Our vision is to meet the rapidly rising demand for specialists who may serve as regional or national experts in the field of heritable CV disorders.
The curriculum will be tailored to the interests of the fellow to allow in-depth training in aortopathies, genetic forms of arrhythmias, sudden cardiac death, familial hypercholesterolemia, hypertrophic, and dilated cardiomyopathy, as well as heritable complex diseases such as coronary heart disease, atrial fibrillation, and congenital heart disease.
As a CV genomics fellow, you will play an integral role in the management of a wide spectrum of heritable CV disorders, including diagnostic and treatment strategies, interpretation of genomic testing including whole genome/exome sequencing, panel tests, polygenic risk scores, and DTC tests, referral for cardiac procedures such as septal reduction, surgery for HCM, ICD placement for arrhythmias, novel biologics for lipid disorders, lipoprotein apheresis, and close collaboration with multi-disciplinary teams.
This program includes exposure to research in the field of heritable CV disorders, including opportunities to advance understanding of the genomic basis of a wide variety of CV disorders (including rare monogenic diseases and more common ‘complex’ diseases such as coronary heart disease (CHD)), polygenic risk scores, rare variant interpretation including functional assays, and training in clinical trial management.