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Journal Articles

Genotypes of the Gene Encoding the Membrane Transporter SLC22A4 Are Associated with Molecular Relapse-Free Survival after Discontinuation of Imatinib Therapy in Patients with Chronic Myeloid Leukemia

Blood (2019) 134 (Supplement_1): 1647.

https://doi.org/10.1182/blood-2019-129710

Published: 2019

Journal Articles

Characterization of Pathogenic Variants Associated with Hereditary Thrombocytopenias in Families from the Czech Republic

Zuzana Vrzalova, PhD, Katerina Stano Kozubik, PhD, Lenka Radova, PhD, Jakub Trizuljak, MD, Sarka Pospisilova, Prof PhD, Michael Doubek, MD PhD

Blood (2019) 134 (Supplement_1): 2343.

https://doi.org/10.1182/blood-2019-122696

Published: 2019

Journal Articles

Evaluation of Newborns Screening Laboratory Tests for Sickle Cell Disease and Other Haemoglobinopathies in Tanzania

Heavenlight Hebron Christopher, BSc, Adam Burns, BSc, PhD, Emmanuel Josephat, BSc, Sephord Saul, BSc, Josephine Mgaya, BSc, Julie Makani, MD PhD FRCP, Siana Watoky Nkya, PhD MSc, BSc, Anna Schuh, PhD

Blood (2019) 134 (Supplement_1): 4817.

https://doi.org/10.1182/blood-2019-129900

Published: 2019

Journal Articles

De Novo Myelodysplastic Syndromes in Patients 20-50 Years Old Characterized By Frequent Mutations in TP53 and Transcription-Related Genes

Zachary D. Epstein-Peterson, MD, Barbara Spitzer, MD, Joseph McCarter, PhD, Erin McGovern, BA, Ross L. Levine, MD, Martin S. Tallman, MD

Blood (2019) 134 (Supplement_1): 2708.

https://doi.org/10.1182/blood-2019-123400

Published: 2019

Journal Articles

Monitoring Minimal Residual Disease in Acute Myeloid Leukemia Using Genomic or cfDNA with MyMRD ® , a Targeted NGS Panel

Zhiyi Xie, PhD, Lisa Chamberlain, PhD, Andrew Carson, PhD, Veronika Atkinson, MS, Valerie McClain, MS, James Sprague, Ogeen Kiya, Peng Xia, MS, Wenli Huang, Bradley Patay, MD, Martin Blankfard, Jeffrey E Miller, PhD

Blood (2018) 132 (Supplement 1): 5268.

https://doi.org/10.1182/blood-2018-99-118971

Published: 2018

Journal Articles

A Novel α-Thalassemia Screening Scheme in Neonates with Higher Sensitivity and Specificity Using a Combination of Hb Bart's Quantity and Red Blood Cell Indices

Thidarat Suksangpleng, PhD, Suchada Riolueang, MSc, Jiraporn Korchuenjit, BSc, Supachai Ekwattanakit, PhD MD, Vip Viprakasit, MD DPhil

Blood (2018) 132 (Supplement 1): 1059.

https://doi.org/10.1182/blood-2018-99-118216

Published: 2018

Journal Articles

Driver Mutation Profile By MLPA in Myelofibrosis Patients

Minuncio Juliana, MD, Alexandre Nonino, MD, Juliana Forte Mazzeu, PhD, Cintia do Couto Mascarenhas, MD PhD

Blood (2018) 132 (Supplement 1): 5494.

https://doi.org/10.1182/blood-2018-99-119776

Published: 2018

Journal Articles

A Novel Filtering Tool for Detecting Sickle Cell Disease in the Pediatric Population

Evashin Pillay, MD, Theresa Louise Coetzer, PhD

Blood (2018) 132 (Supplement 1): 2238.

https://doi.org/10.1182/blood-2018-99-119121

Published: 2018

Journal Articles

Next Generation Myelofibrosis Risk Analysis in the Electronic Health Record

Andrew Sochacki, MD, Cosmin Adrian Bejan, PhD, Shilin Zhao, PhD, Travis Spaulding, MD, Thomas Stricker, MD PhD, Yaomin Xu, PhD, Michael R. Savona, MD

Blood (2018) 132 (Supplement 1): 3038.

https://doi.org/10.1182/blood-2018-99-113692

Published: 2018

Journal Articles

Identification of a Digenic Inheritance of Pklr and KLF1 Mutations Resulting in Hemolytic Anemia in a Neonate from a Study of Genotype-Phenotype Correlation of Globin, Pklr and KLF1 in Thai Patients with Pyruvate Kinase (PK) Deficiency

