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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Massively parallel sequencing: the new frontier of hematologic genomicsRare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFGuidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.A variational Bayes discrete mixture test for rare variant associationMAFsnp: A Multi-Sample Accurate and Flexible SNP Caller Using Next-Generation Sequencing Data.Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.The impact of rare and low-frequency genetic variants in common diseaseVon Willebrand factor regulation in patients with acute and chronic cerebrovascular disease: a pilot, case-control study.A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in miceA genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC StudyAssociation of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity.New insights into genotype and phenotype of VWD.Group association test using a hidden Markov model.A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersPossible race and gender divergence in association of genetic variations with plasma von Willebrand factor: a study of ARIC and 1000 genome cohorts.Laboratory diagnosis of von Willebrand disease.Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients.Regulation of plasma von Willebrand factor.The O-linked glycans of human von Willebrand factor modulate its interaction with ADAMTS-13.Common sequence variants associated with higher VWF and FVIII are less frequent in subjects diagnosed with type 1 VWD
P2860
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P2860
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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2013 nî lūn-bûn
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2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2013 թվականի մայիսին հրատարակված գիտական հոդված
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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name
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@ast
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@en
type
label
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@ast
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@en
prefLabel
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@ast
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@en
P2093
P2860
P50
P1433
P1476
Common and rare von Willebrand ...... HLBI Exome Sequencing Project.
@en
P2093
Alex P Reiner
Christopher S Carlson
David Green
Deborah A Nickerson
Jeffrey Haessler
Jill M Johnsen
Joshua D Smith
NHLBI Exome Sequencing Project
Nicholas Smith
P2860
P304
P356
10.1182/BLOOD-2013-02-485094
P407
P577
2013-05-20T00:00:00Z