Keyphrases
All-cause Mortality
100%
Syncope
71%
Exome
64%
Non-carriers
54%
American College of Medical Genetics
53%
Genetic Variants
52%
Hemoglobin A1c (HbA1c)
46%
Type 2 Diabetes Mellitus (T2DM)
42%
Monogenic
38%
Ventricular Arrhythmia
36%
Diabetes Duration
32%
Older Adults
32%
Population-based Cohort
32%
Glycemic Control
32%
Sudden Infant Death Syndrome
32%
Long QT Syndrome
32%
Cardiac Disease
32%
Inter99
32%
Brugada Syndrome
32%
Major Adverse Cardiovascular Events
32%
Congenital Long QT Syndrome
32%
QT Interval
32%
Congenital Disorders
32%
Without Diabetes
32%
Rare Genetic Variants
32%
Risk of Death
32%
J-point Elevation
32%
Pathogenicity
25%
Malignant Ventricular Arrhythmia
25%
QTc Interval
24%
UK Biobank
21%
Biochemistry, Genetics and Molecular Biology
Genetic Divergence
80%
Cardiac Dysrhythmia
68%
All Cause Mortality
64%
Medical Genetics
64%
Exome
32%
Zinc Finger Protein 804A
32%
Long QT Syndrome
32%
Brugada Syndrome
32%
Catecholaminergic Polymorphic Ventricular Tachycardia
32%
QT Interval
32%
QTc Interval
28%
Ion Channel
16%
Family Aggregation
16%
