Patient-Reported Outcomes Among Adults With Congenital Heart Disease in the Congenital Heart Initiative RegistryScott Leezer, Anitha S. John, Rittal Mehta 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, Danielle Hile et al.|Current Cardiology Reports|2023Cited by 6
Impact of Adult Congenital Heart Disease Specialist Visits on Emergent AdmissionsAnushree Agarwal, Thomas W. Carton, Rong Duan et al.|JACC Advances|2025Cited by 4
Understanding gaps in guideline-recommended adult congenital heart disease care: Data from 12 US health care centersJoseph Bayne, Anushree Agarwal, Rong Duan et al.|American Heart Journal|2025Cited by 1
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