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Journal Articles

F5 Sequence Variant Identified in 7 Patients Evaluated for Hypercoagulable State with a Factor V (FV) HR2 Assay

Margaret M. Leech, BA, Daniel B. Bellissimo, PhD, John A. Uhrmacher, PhD, Sriya W. Gunawardena, MD, Michael J. Meyer, BA, MS, Franklin A. Bontempo, MD

Blood (2018) 132 (Supplement 1): 5053.

https://doi.org/10.1182/blood-2018-99-114203

Published: 2018

Journal Articles

Genotype-Phenotype Relationship and the Role of Alloantibodies in Type 3 VWD in the Zimmerman Program

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

Blood (2017) 130 (Supplement 1): 19.

https://doi.org/10.1182/blood.V130.Suppl_1.19.19

Published: 2017

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

Domain Distribution of Type 1 VWD Sequence Variants and Impact on Clinical and Laboratory Phenotype in the Zimmerman Program

Pamela A Christopherson, Veronica H Flood, MD, Sandra L Haberichter, PhD, Daniel B Bellissimo, PhD, Kenneth D Friedman, MD, Joan Cox Gill, MD, Rupa A Udani, PhD, Robert R Montgomery, MD

Blood (2015) 126 (23): 758.

https://doi.org/10.1182/blood.V126.23.758.758

Published: 2015

Journal Articles

Phenotypic Variability in Carriers of Von Willebrand Factor Truncating Sequence Variants in the Zimmerman Program

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

Blood (2014) 124 (21): 2833.

https://doi.org/10.1182/blood.V124.21.2833.2833

Published: 2014

Journal Articles

Regions on Chromosomes 1 and 14 Are Associated with VWF:Ag Levels in African Americans Using Mapping By Admixture Linkage Disequilibrium

Andrew D Paterson, MD, Nicole M Roslin, Pamela A. Christopherson, Daniel B Bellissimo, PhD, Veronica H Flood, MD, Sandra L. Haberichter, PhD, Robert R Montgomery, MD, Zimmerman Program Investigators

Blood (2014) 124 (21): 2840.

https://doi.org/10.1182/blood.V124.21.2840.2840

Published: 2014

Journal Articles

The Management of Bleeding Risk in Von Willebrand Disease: Should Blood Group O Make a Difference?

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

Blood (2014) 124 (21): 2829.

https://doi.org/10.1182/blood.V124.21.2829.2829

Published: 2014

Journal Articles

Spectrum of Type 2 Von Willebrand Disease in the Zimmerman Program

Veronica H Flood, MD, Pamela A Christopherson, Daniel B Bellissimo, PhD, Joan Cox Gill, MD, Sandra L Haberichter, PhD, Kenneth D Friedman, MD, Rupa A Udani, PhD, Jonathan C Roberts, Robert R Montgomery, MD, The Zimmerman Program Investigators

Blood (2014) 124 (21): 472.

https://doi.org/10.1182/blood.V124.21.472.472

Published: 2014

Journal Articles

Assessment of Erythroid Chimerism in Sickle Cell Patients Undergoing HSCT By Digital Droplet PCR

Lihui Yin, PhD, Rupa A Udani, PhD, Mary Parlow, Daniel B Bellissimo, PhD, Joel A Brochstein, MD FAAP

Blood (2014) 124 (21): 563.

https://doi.org/10.1182/blood.V124.21.563.563

Published: 2014

Journal Articles

Binding Of VWF To Type IV Collagen: An Additional Collagen Binding Mechanism Beyond Types I, III, and VI Collagen?

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

Blood (2013) 122 (21): 333.

https://doi.org/10.1182/blood.V122.21.333.333

Published: 2013

Journal Articles

Novel Germline CEBPA Sequence Variations in Familial AML and Cytogenetically Normal AML.

Rupa A. Udani, PhD, Mary Parlow, Lihui Yin, PhD, Daniel B. Bellissimo, PhD

Blood (2012) 120 (21): 2566.

https://doi.org/10.1182/blood.V120.21.2566.2566

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

Quantitative Analysis of VWF Multimer Structure: Discrimination Between VWD Subtypes

Sandra L Haberichter, PhD, Paula M Jacobi, BA, Veronica H Flood, MD, Pamela A. Christopherson, Joan Cox Gill, MD, Daniel B. Bellissimo, PhD, Kenneth D Friedman, MD, The Zimmerman Program Investigators

Blood (2011) 118 (21): 1215.

