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von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene
Zimmerman Program Investigators
Division of Hematology & Oncology
Institute of Clinical and Translational Sciences (ICTS)
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Siteman Cancer Center
COVID-19 Researchers
Division of Pediatric Neurosurgery
Department of Pediatrics
DBBS - Computational and Systems Biology
DBBS - Neurosciences
DBBS - Human and Statistical Genetics
DBBS - Molecular Genetics and Genomics
DBBS - Molecular Cell Biology
Hope Center for Neurological Disorders
Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
Research output
:
Contribution to journal
›
Article
›
peer-review
20
Scopus citations
Overview
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Dive into the research topics of 'von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene'. Together they form a unique fingerprint.
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Keyphrases
Von Willebrand Factor
100%
Synonymous Variant
100%
Antigen Levels
100%
Von Willebrand Factor Antigen
100%
Von Willebrand Disease
21%
Pathogenic Variants
15%
Nonsynonymous
15%
Combined Annotation-dependent Depletion
15%
P Factor
10%
Next-generation Sequencing
5%
Bleeding
5%
Coding Variants
5%
Healthy Controls
5%
Pathogenicity
5%
Rare Variants
5%
Disease Risk
5%
Gene Variants
5%
Factor Level
5%
Biochemistry, Genetics and Molecular Biology
Von Willebrand Factor
100%
Von Willebrand Disease
19%
Normal Human
9%
Next Generation Sequencing
4%
Rare Variant
4%
Medicine and Dentistry
Von Willebrand Factor
100%
Von Willebrand Disease
19%
Bleeding
4%
Next Generation Sequencing
4%
Pathogenicity
4%