| Issue Date | Title | Author(s) |
| 2023-02-06 | How should severity be understood in the context of reproductive genetic carrier screening? | Dive, L; Archibald, AD; Freeman, L; Newson, AJ |
| 2022-12 | Do online decision aids reflect new prenatal screening and testing options? An environmental scan and content analysis | Lu, JYT; McKinn, S; Freeman, L; Turbitt, E; Bonner, C |
| 2022-09 | O59 Psychological benefits and harms of Non-Invasive Prenatal Screening (NIPS): Women’s perspectives | Javid, N; McKinn, S; Newson, A; Bonner, C; Nassar, N; Shand, A; Freeman, L; Bell, K |
| 2022-11-07 | Genetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening. | Dive, L; Freeman, L; McEwen, A |
| 2022-05-10 | Clinician views and experiences of non-invasive prenatal genetic screening tests in Australia. | McKinn, S; Javid, N; Newson, AJ; Freeman, L; Bonner, C; Shand, AW; Nassar, N; Bell, KJL |
| 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 |
| 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 |
| 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 |
| 2023-08-02 | Should 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 |
