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AT1 mutations and risk of atrial fibrillation based on genotypes from 71,000 individuals from the general population
S C W Marott,
B G Nordestgaard
, G B Jensen,
A Tybjaerg-Hansen
,
M Benn
Østerbroundersøgelsen BFH
Hjertemedicinsk Afdeling AHH
Afdeling for Klinisk Biokemi DIA
7
Citationer (Scopus)
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Keyphrases
Genotype
100%
Atrial Fibrillation
100%
AT-1
85%
Genetic Variants
28%
Myocardial Infarction
14%
Hypertension
14%
Copenhagen City Heart Study
14%
Copenhagen
14%
General Population Studies
14%
Ischemic Heart Disease
14%
Heterozygote
14%
AIMS™
14%
Nonsynonymous
14%
Synonymous Variant
14%
Heart Failure
14%
Angiotensin II Type 1 Receptor (AT1R)
14%
Pharmaceutical Industry
14%
Heterozygosity
14%
Non-carriers
14%
Atrial Myocardium
14%
Structural Remodeling
14%
Electrical Remodeling
14%
Atrial Disease
14%
Genotypic Variation
14%
Biochemistry, Genetics and Molecular Biology
Population
100%
Atrial Fibrillation
100%
Genetic Divergence
42%
Population Research
14%
Angiotensin II Receptor Type 1
14%
Heterozygosity
14%