| Issue Date | Title | Author(s) |
| 2022-07-29 | Clinical impact of whole-genome sequencing in patients with early-onset dementia. | Huq, AJ; Thompson, B; Bennett, MF; Bournazos, A; Bommireddipalli, S; Gorelik, A; Schultz, J; Sexton, A; Purvis, R; West, K; Cotter, M; Valente, G; Hughes, A; Riaz, M; Walsh, M; Farrand, S; Loi, SM; Kilpatrick, T; Brodtmann, A; Darby, D; Eratne, D; Walterfang, M; Delatycki, MB; Storey, E; Fahey, M; Cooper, S; Lacaze, P; Masters, CL; Velakoulis, D; Bahlo, M; James, PA; Winship, I |
| 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, |
| 2019-11-01 | Predicting Biopsy Outcomes During Active Surveillance for Prostate Cancer: External Validation of the Canary Prostate Active Surveillance Study Risk Calculators in Five Large Active Surveillance Cohorts | Drost, FJH; Nieboer, D; Morgan, TM; Carroll, PR; Roobol, MJ; Trock, B; Ehdaie, B; Carroll, P; Filson, C; Kim, J; Logothetis, C; Morgan, T; Klotz, L; Pickles, T; Hyndman, E; Moore, CM; Gnanapragasam, V; Van Hemelrijck, M; Dasgupta, P; Bangma, C; Roobol, M; Villers, A; Rannikko, A; Valdagni, R; Perry, A; Hugosson, J; Rubio-Briones, J; Bjartell, A; Hefermehl, L; Shiong, LL; Frydenberg, M; Kakehi, Y; Chung, BH; van der Kwast, T; van der Linden, W; Hulsen, T; de Jonge, C; Kattan, M; Xinge, J; Muir, K; Lophatananon, A; Fahey, M; Steyerberg, E; Zhang, L; Beckmann, K; Denton, B; Hayen, A; Boutros, P; Guo, W; Benfante, N; Cowan, J; Patil, D; Tolosa, E; Kim, TK; Mamedov, A; Lapointe, V; Crump, T; Kimberly-Duffell, J; Santaolalla, A; Olivier, J; Rancati, T; Ahlgren, H; Mascarós, J; Löfgren, A; Lin, CH; Hirama, H; Lee, KS; Jenster, G; Auvinen, A; Haider, M; van Bochove, K; Carter, B; Gledhill, S; Buzza, M; Bruinsma, S; Helleman, J |
| 2021-11 | Suicide in frontotemporal dementia and Huntington disease: analysis of family-reported pedigree data and implications for genetic healthcare for asymptomatic relatives. | Sexton, A; West, K; Gill, G; Wiseman, A; Taylor, J; Purvis, R; Fahey, M; Storey, E; Walsh, M; James, P |
| 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 |
