| Issue Date | Title | Author(s) |
| 2022-08 | Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting. | Best, MC; Butow, P; Savard, J; Jacobs, C; Bartley, N; Davies, G; Napier, CE; Ballinger, ML; Thomas, DM; Biesecker, B; Tucker, KM; Juraskova, I; Meiser, B; Schlub, T; Newson, AJ |
| 2022-06 | Psychological predictors of cancer patients' and their relatives' attitudes towards the return of genomic sequencing results. | Meiser, B; Butow, P; Davies, G; Napier, CE; Schlub, TE; Bartley, N; Juraskova, I; Ballinger, ML; Thomas, DM; Best, MC; members of the Psychosocial Issues in Genomics in Oncology (PiGeOn) Project,; Jacobs, C |
| 2022-11-07 | Genetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening. | Dive, L; Freeman, L; McEwen, A |
| 2022-04 | Genetic counselling and testing for neurodegenerative disorders using a proposed standard of practice for ALS/MND: diagnostic testing comes first. | Crook, A; McEwen, A |
| 2023-04 | Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia. | DeBortoli, E; McInerney-Leo, AM; Ayres, S; Boyle, J; Jacobs, C; Newson, AJ; Education, Ethics and Social Issues Committee of the Human Genetics Society of Australasia, |
| 2023-04 | Human Genetics Society of Australasia Position Statement: Genetic Carrier Testing for Recessive Conditions. | Vears, DF; Boyle, J; Jacobs, C; McInerney-Leo, A; Newson, AJ; Education, Ethics and Social Issues Committee of the Human Genetics Society of Australasia, |
| 2023-01 | Models of communication for polygenic scores and associated psychosocial and behavioral effects on recipients: A systematic review. | Wallingford, CK; Kovilpillai, H; Jacobs, C; Turbitt, E; Primiero, CA; Young, M-A; Brockman, DG; Soyer, HP; McInerney-Leo, AM; Yanes, T |
| 2022-09-01 | Addressing underrepresentation in genomics research through community engagement. | Lemke, AA; Esplin, ED; Goldenberg, AJ; Gonzaga-Jauregui, C; Hanchard, NA; Harris-Wai, J; Ideozu, JE; Isasi, R; Landstrom, AP; Prince, AER; Turbitt, E; Sabatello, M; Schrier Vergano, SA; Taylor, MRG; Yu, J-H; Brothers, KB; Garrison, NA |
| 2023-06 | Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready? | White, S; Mossfield, T; Fleming, J; Barlow-Stewart, K; Ghedia, S; Dickson, R; Richards, F; Bombard, Y; Wiley, V |
| 2023-07-13 | What's in a name? Justifying terminology for genomic findings beyond the initial test indication: A scoping review. | White, S; Haas, M; Laginha, K-J; Laurendet, K; Gaff, C; Vears, D; Newson, AJ |
