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Fiona Lynch

Showing results (41-50 of 56) 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.
Psycho-Oncology|February 15, 2025
Feasibility and Acceptability of the Fear-Less Screening and Stratified-Care Model for Fear of Cancer Recurrence Among People Affected by Early-Stage CancerMei Jun Tran, Michael Jefford, Tsien Fua, 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.
Science Advances|March 14, 2025
Assessing <i>E. coli</i> levels in surface soils of informal settlements using boot sock and standard grab methodsLamiya Bata, Rebekah Henry, S Fiona Barker, et al.
Psycho-Oncology|April 30, 2023
Evaluation of the validity and screening performance of a revised single-item fear of cancer recurrence screening measure (FCR-1r)Allan 'Ben' Smith, Mingbo Gao, Mei Tran, et al.
European Journal of Human Genetics : EJHG|June 1, 2019
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive careZornitza Stark, Amy Nisselle, Belinda McClaren, et al.
Genetics in Medicine Open|December 23, 2024
Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national programKirsten Boggs, Fiona Lynch, Michelle Ward, et al.
Plos One|February 1, 2013
Age-associated changes in monocyte and innate immune activation markers occur more rapidly in HIV infected womenGenevieve E Martin, Maelenn Gouillou, Anna C Hearps, et al.
Nursing in Critical Care|March 30, 2026
Key Insights From the International ICU Diary Conference 2025Peter Nydahl, Bev Ewens, Anne-Sophie Debue, et al.
European Journal of Human Genetics : EJHG|May 25, 2024
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics servicesStephanie Best, Zoe Fehlberg, Christopher Richards, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
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.
Psycho-Oncology|February 15, 2025
Feasibility and Acceptability of the Fear-Less Screening and Stratified-Care Model for Fear of Cancer Recurrence Among People Affected by Early-Stage CancerMei Jun Tran, Michael Jefford, Tsien Fua, 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.
Science Advances|March 14, 2025
Assessing <i>E. coli</i> levels in surface soils of informal settlements using boot sock and standard grab methodsLamiya Bata, Rebekah Henry, S Fiona Barker, et al.
Psycho-Oncology|April 30, 2023
Evaluation of the validity and screening performance of a revised single-item fear of cancer recurrence screening measure (FCR-1r)Allan 'Ben' Smith, Mingbo Gao, Mei Tran, et al.
European Journal of Human Genetics : EJHG|June 1, 2019
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive careZornitza Stark, Amy Nisselle, Belinda McClaren, et al.
Genetics in Medicine Open|December 23, 2024
Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national programKirsten Boggs, Fiona Lynch, Michelle Ward, et al.
Plos One|February 1, 2013
Age-associated changes in monocyte and innate immune activation markers occur more rapidly in HIV infected womenGenevieve E Martin, Maelenn Gouillou, Anna C Hearps, et al.
Nursing in Critical Care|March 30, 2026
Key Insights From the International ICU Diary Conference 2025Peter Nydahl, Bev Ewens, Anne-Sophie Debue, et al.
European Journal of Human Genetics : EJHG|May 25, 2024
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics servicesStephanie Best, Zoe Fehlberg, Christopher Richards, et al.
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