Opening Panel: Dr Robert Green welcomes Nobel Laureate, Walter Gilbert, genomics and synthetic biology pioneer, George Church, and initiator of the Human Genome Project, Charles DeLisi.

Integrating Untargeted Metabolomics as a Second-Tier Functional Tool for Variant Interpretation in Genomic Newborn Screening

Speaker: José ManuelGonzález de Aledo Castillo

Eight genomic newborn screening implementation challenges observed in Early Check

Speaker: Heidi Cope

Parental Perspectives and Experiences with Genetic Testing and Surveillance for Cancer Predisposition in Healthy Young Children

Speaker: Kayla Hamilton

Genetic Privacy & Law

Speaker: Natalie Ram

1. Genetically-driven Immune Disease Genes in BEACONS Multi-State Genomic Newborn Screening. Jennifer Puck

2. Implementation Considerations for Pediatric Cancer Predisposition Focused Newborn Screening: Preliminary Qualitative Findings from the INSPECT Study. Stacey Pereira

3. CRINGENES: Advancing Newborn Screening in Spain through Genomic and Metabolomic integration. Hugo Rocha

4. Returning condition suspected results in genomic newborn screening: early experiences of parents and clinicians in the Generation Study. Emma Beecham

5. Multi-omic Newborn Screening: preliminary data on 25,000 newborns from the Puglia Genome Program. Paola Orsini

6. Result interpretation for autosomal recessive conditions identified by the GUARDIAN expanded genomic newborn screening study. Brenna Boyd

7. Toward Population-Scale Opt-Out Newborn Genetic Screening: Implementation Framework and Transition Readiness from Abu Dhabi. Sahar Almarzooqi

8. High expectations, deep concerns: South Korean parental perceptions of WGS-based newborn screening. Wonhoo Yoo

9. Results of assessment of infants with Long QT syndrome (LQTS) identified by the GUARDIAN (Genomic Uniform-screening Against Rare Disease in All Newborns) genomic newborn screening (gNBS) study. Brenna Boyd

10. Establishing a core outcome set for type 1 diabetes screening in infants and children. Whiwon Lee

11. GENETIC COUNSELING CHALLENGES FOR PEDIATRIC CANCER SUSCEPTIBILITY GENETIC TESTING IN THE NEWBORN SCREENING: SPANISH CONSENSUS-CANGUR PROJECT. Estela Carrasco López

12. Selection of Genetic Conditions for the BEACONS-NBS study: The First U.S. Multi-State Genomic Newborn Screening Initiative. Harini Somanchi

13. Genetic counseling challenges following genomic newborn screening: Early experience from the PERIGENOMED project. Laurent PASQUIER

14. A Regionally Informed Master Gene List for Genomic Newborn Screening Identifies Actionable and Founder Variants in Middle Eastern Populations. Ammira Al-Shabeeb AKIL

15. Double-Stranded Politics: Partisan Trends in Genetics and Rare Disease Legislation from 2009-2025. Alexandra Crocker