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Denise M. Avard

FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project
2014 · Chandree L. Beaulieu, Jacek Majewski, et al. · The American Journal of Human Genetics · 239
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Cohort Profile: The Maternal‐Infant Research on Environmental Chemicals Research Platform
2013 · Tye E. Arbuckle, William D. Fraser, et al. · Paediatric and Perinatal Epidemiology · 202
Attitudes of parents toward the return of targeted and incidental genomic research findings in children
2014 · Conrad V. Fernandez, Eric Bouffet, et al. · Genetics in Medicine · 96
Whole-Genome Sequencing in Newborn Screening Programs
2014 · Bartha M. Knoppers, Karine Sénécal, et al. · Science Translational Medicine · 86
Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases
2013 · Erika Kleiderman, Bartha Maria Knoppers, et al. · Journal of Medical Ethics · 86
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Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer
2006 · Jacques Simard, Jacques Simard, et al. · Journal of Medical Genetics · 79
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Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information
2009 · Gillian Nycum, Denise Avard, et al. · European Journal of Human Genetics · 69
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Public views on participating in newborn screening using genome sequencing
2014 · Yvonne Bombard, Fiona A Miller, et al. · European Journal of Human Genetics · 68
Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform
2013 · Ma'n H Zawati along with the P3G International Paediatrics Platform members, Bartha Maria Knoppers, et al. · European Journal of Human Genetics · 64
Health-related direct-to-consumer genetic testing: a review of companies’ policies with regard to genetic testing in minors
2009 · Pascal Borry, Heidi C. Howard, et al. · Familial Cancer · 62
Personalized medicine and access to health care: potential for inequitable access?
2012 · Kelly A McClellan, Denise Avard, et al. · European Journal of Human Genetics · 55
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Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening
2010 · Yvonne Bombard, Fiona A Miller, et al. · European Journal of Human Genetics · 53
Clinical Management Recommendations for Surveillance and Risk-Reduction Strategies for Hereditary Breast and Ovarian Cancer Among Individuals Carrying a Deleterious BRCA1 or BRCA2 Mutation
2007 · Doug Horsman, Brenda J. Wilson, et al. · Journal of Obstetrics and Gynaecology Canada · 49
Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting
2013 · Conrad V. Fernandez, Caron Strahlendorf, et al. · Genetics in Medicine · 48
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Citizens’ Values Regarding Research With Stored Samples From Newborn Screening in Canada
2012 · Yvonne Bombard, Fiona A. Miller, et al. · PEDIATRICS · 46
Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?
2011 · Heidi Carmen Howard, Denise Avard, et al. · European Journal of Human Genetics · 43
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Children and incompetent adults in genetic research: consent and safeguards
2002 · Bartha Maria Knoppers, Denise Avard, et al. · Nature Reviews Genetics · 40
Pediatric Research and the Return of Individual Research Results
2011 · Denise Avard, Karine Sénécal, et al. · The Journal of Law Medicine & Ethics · 37
Researchers’ Perceptions of the Ethical Implications of Pharmacogenomics Research with Children
2009 · D. Avard, T. Silverstein, et al. · Public Health Genomics · 36
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Direct-to-consumer genome scanning services. Also for children?
2008 · Pascal Borry, Heidi C. Howard, et al. · Nature Reviews Genetics · 36
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Public Health Genomics (PHG) and Public Participation: Points to Consider
2009 · Denise Avard, Lucie M. Bucci, et al. · Journal of Deliberative Democracy · 35
Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider
2012 · Lee Black, Kelly A. McClellan, et al. · Journal of Community Genetics · 34
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Expectations and values about expanded newborn screening: a public engagement study
2013 · Robin Z. Hayeems, Fiona A. Miller, et al. · Health Expectations · 33
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Framing Genomics, Public Health Research and Policy: Points to Consider
2010 · B.M. Knoppers, T. Leroux, et al. · Public Health Genomics · 33
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Storing Newborn Blood Spots: Modern Controversies
2004 · Linda Kharaboyan, Denise Avard, et al. · The Journal of Law Medicine & Ethics · 33
Works count: 166
Citation count: 2,537
H-index: 29
I10-index: 62
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