OpenAI for helping find 18 new diagnoses across 376 previously unsolved medical cases.
Includes diagnosing Kyra, who has been trying to understand her muscle weakness since age 9, with a rare form of myofibrillar myopathy shortly before her 28th birthday.
Together with researchers at Boston Children’s Hospital and Harvard, we published a study in NEJM AI showing how o3 Deep Research helped clinicians revisit previously unsolved rare pediatric disease cases, and find answers for families who had waited years.