The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments

per Goranitis, Ilias, Best, Stephanie, Christodoulou, John, Stark, Zornitza, Boughtwood, Tiffany
Publicat a Genet Med (2020)

Investigating the Adoption of Clinical Genomics in Australia. An Implementation Science Case Study

per Best, Stephanie, Long, Janet C., Gaff, Clara, Braithwaite, Jeffrey, Taylor, Natalie
Publicat a Genes (Basel) (2021)

Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy

per Crellin, Erin, McClaren, Belinda, Nisselle, Amy, Best, Stephanie, Gaff, Clara, Metcalfe, Sylvia
Publicat a Front Genet (2019)

Decreased Amygdalar Activation to NSSI-Stimuli in People Who Engage in NSSI: A Neuroimaging Pilot Study

per Hooley, Jill M., Dahlgren, Mary Kathryn, Best, Stephanie G., Gonenc, Atilla, Gruber, Staci A.
Publicat a Front Psychiatry (2020)

A transformative translational change programme to introduce genomics into healthcare: a complexity and implementation science study protocol

per Taylor, Natalie, Best, Stephanie, Martyn, Melissa, Long, Janet C, North, Kathryn N, Braithwaite, Jeffrey, Gaff, Clara
Publicat a BMJ Open (2019)

Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review

per Best, Stephanie, Long, Janet, Theodorou, Tahlia, Hatem, Sarah, Lake, Rebecca, Archibald, Alison, Freeman, Lucinda, Braithwaite, Jeffrey
Publicat a Prenat Diagn (2021)

The leadership behaviors needed to implement clinical genomics at scale: a qualitative study

per Best, Stephanie, Stark, Zornitza, Brown, Helen, Long, Janet C., Hewage, Kushani, Gaff, Clara, Braithwaite, Jeffrey, Taylor, Natalie
Publicat a Genet Med (2020)

The long and winding road: perspectives of people and parents of children with mitochondrial conditions negotiating management after diagnosis

per Long, Janet C., Best, Stephanie, Hatem, Sarah, Theodorou, Tahlia, Catton, Toni, Murray, Sean, Braithwaite, Jeffrey, Christodoulou, John
Publicat a Orphanet J Rare Dis (2021)

Building a learning community of Australian clinical genomics: a social network study of the Australian Genomic Health Alliance

per Long, Janet C., Pomare, Chiara, Best, Stephanie, Boughtwood, Tiffany, North, Kathryn, Ellis, Louise A., Churruca, Kate, Braithwaite, Jeffrey
Publicat a BMC Med (2019)

Clinical genomic testing: what matters to key stakeholders?

per Best, Stephanie, Stark, Zornitza, Phillips, Peta, Wu, You, Long, Janet C., Taylor, Natalie, Braithwaite, Jeffrey, Christodoulou, John, Goranitis, Ilias
Publicat a Eur J Hum Genet (2020)

A dynamic systems view of clinical genomics: a rich picture of the landscape in Australia using a complexity science lens

per Long, Janet C., Gul, Hossai, McPherson, Elise, Best, Stephanie, Augustsson, Hanna, Churruca, Kate, Ellis, Louise A., Braithwaite, Jeffrey
Publicat a BMC Med Genomics (2021)

Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics

per Jayasinghe, Kushani, Quinlan, Catherine, Mallett, Andrew J., Kerr, Peter G., McClaren, Belinda, Nisselle, Amy, Mallawaarachchi, Amali, Polkinghorne, Kevan R., Patel, Chirag, Best, Stephanie, Stark, Zornitza
Publicat a Kidney Int Rep (2020)

Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level

per Best, Stephanie, Brown, Helen, Lunke, Sebastian, Patel, Chirag, Pinner, Jason, Barnett, Christopher P., Wilson, Meredith, Sandaradura, Sarah A., McClaren, Belinda, Brett, Gemma R., Braithwaite, Jeffrey, Stark, Zornitza
Publicat a NPJ Genom Med (2021)

Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care

per Stark, Zornitza, Nisselle, Amy, McClaren, Belinda, Lynch, Fiona, Best, Stephanie, Long, Janet C., Martyn, Melissa, Patel, Chirag, Schlapbach, Luregn J., Barnett, Christopher, Theda, Christiane, Pinner, Jason, Dinger, Marcel E., Lunke, Sebastian, Gaff, Clara L.
Publicat a Eur J Hum Genet (2019)

Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol

per Jayasinghe, Kushani, Stark, Zornitza, Patel, Chirag, Mallawaarachchi, Amali, McCarthy, Hugh, Faull, Randall, Chakera, Aron, Sundaram, Madhivanan, Jose, Matthew, Kerr, Peter, Wu, You, Wardrop, Louise, Goranitis, Ilias, Best, Stephanie, Martyn, Melissa, Quinlan, Catherine, Mallett, Andrew J
Publicat a BMJ Open (2019)

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System

per Lunke, Sebastian, Eggers, Stefanie, Wilson, Meredith, Patel, Chirag, Barnett, Christopher P., Pinner, Jason, Sandaradura, Sarah A., Buckley, Michael F., Krzesinski, Emma I., de Silva, Michelle G., Brett, Gemma R., Boggs, Kirsten, Mowat, David, Kirk, Edwin P., Adès, Lesley C., Akesson, Lauren S., Amor, David J., Ayres, Samantha, Baxendale, Anne, Borrie, Sarah, Bray, Alessandra, Brown, Natasha J., Chan, Cheng Yee, Chong, Belinda, Cliffe, Corrina, Delatycki, Martin B., Edwards, Matthew, Elakis, George, Fahey, Michael C., Fennell, Andrew, Fowles, Lindsay, Gallacher, Lyndon, Higgins, Megan, Howell, Katherine B., Hunt, Lauren, Hunter, Matthew F., Jones, Kristi J., King, Sarah, Kumble, Smitha, Lang, Sarah, Le Moing, Maelle, Ma, Alan, Phelan, Dean, Quinn, Michael C. J., Richards, Anna, Richmond, Christopher M., Riseley, Jessica, Rodgers, Jonathan, Sachdev, Rani, Sadedin, Simon, Schlapbach, Luregn J., Smith, Janine, Springer, Amanda, Tan, Natalie B., Tan, Tiong Y., Temple, Suzanna L., Theda, Christiane, Vasudevan, Anand, White, Susan M., Yeung, Alison, Zhu, Ying, Martyn, Melissa, Best, Stephanie, Roscioli, Tony, Christodoulou, John, Stark, Zornitza
Publicat a JAMA (2020)