Provides updates and reviews data from the All of Us Research Program, an effort by the National Institute of Health (NIH), where health data, habits, and the physical environment of … More →
Addresses difficulties that can arise from genomic testing and identifies strategies to mitigate unexpected consequences.
Discusses knowledge gaps of Hepatic Glycogen Storage Diseases.
Discusses how families advocate for the advancement of newborn screening.
Provides the historical context of medical genetics and discusses the future of the genetics workforce.
Discusses the principles of community engagement, highlighting key strategies to help health professionals build trustworthiness with families, and promote health equity when addressing genetic conditions.
Overview of the Rare Disease Advisory Council (RDAC) and how families can get involved in their state’s organization. Find Your State’s RDAC