Keyphrases
Von Willebrand Factor
100%
Chiari Malformation
63%
Von Willebrand Disease
58%
Coding Variants
49%
Chromodomain
47%
African American
47%
Scoliosis
44%
Syringomyelia
42%
Synonymous Variant
41%
European American
35%
Genetic Contribution
34%
Human Genetics
33%
Von Willebrand Factor Antigen
32%
Posterior Fossa Decompression
31%
Antigen Levels
31%
Clubfoot
31%
Environmental Contribution
31%
CHRNB3
31%
CHRNA6
31%
Nicotine Dependence
31%
Adolescent Idiopathic Scoliosis
29%
Neurological Diseases
23%
Alzheimer's Disease
23%
Cerebrospinal Fluid
23%
Syrinx
22%
Copy number Variation
20%
SNP
20%
COVID-19
19%
Alcohol Dependence
18%
Syndromic
18%
Neurological Disorders
18%
Duplication
18%
Obex
18%
Idiopathic Scoliosis
18%
Large Cohort
17%
Missense Variants
17%
Genetic Basis
17%
Factor Level
17%
Pediatric Population
15%
Region Types
15%
Cofactor Activity
15%
Interleukin-7 (IL-7)
15%
Ristocetin
15%
Human Dentition
15%
Inborn Errors
15%
T Cell Activation
15%
Pygathrix
15%
Extradural
15%
Connective Tissue Disease
15%
Duraplasty
15%
Biochemistry, Genetics and Molecular Biology
Genetics
87%
Von Willebrand Factor
71%
Chromodomain
47%
Von Willebrand Disease
37%
Adolescence
35%
Genetic Divergence
34%
Human Genetics
31%
Exome
27%
Liquid
23%
Single Nucleotide Polymorphism
22%
Genetic Variation
19%
Missense
17%
Nicotinic Receptor
15%
Receptor Gene
15%
Genetic Association
15%
Quantitative Trait Locus
15%
Proteome
15%
Iron Poisoning
15%
Iron Overload
15%
Morphological Trait
15%
Iron Homeostasis
15%
Menstruation
15%
Limb Development
15%
Cigarette Smoking
15%
PICALM
15%
BIN1
15%
Genomics
15%
Blood Plasma
15%
CHD8
11%
Chromosome 8
10%
Chromosome 15
10%
Gene Cluster
10%
Natural Selection
10%
Cerebrospinal Fluid Level
10%
Exon
9%
Genome-Wide Association Study
9%
Myelination
7%
Neurotransmitter
7%
GenBank
7%
Maturation
7%
Mastication
7%
Iron Metabolism
7%
Brain Development
7%
PITX1
7%
Iron Transport
7%
Body Height
7%
Coding Region
7%
Reconstruction
7%
Dysplasia
7%
Enhancer Region
7%
Medicine and Dentistry
Von Willebrand Factor
95%
Von Willebrand Disease
53%
Arnold Chiari Malformation
47%
Scoliosis
42%
Syringomyelia
37%
Posterior Fossa
31%
Clubfoot
31%
COVID-19
23%
Exome
20%
Neurologic Disease
17%
Tonsil
17%
Dentition
15%
Tooth Size
15%
Genetic Association
15%
Ristocetin
15%
Cell Function
15%
Pediatrics
15%
Lymphocytopenia
15%
Diagnosis
15%
Menorrhagia
15%
T Cell
15%
Toll Like Receptor 3
15%
Interleukin 7
15%
Connective Tissue Disease
15%
Molecular Pathology
15%
Prevalence
15%
Adolescent Idiopathic Scoliosis
15%
Adolescence
15%
Comorbidity
15%
Bleeding
13%
Oral Processing
9%
Anemia
7%
Congenital Malformation
7%
Diseases
6%
Digestive Function
6%
Immunosuppressive Drug
6%
Mouth
6%
Digestive System
6%
Surgery
5%
Bleeding Disorder
5%
Exome Sequencing
5%
Pathophysiology
5%
