Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis and treatment, according to a new study. A baby's genome ...
If you have ever welcomed a new baby into the world, you know the mix of hope and uncertainty that comes with those first days. For decades, newborn screening has been a quiet triumph of public health ...
‘BEACONS,’ a multi-state collaboration led by Mass General Brigham and Ariadne Labs, will enroll up to 30,000 newborns to explore adding genomic sequencing in U.S. newborn screening GAITHERSBURG, Md.- ...
The goal of this workshop was to examine the types of evidence being collected as part of genomics-based programs at health care systems, consider near-term opportunities for advancing knowledge about ...
In Destiny’s Child No Longer: Rewriting Genetic Fate, we envisioned a world where every newborn would be screened for genetic risks. We see a future in which the randomness of genetic inheritance ...
Genetic conditions with actionable interventions affect nearly 10% of populations in the United States and internationally - ...
Data from more than 22,000 newborns reinforce GeneDx’s role spearheading the adoption of genomic newborn screening (gNBS) from research to clinical practice GeneDx (Nasdaq: WGS), a leader in ...
Prestigious recognition underscores the impact of large-scale genomic screening in identifying serious childhood genetic conditions in conjunction with traditional newborn screening GeneDx (Nasdaq: ...
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