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The application of genetics to inherited bleeding disorders
P. James,
J. Di Paola
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Siteman Cancer Center
COVID-19 Researchers
Division of Hematology & Oncology
Department of Pediatrics
DBBS - Molecular Cell Biology
DBBS - Molecular Genetics and Genomics
Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
Research output
:
Contribution to journal
›
Article
›
peer-review
5
Scopus citations
Overview
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Keyphrases
Bleeding
50%
Bleeding Disorders
50%
Blood Coagulation
50%
Bruise
50%
Carrier Status
50%
Clinical Management
50%
Clinical Practice
50%
Coagulation Factors
50%
Diagnostic Purposes
50%
General Symptoms
50%
Genetic Basis
50%
Genome-wide Approaches
50%
Genome-wide Association Study
50%
Genotype-phenotype Correlation
50%
Hemophilia
50%
High Density
50%
Inherited Bleeding Disorders
100%
Inhibitor Development
50%
Molecular Diagnostics
50%
Molecular Genetic Testing
50%
Phenotypic Assay
50%
Prenatal Diagnosis
50%
Prenatal Prediction
50%
Recent Advances
50%
Single nucleotide Polymorphism
50%
Therapeutic Goals
50%
Von Willebrand Disease
100%
Medicine and Dentistry
Bleeding Disorder
100%
Blood Clotting
50%
Blood Clotting Factor
50%
Clinical Management
50%
Diseases
50%
Genetic Screening
50%
Genome Wide Association Study
50%
Genotype Phenotype Correlation
50%
Haemophilia A
50%
Molecular Diagnostics
50%
Prenatal Diagnosis
50%
Single Nucleotide Polymorphism
50%
Translating (Language)
50%
Von Willebrand Disease
100%
Biochemistry, Genetics and Molecular Biology
Blood Coagulation Factor
50%
Coagulation System
50%
Genetic Screening
50%
Genetics
100%
Genome-Wide Association Study
50%
Genotype Phenotype Correlation
50%
Haemophilia A
50%
Molecular Genetics
50%
Single-Nucleotide Polymorphism
50%
Translating (Language)
50%
Von Willebrand Disease
100%
Neuroscience
Blood Clotting Factor
100%
Coagulation System
100%
Genome-Wide Association Study
100%
Single-Nucleotide Polymorphism
100%