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Journal Articles

SNP Analysis Of The VWF GENE Identifies Multiple Common Variants THAT Affect VWF Levels and OCCUR At Different Frequencies In Patients With TYPE 1 VWD

Jesse Hinckley, PhD, Trudy Burns, PhD, Kai Wang, PhD, Ayse Bilge Ozel, PhD, Meadow Heiman, Amy Shapiro, MD, Robert R. Montgomery, MD, Lawrence Brody, PhD, Karl C. Desch, MD, Jorge Di Paola, MD

Blood (2013) 122 (21): 334.

https://doi.org/10.1182/blood.V122.21.334.334

Published: 2013

Journal Articles

Quantitative Trait Locus (QTL) Linkage Analysis of a Large Pedigree with Von Willebrand Disease Identifies Novel Modifier Loci of Von Willebrand Factor Levels and Confirms Some Previously Reported Modifier Loci

Jesse Hinckley, Kai Wang, PhD, Trudy Burns, PhD, Amy D. Shapiro, MD, Jorge A Di Paola, MD

Blood (2010) 116 (21): 240.

https://doi.org/10.1182/blood.V116.21.240.240

Published: 2010

Journal Articles

An Association Study of Candidate Modifier Genes in a Large Pedigree with Von Willebrand Disease.

Jorge Di Paola, MD, Kayelyn Wagner, MD, Brie Nixon, BS, Jacob Kline, Amy Shapiro, MD, Diana Abbott, Trudy Burns, PhD, Kai Wang, PhD

Blood (2007) 110 (11): 2135.

https://doi.org/10.1182/blood.V110.11.2135.2135

Published: 2007

Journal Articles

Genome Wide Scan of Complete Blood Count (CBC) Measures Suggests Strong Linkage of Red Blood Cell (RBC) Count to Chromosome 4q25.

Diana Abbott, PhD, Kai Wang, PhD, Amy Shapiro, MD, Trudy Burns, PhD, Jorge Di Paola, MD

Blood (2007) 110 (11): 1729.

https://doi.org/10.1182/blood.V110.11.1729.1729

Published: 2007

Journal Articles

Genetic Polymorphisms and Incidence of Thrombotic and Hemorrhagic Events in Patients with Essential Thrombocythemia (ET).

Alejandro Raimondi, MD, Paula Heller, MD, Felisa Molinas, MD, Maria Castañon, PhD, Trudy Burns, PhD, Jorge Di Paola, MD

Blood (2006) 108 (11): 4917.

https://doi.org/10.1182/blood.V108.11.4917.4917

Published: 2006

Journal Articles

A Genome-Wide Linkage Scan of a Large Amish Pedigree with Von Willebrand Disease (VWD) Identified Several Chromosomal Regions That May Contain Potential Modifiers of Von Willebrand Factor (VWF) Levels and Disease Variability.

Jorge Di Paola, MD, Mary Rickard, BS, Jeffrey Murray, MD, Trudy Burns, PhD, Kai Wang, PhD, Amy Shapiro, MD

Blood (2006) 108 (11): 176.

https://doi.org/10.1182/blood.V108.11.176.176

Published: 2006

NARROW

SNP Analysis Of The VWF GENE Identifies Multiple Common Variants THAT Affect VWF Levels and OCCUR At Different Frequencies In Patients With TYPE 1 VWD

Quantitative Trait Locus (QTL) Linkage Analysis of a Large Pedigree with Von Willebrand Disease Identifies Novel Modifier Loci of Von Willebrand Factor Levels and Confirms Some Previously Reported Modifier Loci

An Association Study of Candidate Modifier Genes in a Large Pedigree with Von Willebrand Disease.

Genome Wide Scan of Complete Blood Count (CBC) Measures Suggests Strong Linkage of Red Blood Cell (RBC) Count to Chromosome 4q25.

Genetic Polymorphisms and Incidence of Thrombotic and Hemorrhagic Events in Patients with Essential Thrombocythemia (ET).

A Genome-Wide Linkage Scan of a Large Amish Pedigree with Von Willebrand Disease (VWD) Identified Several Chromosomal Regions That May Contain Potential Modifiers of Von Willebrand Factor (VWF) Levels and Disease Variability.

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ASH Publications

American Society of Hematology

SNP Analysis Of The VWF GENE Identifies Multiple Common Variants THAT Affect VWF Levels and OCCUR At Different Frequencies In Patients With TYPE 1 VWD

Quantitative Trait Locus (QTL) Linkage Analysis of a Large Pedigree with Von Willebrand Disease Identifies Novel Modifier Loci of Von Willebrand Factor Levels and Confirms Some Previously Reported Modifier Loci

An Association Study of Candidate Modifier Genes in a Large Pedigree with Von Willebrand Disease.

Genome Wide Scan of Complete Blood Count (CBC) Measures Suggests Strong Linkage of Red Blood Cell (RBC) Count to Chromosome 4q25.

Genetic Polymorphisms and Incidence of Thrombotic and Hemorrhagic Events in Patients with Essential Thrombocythemia (ET).

A Genome-Wide Linkage Scan of a Large Amish Pedigree with Von Willebrand Disease (VWD) Identified Several Chromosomal Regions That May Contain Potential Modifiers of Von Willebrand Factor (VWF) Levels and Disease Variability.

Email alerts

ASH Publications

American Society of Hematology

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