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Denise Avard

Showing results (31-40 of 44) with videos related to

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Journal of Medical Ethics|December 21, 2013
Returning incidental findings from genetic research to children: views of parents of children affected by rare diseasesErika Kleiderman, Bartha Maria Knoppers, Conrad V Fernandez, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|March 10, 2007
Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutationDoug Horsman, Brenda J Wilson, Denise Avard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2013
Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research settingConrad V Fernandez, Caron Strahlendorf, Denise Avard, et al.
Journal of Population Therapeutics and Clinical Pharmacology = Journal De La Therapeutique Des Populations Et De La Pharmacologie Clinique|April 7, 2011
The communication of pharmacogenetic research results: participants weigh in on their informational needs in a pilot studyParvaz Madadi, Yann Joly, Denise Avard, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 2, 2013
Expectations and values about expanded newborn screening: a public engagement studyRobin Z Hayeems, Fiona A Miller, Yvonne Bombard, et al.
Pediatrics|January 18, 2012
Citizens' values regarding research with stored samples from newborn screening in CanadaYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Pediatrics|June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy OptionsRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
International Journal of Technology Assessment in Health Care|October 3, 2008
Guidance for considering ethical, legal, and social issues in health technology assessment: application to genetic screeningBeth K Potter, Denise Avard, Ian D Graham, et al.
European Journal of Human Genetics : EJHG|February 20, 2014
Public views on participating in newborn screening using genome sequencingYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 18, 2014
Attitudes of parents toward the return of targeted and incidental genomic research findings in childrenConrad V Fernandez, Eric Bouffet, David Malkin, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Journal of Medical Ethics|December 21, 2013
Returning incidental findings from genetic research to children: views of parents of children affected by rare diseasesErika Kleiderman, Bartha Maria Knoppers, Conrad V Fernandez, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|March 10, 2007
Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutationDoug Horsman, Brenda J Wilson, Denise Avard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2013
Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research settingConrad V Fernandez, Caron Strahlendorf, Denise Avard, et al.
Journal of Population Therapeutics and Clinical Pharmacology = Journal De La Therapeutique Des Populations Et De La Pharmacologie Clinique|April 7, 2011
The communication of pharmacogenetic research results: participants weigh in on their informational needs in a pilot studyParvaz Madadi, Yann Joly, Denise Avard, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|February 2, 2013
Expectations and values about expanded newborn screening: a public engagement studyRobin Z Hayeems, Fiona A Miller, Yvonne Bombard, et al.
Pediatrics|January 18, 2012
Citizens' values regarding research with stored samples from newborn screening in CanadaYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Pediatrics|June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy OptionsRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
International Journal of Technology Assessment in Health Care|October 3, 2008
Guidance for considering ethical, legal, and social issues in health technology assessment: application to genetic screeningBeth K Potter, Denise Avard, Ian D Graham, et al.
European Journal of Human Genetics : EJHG|February 20, 2014
Public views on participating in newborn screening using genome sequencingYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 18, 2014
Attitudes of parents toward the return of targeted and incidental genomic research findings in childrenConrad V Fernandez, Eric Bouffet, David Malkin, et al.
Pageof 5