Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project
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Title
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project
Authors
Keywords
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Journal
BLOOD
Volume 122, Issue 4, Pages 590-597
Publisher
American Society of Hematology
Online
2013-05-21
DOI
10.1182/blood-2013-02-485094
References
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Note: Only part of the references are listed.- Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project
- (2012) Paul L. Auer et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score
- (2012) Hayan Lee et al. BIOINFORMATICS
- Sequence and structure relationships within von Willebrand factor
- (2012) Y.-F. Zhou et al. BLOOD
- O-linked glycosylation of von Willebrand factor modulates the interaction with platelet receptor glycoprotein Ib under static and shear stress conditions
- (2012) A. A. Nowak et al. BLOOD
- von Willebrand factor: at the crossroads of bleeding and thrombosis
- (2012) Cécile V. Denis et al. INTERNATIONAL JOURNAL OF HEMATOLOGY
- von Willebrand factor plasma levels, genetic variations and coronary heart disease in an older population
- (2012) J. E. van LOON et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Characterizing polymorphisms and allelic diversity of von Willebrand factor gene in the 1000 Genomes
- (2012) Q. Y. Wang et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
- (2012) Bryan Howie et al. NATURE GENETICS
- In Vivo Analysis of the Role of O-Glycosylations of Von Willebrand Factor
- (2012) Idinath Badirou et al. PLoS One
- Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
- (2012) K. C. Desch et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- Improving the Assessment of the Outcome of Nonsynonymous SNVs with a Consensus Deleteriousness Score, Condel
- (2011) Abel González-Pérez et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genetic Variants Associated with von Willebrand Factor Levels in Healthy Men and Women Identified Using the HumanCVD BeadChip
- (2011) Delilah Zabaneh et al. ANNALS OF HUMAN GENETICS
- Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort
- (2011) M. Campos et al. BLOOD
- VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population
- (2011) D. B. Bellissimo et al. BLOOD
- A comparison of approaches to account for uncertainty in analysis of imputed genotypes
- (2011) Jin Zheng et al. GENETIC EPIDEMIOLOGY
- Genetic determinants of von Willebrand factor levels and activity in relation to the risk of cardiovascular disease: a review
- (2011) M. C. VAN SCHIE et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
- (2011) Guillaume Lettre et al. PLoS Genetics
- Gain-of-function GPIb ELISA assay for VWF activity in the Zimmerman Program for the Molecular and Clinical Biology of VWD
- (2010) V. H. Flood et al. BLOOD
- Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor
- (2010) V. H. Flood et al. BLOOD
- Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor
- (2010) Nicholas L. Smith et al. CIRCULATION
- A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand’s disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation
- (2010) M. S. ENAYAT et al. HAEMOPHILIA
- Factor VIII and von Willebrand factor - too sweet for their own good
- (2010) P. J. LENTING et al. HAEMOPHILIA
- Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study
- (2009) J. EIKENBOOM et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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