Lucinda Freeman
6PUBLICATIONS
11CO-AUTHORS
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Publications (6)
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|Aug 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.Michael P Mackley, Pankaj B Agrawal, Sara S Ali
|Aug 03, 2023
Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.Lucinda Freeman, Lisa Bristowe, Edwin P Kirk
|Feb 09, 2023
Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening.Lucinda Freeman, Martin B Delatycki, Jackie Leach Scully
|Feb 06, 2023
How should severity be understood in the context of reproductive genetic carrier screening?Lisa Dive, Alison D Archibald, Lucinda Freeman
|Nov 06, 2022
Genetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening.Lisa Dive, Lucinda Freeman, Alison McEwen
|Oct 27, 2022
Views of reproductive genetic carrier screening participants regarding screening for genes associated with non-syndromic hearing loss.Lucinda Freeman, Martin B Delatycki, Jackie Leach Scully
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Frequent Collaborators
2 joint publications
Lisa Dive
2 joint publications
Alison McEwen
2 joint publications
Alison D Archibald
2 joint publications
Edwin P Kirk
1 joint publications
Ainsley J Newson
1 joint publications
Michael P Mackley
1 joint publications
Pankaj B Agrawal
1 joint publications
Belinda Dawson-McClaren
1 joint publications
Holly Ellard
1 joint publications
Celine Lewis
