Stephanie Best

Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 47

Top Topics

Systematic Review

Decision Making

Cognitive Decline

Top Venues

European journal of human genetics : EJHG

NPJ genomic medicine

Journal of medical Internet research

Journal of community genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Angela Pearce, Lucas A Mitchell, Stephanie Best, Mary-Anne Young, Bronwyn Terrill
Publics' knowledge of, attitude to and motivation towards health-related genomics: a scoping review. European journal of human genetics : EJHG (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Zoe Fehlberg, Zornitza Stark, Stephanie Best
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study. European journal of human genetics : EJHG (2024)
Zoe Fehlberg, Zornitza Stark, Stephanie Best
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study. European journal of human genetics : EJHG 32 (5) (2024)
Zoe Fehlberg, Zornitza Stark, Stephanie Best
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study. European journal of human genetics : EJHG 32 (5) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG (2024)
Julia Lai-Kwon, Michael Jefford, Stephanie Best, Iris Zhang, Claudia Rutherford
Selecting Immune Checkpoint Inhibitor Side Effects for Real-Time Monitoring in Routine Cancer Care: A Modified Delphi Study. JCO oncology practice (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Angela Pearce, Lucas A Mitchell, Stephanie Best, Mary-Anne Young, Bronwyn Terrill
Publics' knowledge of, attitude to and motivation towards health-related genomics: a scoping review. European journal of human genetics : EJHG 32 (7) (2024)
Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie E Bouffler, Yvonne Bombard, Clara L Gaff, Zornitza Stark
Eliciting parental preferences and values for the return of additional findings from genomic sequencing. NPJ genomic medicine 9 (1) (2024)
Stephanie Best, Zoe Fehlberg, Christopher Richards, Michael C J Quinn, Sebastian Lunke, Amanda B Spurdle, Karin S Kassahn, Chirag Patel, Danya F Vears, Ilias Goranitis, Fiona Lynch, Alan Robertson, Emma Tudini, John Chrisodoulou, Hamish S Scott, Julie McGaughran, Zornitza Stark
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services. European journal of human genetics : EJHG (2024)
Stephanie Best, Sanne Peters, Lisa Guccione, Jillian Francis, Marlena Klaic
Developing a shared language: a proposed guide to frame early implementation science collaboration discussions. Translational behavioral medicine (2024)
Angela Pearce, Lucas A Mitchell, Stephanie Best, Mary-Anne Young, Bronwyn Terrill
Publics' knowledge of, attitude to and motivation towards health-related genomics: a scoping review. European journal of human genetics : EJHG 32 (7) (2024)
Angela Pearce, Lucas A Mitchell, Stephanie Best, Mary-Anne Young, Bronwyn Terrill
Publics' knowledge of, attitude to and motivation towards health-related genomics: a scoping review. European journal of human genetics : EJHG 32 (7) (2024)
Zoe Fehlberg, Zornitza Stark, Stephanie Best
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study. European journal of human genetics : EJHG 32 (5) (2024)
Angela Pearce, Lucas A Mitchell, Stephanie Best, Mary-Anne Young, Bronwyn Terrill
Publics' knowledge of, attitude to and motivation towards health-related genomics: a scoping review. European journal of human genetics : EJHG (2024)
Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie E Bouffler, Yvonne Bombard, Clara L Gaff, Zornitza Stark
Eliciting parental preferences and values for the return of additional findings from genomic sequencing. NPJ genomic medicine 9 (1) (2024)
Erin Tutty, Alison D Archibald, Lilian Downie, Clara L Gaff, Sebastian Lunke, Danya F Vears, Zornitza Stark, Stephanie Best
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework. European journal of human genetics : EJHG (2024)
Zoe Fehlberg, Zornitza Stark, Stephanie Best
Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study. European journal of human genetics : EJHG 32 (5) (2024)
Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie E Bouffler, Yvonne Bombard, Clara L Gaff, Zornitza Stark
Eliciting parental preferences and values for the return of additional findings from genomic sequencing. NPJ genomic medicine 9 (1) (2024)
Zoe Fehlberg, Stephanie Best, Janet C Long, Tahlia Theodorou, Catherine Pope, Peter Hibbert, Sharon Williams, Lucinda Freeman, Sarah Righetti, Alison D Archibald, Jeffrey Braithwaite
Scaling-up and future sustainability of a national reproductive genetic carrier screening program. NPJ genomic medicine 8 (1) (2023)
Inez Beadell, Malia Byun, Hollie Feller, Monica Ferrie, Stephanie Best
Co-designing interventions to 'live well': experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community. Journal of community genetics (2023)
Stephanie Best, Abdullah Al Mahmud, Shivani Tyagi, Jack C W Wheeler, Abdur Rahim Mohammad Forkan, Alexandra Lewis, Nadeem Shuakat, Rohit Kaul, Aisha Ward, Nilmini Wickramasinghe, Prem Prakash Jayaraman, Alison H Trainer
Development of a person-centred digital platform for the long-term support of people living with an adult-onset genetic disease predisposition: a mixed-methods study protocol. BMJ open 13 (7) (2023)
Ann Dadich, Rebecca Wells, Sharon J Williams, Nazim Taskin, Mustafa Coskun, Corinne Grenier, Frederic Ponsignon, Shane L Scahil, Stephanie Best
