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Journal Articles

Myelodysplastic Syndrome with Excess Blasts and Secondary Acute Myeloid Leukemia: Same Disease with Different Blast Count

Xueyan Chen, MD, Megan Othus, PhD, Brent L Wood, MD PhD, Roland B. Walter, MD PhD MS, Pamela S. Becker, MD PhD, Mary-Elizabeth M. Percival, MD, Janis L. Abkowitz, MD, Frederick R. Appelbaum, MD, Elihu H. Estey, MD

Blood (2019) 134 (Supplement_1): 2692.

https://doi.org/10.1182/blood-2019-124977

Published: 2019

Journal Articles

Disruption of a GATA1-binding motif upstream of XG / PBDX abolishes Xg a expression and resolves the Xg blood group system

Mattias Möller, Yan Quan Lee, Karina Vidovic, Sven Kjellström, Linda Björkman, Jill R. Storry, Martin L. Olsson

Blood (2018) 132 (3): 334–338.

https://doi.org/10.1182/blood-2018-03-842542

Published: 2018

Includes: Supplemental data

Journal Articles

Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT

Julia S. Westman, Linn Stenfelt, Karina Vidovic, Mattias Möller, Åsa Hellberg, Sven Kjellström, Martin L. Olsson

Blood (2018) 131 (14): 1611–1616.

https://doi.org/10.1182/blood-2017-08-803080

Published: 2018

Includes: Supplemental data

Journal Articles

Towards the Development of a Noninvasive Prenatal Test for Beta-Thalassemia: Utilization of Probe Capture Enrichment and Next Generation Sequencing

Katie Carlberg, MD, Nikhil Bose, Jingyi Deng, Ashutosh Lal, MD, Henry Erlich, PhD, Cassandra Calloway, PhD

Blood (2016) 128 (22): 3622.

https://doi.org/10.1182/blood.V128.22.3622.3622

Published: 2016

Journal Articles

Identification of Copy Number Variants in Type 1 and Type 3 VWD by aCGH in the Zimmerman Program

Pamela A Christopherson, Rupa A Udani, PhD, Crystal Perry, BS, Daniel B Bellissimo, PhD, Sandra L Haberichter, PhD, Veronica H Flood, MD, Kenneth D Friedman, MD, Joan Cox Gill, MD, Robert R. Montgomery, MD, Zimmerman Program Investigators

Blood (2016) 128 (22): 872.

https://doi.org/10.1182/blood.V128.22.872.872

Published: 2016

Journal Articles

A Second Generation, Multiple Myeloma-Specific, Targeted Sequencing Platform for Detecting Translocations, Copy Number Alterations, and Single Nucleotide Variants

Brian S White, PhD, Irena Lanc, PhD, Daniel Auclair, PhD, Robert Fulton, PhD, Mark A Fiala, BS, CCRP, Justin King, Gregory Ahmann, BS, Mary Derome, MS, Elaine R Mardis, PhD, Joan Levy, PhD, Ravi Vij, MD MBA, John F. DiPersio, MD PhD, Michael Tomasson, MD

Blood (2015) 126 (23): 4207.

https://doi.org/10.1182/blood.V126.23.4207.4207

Published: 2015

Journal Articles

High-Sensitivity Genomic Minimal Residual Disease Detection Reveals Multiclonal Hematopoiesis and Is Associated with Survival in Adult AML

Brian Parkin, Angelina Londoño Joshi, PhD, Qing Kang, PhD, Andrew D. Rhim, MD, Sami N. Malek

Blood (2015) 126 (23): 225.

https://doi.org/10.1182/blood.V126.23.225.225

Published: 2015

Journal Articles

Rapid Simultaneous Detection of Multiple Micro-Ribonucleic Acids By Surface Plasmon Resonance Array in Cell Lysates of Myelodysplastic Syndromes Patients

Jan E. Dyr, professor, Jaroslav Cermak, Hana Vaisocherova, Zdenek Krejcik, Hana Sipova, Marketa Bockova, Ivana Visova, Tomas Springer, Marie Laura Ermini, Leona Chrastinova, Ondrej Pastva, Kristyna Pimkova, Roman Kotlin, Jaromir Novak, Jiri Homola

