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European Journal of Human Genetics : EJHG|January 23, 2019
Australians' views and experience of personal genomic testing: survey findings from the Genioz studyJacqueline Savard, Chriselle Hickerton, Rigan Tytherleigh, et al.
European Journal of Medical Genetics|November 16, 2018
Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz studySylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 26, 2021
The expectations and realities of nutrigenomic testing in australia: A qualitative studyErin Tutty, Chriselle Hickerton, Bronwyn Terrill, et al.
European Journal of Human Genetics : EJHG|April 17, 2025
Empowering human research ethics committees to review genomics applications: evaluating the utility of a custom online education resourceElla McGahan, Jennifer Berkman, David Milne, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2023
Development and evaluation of a novel educational program for providers on the use of polygenic risk scoresTatiane Yanes, Courtney K Wallingford, Mary-Anne Young, et al.
Frontiers in Medicine|May 15, 2025
Building capacity for genomics in primary care: a scoping review of practitioner attitudes, education needs, and enablersKate L A Dunlop, Nehal Singh, Amelia K Smit, et al.
European Journal of Human Genetics : EJHG|January 11, 2023
Community Genetics screening in a pandemic: solutions for pre-test education, informed consent, and specimen collectionBronwyn Terrill, Lauren McKnight, Angela Pearce, et al.
American Journal of Human Genetics|June 6, 2025
Consultation informs strategies for improving the use of functional evidence in variant classificationRehan M Villani, Bronwyn Terrill, Emma Tudini, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Consultation informs strategies to improve functional evidence use in variant classificationRehan M Villani, Bronwyn Terrill, Emma Tudini, et al.
European Journal of Human Genetics : EJHG|August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementationMichael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
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