| Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research L Ioannou, BJ McClaren, J Massie, S Lewis, SA Metcalfe, L Forrest, ... Genetics in Medicine 16 (3), 207-216, 2014 | 85 | 2014 |
| 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 | 76 | 2016 |
| Parental experiences after prenatal diagnosis of fetal abnormality J Hodgson, BJ McClaren Seminars in Fetal and Neonatal Medicine 23 (2), 150-154, 2018 | 70 | 2018 |
| ĦIt is not in my world˘: an exploration of attitudes and influences associated with cystic fibrosis carrier screening BJ McClaren, MB Delatycki, V Collins, SA Metcalfe, MA Aitken European Journal of Human Genetics 16 (4), 435-444, 2008 | 62 | 2008 |
| Preparing medical specialists for genomic medicine: continuing education should include opportunities for experiential learning BJ McClaren, E Crellin, M Janinski, AE Nisselle, L Ng, SA Metcalfe, ... Frontiers in genetics 11, 151, 2020 | 59 | 2020 |
| Preparing medical specialists to practice genomic medicine: education an essential part of a broader strategy E Crellin, B McClaren, A Nisselle, S Best, C Gaff, S Metcalfe Frontiers in Genetics 10, 468050, 2019 | 58 | 2019 |
| A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy SH Wong, BJ McClaren, AD Archibald, A Weeks, T Langmaid, MM Ryan, ... European journal of human genetics 23 (10), 1294-1300, 2015 | 54 | 2015 |
| ĦA short time but a lovely little short time˘: Bereaved parents' experiences of having a child with spinal muscular atrophy type 1 EJ Higgs, BJ McClaren, MAR Sahhar, MM Ryan, R Forbes Journal of paediatrics and child health 52 (1), 40-46, 2016 | 46 | 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 |
| Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening BJ McClaren, SA Metcalfe, MA Aitken, RJ Massie, OC Ukoumunne, ... European Journal of Human Genetics 18 (10), 1084-1089, 2010 | 40 | 2010 |
| Population-based genetic screening for cystic fibrosis: attitudes and outcomes L Ioannou, J Massie, V Collins, B McClaren, MB Delatycki Public Health Genomics 13 (7-8), 449-456, 2010 | 38 | 2010 |
| Attitudes and practices of Australian nephrologists toward implementation of clinical genomics K Jayasinghe, C Quinlan, AJ Mallett, PG Kerr, B McClaren, A Nisselle, ... Kidney international reports 6 (2), 272-283, 2021 | 33 | 2021 |
| Readiness of clinical genetic healthcare professionals to provide genomic medicine: an Australian census A Nisselle, I Macciocca, F McKenzie, H Vuong, K Dunlop, B McClaren, ... Journal of Genetic Counseling 28 (2), 367-377, 2019 | 33 | 2019 |
| Measuring physician practice, preparedness and preferences for genomic medicine: a national survey A Nisselle, EA King, B McClaren, M Janinski, S Metcalfe, C Gaff BMJ open 11 (7), e044408, 2021 | 32 | 2021 |
| Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care Z Stark, A Nisselle, B McClaren, F Lynch, S Best, JC Long, M Martyn, ... European Journal of Human Genetics 27 (10), 1493-1501, 2019 | 32 | 2019 |
| Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination P Pitt, BJ McClaren, J Hodgson Reproductive health matters 24 (47), 168-177, 2016 | 32 | 2016 |
| Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention JM Hodgson, SA Metcalfe, MA Aitken, SM Donath, CL Gaff, IM Winship, ... BMC Medical Genetics 15, 1-6, 2014 | 32 | 2014 |
| Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing BJ McClaren, MA Aitken, J Massie, D Amor, OC Ukoumunne, SA Metcalfe Genetics in medicine 15 (7), 533-540, 2013 | 28 | 2013 |
| Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics) A Nisselle, M Janinski, M Martyn, B McClaren, N Kaunein, J Maguire, ... Genetics in medicine 23 (7), 1356-1365, 2021 | 27 | 2021 |
| Development of an evidence-based, theory-informed national survey of physician preparedness for genomic medicine and preferences for genomics continuing education BJ McClaren, EA King, E Crellin, C Gaff, SA Metcalfe, A Nisselle Frontiers in genetics 11, 488188, 2020 | 26 | 2020 |
