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Family studies to find rare high risk variants in migraine
Rikke Dyhr Hansen, Anne Francke Christensen,
Jes Olesen
Institut for Klinisk Medicin
12
Citationer (Scopus)
74
Downloads (Pure)
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Keyphrases
Migraine
100%
Family Study
100%
High Risk
100%
Risk Variant
100%
Next-generation Sequencing
60%
Common Complex Disease
50%
Rare Variants
30%
Candidate Gene Approach
20%
Rare Genetic Variants
20%
Disease Risk
10%
Pedigree
10%
Promising Applications
10%
Genetic Variation
10%
Family-based Design
10%
Linkage Analysis
10%
PubMed
10%
Heritability
10%
Family-based Approaches
10%
De-novo mutations
10%
Common Variants
10%
Large Families
10%
Odds Ratio
10%
Large Degree
10%
Exome
10%
Potassium Channel
10%
Candidate Gene Study
10%
Migraine without Aura (MWoA)
10%
Environmental Factors
10%
Small Parts
10%
Pathophysiology
10%
Genetic Susceptibility
10%
Genetic Factors
10%
Rare mutation
10%
Biochemistry, Genetics and Molecular Biology
Next Generation Sequencing
100%
Rare Variant
50%
Genetic Divergence
50%
Genetics
50%
Candidate Gene
33%
Linkage Analysis
16%
Medline
16%
Exome
16%
Potassium Channel
16%
Genetic Variation
16%
Genetic Susceptibility
16%
Pedigree
16%
Medicine and Dentistry
Migraine
100%
Diseases
90%
Next Generation Sequencing
60%
Migraine with Aura
10%
Heritability
10%
Pathophysiology
10%
Exome
10%
Pedigree
10%
Odds Ratio
10%
Genetic Susceptibility
10%
Environmental Factor
10%
Linkage Analysis
10%
Effect Size
10%
Malignant Neoplasm
10%
Potassium Channel
10%
Genetic Variation
10%