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Stephanie Best

Showing results (101-110 of 136) with videos related to

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Human Genomics|May 9, 2024
Australian public perspectives on genomic newborn screening: which conditions should be included?Fiona Lynch, Stephanie Best, Clara Gaff, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
How parents decide whether to have genomic newborn screening: experiences from BabyScreenAnaita Kanga-Parabia, Erin Tutty, Nathasha Kugenthiran, et al.
International Journal of Neonatal Screening|January 22, 2024
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for ImplementationFiona Lynch, Stephanie Best, Clara Gaff, et al.
NPJ Genomic Medicine|January 29, 2021
Learning from scaling up ultra-rapid genomic testing for critically ill children to a national levelStephanie Best, Helen Brown, Sebastian Lunke, et al.
Public Health Genomics|January 2, 2025
Adopting Public Health Genomics when the House Is on Fire: How Will We Navigate to 2030?Jeffrey Braithwaite, Samantha Spanos, Klay Lamprell, et al.
BMJ Open|October 26, 2022
Acceptability and feasibility of an online information linker service for caregivers who have a child with genetic epilepsy: a mixed-method pilot study protocolEden G Robertson, Lauren Kelada, Stephanie Best, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2023
"Somewhere to turn to with my questions": A pre-post pilot of an information linker service for caregivers who have a child with a Developmental and Epileptic EncephalopathyEden G Robertson, Natalie J Roberts, Fleur Le Marne, et al.
Internal Medicine Journal|July 2, 2025
Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromesLucy C Fox, Erin Goode, Nicole Den Elzen, et al.
BMJ Open|July 30, 2023
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 protocolStephanie Best, Abdullah Al Mahmud, Shivani Tyagi, et al.
BMJ Open|June 18, 2025
Evaluation of a telehealth service to support breast cancer prevention medication uptake: a protocol of a mixed methods studyKatrina Louise West, Tim Spelman, Wanda Cui, et al.
Pageof 14

Showing results (101-110 of 136) with videos related to

Sort By:
Pageof 14
Human Genomics|May 9, 2024
Australian public perspectives on genomic newborn screening: which conditions should be included?Fiona Lynch, Stephanie Best, Clara Gaff, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
How parents decide whether to have genomic newborn screening: experiences from BabyScreenAnaita Kanga-Parabia, Erin Tutty, Nathasha Kugenthiran, et al.
International Journal of Neonatal Screening|January 22, 2024
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for ImplementationFiona Lynch, Stephanie Best, Clara Gaff, et al.
NPJ Genomic Medicine|January 29, 2021
Learning from scaling up ultra-rapid genomic testing for critically ill children to a national levelStephanie Best, Helen Brown, Sebastian Lunke, et al.
Public Health Genomics|January 2, 2025
Adopting Public Health Genomics when the House Is on Fire: How Will We Navigate to 2030?Jeffrey Braithwaite, Samantha Spanos, Klay Lamprell, et al.
BMJ Open|October 26, 2022
Acceptability and feasibility of an online information linker service for caregivers who have a child with genetic epilepsy: a mixed-method pilot study protocolEden G Robertson, Lauren Kelada, Stephanie Best, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2023
"Somewhere to turn to with my questions": A pre-post pilot of an information linker service for caregivers who have a child with a Developmental and Epileptic EncephalopathyEden G Robertson, Natalie J Roberts, Fleur Le Marne, et al.
Internal Medicine Journal|July 2, 2025
Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromesLucy C Fox, Erin Goode, Nicole Den Elzen, et al.
BMJ Open|July 30, 2023
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 protocolStephanie Best, Abdullah Al Mahmud, Shivani Tyagi, et al.
BMJ Open|June 18, 2025
Evaluation of a telehealth service to support breast cancer prevention medication uptake: a protocol of a mixed methods studyKatrina Louise West, Tim Spelman, Wanda Cui, et al.
Pageof 14