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Journal Articles

Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β 0 -Thalassemia Mutation

Zhihua Jiang, PhD, Shengwen Huang, MD PhD, Hong Yuan Luo, MB, PhD, Nejat Akar, MD, A.Nazli Basak, MD, Nasir Al-Allawi, MD PhD, Sule Unal, MD, Fatma Gumruk, MDProf, Lance Davis, MD, Tasha Morrison, MPH,BA, Andrew Campbell, MD, Patrick G. Gallagher, MD, Bernard G Forget, MD, Martin H. Steinberg, MD, David H.K. Chui, MD

Blood (2014) 124 (21): 2690.

https://doi.org/10.1182/blood.V124.21.2690.2690

Published: 2014

Journal Articles

Analysis of (δβ) 0 Thalassemia and HPFH Deletions Suggest a Hierarchy of Cis-Acting Elements Regulating Fetal Hemoglobin Gene Expression.

Heather L Edward, BA, Tasha Morrison, MPH,BA, Jacqueline N Milton, MS, Hong-yuan Luo, MB, PhD, Lance Davis, MD, Bernard G Forget, MD, Martin H. Steinberg, MD, David H.K. Chui, MD

Blood (2014) 124 (21): 54.

https://doi.org/10.1182/blood.V124.21.54.54

Published: 2014

Journal Articles

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

Kimberly Lezon-Geyda, PhD, Yelena Maksimova, MS, Vincent P Schulz, PhD, Bernard G Forget, MD, Patrick G Gallagher, MD

Blood (2014) 124 (21): 4011.

https://doi.org/10.1182/blood.V124.21.4011.4011

Published: 2014

Journal Articles

Downregulation of Prdm16 mRNA is a specific antileukemic mechanism during HOXB4-mediated HSC expansion in vivo

Hui Yu, Geoffrey Neale, Hui Zhang, Han M. Lee, Zhijun Ma, Sheng Zhou, Bernard G. Forget, Brian P. Sorrentino

Blood (2014) 124 (11): 1737–1747.

https://doi.org/10.1182/blood-2013-10-534735

Published: 2014

Includes: Supplemental data

Journal Articles

Neonatal Hemolytic Anemia and (δβ) 0 -Thalassemia Caused By Novel Deletions Involving The β-Globin Gene Cluster

Morrison Tasha, MPH, Hong-yuan Luo, MB, PhD, Lance Davis, MD, Roger Theberge, PhD, Mark E McComb, PhD, Catherine E. Costello, PhD, Jeanne Boudreaux, MD, Zeqiu Han, MD, Martin H. Steinberg, MD, Bernard G. Forget, MD, David H.K. Chui, MD

Blood (2013) 122 (21): 3452.

https://doi.org/10.1182/blood.V122.21.3452.3452

Published: 2013

Journal Articles

Patients Homozygous For Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation With Markedly Increased HbF

Zhihua Jiang, PhD, Hong-yuan Luo, MB, PhD, Nasir Al-Allawi, MD, PhD, Sule Unal, MD, Fatma Gumruk, MD, Leonor Osorio-Almeida, PhD, Lance Davis, MD, Tasha Morrison, MPH, Andrew D. Campbell, MD, Martin H. Steinberg, MD, Patrick G Gallagher, MD, Bernard G. Forget, MD, David H.K. Chui, MD

Blood (2013) 122 (21): 3455.

https://doi.org/10.1182/blood.V122.21.3455.3455

Published: 2013

Journal Articles

Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation

Andrew Campbell, MD, Hong-yuan Luo, Katherine Benson, Lance Davis, Patrick G. Gallagher, MD, Martin H. Steinberg, MD, Peter Fraser, PhD, Bernard G. Forget, MD, David H.K. Chui, MD

Blood (2012) 120 (21): 1022.

https://doi.org/10.1182/blood.V120.21.1022.1022

Published: 2012

Journal Articles

Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy

Hannah Bogardus, Vincent P Schulz, Yelena Maksimova, Barbara A Miller, Bernard G. Forget, MD, Patrick G. Gallagher, MD

Blood (2011) 118 (21): 1030.

https://doi.org/10.1182/blood.V118.21.1030.1030

Published: 2011

Journal Articles

Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells

Han M. Lee, Hui Zhang, Vincent Schulz, David P. Tuck, Bernard G. Forget

Blood (2010) 116 (5): 720–730.

https://doi.org/10.1182/blood-2009-11-253872

Published: 2010

Includes: Supplemental data

Journal Articles

Acute Myeloid Leukemia in Mice Associated with Retrovirally-Mediated Overexpression of HOXB4

Hui Zhang, MD, PhD, Wendy Chen, DO, Svetlana Rogulina, Han M. Lee, Bernard G. Forget, MD

Blood (2008) 112 (11): 4484.

https://doi.org/10.1182/blood.V112.11.4484.4484

Published: 2008

Journal Articles

Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.

