| Issue Date | Title | Author(s) |
| 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 |
| 2022-01-01 | Reproductive carrier screening: responding to the eugenics critique. | Dive, L; Newson, AJ |
| 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 |
| 2021-07 | One size does not fit all: The case for targeted education in genetics and genomics for cancer nurses. | Jacobs, C; Rahman, B |
| 2021-10 | Mendelian randomisation study of smoking exposure in relation to breast cancer risk. | Park, HA; Neumeyer, S; Michailidou, K; Bolla, MK; Wang, Q; Dennis, J; Ahearn, TU; Andrulis, IL; Anton-Culver, H; Antonenkova, NN; Arndt, V; Aronson, KJ; Augustinsson, A; Baten, A; Beane Freeman, LE; Becher, H; Beckmann, MW; Behrens, S; Benitez, J; Bermisheva, M; Bogdanova, NV; Bojesen, SE; Brauch, H; Brenner, H; Brucker, SY; Burwinkel, B; Campa, D; Canzian, F; Castelao, JE; Chanock, SJ; Chenevix-Trench, G; Clarke, CL; NBCS Collaborators,; Conroy, DM; Couch, FJ; Cox, A; Cross, SS; Czene, K; Daly, MB; Devilee, P; Dörk, T; Dos-Santos-Silva, I; Dwek, M; Eccles, DM; Eliassen, AH; Engel, C; Eriksson, M; Evans, DG; Fasching, PA; Flyger, H; Fritschi, L; García-Closas, M; García-Sáenz, JA; Gaudet, MM; Giles, GG; Glendon, G; Goldberg, MS; Goldgar, DE; González-Neira, A; Grip, M; Guénel, P; Hahnen, E; Haiman, CA; Håkansson, N; Hall, P; Hamann, U; Han, S; Harkness, EF; Hart, SN; He, W; Heemskerk-Gerritsen, BAM; Hopper, JL; Hunter, DJ; ABCTB Investigators,; kConFab Investigators,; Jager, A; Jakubowska, A; John, EM; Jung, A; Kaaks, R; Kapoor, PM; Keeman, R; Khusnutdinova, E; Kitahara, CM; Koppert, LB; Koutros, S; Kristensen, VN; Kurian, AW; Lacey, J; Lambrechts, D; Le Marchand, L; Lo, W-Y; Lubiński, J; Mannermaa, A; Manoochehri, M; Margolin, S; Martinez, ME; Mavroudis, D; Meindl, A; Menon, U; Milne, RL; Muranen, TA; Nevanlinna, H; Newman, WG; Nordestgaard, BG; Offit, K; Olshan, AF; Olsson, H; Park-Simon, T-W; Peterlongo, P; Peto, J; Plaseska-Karanfilska, D; Presneau, N; Radice, P; Rennert, G; Rennert, HS; Romero, A; Saloustros, E; Sawyer, EJ; Schmidt, MK; Schmutzler, RK; Schoemaker, MJ; Schwentner, L; Scott, C; Shah, M; Shu, X-O; Simard, J; Smeets, A; Southey, MC; Spinelli, JJ; Stevens, V; Swerdlow, AJ; Tamimi, RM; Tapper, WJ; Taylor, JA; Terry, MB; Tomlinson, I; Troester, MA; Truong, T; Vachon, CM; van Veen, EM; Vijai, J; Wang, S; Wendt, C; Winqvist, R; Wolk, A; Ziogas, A; Dunning, AM; Pharoah, PDP; Easton, DF; Zheng, W; Kraft, P; Chang-Claude, J |
| 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 |
| 2021-11 | A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study. | Bancroft, EK; Page, EC; Brook, MN; Thomas, S; Taylor, N; Pope, J; McHugh, J; Jones, A-B; Karlsson, Q; Merson, S; Ong, KR; Hoffman, J; Huber, C; Maehle, L; Grindedal, EM; Stormorken, A; Evans, DG; Rothwell, J; Lalloo, F; Brady, AF; Bartlett, M; Snape, K; Hanson, H; James, P; McKinley, J; Mascarenhas, L; Syngal, S; Ukaegbu, C; Side, L; Thomas, T; Barwell, J; Teixeira, MR; Izatt, L; Suri, M; Macrae, FA; Poplawski, N; Chen-Shtoyerman, R; Ahmed, M; Musgrave, H; Nicolai, N; Greenhalgh, L; Brewer, C; Pachter, N; Spigelman, AD; Azzabi, A; Helfand, BT; Halliday, D; Buys, S; Ramon Y Cajal, T; Donaldson, A; Cooney, KA; Harris, M; McGrath, J; Davidson, R; Taylor, A; Cooke, P; Myhill, K; Hogben, M; Aaronson, NK; Ardern-Jones, A; Bangma, CH; Castro, E; Dearnaley, D; Dias, A; Dudderidge, T; Eccles, DM; Green, K; Eyfjord, J; Falconer, A; Foster, CS; Gronberg, H; Hamdy, FC; Johannsson, O; Khoo, V; Lilja, H; Lindeman, GJ; Lubinski, J; Axcrona, K; Mikropoulos, C; Mitra, AV; Moynihan, C; Ni Raghallaigh, H; Rennert, G; Collier, R; IMPACT Study Collaborators,; Offman, J; Kote-Jarai, Z; Eeles, RA |
| 2016-01-29 | Antenatal screening for aneuploidy--surveying the current situation and planning for non-invasive prenatal diagnosis in New Zealand. | Eastwood, A; Webster, D; Taylor, J; Mckay, R; McEwen, A; Sullivan, J; Pope-Couston, R; Stone, P |
| 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 |
