Summary
This NIH funding opportunity announcement (PAR-25-185) solicits R01 research grant applications focused on the screening and functional validation of genomic variants associated with human congenital anomalies. Clinical trials are explicitly excluded. The opportunity is issued by the National Institutes of Health (HHS) and is open for a multi-year window from October 2024 through January 2028, suggesting multiple receipt/review cycles. Applicants are expected to conduct genomic and functional biology research aimed at understanding the genetic underpinnings of birth defects and developmental disorders.