https://doi.org/10.1182/blood.V118.21.1215.1215

Published: 2011

Journal Articles

Fourteen Percent of Healthy African Americans Participating In the Zimmerman Program for the Molecular and Clinical Biology of VWD (ZPMCB VWD) Are Heterozygous for the VWF Gene Mutation H817Q Associated with Type 2N Von Willebrand Disease

Kenneth D Friedman, MD, Daniel B. Bellissimo, PhD, Pamela A. Christopherson, Veronica H Flood, MD, Joan Cox Gill, MD, Robert R. Montgomery, MD, Sandra L Haberichter, PhD, Primary Clinical Center Directors

Blood (2010) 116 (21): 239.

https://doi.org/10.1182/blood.V116.21.239.239

Published: 2010

Journal Articles

Low VWF:RCo In Subjects with VWF Polymorphisms D1472H and P1467S Due to Decreased Binding of Ristocetin to the VWF A1 Domain

Veronica H Flood, MD, Jeffrey S Wren, Sandra L Haberichter, PhD, Kenneth D Friedman, MD, Daniel B. Bellissimo, PhD, Joan Cox Gill, MD, Raymond G Hoffmann, PhD, J. Paul Scott, MD, Robert R Montgomery, MD

Blood (2010) 116 (21): 2208.

https://doi.org/10.1182/blood.V116.21.2208.2208

Published: 2010

Journal Articles

Novel VWF Sequence Variations Identified in a Second Cohort of Index Cases Enrolled in the TS Zimmerman Program for the Molecular and Clinical Biology of VWD (ZPMCB-VWD).

Daniel B. Bellissimo, PhD, Pamela A. Christopherson, Sandra L. Haberichter, PhD, Veronica H. Flood, MD, Joan Cox Gill, MD, Kenneth D. Friedman, MD, Robert R. Montgomery, MD, The Zimmerman Project Investigators

Blood (2008) 112 (11): 3379.

https://doi.org/10.1182/blood.V112.11.3379.3379

Published: 2008

Journal Articles

Superdonors Have Decreased Iron Stores but Can Repeatedly Donate Whole Blood through Use of Iron Supplements and Decreased Serum Hepcidin Concentration.

Alan E. Mast, MD, PhD, Tisha Foster, MD, Holly L. Pinder, Craig A. Beczkiewicz, Daniel B. Bellissimo, PhD, Anthony T. Murphy, Steve Kovacevic, Victor J. Wroblewski, PhD, Derrick R. Witcher, PhD

Blood (2007) 110 (11): 2887.

https://doi.org/10.1182/blood.V110.11.2887.2887

Published: 2007

NARROW

F5 Sequence Variant Identified in 7 Patients Evaluated for Hypercoagulable State with a Factor V (FV) HR2 Assay

Genotype-Phenotype Relationship and the Role of Alloantibodies in Type 3 VWD in the Zimmerman Program

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

Domain Distribution of Type 1 VWD Sequence Variants and Impact on Clinical and Laboratory Phenotype in the Zimmerman Program

Phenotypic Variability in Carriers of Von Willebrand Factor Truncating Sequence Variants in the Zimmerman Program

Regions on Chromosomes 1 and 14 Are Associated with VWF:Ag Levels in African Americans Using Mapping By Admixture Linkage Disequilibrium

The Management of Bleeding Risk in Von Willebrand Disease: Should Blood Group O Make a Difference?

Spectrum of Type 2 Von Willebrand Disease in the Zimmerman Program

Assessment of Erythroid Chimerism in Sickle Cell Patients Undergoing HSCT By Digital Droplet PCR

Binding Of VWF To Type IV Collagen: An Additional Collagen Binding Mechanism Beyond Types I, III, and VI Collagen?

Novel Germline CEBPA Sequence Variations in Familial AML and Cytogenetically Normal AML.

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

Quantitative Analysis of VWF Multimer Structure: Discrimination Between VWD Subtypes

Fourteen Percent of Healthy African Americans Participating In the Zimmerman Program for the Molecular and Clinical Biology of VWD (ZPMCB VWD) Are Heterozygous for the VWF Gene Mutation H817Q Associated with Type 2N Von Willebrand Disease

Low VWF:RCo In Subjects with VWF Polymorphisms D1472H and P1467S Due to Decreased Binding of Ristocetin to the VWF A1 Domain

Novel VWF Sequence Variations Identified in a Second Cohort of Index Cases Enrolled in the TS Zimmerman Program for the Molecular and Clinical Biology of VWD (ZPMCB-VWD).

Superdonors Have Decreased Iron Stores but Can Repeatedly Donate Whole Blood through Use of Iron Supplements and Decreased Serum Hepcidin Concentration.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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