| Early childhood education participation: A mixed-methods study of parent and provider perceived barriers and facilitators R Beatson, C Molloy, Z Fehlberg, N Perini, C Harrop, S Goldfeld Journal of Child and Family Studies 31 (11), 2929-2946, 2022 | 20 | 2022 |
| Needs of people with rare diseases that can be supported by electronic resources: a scoping review JC Long, S Best, BNG Easpaig, S Hatem, Z Fehlberg, J Christodoulou, ... BMJ open 12 (9), e060394, 2022 | 12 | 2022 |
| The more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening S Best, JC Long, Z Fehlberg, T Theodorou, S Hatem, A Archibald, ... European Journal of Human Genetics 31 (4), 430-444, 2023 | 10 | 2023 |
| Mobile apps for people with rare diseases: Review and quality assessment using mobile app rating scale S Hatem, JC Long, S Best, Z Fehlberg, B Nic Giolla Easpaig, J Braithwaite Journal of Medical Internet Research 24 (7), e36691, 2022 | 8 | 2022 |
| Correspondence on “Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics … S Righetti, L Dive, AD Archibald, L Freeman, B McClaren, ... Genetics in Medicine 24 (5), 1158-1161, 2022 | 8 | 2022 |
| Determining the utility of diagnostic genomics: a conceptual framework A Mallett, Z Stark, Z Fehlberg, S Best, I Goranitis Human Genomics 17 (1), 75, 2023 | 6 | 2023 |
| Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study Z Fehlberg, Z Stark, S Best European Journal of Human Genetics 32 (5), 521-528, 2024 | 2 | 2024 |
| Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services S Best, Z Fehlberg, C Richards, MCJ Quinn, S Lunke, AB Spurdle, ... European Journal of Human Genetics, 1-8, 2024 | 1 | 2024 |
| Scaling-up and future sustainability of a national reproductive genetic carrier screening program Z Fehlberg, S Best, JC Long, T Theodorou, C Pope, P Hibbert, S Williams, ... npj Genomic Medicine 8 (1), 18, 2023 | 1 | 2023 |
| Determining priority indicators of utility for genomic testing in rare disease: A Delphi study Z Fehlberg, I Goranitis, AJ Mallett, Z Stark, S Best Genetics in Medicine 26 (6), 101116, 2024 | | 2024 |
| Using a theory informed approach to design, execute, and evaluate implementation strategies to support offering reproductive genetic carrier screening in Australia S Best, JC Long, Z Fehlberg, N Taylor, LA Ellis, K Boggs, J Braithwaite BMC Health Services Research 23 (1), 1276, 2023 | | 2023 |
| Supporting healthcare professionals to offer reproductive genetic carrier screening: a behaviour change theory approach S Best, JC Long, Z Fehlberg, AD Archibald, J Braithwaite Australian Journal of Primary Health 29 (5), 480-489, 2023 | | 2023 |
| Implementing a national reproductive genetic carrier screening programme for high quality care: Mackenzie’s Mission, Australia S Best, JC Long, Z Fehlberg, J Braithwaite ISQua 38th International Conference 2022, 2022 | | 2022 |
| Parenting programs: A study of barriers, facilitators, & strategies to improve participation C MOLLOY, C Macmillan, R McNeil, Z Fehlberg, R Beatson, C Harrop, ... Melbourne: Murdoch Children's Research Institute, 2021 | | 2021 |
