaw P. Maciejewski, MD, PhD

Blood (2008) 112 (11): 1483.

https://doi.org/10.1182/blood.V112.11.1483.1483

Published: 2008

NARROW

WHO2016 Vs. WHO2008 Criteria for the Diagnosis of Chronic Myelomonocytic Leukemia

Different Characteristics Identified by Single Nucleotide Polymorphism Array Analsysis in Leukemia Suggest the Need for Different Application Strategics Depending On Disease Category.

NPM1, IDH1/2 and DNAH11 Gene Mutations Can Improve a Prognostic Stratification of Acute Myeloid Leukemia Patients with Normal Karyotype but Not Harboring FLT3/ITD Mutation.

Whole Exome Sequencing Analysis in AML with Normal Karyotype Not Harboring FLT3/ITD Mutation Reveals Novel Genetic Alterations.

Definition of Commonly Deleted Regions and Identification of Candidate Genes of Chromosome 20 in Myeloid Malignancies Using Genome-Wide Single Nucleotide Polymorphism (SNP) Array.

Using Combined High Density SNP/CNV Arrays as a Clinical Karyotyping Tool in Myeloid Malignancies.

SNP-Array Based Karyotyping Complements Routine Cytogenetics in Diagnosis and Risk Stratification Schemes of MDS

FISH and SNP-Array Karyotyping Improve the Detection of Recurrent Chromosomal Defects Including Del(5q), Monosomy 7, Del(7q), Trisomy 8, and Del(20q) in Myelodysplastic Syndromes.

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ASH Publications

American Society of Hematology

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ASH Publications

American Society of Hematology

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