Blood (2014) 124 (21): 5605.

https://doi.org/10.1182/blood.V124.21.5605.5605

Published: 2014

Journal Articles

Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia

Amber Hogart Begtrup, PhD, Neha Dagaonkar, Suvarnamala Pushkaran, M.Sc., Katie M. Giger, PhD, Ammar Husami, Diane Kissell, Clinton H. Joiner, MD, PhD, Mehdi Keddache, Ph.D., Kejian Zhang, M.D., M.B.A., Theodosia A. Kalfa, M.D., Ph.D.

Blood (2013) 122 (21): 949.

https://doi.org/10.1182/blood.V122.21.949.949

Published: 2013

Journal Articles

Clinical and Biological Characteristics According to the Burden of JAK2V617F Mutated Allele in BCR-ABL Negative MPNs

Blood (2012) 120 (21): 1437.

https://doi.org/10.1182/blood.V120.21.1437.1437

Published: 2012

Journal Articles

Detection of VWF Copy Number Variations by Microarray Analysis in Von Willebrand Disease Type 3 Index Cases

Daniel B. Bellissimo, PhD, Ephrem Chin, Madhuri Hegde, PhD, Pamela A. Christopherson, Sandra L. Haberichter, PhD, Robert R. Montgomery, MD

Blood (2011) 118 (21): 380.

https://doi.org/10.1182/blood.V118.21.380.380

Published: 2011

Journal Articles

Impact of KIR B/X Genotype and Missing KIR Ligands in HLA-Matched Unrelated Donor HSCT

Weiyang Li, Jun He, Xiaojing Bao, Lina Zhou, Wu Depei, MD, PhD, Aining Sun

Blood (2011) 118 (21): 4488.

https://doi.org/10.1182/blood.V118.21.4488.4488

Published: 2011

Journal Articles

The Effect of KIR B/X Genotype and Missing KIR Ligands In Haploidentical Hematopoietic Stem Cell Transplantation.

Aining Sun, Jun He, Lina Zhou, Wu Depei, MD, PhD, Weiyang Li, Xiaojing Bao

Blood (2010) 116 (21): 4578.

https://doi.org/10.1182/blood.V116.21.4578.4578

Published: 2010

Journal Articles

Impact of Missing KIR Ligands in HLA-Matched Unrelated Donor HSCT.

Aining Sun, Weiyang Li, Wu Depei, Jun He, Xiaojing Bao, Lina Zhou

Blood (2009) 114 (22): 1185.

https://doi.org/10.1182/blood.V114.22.1185.1185

Published: 2009

Journal Articles

The Research of Phenylhexyl Isothiocyanate’s Influence on p16 Gene Methylation of Leukaemia Cell

Blood (2008) 112 (11): 4497.

https://doi.org/10.1182/blood.V112.11.4497.4497

Published: 2008

Journal Articles

Cytogenetically Cryptic Tyrosine Kinase Fusion Genes Are Rare in Atypical Myeloproliferative Neoplasms: An Analysis by Targeted Array Comparative Genomic Hybridization

Thomas Ernst, MD, Andrew Chase, PhD, Francis Grand, PhD, Andreas Reiter, MD, Nicholas C.P. Cross, PhD

Blood (2008) 112 (11): 2791.

https://doi.org/10.1182/blood.V112.11.2791.2791

Published: 2008

Journal Articles

MicroRNA Is Prognostic Indicator in Patients with Diffuse Large B Cell Lymphoma

Meir Lahav, MD, Ron Ram, Michal Kushnir, Rosetta Genomics Israel, Ofer Spilberg, Gila Lithwick Yanai, Osnat Beeri, Moshe Hoshen, Maora Feinmesser

Blood (2008) 112 (11): 806.

https://doi.org/10.1182/blood.V112.11.806.806

Published: 2008

Journal Articles

ChIP-on-Chip Analysis Using Dominant Negative Form of PAX5 Fusion Gene Revealed Genes Associated with Tumorigenesis Were Directly Regulated by PAX5 in a Human B Cell Line, NALM6

