Australian public perspectives on genomic newborn screening: which conditions should be included?

Reference

Lynch, F., Best, S., Gaff, C. L., Downie, L., Archibald, A. D., Gyngell, C., Goranitis, I., Peters, R., Savulescu, J., Lunke, S., Startk, Z. and Vears, D. F., (2024), 'Australian public perspectives on genomic newborn screening: which conditions should be included?', Human Genomics, Vol: 18(4): Article 45 [PMC11077791]  

Abstract

Implementing genomic sequencing into newborn screening programs allows for significant expansion in the number and scope of conditions detected. We sought to explore public preferences and perspectives on which conditions to include in genomic newborn screening (gNBS).

We recruited English-speaking members of the Australian public over 18 years of age, using social media, and invited them to participate in online focus groups.

Links

Publisher website: https://humgenomics.biomedcentral.com/articles/10.1186/s40246-024-00611-x

Europe PMC: https://europepmc.org/article/MED/38720401

All OUCs Open Access papers are available on our Open Access webpage

Funders

Wellcome Trust WT203132 [Wellcome Centre for Ethics and Humanities]