Patient-Reported Outcomes Among Adults With Congenital Heart Disease in the Congenital Heart Initiative RegistryScott Leezer, Anitha S. John, Adam M. Lubert et al.|JAMA Network Open|2024Cited by 21
Patient Engagement in Research: Considerations in Creating a Registry for Adults with Congenital Heart DiseaseRuth Phillippi, Anitha S. John, Scott Leezer et al.|Current Cardiology Reports|2023Cited by 6
Prioritizing patient‐centered research in adult congenital heart disease and pregnancy: Findings from Phase 3 of a multiphase national initiativeKashvi Singh, Anitha S. John, Mindi Messmer et al.|Pregnancy|2026Cited by 1
Abstract 15763: Increasing Diversity Among Research Participants Through Patient Engagement in the Congenital Heart InitiativeMindi Messmer, Anitha S. John, Scott Leezer et al.|Circulation|2023Cited by 1