Keyphrases
Adolescent Idiopathic Scoliosis
100%
Coding Variants
61%
Nicotine Dependence
60%
Chiari Malformation
58%
Synonymous Variant
54%
Missense Variants
54%
Syringomyelia
53%
Rare Variants
48%
Von Willebrand Factor
48%
Scoliosis
44%
Chromodomain
43%
CHRNB3
39%
Copy number Variation
38%
Posterior Fossa Decompression
38%
African American
32%
Idiopathic Scoliosis
31%
Human Genetics
29%
Research Consortium
29%
Chiari 1 Malformation
29%
Von Willebrand Factor Antigen
29%
CHRNB4
29%
Antigen Levels
29%
Functional Characterization
29%
Clubfoot
29%
Cerebrospinal Fluid
29%
Alcohol Dependence
29%
Genetic Variants
28%
CHRNA6
27%
Variants of Uncertain Significance
27%
Cocaine Dependence
25%
Genome-wide Association Study
25%
Exome Sequencing
23%
Functional Impact
22%
Fibrillin-1 (FBN1)
21%
Syrinx
21%
Von Willebrand Disease
20%
CHRNA3
20%
Risk Reduction
19%
Single nucleotide Variant
18%
Joint Hypermobility
18%
Duplication
17%
Functional Score
17%
Comorbidity
17%
Nicotine
16%
CHRNA5
16%
Obex
16%
Genetic Risk
16%
Nicotinic Receptor Genes
16%
Pathogenicity
16%
Large Cohort
15%
Biochemistry, Genetics and Molecular Biology
Adolescence
72%
Missense
64%
Genetic Divergence
61%
Genetics
54%
Von Willebrand Factor
51%
Rare Variant
48%
Chromodomain
43%
CHRNB4
34%
Receptor Gene
29%
Human Genetics
29%
Single-Nucleotide Polymorphism
29%
CHRNA3
27%
Exome
27%
Single Nucleotide Polymorphism
22%
Exome Sequencing
21%
Genome-Wide Association Study
21%
Nicotinic Receptor
21%
Von Willebrand Disease
20%
Smoking
19%
Coding Region
18%
CHRNA5
18%
Genetic Variation
16%
Next Generation Sequencing
15%
Sarcoglycan
14%
Amino Acids
14%
Erethism
14%
Genetic Association
14%
Osteoclast
14%
Cell Viability
14%
Quantitative Technique
14%
Prenylation
14%
Gene Mutation
14%
GLUT1
14%
Menstruation
14%
Olfactory Receptor
14%
Pyrophosphate
14%
Genetic Test
14%
Synthase
14%
Protein Prenylation
14%
Transcription Factors
14%
Senescence
14%
Androgen Receptor
14%
Human Leukocyte Antigen
14%
Limb Development
14%
Mutagenesis
14%
Inosine
14%
Cohesin
14%
Fibrillin
14%
Gene Cluster
12%
Allele
11%
Medicine and Dentistry
Arnold Chiari Malformation
58%
Adolescent Idiopathic Scoliosis
58%
Syringomyelia
49%
Scoliosis
44%
Posterior Fossa
43%
Von Willebrand Factor
43%
Surgery
21%
Exome
20%
Cell Surface
18%
Joint Laxity
18%
Tonsil
16%
Pathogenicity
15%
Single Nucleotide Polymorphism
14%
Menorrhagia
14%
Tobacco Dependence
14%
Glucose Transporter 1
14%
Genetic Association
14%
Aortic Aneurysm
14%
Genetic Risk
14%
Clubfoot
14%
Limb Girdle Muscular Dystrophy
14%
Fibrillin 1
14%
Fibrillin 2
14%
Prevalence
14%
Adolescence
14%
Comorbidity
14%
Myopathy
10%
Early Diagnosis
9%
Marfan Syndrome
8%
Cell Population
7%
In Vitro
7%
Cas9
7%
Sarcoglycan
7%
Cell Growth
7%
Cell Culture
7%
Anemia
7%
Clustered Regularly Interspaced Short Palindromic Repeat
7%
Blood Glucose
7%
Genetic Screening
7%
Amino Acid
7%
Cerebrospinal Fluid
7%
Clinical Trial
6%
Bleeding
6%
Basilar Invagination
5%
Von Willebrand Disease
5%
Congenital Malformation
5%
Disease Severity
5%
Disease
5%