Browsing byAuthorCrook, A

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Issue DateTitleAuthor(s)
2023A 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
2018-11Bayesian 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
2019-07-03The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counselingCrook, A; McEwen, A; Fifita, JA; Zhang, K; Kwok, JB; Halliday, G; Blair, IP; Rowe, DB
2023-10Clinical 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
2019-11CMS-01 Genetic testing for familial amyotrophic lateral sclerosis (ALS): insights and challenges.Crook, A; Hogden, A; Mumford, V; Blair, IP; Williams, KL; Rowe, DB
2022-07Correction: 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
2019-12-01Development and validation of a targeted gene sequencing panel for application to disparate cancersMcCabe, MJ; Gauthier, MEA; Chan, CL; Thompson, TJ; De Sousa, SMC; Puttick, C; Grady, JP; Gayevskiy, V; Tao, J; Ying, K; Cipponi, A; Deng, N; Swarbrick, A; Thomas, ML; Lord, RV; Johns, AL; Kohonen-Corish, M; O’Toole, SA; Clark, J; Mueller, SA; Gupta, R; McCormack, AI; Dinger, ME; Cowley, MJ; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Armitage, S; Arnold, L; Balleine, R; Bastick, P; Beesley, J; Beilby, J; Bennett, I; Blackburn, A; Bogwitz, M; Botes, L; Brennan, M; Brown, M; Buckley, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Callen, D; Campbell, I; Chauhan, D; Chauhan, M; Chenevix-Trench, G; Christian, A; Clarke, C; Cohen, P; Colley, A; Crook, A; Cui, J; Culling, B; Cummings, M; Dawson, SJ; deFazio, A; Delatycki, M; Dickson, R; Dixon, J; Dobrovic, A; Dudding, T; Edkins, T; Edwards, S; Eisenbruch, M; Farshid, G; Fellows, A; Fenton, G; Field, M; Flanagan, J; Fong, P; Forrest, L; Fox, S; French, J; Friedlander, M; Gaff, C; Ortega, DG; Gattas, M; George, P; Giles, G; Gill, G; Greening, S; Haan, E; Harris, M; Hart, S; Hayward, N; Heiniger, L; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kidd, A; Kirk, J; Koehler, J; Kollias, J; Lakhani, S
2022-10Genetic 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
2021-03-01Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic reviewCrook, A; Jacobs, C; Newton-John, T; O’Shea, R; McEwen, A
2022-04Genetic counselling and testing for neurodegenerative disorders using a proposed standard of practice for ALS/MND: diagnostic testing comes first.Crook, A; McEwen, A
2021-05-19Health system interventions to integrate genetic testing in routine oncology services: A systematic reviewO’Shea, R; Taylor, N; Crook, A; Jacobs, C; Kang, YJ; Lewis, S; Rankin, NM
2021-08Helping young children understand inherited cancer predisposition syndromes using bibliotherapy.Schlub, GM; Crook, A; Barlow-Stewart, K; Fleming, J; Kirk, J; Tucker, K; Greening, S
2019-12-01Homologous recombination DNA repair defects in PALB2-associated breast cancersLi, 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
2020-11-09Implementing 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
2023-10Incorporating 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
2022-07Incorporating 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
2017-08Lessons 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
2022-08-12Outcomes 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
2021-10Patient 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
2017-12Patient-centered decision making in amyotrophic lateral sclerosis: where are we?Hogden, A; Crook, A