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Clara Gaff

Showing results (61-70 of 109) with videos related to

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European Journal of Human Genetics : EJHG|May 7, 2025
Opportunities and challenges for paediatricians requesting funded genomic tests for childrenBelinda Dawson-McClaren, Melissa Martyn, Jessica Ince, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disordersOliver James Dillon, Sebastian Lunke, Zornitza Stark, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 17, 2016
The Impact of Receiving Predictive Genetic Information about Lynch Syndrome on Individual Colonoscopy and Smoking BehaviorsJoanne Soo-Min Kim, Peter C Coyte, Michelle Cotterchio, et al.
Journal of Genetic Counseling|February 24, 2007
Development and pilot testing of two decision aids for individuals considering genetic testing for cancer riskClaire E Wakefield, Bettina Meiser, Judi Homewood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursementZornitza Stark, Deborah Schofield, Khurshid Alam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing projectLilian Downie, Jane Halliday, Sharon Lewis, et al.
Journal of Paediatrics and Child Health|November 20, 2025
Exomes in Paediatrics: Co-Design and Implementation of Interventions to Support Paediatricians to Provide Genomic CareBelinda Dawson-McClaren, Melissa Martyn, Emma Weisz, et al.
European Journal of Human Genetics : EJHG|February 13, 2026
Impact of a digital platform on genetic counselling encounters in the screening contextChloe Mighton, Alli Jan, Ling Lee, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|June 28, 2026
Content validity, face validity and comprehensiveness of generic quality-of-life measures in adults and children with rare genetic conditions and their carers: a think aloud qualitative studyMackenzie Bourke, Xuemin Zhu, Tiffany Boughtwood, et al.
Frontiers in Genetics|November 30, 2019
Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic ApproachAmy Nisselle, Melissa Martyn, Helen Jordan, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|May 7, 2025
Opportunities and challenges for paediatricians requesting funded genomic tests for childrenBelinda Dawson-McClaren, Melissa Martyn, Jessica Ince, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disordersOliver James Dillon, Sebastian Lunke, Zornitza Stark, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 17, 2016
The Impact of Receiving Predictive Genetic Information about Lynch Syndrome on Individual Colonoscopy and Smoking BehaviorsJoanne Soo-Min Kim, Peter C Coyte, Michelle Cotterchio, et al.
Journal of Genetic Counseling|February 24, 2007
Development and pilot testing of two decision aids for individuals considering genetic testing for cancer riskClaire E Wakefield, Bettina Meiser, Judi Homewood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursementZornitza Stark, Deborah Schofield, Khurshid Alam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing projectLilian Downie, Jane Halliday, Sharon Lewis, et al.
Journal of Paediatrics and Child Health|November 20, 2025
Exomes in Paediatrics: Co-Design and Implementation of Interventions to Support Paediatricians to Provide Genomic CareBelinda Dawson-McClaren, Melissa Martyn, Emma Weisz, et al.
European Journal of Human Genetics : EJHG|February 13, 2026
Impact of a digital platform on genetic counselling encounters in the screening contextChloe Mighton, Alli Jan, Ling Lee, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|June 28, 2026
Content validity, face validity and comprehensiveness of generic quality-of-life measures in adults and children with rare genetic conditions and their carers: a think aloud qualitative studyMackenzie Bourke, Xuemin Zhu, Tiffany Boughtwood, et al.
Frontiers in Genetics|November 30, 2019
Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic ApproachAmy Nisselle, Melissa Martyn, Helen Jordan, et al.
Pageof 11