Supachai Ekwattanakit, BSc, PhD MD, Suchada Riolueang, M.Sc., Kalaya Tachavanich, Hitoshi Kanno, MDPhD, Vip Viprakasit, MD DPhil, Thidarat Suksangpleng, PhD, Vorravarn S Tanphaichitr

Blood (2017) 130 (Supplement 1): 3477.

https://doi.org/10.1182/blood.V130.Suppl_1.3477.3477

Published: 2017

Journal Articles

Biallelic Mutations in Hamp in Type 2b Hemochromatosis

Serge Pissard, MDPhD, Ka Chandran, Florence Houriez, Ichrache Benmaad, Martial Saunier, Thibault Lefebvre, Patricia Aguilar-Martinez, MD PhD, Patricia A. Bignell, Gerald Le Gac, MDPhD, Jacques Rochette, MB, DSc

Blood (2016) 128 (22): 1279.

https://doi.org/10.1182/blood.V128.22.1279.1279

Published: 2016

Journal Articles

Next-Generation Sequencing Based Minimal Residual Disease Assessment in Peripheral Blood RNA from Multiple Myeloma Patients

Jeffrey L. Wolf, MD, Katherine A. Kong, PhD, Jenai Wilmoth, RN, Joshua Bayes, Amy Marsala, ANP,MPH, Victoria Carlton, PhD, Aaron Logan, MDPhD, Thomas G. Martin, III, MD

Blood (2016) 128 (22): 3286.

https://doi.org/10.1182/blood.V128.22.3286.3286

Published: 2016

Journal Articles

Blood Group Genotyping to Prevent Alloimmunization in Children with Sickle Cell Disease

Nancy Robitaille, MD, Yves D. Pastore, MD, Anne-Julie Landry, M.Sc, Catherine Latour, MD, Josée Lavoie, M.Sc, Geneviève Laflamme, M.Sc, Josée Perreault, PhD, Maryse St-Louis, PhD

Blood (2016) 128 (22): 2486.

https://doi.org/10.1182/blood.V128.22.2486.2486

Published: 2016

Journal Articles

Asymptomatic Dysprothrombinemia (Prothtombin Himi) with p.M380T and p.R431H Shows Severely Reduced Clotting Activity, Moderate Antithrombin Resistance and Severe Thrombomodulin Binding Defect

Eriko Morishita, MD PhD, Mao Takata, BSc, Fumina Taniguchi, BSc, Masashi Akiyama, PhD, Akiko Sekiya, PhD, Akira Takagi, PhD, Toshiyuki Miyata, PhD, Tetsuhito Kojima, MD PhD

Blood (2016) 128 (22): 2574.

https://doi.org/10.1182/blood.V128.22.2574.2574

Published: 2016

Journal Articles

Correlation of Toll-like Receptor (TLR) and PD-1 Pathways in Central Nervous System Lymphoma: A Clinicopathological Study on Outcomes

Tarsheen Sethi, MD MBBS, Alexandra E. Kovach, MD, Samuel M Rubinstein, MD, Laura Lee, MDPhD, Yang Wang, PhD, David S. Morgan, MD, John P Greer, MD, Cindy Vnencak-Jones, PhD, Nishitha Reddy, MD MSCI, MBBS

Blood (2016) 128 (22): 929.

https://doi.org/10.1182/blood.V128.22.929.929

Published: 2016

Journal Articles

Detection of Hemoglobin (Hb) Variants By HPLC Screening in Cord Blood Units (CBU) Donated to the National Cord Blood Program (NCBP)

Ludy Dobrila, PhD, Tracy Zhu, Dan Zamfir, MS, Michal Tarnawski, MD, Rodica Ciubotariu, MD PhD, Maria S Albano, PhD, Maryely DeLeon, Kelsey Turner, Mahin Azimi, Carolyn C. Hoppe, MD, Andromachi Scaradavou, MD, Pablo Rubinstein, MD

Blood (2016) 128 (22): 2182.

https://doi.org/10.1182/blood.V128.22.2182.2182

Published: 2016

Journal Articles

Landscape of Subclonal Mutations in Myelodysplastic Syndromes (MDS) Allows for a Novel Hierarchy of Clonal Advantage By Combining Germline and Somatic Mutations

Blood (2016) 128 (22): 957.

https://doi.org/10.1182/blood.V128.22.957.957

Published: 2016

Journal Articles

Genome Editing Recreates Hereditary Persistence of Fetal Hemoglobin in Primary Human Erythroblasts