Norihiko Kawamata, MD, Fabienne Isken, Stefanie Goellner, C. Müller-Tidow, MD, H. Phillip Koeffler, MD

Blood (2008) 112 (11): 3585.

https://doi.org/10.1182/blood.V112.11.3585.3585

Published: 2008

Journal Articles

Simultaneous Phenotype-Specific Telomere Length Measured by Flow-FISH Using Thermally Stable Quantum Dots

Veena Kapoor, B.S., Fran Hakim, Ph.D., Najibah Rehman, Ronald E Gress, M.D., William G Telford, Ph.D.

Blood (2008) 112 (11): 4908.

https://doi.org/10.1182/blood.V112.11.4908.4908

Published: 2008

Journal Articles

Utility of Oligonucleotide Array Comparative Genomic Hybridization to Identify Cryptic Copy Number Alterations in Myelodysplastic Syndromes

Wendy K Chung, MD, PhD, James Weisberger, M.D., Yi Sun, PhD, Pauline Brenholz, MD, Stephanie Warren, MS, Brigette A Brown-Kipphut, MS, Swaroop Aradhya, PhD, Charles A LeDuc, PhD, Marc Grodman, MD, Richard Burack, MD, PhD, M. Anwar Iqbal, PhD, John M. Bennett, MD

Blood (2008) 112 (11): 5076.

https://doi.org/10.1182/blood.V112.11.5076.5076

Published: 2008

NARROW

Myelodysplastic Syndrome with Excess Blasts and Secondary Acute Myeloid Leukemia: Same Disease with Different Blast Count

Disruption of a GATA1-binding motif upstream of XG / PBDX abolishes Xg a expression and resolves the Xg blood group system

Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT

Towards the Development of a Noninvasive Prenatal Test for Beta-Thalassemia: Utilization of Probe Capture Enrichment and Next Generation Sequencing

Identification of Copy Number Variants in Type 1 and Type 3 VWD by aCGH in the Zimmerman Program

A Second Generation, Multiple Myeloma-Specific, Targeted Sequencing Platform for Detecting Translocations, Copy Number Alterations, and Single Nucleotide Variants

High-Sensitivity Genomic Minimal Residual Disease Detection Reveals Multiclonal Hematopoiesis and Is Associated with Survival in Adult AML

Rapid Simultaneous Detection of Multiple Micro-Ribonucleic Acids By Surface Plasmon Resonance Array in Cell Lysates of Myelodysplastic Syndromes Patients

Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia

Clinical and Biological Characteristics According to the Burden of JAK2V617F Mutated Allele in BCR-ABL Negative MPNs

Detection of VWF Copy Number Variations by Microarray Analysis in Von Willebrand Disease Type 3 Index Cases

Impact of KIR B/X Genotype and Missing KIR Ligands in HLA-Matched Unrelated Donor HSCT

The Effect of KIR B/X Genotype and Missing KIR Ligands In Haploidentical Hematopoietic Stem Cell Transplantation.

Impact of Missing KIR Ligands in HLA-Matched Unrelated Donor HSCT.

The Research of Phenylhexyl Isothiocyanate’s Influence on p16 Gene Methylation of Leukaemia Cell

Cytogenetically Cryptic Tyrosine Kinase Fusion Genes Are Rare in Atypical Myeloproliferative Neoplasms: An Analysis by Targeted Array Comparative Genomic Hybridization

MicroRNA Is Prognostic Indicator in Patients with Diffuse Large B Cell Lymphoma

ChIP-on-Chip Analysis Using Dominant Negative Form of PAX5 Fusion Gene Revealed Genes Associated with Tumorigenesis Were Directly Regulated by PAX5 in a Human B Cell Line, NALM6

Simultaneous Phenotype-Specific Telomere Length Measured by Flow-FISH Using Thermally Stable Quantum Dots

Utility of Oligonucleotide Array Comparative Genomic Hybridization to Identify Cryptic Copy Number Alterations in Myelodysplastic Syndromes

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American Society of Hematology

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