Biochemistry, Genetics and Molecular Biology
Genome-Wide Association Study
100%
Blood Pressure
95%
Genetic Divergence
95%
Genotyping
93%
Single-Nucleotide Polymorphism
85%
Exome Sequencing
53%
Allele
51%
Single Nucleotide Polymorphism
43%
Cardiac Muscle Cell
41%
Proband
41%
Candidate Gene
38%
Promoter Region
36%
Haplotype
33%
Heart Left Ventricle Mass
32%
Prevalence
30%
Genome Wide Association Study
30%
Gene Expression
28%
Genetic Association
28%
FLT4
27%
Angiotensin
26%
Genetic Determinism
25%
Genetic Risk
24%
Genetic Variation
24%
Embryonic Stem Cell
24%
Indel
24%
Mouse
23%
Genetic Architecture
22%
Next Generation Sequencing
21%
Case-Control Study
20%
Body Mass
20%
Gene Linkage
20%
Gene Polymorphism
19%
Induced Pluripotent Stem Cell
18%
Systolic Blood Pressure
18%
Angiotensin-Converting Enzyme
18%
Renin Angiotensin Aldosterone System
18%
Atrial Fibrillation
18%
Mendelian Randomization
17%
TBX1
16%
Genetic Association Study
16%
Sample Size
16%
Magnetism
15%
Diastolic Blood Pressure
15%
Genetic Polymorphism
15%
Linkage Analysis
15%
Mass Spectrometry
14%
Quantitative Trait Locus
14%
Phenotype
14%
Aldosterone
14%
Regulatory Element
14%
Medicine and Dentistry
Persistent Truncus Arteriosus
83%
Cardiovascular System
46%
Meta-Analysis
41%
Percutaneous Coronary Intervention
34%
Coronary Artery Disease
31%
Tetralogy of Fallot
28%
Diseases
26%
Genome Wide Association Study
25%
Myocardial Infarction
21%
Cardiac Muscle Cell
20%
Cardiovascular Disease
19%
Heart Development
19%
Atrial Septal Defect
18%
In Vitro
18%
Heritability
18%
Genetic Association
18%
Single Nucleotide Polymorphism
18%
Lymph Duct
18%
Prevalence
17%
Odds Ratio
15%
Heart Left Ventricle Function
14%
Blood Pressure
14%
UK Biobank
14%
Long Untranslated RNA
13%
Genetic Variability
13%
Ebstein's Anomaly
12%
MYH7
12%
Endothelial Progenitor Cell
12%
Dipeptidyl Carboxypeptidase
12%
Disorders of Mitochondrial Functions
12%
Milroy's Disease
11%
Apoplexy
11%
Population Stratification
10%
Congenital Malformation
10%
Noncompaction Cardiomyopathy
9%
COVID-19
9%
Absence
9%
Autosomal Dominant Inheritance
9%
Coarctation of the Aorta
8%
Drug Therapy
8%
Atherosclerosis
8%
Brain Ischemia
8%
Lymphangiogenesis
8%
Exome
8%
Case-Control Study
8%
ST Segment Elevation Myocardial Infarction
7%
Heart Failure
7%
Creatine Phosphate
7%
Intima-Media Thickness
7%
Left Ventricular Hypertrophy
7%