| Issue Date | Title | Author(s) |
| 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 |
| 2018-11 | Bayesian approach to determining penetrance of pathogenic SDH variants. | Benn, DE; Zhu, Y; Andrews, KA; Wilding, M; Duncan, EL; Dwight, T; Tothill, RW; Burgess, J; Crook, A; Gill, AJ; Hicks, RJ; Kim, E; Luxford, C; Marfan, H; Richardson, AL; Robinson, B; Schlosberg, A; Susman, R; Tacon, L; Trainer, A; Tucker, K; Maher, ER; Field, M; Clifton-Bligh, RJ |
| 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 |
| 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 | A mainstreaming oncogenomics model: improving the identification of Lynch syndrome. | O'Shea, R; Crook, A; Jacobs, C; Kentwell, M; Gleeson, M; Tucker, KM; Hampel, H; Rahm, AK; Taylor, N; Lewis, S; Rankin, NM |
| 2023-10 | Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1. | Wilding, M; Fleming, J; Moore, K; Crook, A; Reddy, R; Choi, S; Schlub, TE; Field, M; Thiyagarajan, L; Thompson, J; Berman, Y |
| 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 |
| 2022-10 | Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences. | Crook, A; Jacobs, C; Newton-John, T; McEwen, A |
| 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 |
| 2022-07 | Correction: 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 |
