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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

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

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

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

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

NARROW

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

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

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

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

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

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

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American Society of Hematology

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American Society of Hematology

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