| Identification of six new susceptibility loci for invasive epithelial ovarian cancer KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ... Nature genetics 47 (2), 164-171, 2015 | 307 | 2015 |
| BRAFV600E immunohistochemistry facilitates universal screening of colorectal cancers for Lynch syndrome CW Toon, MJ Walsh, A Chou, D Capper, A Clarkson, L Sioson, S Clarke, ... The American journal of surgical pathology 37 (10), 1592, 2013 | 147 | 2013 |
| Fumarate hydratase–deficient uterine leiomyomas occur in both the syndromic and sporadic settings WJ Harrison, J Andrici, F Maclean, R Madadi-Ghahan, M Farzin, L Sioson, ... The American journal of surgical pathology 40 (5), 599, 2016 | 133 | 2016 |
| Bayesian approach to determining penetrance of pathogenic SDH variants DE Benn, Y Zhu, KA Andrews, M Wilding, EL Duncan, T Dwight, ... Journal of medical genetics 55 (11), 729-734, 2018 | 56 | 2018 |
| Breast cancer polygenic risk score and contralateral breast cancer risk I Kramer, MJ Hooning, N Mavaddat, M Hauptmann, R Keeman, ... The American Journal of Human Genetics 107 (5), 837-848, 2020 | 51 | 2020 |
| Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy F Najdawi, A Crook, J Maidens, C McEvoy, A Fellowes, J Pickett, M Ho, ... Pathology 49 (5), 457-464, 2017 | 39 | 2017 |
| Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations A Crook, K Williams, L Adams, I Blair, DB Rowe Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18 (7-8), 475-485, 2017 | 33 | 2017 |
| The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling A Crook, A McEwen, JA Fifita, K Zhang, JB Kwok, G Halliday, IP Blair, ... Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20 (5-6), 310-316, 2019 | 20 | 2019 |
| Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review A Crook, C Jacobs, T Newton-John, R O’Shea, A McEwen Journal of Neurology, 1-17, 2022 | 18 | 2022 |
| Health system interventions to integrate genetic testing in routine oncology services: A systematic review R O’Shea, N Taylor, A Crook, C Jacobs, Y Jung Kang, S Lewis, ... PloS one 16 (5), e0250379, 2021 | 16 | 2021 |
| Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS) A Crook, L Plunkett, LE Forrest, N Hallowell, S Wake, K Alsop, M Gleeson, ... European Journal of Human Genetics 23 (2), 152-158, 2015 | 16 | 2015 |
| Surveillance Improves Outcomes for Carriers of SDHB Pathogenic Variants: A Multicenter Study DF Davidoff, DE Benn, M Field, A Crook, BG Robinson, K Tucker, ... The Journal of Clinical Endocrinology & Metabolism 107 (5), e1907-e1916, 2022 | 15 | 2022 |
| Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD: A Systematic Scoping Review A Crook, C Jacobs, T Newton-John, E Richardson, A McEwen Alzheimer Disease & Associated Disorders 35 (4), 374-385, 2021 | 12 | 2021 |
| The psychological impact and experience of breast cancer screening in young women with an increased risk of breast cancer due to neurofibromatosis type 1 A Crook, R Kwa, S Ephraums, M Wilding, L Thiyagarajan, J Fleming, ... Familial cancer 21 (2), 241-253, 2022 | 10 | 2022 |
| Systematic review of outcomes in studies of reproductive genetic carrier screening: Towards development of a core outcome set E Richardson, A McEwen, T Newton-John, A Crook, C Jacobs Genetics in Medicine, 2021 | 10 | 2021 |
| Patient-centered decision making in amyotrophic lateral sclerosis: where are we? A Hogden, A Crook Neurodegenerative disease management 7 (6), 377-386, 2017 | 7 | 2017 |
| Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences A Crook, C Jacobs, T Newton‐John, A McEwen Journal of Genetic Counseling 31 (5), 1206-1218, 2022 | 6 | 2022 |
| Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: A sequential systematic review E Richardson, A McEwen, T Newton-John, A Crook, C Jacobs European Journal of Human Genetics 30 (7), 756-765, 2022 | 6 | 2022 |
| Predictive genetic testing for Motor neuron disease: time for a guideline? A McNeill, MM Amador, H Bekker, A Clarke, A Crook, C Cummings, ... European Journal of Human Genetics 30 (6), 635-636, 2022 | 6 | 2022 |
| Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility E Tudini, AL Davidson, U Dressel, L Andrews, Y Antill, A Crook, M Field, ... Journal of medical genetics 58 (12), 853-858, 2021 | 6 | 2021 |
