Author
University of MichiganORCID 0000-0003-4855-9260Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
4 papers
Recent·Most cited
Sophie Hespe, G. Powell, Laura Catto…·Jodie Ingles
The paper reclassifies genetic variants in HCM patients using a large registry, finding 10% of variants were reclassified, with most VUS unlikely to be causal.
Marin Jacobwitz, Hongbo Michael Xie, Jamie L. Catalano…·Ana G. Cristancho
The paper identifies DNA methylation differences associated with normalized fetal/placental weight ratios and links them to neurodevelopmental outcomes in neonates with congenital heart disease.
Megan J. Puckelwartz, Lorenzo L. Pesce, Edgar Javier Hernandez…·Elizabeth M. McNally
This study identifies genetic variants in epilepsy, cardiomyopathy, and arrhythmia genes in a sudden death in the young cohort, finding enrichment of damaging variants and a correlation with younger age at death.
Thomas A. Miller, Edgar Javier Hernandez, James William Gaynor…·Martin Tristani‐Firouzi
The paper examines how genetic, demographic, and clinical factors interact to influence neurodevelopmental outcomes in children with single ventricle heart disease.