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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

Calreticulin mRNA Expression Levels and Clinicopathologic Characteristics in Hematologic Malignancies

Sholhui Park, MD, Hee Jin Huh, Yeung Chul Mun, Chu-Myong Seong, Wha Soon Chung, Jungwon Huh

Blood (2014) 124 (21): 5184.

https://doi.org/10.1182/blood.V124.21.5184.5184

Published: 2014

Journal Articles

Oxidation Of Peroxiredoxins By Thioredoxin Inactivation Is Mediated In Arsenic Trioxide-Induced Reactive Oxygen Species Formation and Its Cytotoxicity In Acute Promyelocytic Leukemia Cells

Yeung-Chul Mun, Jee-Young Ahn, Eun-Sun Yoo, Jungwon Huh, Kyoung Eun Lee, Eunmi Nam, Soon Nam Lee, Chu-Myong Seong

Blood (2013) 122 (21): 3858.

https://doi.org/10.1182/blood.V122.21.3858.3858

Published: 2013

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

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

Genome-Wide Single-Nucleotide Polymorphism-Array Can Improve Prognostic Stratification of Core Binding Factor Acute Myeloid Leukemia, Especially in the Subgroup with Inv(16)/t(16;16) or without D816 C-KIT Mutation,

Jungwon Huh, Heeje Kim, Woo-Sung Min, Chul Won Jung, Hee-Jin Kim, Sun-Hee Kim, Yeo-Kyeoung Kim, Hyeoung Joon Kim, Joon Ho Moon, Sang Kyun Sohn, Sung Hyun Kim, Won Sik Lee, Jong-Ho Won, Yeung-Chul Mun, Hawk Kim, Jeeny Park, Dennis Dong Hwan Kim

Blood (2011) 118 (21): 3515.

https://doi.org/10.1182/blood.V118.21.3515.3515

Published: 2011

Journal Articles

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

Ramon V. Tiu, Lukasz P. Gondek, Christine L. O'Keefe, Paul Elson, Jungwon Huh, Azim Mohamedali, Austin Kulasekararaj, Anjali S. Advani, Ronald Paquette, Alan F. List, Mikkael A. Sekeres, Michael A. McDevitt, Ghulam J. Mufti, Jaroslaw P. Maciejewski

Blood (2011) 117 (17): 4552–4560.

https://doi.org/10.1182/blood-2010-07-295857

Published: 2011

Includes: Supplemental data

Journal Articles

Genome-Wide Single-Nucleotide Polymorphism-Array Based Karyotyping Detects Clonal Aberrations, and Predicts the Risk of Imatinib Failure In Chronic Myeloid Leukemia.

Boram Han, Jungwon Huh, Jun Ho Yi, Ha Yeon Lee, Jong-Won Kim, Hee-Jin Kim, Yeo-Kyeoung Kim, Hyeoung Joon Kim, MD, PhD, Joon Ho Moon, Sang Kyun Sohn, Chul Won Jung, Dong Hwan (Dennis) Kim

Blood (2010) 116 (21): 3387.

https://doi.org/10.1182/blood.V116.21.3387.3387

Published: 2010

Journal Articles

Genome-Wide Single-Nucleotide Polymorphism-Array Based Karyotyping Detects Clonal Aberrations Including Uniparental Disomy (UPD), Gain or Loss Which Were Unfavorable Prognostic Factor In Acute Myeloid Leukemia with Normal Karyotype.

Dong Hwan (Dennis) Kim, Jungwon Huh, Boram Han, Ha Yeon Lee, Jun Ho Yi, Jun Ho Jang, Kihyun Kim, Hyeoung Joon Kim, MD, PhD, Yeo-Kyeoung Kim, Sang Kyun Sohn, Joon Ho Moon, Sung Hyun Kim, Chul Won Jung

Blood (2010) 116 (21): 1669.

https://doi.org/10.1182/blood.V116.21.1669.1669

Published: 2010

Journal Articles

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

Anna M. Jankowska, Hadrian Szpurka, Ramon V. Tiu, Hideki Makishima, Manuel Afable, Jungwon Huh, Christine L. O'Keefe, Rebecca Ganetzky, Michael A. McDevitt, Jaroslaw P. Maciejewski

Blood (2009) 113 (25): 6403–6410.

https://doi.org/10.1182/blood-2009-02-205690

Published: 2009

Journal Articles

SNP Array-Based Analysis of Chromosome 17 Reveals Biallelic TP53 Mutations Due to Uniparental Disomy 17p in Advanced MDS and AML with Cooperating Deletions of Chromosomes 5 and 7

Monika Jasek, Lukasz P. Gondek, Nelli Bejanyan, Ramon V. Tiu, Jungwon Huh, Karl S. Theil, Christine O’ Keefe, Michael A. McDevitt, Jaroslaw P. Maciejewski

Blood (2008) 112 (11): 2521.

https://doi.org/10.1182/blood.V112.11.2521.2521

Published: 2008

Journal Articles

SNP Karyotyping Can Detect Clonality of Stem Cell Compartment and Early Malignant Evolution in Aplastic Anemia

Marcin Wlodarski, Sanjay Mohan, Lukasz Gondek, Jungwon Huh, Michael Clemente, Ramon Tiu, Jaroslaw Maciejewski

Blood (2008) 112 (11): 443.

https://doi.org/10.1182/blood.V112.11.443.443

Published: 2008

Journal Articles

High Resolution Karyotyping of Large Granular Lymphocyte Leukemia by SNP Arrays Reveals Clonal Defects Leading to LOH at Loci Integral to Lymphocyte Function.

Aaron D. Viny, BS, Hideki Makashima, Jungwon Huh, Karl S. Theil, MD, Lukasz Gondek, MD, Jaroslaw Maciejewski

Blood (2008) 112 (11): 1513.

https://doi.org/10.1182/blood.V112.11.1513.1513

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

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

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

NARROW

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

Calreticulin mRNA Expression Levels and Clinicopathologic Characteristics in Hematologic Malignancies

Oxidation Of Peroxiredoxins By Thioredoxin Inactivation Is Mediated In Arsenic Trioxide-Induced Reactive Oxygen Species Formation and Its Cytotoxicity In Acute Promyelocytic Leukemia Cells

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

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.

Genome-Wide Single-Nucleotide Polymorphism-Array Can Improve Prognostic Stratification of Core Binding Factor Acute Myeloid Leukemia, Especially in the Subgroup with Inv(16)/t(16;16) or without D816 C-KIT Mutation,

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

Genome-Wide Single-Nucleotide Polymorphism-Array Based Karyotyping Detects Clonal Aberrations, and Predicts the Risk of Imatinib Failure In Chronic Myeloid Leukemia.

Genome-Wide Single-Nucleotide Polymorphism-Array Based Karyotyping Detects Clonal Aberrations Including Uniparental Disomy (UPD), Gain or Loss Which Were Unfavorable Prognostic Factor In Acute Myeloid Leukemia with Normal Karyotype.

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

SNP Array-Based Analysis of Chromosome 17 Reveals Biallelic TP53 Mutations Due to Uniparental Disomy 17p in Advanced MDS and AML with Cooperating Deletions of Chromosomes 5 and 7

SNP Karyotyping Can Detect Clonality of Stem Cell Compartment and Early Malignant Evolution in Aplastic Anemia

High Resolution Karyotyping of Large Granular Lymphocyte Leukemia by SNP Arrays Reveals Clonal Defects Leading to LOH at Loci Integral to Lymphocyte Function.

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.

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

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.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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