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Vears, D, Amor, DJ.
A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?.
Prenat Diagn
42(6)
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697 -704
2022
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Elliott, K, Vears, DF, Sung, V, Poulakis, Z, Sheehan, J.
Exploring Parent Support Needs during the Newborn Hearing Diagnosis Pathway..
J Clin Med
11(5)
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2022
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Lynch, F, Meng, Y, Best, S, Goranitis, I, Savulescu, J, Gyngell, C, Vears, DF.
Australian Public Perspectives on Genomic Data Storage and Sharing: Benefits, Concerns and Access Preferences.
2022
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Notini, L, Gaff, CL, Savulescu, J, Vears, DF.
Clinicians' Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss..
J Clin Med
11(1)
:
2021
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Gyngell, C, Lynch, F, Stark, Z, Vears, D.
Consent for rapid genomic sequencing for critically ill children: legal and ethical issues..
Monash Bioeth Rev
39(Suppl 1)
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117 -129
2021
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