Biochemistry, Genetics and Molecular Biology
Amyloidosis
14%
Candidate Gene
10%
Cardiac Dysrhythmia
37%
Cardiac Muscle Cell
17%
Cohort Study
7%
Desmosome
9%
DPP6
7%
DSC2
9%
Dysplasia
64%
Electric Potential
13%
Electrocardiogram
25%
Exome Sequencing
52%
Filamin
14%
Gene Mutation
12%
Genetic Counseling
7%
Genetic Determinism
7%
Genetic Disorder
10%
Genetic Divergence
22%
Genetic Screening
24%
Genetics
89%
Genotyping
40%
Haplotype
35%
Heavy Meromyosin
7%
Indel
15%
Kinase
9%
Medical Genetics
7%
Medical Genomics
7%
Missense
34%
Missense Mutation
9%
Mouse
9%
Next Generation Sequencing
17%
Penetrance
22%
Phospholamban
78%
Phosphotransferase
9%
PKP2
25%
Plakophilin
25%
Population Dynamics
9%
Prevalence
16%
Proband
27%
Quantitative Technique
7%
RNA
8%
Standing
7%
Sudden Cardiac Death
10%
T Wave
8%
Titin
14%
TMEM43
16%
TPM1
8%
Transthyretin
12%
Tropomyosin
7%
Ventricular Fibrillation
7%
Keyphrases
Arrhythmogenic Cardiomyopathy
21%
Arrhythmogenic Right Ventricular Cardiomyopathy
22%
Arrhythmogenic Right Ventricular Dysplasia
42%
Asymptomatic Carriers
9%
ATTR Amyloidosis
12%
Cardiac Phenotype
8%
Cardiomyopathy
63%
Cell nucleus
7%
Cerebellar Dysgenesis
7%
Clinical Characterization
7%
Common Haplotype
8%
Desmosomal Genes
7%
Desmosome
9%
Diagnostic Performance
8%
Dilated Cardiomyopathy
32%
DNA Analysis
8%
Dutch
41%
Europe
10%
Family Members
10%
Founder mutation
24%
Gene Variants
9%
Genetic Causes
7%
Haplotype Analysis
12%
Haplotype Sharing
8%
Heart Failure
21%
Heart Failure Therapy
14%
Highly Sensitive
7%
Immunostaining
7%
Index Patient
26%
Large Series
9%
Likely Pathogenic Variant
7%
Malignant Ventricular Arrhythmia
12%
Mutation Carriers
28%
Myosin Heavy Chain 7
7%
Netherlands
25%
PACS2
7%
Pathogenic mutations
8%
Pathogenic Variants
18%
Peripartum Cardiomyopathy
7%
Phenotypic Variation
8%
Phospholamban
71%
PKP2
12%
Plakophilin-2
25%
Recurrent mutation
21%
Risk Model
9%
Shift-share Analysis
7%
Stiffness
7%
Task Force Criteria
8%
TMEM43
13%
Ventricular Arrhythmia
21%
Medicine and Dentistry
Amyloidosis
8%
Arrhythmogenic Right Ventricular Dysplasia
22%
Ascertainment Bias
7%
ATTR Amyloidosis
14%
Bone Scintigraphy
7%
Cardiac Fibrosis
9%
Cardiac Magnetic Resonance Imaging
11%
Cardiomyopathy
100%
Cardiovascular Condition
7%
Cohort Analysis
8%
Congenital Heart Defect
7%
Desmosome
7%
Diagnosis
11%
Dilated Cardiomyopathy
17%
Disease
12%
Ejection Fraction
7%
Electrocardiogram
18%
Filamin
14%
Gadolinium
7%
Heart Disease
8%
Heart Failure
17%
Heart Left Ventricle Ejection Fraction
7%
Heart Ventricle Arrhythmia
41%
Heavy Meromyosin
7%
Immunohistochemistry
7%
Implantable Automatic Defibrillator
7%
Intervention Study
7%
Light Chain
7%
Neurofilament
7%
Noncompaction Cardiomyopathy
7%
Patient Care
7%
Pediatrics
8%
Phospholamban
71%
Rib
5%
Sudden Cardiac Death
5%
Technetium-99
7%
Transthyretin
7%