A. Miron

Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy

S. Scherer, Marta Melé, B. Thiruvahindrapuram, 2020, medRxiv.

A Validated Model for Sudden Cardiac Death Risk Prediction in Pediatric Hypertrophic Cardiomyopathy

S. Colan, M. Lafreniere-Roula, R. Weintraub, 2020, Circulation.

Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy

A. Need, C. Tregidgo, R. Weintraub, 2022, npj Genomic Medicine.

Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy

S. Scherer, R. Weintraub, Marta Melé, 2022, NPJ genomic medicine.

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

Lisa J. Martin, Julie A. Phillippi, P. Kirshbom, 2021, HGG advances.

Return of genetic and genomic research findings: experience of a pediatric biorepository

M. Reuter, R. Kim, R. Jobling, 2019, BMC Medical Genomics.

Machine Learning Identifies Clinical and Genetic Factors Associated With Anthracycline Cardiotoxicity in Pediatric Cancer Survivors

P. Nathan, M. Lafreniere-Roula, S. Mital, 2020, JACC. CardioOncology.