Cues Disseminated by Professional Associations That Represent 5 Health Care Professions Across 5 Nations: Lexical Analysis of Tweets. Journal of medical Internet research 25 (2023)
Ann Dadich, Rebecca Wells, Sharon J Williams, Nazim Taskin, Mustafa Coskun, Corinne Grenier, Frederic Ponsignon, Shane L Scahil, Stephanie Best
Cues Disseminated by Professional Associations That Represent 5 Health Care Professions Across 5 Nations: Lexical Analysis of Tweets. Journal of medical Internet research 25 (2023)
Fiona Lynch, Yan Meng, Stephanie Best, Ilias Goranitis, Julian Savulescu, Christopher Gyngell, Danya F Vears
Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations. European journal of human genetics : EJHG (2023)
Eden G Robertson, Lauren Kelada, Stephanie Best, Ilias Goranitis, Kristine Pierce, null null, Annie Bye, Emma Elizabeth Palmer
Quality of life in caregivers of a child with a developmental and epileptic encephalopathy. Developmental medicine and child neurology (2023)
Mariana L Lauretta, Anna I Jarmolowicz, David J Amor, Stephanie Best, Angela T Morgan
An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech. Journal of speech, language, and hearing research : JSLHR (2023)
Madeleine Harris, Stephanie Best, Michelle G de Silva, Keri Finlay
"It's fundamental to the work that we do": Genetic counselors' perceptions of their role in clients' mental well-being. Journal of genetic counseling (2023)
Inez Beadell, Malia Byun, Hollie Feller, Monica Ferrie, Stephanie Best
Co-designing interventions to 'live well': experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community. Journal of community genetics (2023)
Ann Dadich, Rebecca Wells, Sharon J Williams, Nazim Taskin, Mustafa Coskun, Corinne Grenier, Frederic Ponsignon, Shane L Scahil, Stephanie Best
Cues Disseminated by Professional Associations That Represent 5 Health Care Professions Across 5 Nations: Lexical Analysis of Tweets. Journal of medical Internet research 25 (2023)
Inez Beadell, Malia Byun, Hollie Feller, Monica Ferrie, Stephanie Best
Co-designing interventions to 'live well': experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community. Journal of community genetics (2023)
Stephanie Best, Janet C Long, Zoe Fehlberg, Tahlia Theodorou, Sarah Hatem, Alison Archibald, Jeffrey Braithwaite
The more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening. European journal of human genetics : EJHG (2022)
Sharon J Williams, Stephanie Best
What Does a Systems Approach to Quality Improvement Look Like in Practice? International journal of environmental research and public health 19 (2) (2022)
Malia Byun, Hollie Feller, Monica Ferrie, Stephanie Best
Living with a genetic, undiagnosed or rare disease: A longitudinal journalling study through the COVID-19 pandemic. Health expectations : an international journal of public participation in health care and health policy 25 (5) (2022)
Isabella A Sherburn, Keri Finlay, Stephanie Best
How does the genomic naive public perceive whole genomic testing for health purposes? A scoping review. European journal of human genetics : EJHG (2022)
Stephanie Best, Nada Vidic, Kim An, Felicity Collins, Susan M White
A systematic review of geographical inequities for accessing clinical genomic and genetic services for non-cancer related rare disease. European journal of human genetics : EJHG 30 (6) (2022)
Sarah Hatem, Janet C Long, Stephanie Best, Zoe Fehlberg, Bróna Nic Giolla Easpaig, Jeffrey Braithwaite
Mobile Apps for People With Rare Diseases: Review and Quality Assessment Using Mobile App Rating Scale. Journal of medical Internet research 24 (7) (2022)
Stephanie Best, Janet C Long, Tahlia Theodorou, Sarah Hatem, Rebecca Lake, Alison Dalton Archibald, Lucinda Freeman, Jeffrey Braithwaite
Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review. Prenatal diagnosis 41 (6) (2021)
Stephanie Best, Helen L Brown, Zornitza Stark, Janet C Long, Larissa Ng, Jeffrey Braithwaite, Natalie Taylor
Teamwork in clinical genomics: A dynamic sociotechnical healthcare setting. Journal of evaluation in clinical practice 27 (6) (2021)
Stephanie Best, Janet C Long, Clara Gaff, Jeffrey Braithwaite, Natalie Taylor
Investigating the Adoption of Clinical Genomics in Australia. An Implementation Science Case Study. Genes 12 (2) (2021)
Ilias Goranitis, Stephanie Best, John Chrisodoulou, Tiffany F Boughtwood, Zornitza Stark
Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment. European journal of human genetics : EJHG 29 (11) (2021)
Stephanie Best, Helen Brown, Sebastian Lunke, Chirag Patel, Jason Pinner, Christopher P Barnett, Meredith Wilson, Sarah A Sandaradura, Belinda McClaren, Gemma R Brett, Jeffrey Braithwaite, Zornitza Stark
Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level. NPJ genomic medicine 6 (1) (2021)
Stephanie Best, Zornitza Stark, Peta Phillips, You Wu, Janet C Long, Natalie Taylor, Jeffrey Braithwaite, John Chrisodoulou, Ilias Goranitis
Clinical genomic testing: what matters to key stakeholders? European journal of human genetics : EJHG 28 (7) (2020)
Stephanie Best, Zornitza Stark, Helen Brown, Janet C Long, Kushani Hewage, Clara Gaff, Jeffrey Braithwaite, Natalie Taylor
The leadership behaviors needed to implement clinical genomics at scale: a qualitative study. Genetics in medicine : official journal of the American College of Medical Genetics 22 (8) (2020)
Stephanie Best, Sharon J Williams
Professional identity in interprofessional teams: findings from a scoping review. Journal of interprofessional care 33 (2) (2018)