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Author Details
Full Name
Tiffany Boughtwood
Affiliation
Murdoch Children's Research Institute
ORCID
Career Start Year
2018
Papers
29
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37169978
Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing.
Eur J Hum Genet
2024
37709947
Evaluation of CTRL: a web application for dynamic consent and engagement with individuals involved in a cardiovascular genetic disorders cohort.
Eur J Hum Genet
2024
37217628
Correction: Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing.
Eur J Hum Genet
2024
37280361
Direct notification by health professionals of relatives at-risk of genetic conditions (with patient consent): views of the Australian public.
Eur J Hum Genet
2024
36868206
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Am J Hum Genet
2023
37479894
Genomics and inclusion of Indigenous peoples in high income countries.
Hum Genet
2023
37868041
Equity, diversity, and inclusion at the Global Alliance for Genomics and Health.
Cell Genom
2023
37366793
Privacy Implications of Contacting the At-Risk Relatives of Patients with Medically Actionable Genetic Predisposition, with Patient Consent: A Hypothetical Australian Case Study.
BioTech (Basel)
2023
34544841
A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratorium.
J Med Genet
2022
36579509
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
J Pers Med
2022
35902697
Health professionals' views and experiences of the Australian moratorium on genetic testing and life insurance: A qualitative study.
Eur J Hum Genet
2022
36332611
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.
Am J Hum Genet
2022
34427008
Paediatric genomic testing: Navigating genomic reports for the general paediatrician.
J Paediatr Child Health
2022
32839572
The value of genomic sequencing in complex pediatric neurological disorders: a discrete choice experiment.
Genet Med
2021
33566436
Paediatric genomic testing: Navigating medicare rebatable genomic testing.
J Paediatr Child Health
2021
33811253
Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment.
Eur J Hum Genet
2021
35072136
GA4GH: International policies and standards for data sharing across genomic research and healthcare.
Cell Genom
2021
34820659
The Data Use Ontology to streamline responsible access to human biomedical datasets.
Cell Genom
2021
34020638
Study protocol: the Australian genetics and life insurance moratorium-monitoring the effectiveness and response (A-GLIMMER) project.
BMC Med Ethics
2021
34205718
A Pathway to Precision Medicine for Aboriginal Australians: A Study Protocol.
Methods Protoc
2021
33408362
'CTRL': an online, Dynamic Consent and participant engagement platform working towards solving the complexities of consent in genomic research.
Eur J Hum Genet
2021
32371919
The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments.
Genet Med
2020
32266555
Parental health spillover effects of paediatric rare genetic conditions.
Qual Life Res
2020
30609404
Integrating Genomics into Healthcare: A Global Responsibility.
Am J Hum Genet
2019
31734945
The ethics approval process for multisite research studies in Australia: changes sought by the Australian Genomics initiative.
Med J Aust
2019
30927468
Preparing Australia for genomic medicine: data, computing and digital health.
Med J Aust
2019
30791916
Building a learning community of Australian clinical genomics: a social network study of the Australian Genomic Health Alliance.
BMC Med
2019
31271757
Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.
Am J Hum Genet
2019
30069064
Registered access: authorizing data access.
Eur J Hum Genet
2018
1 - 29 of 29
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