Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia

Abstract excerpt

Integrating genomic sequencing into newborn screening (NBS) has transformative potential for the identification and management of genetic conditions. Using discrete choice experiment surveys, we elicited the preferences, values, and priorities of 2,509 members of the Australian public about the value (n = 1,504) and implementation (n = 1,005) of genomic NBS (gNBS). The Australian public demonstrated positive...

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