| Issue Date | Title | Author(s) |
| 2017-05 | Diagnostic and cost utility of whole exome sequencing in peripheral neuropathy. | Walsh, M; Bell, KM; Chong, B; Creed, E; Brett, GR; Pope, K; Thorne, NP; Sadedin, S; Georgeson, P; Phelan, DG; Day, T; Taylor, JA; Sexton, A; Lockhart, PJ; Kiers, L; Fahey, M; Macciocca, I; Gaff, CL; Oshlack, A; Yiu, EM; James, PA; Stark, Z; Ryan, MM; Melbourne Genomics Health Alliance, |
| 2024-08-17 | Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023. | Mallawaarachchi, A; Biros, E; Harris, T; Bennetts, B; Boughtwood, T; Elliott, J; Fowles, L; Gardos, R; Garza, D; Goranitis, I; Haas, M; Huntley, V; Jefferis, J; Kassahn, K; Leaver, A; Lundie, B; Lunke, S; O'Connor, C; Pratt, G; Quinlan, C; Shearman, D; Soraru, J; Sundaram, M; Tchan, M; Valente, G; White, J; Wilkins, E; Alexander, SI; Amir, N; Best, S; Gul, H; Jayasinghe, K; McCarthy, H; Patel, C; Stark, Z; Mallett, AJ |
| 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 |
