New genomic studies could screen babies for more rare conditions, making parent information more important than ever.

Page for Spinal Muscular Atrophy (SMA) newborn screening acceptability study, being conducted as part of an in-service evaluation (ISE) for the UK National Screening Committee (UK NSC)

The aim of the network is to promote a positive research culture around Social and Ethical Research in Genomics where collaboration and mutual support is fostered and encouraged.

The aim of the network is to promote a positive research culture around Social and Ethical Research in Genomics where collaboration and mutual support is fostered and encouraged.

The aim of the network is to promote a positive research culture around Social and Ethical Research in Genomics where collaboration and mutual support is fostered and encouraged.

European Journal of Human Genetics - Acceptability of newborn screening for spinal muscular atrophy: views of the UK public, screened families, health professionals and the SMA community

In recent years, the use of remote methods by qualitative researchers has become commonplace. The COVID-19 pandemic forced researchers across the globe to rapidly convert their face-to-face methods t