| Issue Date | Title | Author(s) |
| 2017-07 | Motivators and barriers for paediatricians discharging patients. | Turbitt, E; Kunin, M; Gafforini, S; Freed, GL |
| 2017-08 | Parental preferences for paediatric specialty follow-up care. | Kunin, M; Turbitt, E; Gafforini, SA; Sanci, LA; Spike, NA; Freed, GL |
| 2019-10 | Living with Hereditary Haemorrhagic Telangiectasia: stigma, coping with unpredictable symptoms, and self-advocacy. | Sexton, A; Gargan, B; Taylor, J; Bogwitz, M; Winship, I |
| 2021-05-30 | Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16. | Pakdaman, Y; Berland, S; Bustad, HJ; Erdal, S; Thompson, BA; James, PA; Power, KN; Ellingsen, S; Krooni, M; Berge, LI; Sexton, A; Bindoff, LA; Knappskog, PM; Johansson, S; Aukrust, I |
| 2021-11 | Stakeholders' views of integrating universal tumour screening and genetic testing for colorectal and endometrial cancer into routine oncology. | O'Shea, R; Rankin, NM; Kentwell, M; Gleeson, M; Tucker, KM; Hampel, H; Taylor, N; Lewis, S |
| 2021-06-25 | Evaluation of two population screening programmes for <i>BRCA1/2</i> founder mutations in the Australian Jewish community: a protocol paper. | Cousens, NE; Tiller, J; Meiser, B; Barlow-Stewart, K; Rowley, S; Ko, Y-A; Mahale, S; Campbell, IG; Kaur, R; Bankier, A; Burnett, L; Jacobs, C; James, PA; Trainer, A; Neil, S; Delatycki, MB; Andrews, L |
| 2021-05 | Engagement and return of results preferences among a primarily African American genomic sequencing research cohort. | Lewis, KL; Turbitt, E; Chan, PA; Epps, S; Biesecker, BB; Erby, LAH; Fasaye, G-A; Biesecker, LG |
| 2021-01-15 | The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective. | Eratne, D; Schneider, A; Lynch, E; Martyn, M; Velakoulis, D; Fahey, M; Kwan, P; Leventer, R; Rafehi, H; Chong, B; Stark, Z; Lunke, S; Phelan, DG; O'Keefe, M; Siemering, K; West, K; Sexton, A; Jarmolowicz, A; Taylor, JA; Schultz, J; Purvis, R; Uebergang, E; Chalinor, H; Creighton, B; Gelfand, N; Saks, T; Prawer, Y; Smagarinsky, Y; Pan, T; Goranitis, I; Ademi, Z; Gaff, C; Huq, A; Walsh, M; James, PA; Krzesinski, EI; Wallis, M; Stutterd, CA; Bahlo, M; Delatycki, MB; Berkovic, SF |
| 2017-09 | Defining personal utility in genomics: A Delphi study. | Kohler, JN; Turbitt, E; Lewis, KL; Wilfond, BS; Jamal, L; Peay, HL; Biesecker, LG; Biesecker, BB |
| 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 |
