| Issue Date | Title | Author(s) |
| 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 |
| 2022-10 | Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences. | Crook, A; Jacobs, C; Newton-John, T; McEwen, A |
| 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 |
| 2021-01-15 | 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 |
| 2020-09 | What do we do and how do we do it? Assessing genetic counselling in the modern era. | Yeates, L; McEwen, A; Ingles, J |
| 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 |
| 2022-06 | Predictive genetic testing for Motor neuron disease: time for a guideline? | McNeill, A; Amador, M-D-M; Bekker, H; Clarke, A; Crook, A; Cummings, C; McEwen, A; McDermott, C; Quarrell, O; Renieri, A; Roggenbuck, J; Salmon, K; Volk, A; Weishaupt, J; International Alliance of ALS/MND Associations, |
| 2022-09 | The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review. | Freeman, L; Righetti, S; Delatycki, MB; Scully, JL; Kirk, EP |
| 2023-07 | Is It Just for a Screening Program to Give People All the Information They Want? | Dive, L; Holmes, I; Newson, AJ |
| 2023-03 | Consistency of What? Appropriately Contextualizing Ethical Analysis of Non-Invasive Prenatal Testing. | Newson, AJ; Deans, Z; Dive, L; Holmes, IC |