Whitney Tolpinrud, BS, Massimiliano Gaetani, PhD, Yelena Maksimova, BS, Sara Mootien, PhD, Sandra Harper, PhD, Bernard G. Forget, MD, David W. Speicher, PhD, Patrick G. Gallagher, MD

Blood (2007) 110 (11): 1706.

https://doi.org/10.1182/blood.V110.11.1706.1706

Published: 2007

Journal Articles

Effects of the Homeodomain Gene Pitx2 on Self-Renewal of Hematopoietic Stem Cells.

Hui Z. Zhang, MD, PhD, Svetlana Rogulina, M.D., Wendy Chen, D.O., Barbara A. Degar, M.D., Bernard G. Forget, M.D.

Blood (2007) 110 (11): 95.

https://doi.org/10.1182/blood.V110.11.95.95

Published: 2007

Journal Articles

Expression of Pitx2 in stromal cells is required for normal hematopoiesis

Aurélie Kieusseian, Jalila Chagraoui, Cécile Kerdudo, Philippe-Emmanuel Mangeot, Philip J. Gage, Nicole Navarro, Brigitte Izac, Georges Uzan, Bernard G. Forget, Anne Dubart-Kupperschmitt

Blood (2006) 107 (2): 492–500.

https://doi.org/10.1182/blood-2005-02-0529

Published: 2006

Journal Articles

A novel splicing mutation of the α-spectrin gene in the original hereditary pyropoikilocytosis kindred

Daniel B. Costa, Larisa Lozovatsky, Patrick G. Gallagher, Bernard G. Forget

Blood (2005) 106 (13): 4367–4369.

https://doi.org/10.1182/blood-2005-05-1813

Published: 2005

Journal Articles

Identifying Downstream Targets of HOXB4 Using the EML Primitive Hematopoietic Progenitor Cell Line.

Han M. Lee, Hui Zhang, Bernard G. Forget

Blood (2004) 104 (11): 4150.

https://doi.org/10.1182/blood.V104.11.4150.4150

Published: 2004

Journal Articles

A Position +5 Intronic Mutation in the α-Spectrin Gene Is Associated with Marked Deficiency of α-Spectrin Production in the First Reported Cases of Hereditary Pyropoikilocytosis.

Daniel B. Costa, M.D., Patrick G. Gallagher, M.D., Bernard G. Forget, M.D.

Blood (2004) 104 (11): 576.

https://doi.org/10.1182/blood.V104.11.576.576

Published: 2004

Journal Articles

A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis

Murat O. Arcasoy, Aysen F. Karayal, Harvey M. Segal, Joseph G. Sinning, Bernard G. Forget

Blood (2002) 99 (8): 3066–3069.

https://doi.org/10.1182/blood.V99.8.3066

Published: 2002

Journal Articles

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter

Patrick G. Gallagher, Marc Romana, William T. Tse, Samuel E. Lux, Bernard G. Forget

Blood (2000) 96 (3): 1136–1143.

https://doi.org/10.1182/blood.V96.3.1136

Published: 2000

Journal Articles

The Distal Cytoplasmic Domain of the Erythropoietin Receptor Induces Granulocytic Differentiation in 32D Cells

Kevin W. Harris, Xian-Jue Hu, Suzanne Schultz, Murat O. Arcasoy, Bernard G. Forget, Nanette Clare

Blood (1998) 92 (4): 1219–1224.

https://doi.org/10.1182/blood.V92.4.1219

Published: 1998

Journal Articles

Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene

Murat O. Arcasoy, Barbara A. Degar, Kevin W. Harris, Bernard G. Forget

Blood (1997) 89 (12): 4628–4635.

https://doi.org/10.1182/blood.V89.12.4628

Published: 1997

NARROW

Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β 0 -Thalassemia Mutation

Analysis of (δβ) 0 Thalassemia and HPFH Deletions Suggest a Hierarchy of Cis-Acting Elements Regulating Fetal Hemoglobin Gene Expression.

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

Downregulation of Prdm16 mRNA is a specific antileukemic mechanism during HOXB4-mediated HSC expansion in vivo

Neonatal Hemolytic Anemia and (δβ) 0 -Thalassemia Caused By Novel Deletions Involving The β-Globin Gene Cluster

Patients Homozygous For Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation With Markedly Increased HbF

Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation

Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy

Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells

Acute Myeloid Leukemia in Mice Associated with Retrovirally-Mediated Overexpression of HOXB4

Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.

Effects of the Homeodomain Gene Pitx2 on Self-Renewal of Hematopoietic Stem Cells.

Expression of Pitx2 in stromal cells is required for normal hematopoiesis

A novel splicing mutation of the α-spectrin gene in the original hereditary pyropoikilocytosis kindred

Identifying Downstream Targets of HOXB4 Using the EML Primitive Hematopoietic Progenitor Cell Line.

A Position +5 Intronic Mutation in the α-Spectrin Gene Is Associated with Marked Deficiency of α-Spectrin Production in the First Reported Cases of Hereditary Pyropoikilocytosis.

A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter

The Distal Cytoplasmic Domain of the Erythropoietin Receptor Induces Granulocytic Differentiation in 32D Cells

Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene

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American Society of Hematology

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American Society of Hematology

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