| Issue Date | Title | Author(s) |
| 2016-03-12 | Achieving behaviour change for detection of Lynch syndrome using the Theoretical Domains Framework Implementation (TDFI) approach: A study protocol | Taylor, N; Long, JC; Debono, D; Williams, R; Salisbury, E; O'Neill, S; Eykman, E; Braithwaite, J; Chin, M |
| 2020-09 | How can Australia integrate routine genetic sequencing in oncology: a qualitative study through an implementation science lens. | O'Shea, R; Rankin, NM; Kentwell, M; Gleeson, M; Salmon, L; Tucker, KM; Lewis, S; Taylor, N |
| 2022-07 | Real world outcomes and implementation pathways of exome sequencing in an adult genetic department. | Walsh, M; West, K; Taylor, JA; Thompson, BA; Hopkins, A; Sexton, A; Ragunathan, A; Verma, KP; Panetta, J; Matotek, E; Fahey, MC; Christie, M; Winship, IM; Trainer, AH; James, PA |
| 2022-11 | Toward genetic counseling practice standards for diagnostic testing in amyotrophic lateral sclerosis and frontotemporal dementia. | Crook, A; Jacobs, C; Newton-John, T; McEwen, A |
| 2021-08 | Genetic testing in dementia-A medical genetics perspective. | Huq, AJ; Sexton, A; Lacaze, P; Masters, CL; Storey, E; Velakoulis, D; James, PA; Winship, IM |
| 2016-07 | Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations. | Manchanda, R; Burnell, M; Loggenberg, K; Desai, R; Wardle, J; Sanderson, SC; Gessler, S; Side, L; Balogun, N; Kumar, A; Dorkins, H; Wallis, Y; Chapman, C; Tomlinson, I; Taylor, R; Jacobs, C; Legood, R; Raikou, M; McGuire, A; Beller, U; Menon, U; Jacobs, I |
| 2016-01-12 | Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. | Traylor, M; Zhang, CR; Adib-Samii, P; Devan, WJ; Parsons, OE; Lanfranconi, S; Gregory, S; Cloonan, L; Falcone, GJ; Radmanesh, F; Fitzpatrick, K; Kanakis, A; Barrick, TR; Moynihan, B; Lewis, CM; Boncoraglio, GB; Lemmens, R; Thijs, V; Sudlow, C; Wardlaw, J; Rothwell, PM; Meschia, JF; Worrall, BB; Levi, C; Bevan, S; Furie, KL; Dichgans, M; Rosand, J; Markus, HS; Rost, N; International Stroke Genetics Consortium, |
| 2021-06 | Motivations and barriers to pursue cancer genomic testing: A systematic review. | Smith-Uffen, M; Bartley, N; Davies, G; Best, M |
| 2017-06 | Personal utility in genomic testing: a systematic literature review. | Kohler, JN; Turbitt, E; Biesecker, BB |
| 2022-07 | Ethically robust reproductive genetic carrier screening needs to measure outcomes that matter to patients. | Dive, L; Newson, AJ |
