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Clara Gaff

Showing results (81-90 of 109) with videos related to

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European Journal of Human Genetics : EJHG|January 23, 2019
Australians' views and experience of personal genomic testing: survey findings from the Genioz studyJacqueline Savard, Chriselle Hickerton, Rigan Tytherleigh, et al.
European Journal of Human Genetics : EJHG|February 24, 2026
Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ studyErin Tutty, Anaita Kanga-Parabia, Nathasha Kugenthiran, et al.
Journal of Genetic Counseling|June 11, 2013
Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testingLouisa Flander, Andrew Speirs-Bridge, Alison Rutstein, et al.
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.
European Journal of Human Genetics : EJHG|August 24, 2017
A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES dataZornitza Stark, Harriet Dashnow, Sebastian Lunke, et al.
Genetics in Medicine Open|December 23, 2024
Genetic counseling workforce diversity, inclusion, and capacity in Australia and New ZealandAnaita Kanga-Parabia, Lucas Mitchell, Renee Smyth, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 26, 2021
The expectations and realities of nutrigenomic testing in australia: A qualitative studyErin Tutty, Chriselle Hickerton, Bronwyn Terrill, et al.
European Journal of Medical Genetics|November 16, 2018
Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz studySylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
Pageof 11

Showing results (81-90 of 109) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|January 23, 2019
Australians' views and experience of personal genomic testing: survey findings from the Genioz studyJacqueline Savard, Chriselle Hickerton, Rigan Tytherleigh, et al.
European Journal of Human Genetics : EJHG|February 24, 2026
Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ studyErin Tutty, Anaita Kanga-Parabia, Nathasha Kugenthiran, et al.
Journal of Genetic Counseling|June 11, 2013
Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testingLouisa Flander, Andrew Speirs-Bridge, Alison Rutstein, et al.
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.
European Journal of Human Genetics : EJHG|August 24, 2017
A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES dataZornitza Stark, Harriet Dashnow, Sebastian Lunke, et al.
Genetics in Medicine Open|December 23, 2024
Genetic counseling workforce diversity, inclusion, and capacity in Australia and New ZealandAnaita Kanga-Parabia, Lucas Mitchell, Renee Smyth, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 26, 2021
The expectations and realities of nutrigenomic testing in australia: A qualitative studyErin Tutty, Chriselle Hickerton, Bronwyn Terrill, et al.
European Journal of Medical Genetics|November 16, 2018
Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz studySylvia A Metcalfe, Chriselle Hickerton, Jacqueline Savard, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
Pageof 11