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Biotech (Basel (Switzerland))|June 27, 2023
Privacy Implications of Contacting the At-Risk Relatives of Patients with Medically Actionable Genetic Predisposition, with Patient Consent: A Hypothetical Australian Case StudyJane Tiller, Kristen Nowak, Tiffany Boughtwood, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2020
The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experimentsIlias Goranitis, Stephanie Best, John Christodoulou, et al.Ethics & Human Research|September 27, 2025
Translational Genomics and Community-Driven Research in AustraliaFiona Russo, Keri Finlay, Isabella Sherburn, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 26, 2020
The value of genomic sequencing in complex pediatric neurological disorders: a discrete choice experimentIlias Goranitis, Stephanie Best, Zornitza Stark, et al.European Journal of Human Genetics : EJHG|April 3, 2021
Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experimentIlias Goranitis, Stephanie Best, John Christodoulou, et al.European Journal of Human Genetics : EJHG|September 14, 2023
Evaluation of CTRL: a web application for dynamic consent and engagement with individuals involved in a cardiovascular genetic disorders cohortMatilda A Haas, Evanthia O Madelli, Rosie Brown, et al.European Journal of Human Genetics : EJHG|December 20, 2024
Health professionals contacting patients' relatives directly about genetic risk (with patient consent): current clinical practice and perspectivesAmi Stott, Evanthia O Madelli, Tiffany Boughtwood, et al.BMC Medicine|February 23, 2019
Building a learning community of Australian clinical genomics: a social network study of the Australian Genomic Health AllianceJanet C Long, Chiara Pomare, Stephanie Best, et al.European Journal of Human Genetics : EJHG|January 7, 2021
'CTRL': an online, Dynamic Consent and participant engagement platform working towards solving the complexities of consent in genomic researchMatilda A Haas, Harriet Teare, Megan Prictor, et al.Human Genetics|July 21, 2023
Genomics and inclusion of Indigenous peoples in high income countriesKylie Gwynne, Shirley Jiang, Robertson Venema, et al.Pageof 5