Elizabeth Traxler, Yu Yao, MD, Chunliang Li, Jeremy Grevet, Peng Huang, PhD, Shaela Wright, Gerd A. Blobel, MD PhD, Mitchell J. Weiss, MD PhD

Blood (2015) 126 (23): 640.

https://doi.org/10.1182/blood.V126.23.640.640

Published: 2015

Journal Articles

C5 Polymorphism in a Dutch Patient with Paroxysmal Nocturnal Hemoglobinuria (PNH) and No Asian Ancestry, Resistant to Eculizumab, but in Vitro Sensitive to Coversin

Saskia Langemeijer, MD PhD, Jun-Ichi Nishimura, MD PhD, Wynne Weston-Davies, Miles A Nunn, DPhil, Yuzuru Kanakura, MD PhD, Ian J Mackie, Petra Muus, MD PhD

Blood (2015) 126 (23): 1209.

https://doi.org/10.1182/blood.V126.23.1209.1209

Published: 2015

Journal Articles

Earlier Antenatal Diagnosis of Hemoglobinopathies By Coelocentesis

Antonino Giambona, Gianfranca Damiani, Filippo Leto, Cristina Yakil, Cristina Passarello, Valentina Cigna, Giovanna Schillaci, Massimiliano Sacco, Rosario Di Maggio, Angela Vitrano, Aurelio Maggio

Blood (2015) 126 (23): 2133.

https://doi.org/10.1182/blood.V126.23.2133.2133

Published: 2015

NARROW

Genotypes of the Gene Encoding the Membrane Transporter SLC22A4 Are Associated with Molecular Relapse-Free Survival after Discontinuation of Imatinib Therapy in Patients with Chronic Myeloid Leukemia

Characterization of Pathogenic Variants Associated with Hereditary Thrombocytopenias in Families from the Czech Republic

Evaluation of Newborns Screening Laboratory Tests for Sickle Cell Disease and Other Haemoglobinopathies in Tanzania

De Novo Myelodysplastic Syndromes in Patients 20-50 Years Old Characterized By Frequent Mutations in TP53 and Transcription-Related Genes

Monitoring Minimal Residual Disease in Acute Myeloid Leukemia Using Genomic or cfDNA with MyMRD ® , a Targeted NGS Panel

A Novel α-Thalassemia Screening Scheme in Neonates with Higher Sensitivity and Specificity Using a Combination of Hb Bart's Quantity and Red Blood Cell Indices

Driver Mutation Profile By MLPA in Myelofibrosis Patients

A Novel Filtering Tool for Detecting Sickle Cell Disease in the Pediatric Population

Next Generation Myelofibrosis Risk Analysis in the Electronic Health Record

Identification of a Digenic Inheritance of Pklr and KLF1 Mutations Resulting in Hemolytic Anemia in a Neonate from a Study of Genotype-Phenotype Correlation of Globin, Pklr and KLF1 in Thai Patients with Pyruvate Kinase (PK) Deficiency

Biallelic Mutations in Hamp in Type 2b Hemochromatosis

Next-Generation Sequencing Based Minimal Residual Disease Assessment in Peripheral Blood RNA from Multiple Myeloma Patients

Blood Group Genotyping to Prevent Alloimmunization in Children with Sickle Cell Disease

Asymptomatic Dysprothrombinemia (Prothtombin Himi) with p.M380T and p.R431H Shows Severely Reduced Clotting Activity, Moderate Antithrombin Resistance and Severe Thrombomodulin Binding Defect

Correlation of Toll-like Receptor (TLR) and PD-1 Pathways in Central Nervous System Lymphoma: A Clinicopathological Study on Outcomes

Detection of Hemoglobin (Hb) Variants By HPLC Screening in Cord Blood Units (CBU) Donated to the National Cord Blood Program (NCBP)

Landscape of Subclonal Mutations in Myelodysplastic Syndromes (MDS) Allows for a Novel Hierarchy of Clonal Advantage By Combining Germline and Somatic Mutations

Genome Editing Recreates Hereditary Persistence of Fetal Hemoglobin in Primary Human Erythroblasts

C5 Polymorphism in a Dutch Patient with Paroxysmal Nocturnal Hemoglobinuria (PNH) and No Asian Ancestry, Resistant to Eculizumab, but in Vitro Sensitive to Coversin

Earlier Antenatal Diagnosis of Hemoglobinopathies By Coelocentesis

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American Society of Hematology

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ASH Publications

American Society of Hematology

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