Showing results 11 to 28 of 28
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| Issue Date | Title | Author(s) |
| 2021-05-19 | Health system interventions to integrate genetic testing in routine oncology services: A systematic review | O’Shea, R; Taylor, N; Crook, A; Jacobs, C; Kang, YJ; Lewis, S; Rankin, NM |
| 2021-08 | Helping young children understand inherited cancer predisposition syndromes using bibliotherapy. | Schlub, GM; Crook, A; Barlow-Stewart, K; Fleming, J; Kirk, J; Tucker, K; Greening, S |
| 2019-12-01 | Homologous recombination DNA repair defects in PALB2-associated breast cancers | Li, A; Geyer, FC; Blecua, P; Lee, JY; Selenica, P; Brown, DN; Pareja, F; Lee, SSK; Kumar, R; Rivera, B; Bi, R; Piscuoglio, S; Wen, HY; Lozada, JR; Gularte-Mérida, R; Cavallone, L; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Balleine, R; Beesley, J; Blackburn, A; Bogwitz, M; Brown, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Campbell, I; Christian, A; Clarke, C; Cohen, P; Crook, A; Cui, J; Cummings, M; Dawson, SJ; De Fazio, A; Delatycki, M; Dobrovic, A; Dudding, T; Duijf, P; Edkins, E; Edwards, S; Farshid, G; Fellows, A; Field, M; Flanagan, J; Fong, P; Forbes, J; Forrest, L; Fox, S; French, J; Friedlander, M; Ortega, DG; Gattas, M; Giles, G; Gill, G; Gleeson, M; Greening, S; Haan, E; Harris, M; Hayward, N; Hickie, I; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kentwell, M; Kirk, J; Kollias, J; Lakhani, S; Lindeman, G; Lipton, L; Lobb, L; Lok, S; Macrea, F; Mann, G; Marsh, D; McLachlan, SA; Meiser, B; Milne, R; Nightingale, S; O’Connell, S; Pachter, N; Patterson, B; Phillips, K; Saleh, M; Salisbury, E; Saunders, C; Saunus, J; Scott, C; Scott, R; Sexton, A; Shelling, A; Simpson, P; Spigelman, A; Spurdle, M; Stone, J |
| 2020-11-09 | Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. | Tudini, E; Davidson, AL; Dressel, U; Andrews, L; Antill, Y; Crook, A; Field, M; Gattas, M; Harris, R; Kirk, J; Pachter, N; Salmon, L; Susman, R; Townshend, S; Trainer, AH; Tucker, KM; Mitchell, G; James, PA; Ward, RL; Mar Fan, H; Poplawski, NK; Spurdle, AB |
| 2023-10 | Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders. | Chambers, C; Lichten, L; Crook, A; Uhlmann, WR; Dratch, L |
| 2022-07 | Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review. | Richardson, E; McEwen, A; Newton-John, T; Crook, A; Jacobs, C |
| 2017-08 | Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy. | Najdawi, F; Crook, A; Maidens, J; McEvoy, C; Fellowes, A; Pickett, J; Ho, M; Nevell, D; McIlroy, K; Sheen, A; Sioson, L; Ahadi, M; Turchini, J; Clarkson, A; Hogg, R; Valmadre, S; Gard, G; Dooley, SJ; Scott, RJ; Fox, SB; Field, M; Gill, AJ |
| 2022-08-12 | Outcomes of Importance to Patients in Reproductive Genetic Carrier Screening: A Qualitative Study to Inform a Core Outcome Set. | Richardson, E; McEwen, A; Newton-John, T; Crook, A; Jacobs, C |
| 2021-10 | Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD: A Systematic Scoping Review. | Crook, A; Jacobs, C; Newton-John, T; Richardson, E; McEwen, A |
| 2017-12 | Patient-centered decision making in amyotrophic lateral sclerosis: where are we? | Hogden, A; Crook, A |
| 2017-11 | Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations. | Crook, A; Williams, K; Adams, L; Blair, I; Rowe, DB |
| 2022-06 | Predictive genetic testing for Motor neuron disease: time for a guideline? | McNeill, A; Amador, M-D-M; Bekker, H; Clarke, A; Crook, A; Cummings, C; McEwen, A; McDermott, C; Quarrell, O; Renieri, A; Roggenbuck, J; Salmon, K; Volk, A; Weishaupt, J; International Alliance of ALS/MND Associations, |
| 2019-12-01 | Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9) | Li, A; Geyer, FC; Blecua, P; Lee, JY; Selenica, P; Brown, DN; Pareja, F; Lee, SSK; Kumar, R; Rivera, B; Bi, R; Piscuoglio, S; Wen, HY; Lozada, JR; Gularte-Mérida, R; Cavallone, L; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Balleine, R; Beesley, J; Blackburn, A; Bogwitz, M; Brown, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Campbell, I; Christian, A; Clarke, C; Cohen, P; Crook, A; Cui, J; Cummings, M; Dawson, SJ; De Fazio, A; Delatycki, M; Dobrovic, A; Dudding, T; Duijf, P; Edkins, E; Edwards, S; Farshid, G; Fellows, A; Field, M; Flanagan, J; Fong, P; Forbes, J; Forrest, L; Fox, S; French, J; Friedlander, M; Ortega, DG; Gattas, M; Giles, G; Gill, G; Gleeson, M; Greening, S; Haan, E; Harris, M; Hayward, N; Hickie, I; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kentwell, M; Kirk, J; Kollias, J; Lakhani, S; Lindeman, G; Lipton, L; Lobb, L; Lok, S; Macrea, F; Mann, G; Marsh, D; McLachlan, SA; Meiser, B; Milne, R; Nightingale, S; O’Connell, S; Pachter, N; Patterson, B; Phillips, K; Saleh, M; Salisbury, E; Saunders, C; Saunus, J; Scott, C; Scott, R; Sexton, A; Shelling, A; Simpson, P; Spigelman, A; Spurdle, M; Stone, J |
| 2022-04-19 | Surveillance Improves Outcomes for Carriers of SDHB Pathogenic Variants: A Multicenter Study. | Davidoff, DF; Benn, DE; Field, M; Crook, A; Robinson, BG; Tucker, K; De Abreu Lourenco, R; Burgess, JR; Clifton-Bligh, RJ |
| 2022-01-01 | Systematic review of outcomes in studies of reproductive genetic carrier screening: Towards development of a core outcome set. | Richardson, E; McEwen, A; Newton-John, T; Crook, A; Jacobs, C |
| 2023-09 | The complexity of multidisciplinary respiratory care in amyotrophic lateral sclerosis. | Berlowitz, DJ; Mathers, S; Hutchinson, K; Hogden, A; Carey, KA; Graco, M; Whelan, B-M; Charania, S; Steyn, F; Allcroft, P; Crook, A; Sheers, NL |
| 2021-05-08 | The psychological impact and experience of breast cancer screening in young women with an increased risk of breast cancer due to neurofibromatosis type 1. | Crook, A; Kwa, R; Ephraums, S; Wilding, M; Thiyagarajan, L; Fleming, J; Moore, K; Berman, Y |
| 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 |
