March 17, 2025 GenomeWeb BeginNGS Program Seeks to Improve Pediatric Rare Disease Dx, Treatment via Rapid NGS, Data Curation
October 9, 2023 Precision Medicine Online International Newborn Genome Sequencing Projects Discuss Differences, Future Goals
September 27, 2023 Patient Worthy Rare Community Profiles: Inozyme’s Catherine Nester Discusses Newborn Screening and the GACI Diagnostic Delay
September 25, 2023 Fierce Pharma Why Pharma Should Pay Attention to – and Be Part of – Rapid Whole Genome Sequencing Advancement
May 19, 2025 BeginNGS® Consortium Announces Alexion, AstraZeneca Rare Disease as its First Platinum Member
December 5, 2024 BeginNGS® Newborn Screening by Genome Sequencing Shown to be Safe and Effective in Two Clinical Studies
July 10, 2023 Rady Children’s Institute for Genomic Medicine Launches Phase 2 of BeginNGS Program for Identifying Treatable Genetic Diseases for Newborns
February 9, 2023 Study Finds Association of Genetic Disease and Infant Mortality Higher Than Previously Recognized: 41% of Infant Deaths Associated with Genetic Diseases
August 24, 2022 Novel Newborn Screening System Uses Rapid Whole Genome Sequencing and Acute Management Guidance to Screen and Diagnosis Genetic Diseases
