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Issue DateTitleAuthor(s)
2023A mainstreaming oncogenomics model: improving the identification of Lynch syndrome.O'Shea, R; Crook, A; Jacobs, C; Kentwell, M; Gleeson, M; Tucker, KM; Hampel, H; Rahm, AK; Taylor, N; Lewis, S; Rankin, NM
2023-10Motivations to learn genomic information are not exceptional: Lessons from behavioral science.Taber, JM; Peters, E; Klein, WMP; Cameron, LD; Turbitt, E; Biesecker, BB
2023-08-04Genetic testing and other healthcare use by Black and white individuals in a genomic sequencing study.Saylor, KW; Klein, WM; Calancie, L; Lewis, KL; Biesecker, LG; Turbitt, E; Roberts, MC
2023-06-21A survey of genetic and palliative care health professionals' views of integrating genetics into palliative care.White, S; Turbitt, E; Rogers, K; Tucker, K; McEwen, A; Best, M; Phillips, JL; Jacobs, C
2023-09-04How do women talk about self-funded breast cancer genetic testing?: Small stories and stance-taking strategies.Bechaz, A; Sexton, A; Gill, G; Karidakis, M
2023-08Defining core outcomes of reproductive genetic carrier screening: A Delphi survey of Australian and New Zealand stakeholders.Richardson, E; McEwen, A; Newton-John, T; Jacobs, C
2023-08-02Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.Freeman, L; Bristowe, L; Kirk, EP; Delatycki, MB; Scully, JL
2023-05Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening.Freeman, L; Delatycki, MB; Scully, JL; Briggs, N; Kirk, EP
2023-05-11Models of communication for polygenic scores and associated behavioural and psychological outcomes: a systematic reviewWallingford, C; Kovilpillai, H; Jacobs, C; Turbitt, E; Primiero, C; Brockman, D; Soyer, HP; McInerney-Leo, A; Yanes, T
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