Gemma R Brett

8PUBLICATIONS
38CO-AUTHORS
Infant and child healthTranslation and interpretation studiesImplementation science and evaluationCell and nuclear divisionNeonatology
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Publications (8)

|Jun 08, 2023
Integrated multi-omics for rapid rare disease diagnosis on a national scale.

Sebastian Lunke, Sophie E Bouffler, Chirag V Patel

|Oct 22, 2022
Co-design, implementation, and evaluation of plain language genomic test reports.

Gemma R Brett, Aisha Ward, Sophie E Bouffler

|Jul 13, 2022
'Diagnostic shock': the impact of results from ultrarapid genomic sequencing of critically unwell children on aspects of family functioning.

Hilary Bowman-Smart, Danya F Vears, Gemma R Brett

|Jan 29, 2021
Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level.

Stephanie Best, Helen Brown, Sebastian Lunke

|Nov 10, 2020
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10.

Guy Helman, Alison G Compton, Daniella H Hock

|Jul 29, 2020
Parental experiences of ultrarapid genomic testing for their critically unwell infants and children.

Gemma R Brett, Melissa Martyn, Fiona Lynch

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Frequent Collaborators

7 joint publications

Zornitza Stark

2 joint publications

David R Thorburn

2 joint publications

John Christodoulou

2 joint publications

Meredith Wilson