Genomic Newborn Screening (gNBS) Working Group

• International Consortium on Newborn Sequencing (ICONSeq)
• BEACONs Newborn Screening Initiative
• Genomics England – Newborn Genomes Programme
• APHL Molecular Resources for Newborn Screening
• Early Check
• Guardian Study
• BabyScreen Project – Murdoch Children’s Research Institute
• BEGIN NGS – Rady Genomics
• Genomes2People

Resources listed are for informational purposes only. The inclusion of any external link does not imply a recommendation or endorsement by the University of Minnesota of the views expressed within them. We do not control or guarantee the accuracy, relevance, timeliness, or completeness of any information on these external websites.

• Babies, Incurable Diseases and the Promise of Genomic Screening – The New York Times
• Rewriting Genetic Fate: Universal Newborn Genomic Screening Arrives – Forbes
• Baby genomics: newborn sequencing starts to fulfill its promise
• USF Joins Sunshine Genetics Consortium
• Consensus recommendations from the International Consortium on Newborn Sequencing

Resources listed are for informational purposes only. The inclusion of any external link does not imply a recommendation or endorsement by the University of Minnesota of the views expressed within them. We do not control or guarantee the accuracy, relevance, timeliness, or completeness of any information on these external websites.

• Evidence is building for genomic newborn screening
• What do we mean by actionability? Examining a key criterion in genomic prenatal and newborn screening
• PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France
• A Genomic Sequencing Approach to Newborn Mass Screening and Its Opportunities
• "Jumping too far ahead": Australian healthcare professional, scientist, and policy maker perspectives on using genomics in newborn screening
• Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study
• Genomic Newborn Screening-A Long Road From Pilot to Public Policy
• Newborn screening for rare diseases: expanding the paradigm in the genomic era
• Primary Care Provider Perspectives on Expanded Genomic Screening in Children
• Feasibility and clinical utility of expanded genomic newborn screening in the Early Check program
• Data-driven consideration of genetic disorders for global genomic newborn screening programs
• TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care project
• Genomic newborn screening: exploring opportunities and navigating pitfalls while ensuring inclusivity
• Implementing genomic newborn screening as an effective public health intervention: sidestepping the hype and criticism
• Promises and challenges of genomic newborn screening (NBS) - lessons from public health NBS programs
• Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns
• Exploring the benefits, harms and costs of genomic newborn screening for rare diseases
• Genomic Newborn Screening for Pediatric Cancer Predisposition Syndromes: A Holistic Approach
• Genomic newborn screening: current concerns and challenges
• The case against genomic sequencing of healthy newborns
• Ethics of genomic newborn screening—a child centered public health framework
• Towards genomic newborn screening, part I: Mapping the ethical issues
• Operationalizing the Wilson-Jungner principles for the genomics era: Consensus recommendations from the International Consortium on Newborn Sequencing

Resources listed are for informational purposes only. The inclusion of any external link does not imply a recommendation or endorsement by the University of Minnesota of the views expressed within them. We do not control or guarantee the accuracy, relevance, timeliness, or completeness of any information on these external websites.