Issue Date | Title | Author(s) |
2021-08 | Parent clinical trial priorities for fragile X syndrome: a best-worst scaling. | Turbitt, E; D'Amanda, C; Hyman, S; Weber, JD; Bridges, JFP; Peay, HL; Biesecker, BB |
2021-07 | Enrolling Children in Clinical Trials for Genetic Neurodevelopmental Conditions: Ethics, Parental Decisions, and Children's Identities. | Turbitt, E; Newson, AJ; Biesecker, BB; Wilfond, BS |
2023-09 | (In)visibility of LGBTQIA+ people and relationships in healthcare: A scoping review. | Mitchell, LA; Jacobs, C; McEwen, A |
2023-08 | Defining 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 |
2022-11-01 | The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation | Archibald, AD; McClaren, BJ; Caruana, J; Tutty, E; King, EA; Halliday, JL; Best, S; Kanga-Parabia, A; Bennetts, BH; Cliffe, CC; Madelli, EO; Ho, G; Liebelt, J; Long, JC; Braithwaite, J; Kennedy, J; Massie, J; Emery, JD; McGaughran, J; Marum, JE; Boggs, K; Barlow-Stewart, K; Burnett, L; Dive, L; Freeman, L; Davis, MR; Downes, MJ; Wallis, M; Ferrie, MM; Pachter, N; Scuffham, PA; Casella, R; Allcock, RJN; Ong, R; Edwards, S; Righetti, S; Lunke, S; Lewis, S; Walker, SP; Boughtwood, TF; Hardy, T; Newson, AJ; Kirk, EP; Laing, NG; Delatycki, MB |
2017-02 | A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public. | Smit, AK; Espinoza, D; Newson, AJ; Morton, RL; Fenton, G; Freeman, L; Dunlop, K; Butow, PN; Law, MH; Kimlin, MG; Keogh, LA; Dobbinson, SJ; Kirk, J; Kanetsky, PA; Mann, GJ; Cust, AE |
2023-02-13 | Do Teachers Question the Reality of Pain in Their Students? A Survey Using the Concept of Pain Inventory-Proxy (COPI-Proxy). | Fechner, R; Noel, M; Verhagen, A; Turbitt, E; Pate, JW |
2022-07 | Correction: Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review. | Richardson, E; McEwen, A; Newton-John, T; Crook, A; Jacobs, C |
2022-12 | Views of reproductive genetic carrier screening participants regarding screening for genes associated with non-syndromic hearing loss. | Freeman, L; Delatycki, MB; Leach Scully, J; Kirk, EP |
2020-05 | Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial. | Umstead, KL; Han, PKJ; Lewis, KL; Miller, IM; Hepler, CL; Thompson, LJ; Wolfsberg, TG; Nguyen, A-D; Fredriksen, MT; Gibney, G; Turbitt, E; Biesecker, LG; Biesecker, BB |