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Journal Articles

Molecular Features in the Diagnosis of Myeloid Neoplasms in Down Syndrome Patients Less Than Four Years of Age: Experience from a Single Institution

Chris Ours, MD, Fiorella Iglesias, MD, Erin Morales, MD, Luke Maese, DO, Archana M Agarwal, MD, Anupam Verma, MD

Blood (2018) 132 (Supplement 1): 5180.

https://doi.org/10.1182/blood-2018-99-120304

Published: 2018

Journal Articles

Use of Next Generation Sequencing Panel for Routine Diagnosis of Hereditary Hemolytic Anemias

Archana M Agarwal, MD, Jay L Patel, MD, Adam Clayton, PhD, Noel Scott Reading, PhD

Blood (2018) 132 (Supplement 1): 2325.

https://doi.org/10.1182/blood-2018-99-112589

Published: 2018

Journal Articles

Transcriptional Characterization of Myelofibrotic Bone Marrow Microenvironment Reveals Distinct Tumor Microenvironment in JAK2 + and Calr + PMF Marrows

N. Scott Reading, PhD, Archana M Agarwal, MD, Ronald Hoffman, MD, Josef T. Prchal, MD, Mohamed E Salama, MD

Blood (2016) 128 (22): 1954.

https://doi.org/10.1182/blood.V128.22.1954.1954

Published: 2016

Journal Articles

Using a Next Generation Sequencing Panel to Discover the Obscure Causes of Hereditary Hemolytic Anemias

Archana M Agarwal, MD, N. Scott Reading, PhD, Kimberly Frizzell, PhD, Wei Shen, PhD, Shelly Sorrells, PhD, Mohamed E Salama, MD, Josef T. Prchal, MD, Hassan M. Yaish, Jay L Patel, MD, Robert D. Christensen, MD

Blood (2016) 128 (22): 2433.

https://doi.org/10.1182/blood.V128.22.2433.2433

Published: 2016

Journal Articles

Sickle Cell Anemia in a Child with Three β-Globin Clusters (β-S/β-S, β-A): Loss of LCR and 3' HS1 in the Duplicated Wild-Type β-Globin Cluster Does Not Fully Abrogate Its Transcript

N. Scott Reading, PhD, Barnaby E. Clark, PhD, Jihyun Song, MS, Claire C. Shooter, Robin E. Miller, MD, Archana M Agarwal, MD, Swee Lay Thein, MD, Vladimir Divoky, PhD, Josef T. Prchal, MD

Blood (2015) 126 (23): 3371.

https://doi.org/10.1182/blood.V126.23.3371.3371

Published: 2015

Journal Articles

The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Hereditary Hemolytic Anemias

Roberto H Nussenzveig, PhD, Nikhil Sangle, MD, Robert D. Christensen, MD, Mohamed E Salama, MD, Josef Prchal, MD, Hassan Yaish, MD, Archana M Agarwal, MD

Blood (2013) 122 (21): 3421.

https://doi.org/10.1182/blood.V122.21.3421.3421

Published: 2013

Journal Articles

The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Polycythemia

Roberto H Nussenzveig, PhD, Mohamed E Salama, MD, Sherrie L. Perkins, MD, PhD, Josef Prchal, MD, Archana M Agarwal, MD

Blood (2013) 122 (21): 2185.

https://doi.org/10.1182/blood.V122.21.2185.2185

Published: 2013

Journal Articles

Flow Cytometry Analysis of Peripheral Blood CD34+ Cells in Patients with Primary Myelofibrosis

Archana M Agarwal, MD, Scott James Samuelson, M.D., Sergey Preobrazhensky, PhD, Charles J. Parker, MD, Kimberly Hickman, Sherrie L. Perkins, MD, PhD, Josef T. Prchal, MD, David W. Bahler, MD, PhD.

Blood (2008) 112 (11): 5240.

https://doi.org/10.1182/blood.V112.11.5240.5240

Published: 2008

Journal Articles

Novel Exon 2 Alpha Spectrin Mutation in a Caucasian Family with Pyropoikilocytosis, Elliptocytosis, and Normal Morphology: Three Phenotypes Due to Decreased Spectrin mRNA and Intragenic Crossover

Neeraj Agarwal, MD#, Sabina Swierczek#, PhD, Filipe R. Lorenzo, MD, PhD, Kubendran Naidoo, BScHons, Archana M. Agarwal, MD, Roberto H Nussenzveig, PhD, Jonathan Whisenant, MD, Theresa L. Coetzer, MD, Josef T. Prchal, MD

Blood (2008) 112 (11): 3840.

https://doi.org/10.1182/blood.V112.11.3840.3840

Published: 2008

Journal Articles

In Vitro Erythroid Cell Expansion Analysis in Polycythemia Vera.

Donghoon Yoon, PhD, Hana Bruchova, PhD, Archana M. Agarwal, MD, Josef T. Prchal, MD, Jaroslav F. Prchal, MD

Blood (2006) 108 (11): 4916.

https://doi.org/10.1182/blood.V108.11.4916.4916

Published: 2006

NARROW

Molecular Features in the Diagnosis of Myeloid Neoplasms in Down Syndrome Patients Less Than Four Years of Age: Experience from a Single Institution

Use of Next Generation Sequencing Panel for Routine Diagnosis of Hereditary Hemolytic Anemias

Transcriptional Characterization of Myelofibrotic Bone Marrow Microenvironment Reveals Distinct Tumor Microenvironment in JAK2 + and Calr + PMF Marrows

Using a Next Generation Sequencing Panel to Discover the Obscure Causes of Hereditary Hemolytic Anemias

Sickle Cell Anemia in a Child with Three β-Globin Clusters (β-S/β-S, β-A): Loss of LCR and 3' HS1 in the Duplicated Wild-Type β-Globin Cluster Does Not Fully Abrogate Its Transcript

The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Hereditary Hemolytic Anemias

The Clinical Utility Of Next-Generation Sequencing In The Diagnosis Of Polycythemia

Flow Cytometry Analysis of Peripheral Blood CD34+ Cells in Patients with Primary Myelofibrosis

Novel Exon 2 Alpha Spectrin Mutation in a Caucasian Family with Pyropoikilocytosis, Elliptocytosis, and Normal Morphology: Three Phenotypes Due to Decreased Spectrin mRNA and Intragenic Crossover

In Vitro Erythroid Cell Expansion Analysis in Polycythemia Vera.

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American Society of Hematology

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American Society of Hematology

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