Ashok K. Manickaraj
Toronto, ON, Canada
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Machine Learning Identifies Clinical and Genetic Factors Associated With Anthracycline Cardiotoxicity in Pediatric Cancer Survivors.
Journal: JACC. CardioOncology
Published: March 11, 2020
Clinical genetic testing in pediatric cardiomyopathy: Is bigger better?
Journal: Clinical genetics
Published: February 05, 2017
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Journal: American journal of human genetics
Published: March 03, 2016
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 25, 2014
High throughput exome coverage of clinically relevant cardiac genes.
Journal: BMC medical genomics
Published: August 12, 2014
Rare variants in NR2F2 cause congenital heart defects in humans.
Journal: American journal of human genetics
Published: October 24, 2013
Genetic variations in hypoxia response genes influence hypertrophic cardiomyopathy phenotype.
Journal: Pediatric research
Published: September 26, 2012
Personalized medicine in pediatric cardiology: do little changes make a big difference?
Journal: Current opinion in pediatrics
Published: August 15, 2012
Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair.
Journal: Pediatric research
Published: July 17, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026