Press Releases August 24, 2022 Novel Newborn Screening System Uses Rapid Whole Genome Sequencing and Acute Management Guidance to Screen and Diagnosis Genetic Diseases Study demonstrates feasibility of NBS-rWGS prototype to rapidly screen for several hundred genetic diseases with effective interventions
Press Releases July 26, 2022 Study Supports Potential of Genome-to-Treatment (GTRx™) to Guide Physicians in the Management of 500 Treatable Genetic Diseases
Media Coverage July 25, 2022 The earlier the better: New consortium leverages infant screening to accelerate treatment PharmaVoice PHARMAVOICE: Newborn screening is gaining prominence across the biopharma and healthcare industries amid efforts to detect and treat disease as early as possible.
Press Releases June 14, 2022 RCIGM Launches Program to Advance Newborn Screening for Treatable Genetic Diseases
Media Coverage October 20, 2021 Rady Children’s Team Presents Genomic Medicine Management Tool at ASHG GenomeWeb
Press Releases September 27, 2021 Randomized Trial Demonstrates Whole-Genome Sequencing Leads to Improved Patient Care for Critically Ill Infants from Diverse Backgrounds
Press Releases June 2, 2021 From 13 Years to 13 Hours: Rady Children’s Institute for Genomic Medicine Demonstrates Fastest Time to Life-Changing Diagnosis for Infants with Rare Disease
Press Releases April 24, 2019 Rady Children’s Institute for Genomic Medicine Uses Artificial Intelligence to Diagnose Genetic Diseases