| Experiences of prenatal diagnosis and decision‐making about termination of pregnancy: a qualitative study J Hodgson, P Pitt, S Metcalfe, J Halliday, M Menezes, J Fisher, ... Australian and New Zealand Journal of Obstetrics and Gynaecology 56 (6), 605-613, 2016 | 75 | 2016 |
| A mixed methods exploration of families¢ experiences of the diagnosis of childhood spinal muscular atrophy S Lawton, C Hickerton, AD Archibald, BJ McClaren, SA Metcalfe European Journal of Human Genetics 23 (5), 575-580, 2015 | 46 | 2015 |
| “Did you find that out in time?”: New life trajectories of parents who choose to continue a pregnancy where a genetic disorder is diagnosed or likely CL Hickerton, MA Aitken, J Hodgson, MB Delatycki American Journal of Medical Genetics Part A 158 (2), 373-383, 2012 | 46 | 2012 |
| “It's about having the choice”: Stakeholder perceptions of population‐based genetic carrier screening for fragile X syndrome AD Archibald, CL Hickerton, AM Jaques, S Wake, J Cohen, SA Metcalfe American Journal of Medical Genetics Part A 161 (1), 48-58, 2013 | 32 | 2013 |
| Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes EK Baker, DE Godler, M Bui, C Hickerton, C Rogers, M Field, DJ Amor, ... Journal of neurodevelopmental disorders 10, 1-8, 2018 | 31 | 2018 |
| Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening SA Metcalfe, M Martyn, A Ames, V Anderson, AD Archibald, R Carter, ... Genetics in Medicine 19 (12), 1346-1355, 2017 | 25 | 2017 |
| “It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare AD Archibald, CL Hickerton, SA Wake, AM Jaques, J Cohen, SA Metcalfe Journal of community genetics 7, 159-171, 2016 | 25 | 2016 |
| Australians¢ perspectives on support around use of personal genomic testing: findings from the Genioz study SA Metcalfe, C Hickerton, J Savard, E Stackpoole, R Tytherleigh, E Tutty, ... European Journal of Medical Genetics 62 (5), 290-299, 2019 | 22 | 2019 |
| Australians¢ views on personal genomic testing: focus group findings from the Genioz study SA Metcalfe, C Hickerton, J Savard, B Terrill, E Turbitt, C Gaff, K Gray, ... European Journal of Human Genetics 26 (8), 1101-1112, 2018 | 19 | 2018 |
| Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X M Arpone, EK Baker, L Bretherton, M Bui, X Li, S Whitaker, ... Scientific Reports 8 (1), 3644, 2018 | 18 | 2018 |
| From expectations to experiences: consumer autonomy and choice in personal genomic testing J Savard, C Hickerton, SA Metcalfe, C Gaff, A Middleton, AJ Newson AJOB empirical bioethics 11 (1), 63-76, 2020 | 16 | 2020 |
| Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile … M Field, T Dudding-Byth, M Arpone, EK Baker, SM Aliaga, C Rogers, ... International Journal of Molecular Sciences 20 (16), 3907, 2019 | 14 | 2019 |
| Australians¢ views and experience of personal genomic testing: survey findings from the Genioz study J Savard, C Hickerton, R Tytherleigh, B Terrill, E Turbitt, AJ Newson, ... European Journal of Human Genetics 27 (5), 711-720, 2019 | 14 | 2019 |
| ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible MB Delatycki, M Wolthuizen, V Collins, E Varley, J Craven, KJ Allen, ... European journal of human genetics 20 (5), 505-509, 2012 | 12 | 2012 |
| General practitioners' views on genomics, practice and education: a qualitative interview study MB Cusack, C Hickerton, A Nisselle, B McClaren, B Terrill, C Gaff, ... Australian Journal of General Practice 50 (10), 747-752, 2021 | 8 | 2021 |
| Personal genomic testing for nutrition and wellness in Australia: a content analysis of online information E Tutty, C Hickerton, MM Adamski, SA Metcalfe Nutrition & dietetics 76 (3), 263-270, 2019 | 7 | 2019 |
| The expectations and realities of nutrigenomic testing in australia: A qualitative study E Tutty, C Hickerton, B Terrill, B McClaren, R Tytherleigh, E Stackpoole, ... Health Expectations 24 (2), 670-686, 2021 | 3 | 2021 |
| To tell or not to tell – what to do about p.C282Y heterozygotes identified by HFE screening MB Delatycki, M Wolthuizen, MA Aitken, C Hickerton, SA Metcalfe, ... Clinical Genetics 84 (3), 286-289, 2013 | 2 | 2013 |
| 12 ¡Recreational¢consumer genomics: no such thing as a non-medical test B Wilson, J Savard, C Hickerton, B Terrill, A Newson, C Gaff, K Gray, ... BMJ Evidence-Based Medicine 24 (Suppl 2), A58-A58, 2019 | | 2019 |
| " I just wanted answers": Exploring personal genomic testing for nutrition and wellness E Tutty, C Hickerton, M Adamski, J Savard, B Terrill, A Newson, C Gaff, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 742-743, 2019 | | 2019 |
