D. Avard

D. Avard, J. Lockyer, J. Parboosingh, 1987, Research in medical education : proceedings of the ... annual Conference. Conference on Research in Medical Education.

THC volume 31 issue 6 Cover and Back matter

M. Hallett, D. Avard, D. Husereau, 2015, International Journal of Technology Assessment in Health Care.

Newborn Blood Spot Screening in Four Countries: Stakeholder Involvement

B. Potter, D. Avard, B. Wilson, 2008, Journal of public health policy.

Low-birth-weight symposium: summary of proceedings.

D. Avard, G. Chance, C. Levitt, 1993, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

Improved Understanding of Genetic and Genomic Influences on Drug Disposition and Action

Y. Joly, D. Avard, 2008, Paediatric drugs.

Physicians and genetic malpractice.

B. Knoppers, D. Avard, M. J. Howlett, 2002, Medicine and law.

6.4 Pharmacogenomics

Y. Joly, D. Avard, T. Silverstein, 2014 .

Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

D. Avard, P. Borry, H. Howard, 2011, European Journal of Human Genetics.

Direct-to-consumer genome scanning services. Also for children?

D. Avard, K. Sénécal, P. Borry, 2009, Nature Reviews Genetics.

Newborn Screening by Tandem Mass Spectrometry

B. Potter, C. Greenberg, D. Avard, 2007, Canadian journal of public health = Revue canadienne de sante publique.

The communication of pharmacogenetic research results: participants weigh in on their informational needs in a pilot study.

M. Hayden, B. Carleton, G. Koren, 2011, Journal of population therapeutics and clinical pharmacology = Journal de la therapeutique des populations et de la pharamcologie clinique.

Variability in the storage and use of newborn dried bloodspots in Canada: is it time for national standards?

C. Laberge, C. Greenberg, D. Avard, 2006, Genomics, society, and policy.

Ethical dimensions of genetics in pediatric neurology: a look into the future.

B. Knoppers, D. Avard, 2002, Seminars in pediatric neurology.

Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform

B. Knoppers, D. Avard, K. Sénécal, 2013, European Journal of Human Genetics.

Risks and benefits of obstetric epidural analgesia: a review.

D. Avard, C. M. Nimrod, 1985, Birth.

Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk

B. Knoppers, J. Simard, D. Avard, 2013, European Journal of Human Genetics.

Informed Consent in Genetics

B. Knoppers, A. Thorogood, D. Avard, 2012 .

Genetics and Society Project

B. Knoppers, D. Avard, 2001, Public Health Genomics.

RMGA Statement of Principles on the Return of Research Results and Incidental Findings

B. Knoppers, D. Avard, K. Sénécal, 2013 .

Pharmacogenetics of opioids for the treatment of acute maternal pain during pregnancy and lactation.

G. Koren, D. Avard, P. Madadi, 2012, Current drug metabolism.

Understanding umbilical cord blood banking: what women need to know before deciding.

B. Knoppers, D. Avard, J. Nisker, 2007, Women's health issues : official publication of the Jacobs Institute of Women's Health.

Research Ethics Boards and Challenges for Public Participation

D. Pullman, D. Avard, R. Saginur, 2009 .

Regulatory approval for new pharmacogenomic tests: a comparative overview.

M. Hayden, B. Carleton, A. Issa, 2011, Food and drug law journal.

D. Avard, K. Sénécal, P. Borry, 2010, Familial Cancer.

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

B. Knoppers, B. Godard, D. Easton, 2006, Journal of Medical Genetics.

Attitudes of parents toward the return of targeted and incidental genomic research findings in children

P. Sorensen, B. Knoppers, K. Boycott, 2014, Genetics in Medicine.

Newborn screening for sickle-cell disease : socio-ethical implications

B. Knoppers, D. Avard, Linda Kharaboyan, 2006 .

Family History Tools in Primary Care: Does One Size Fit All?

D. Castle, J. Grimshaw, J. Little, 2012, Public Health Genomics.

Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutation.

D. Horsman, W. Meschino, J. Simard, 2007, Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC.

Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases

B. Knoppers, K. Boycott, D. Avard, 2013, Journal of Medical Ethics.

Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options

Carolyn J. Barg, Y. Bombard, J. Little, 2016, Pediatrics.

Newborn Screening, Banking, and Consent

C. Laberge, D. Avard, Linda Kharaboyan, 2004 .

Personalized medicine and access to health care: potential for inequitable access?

B. Knoppers, J. Simard, D. Avard, 2012, European Journal of Human Genetics.

Citizens’ Values Regarding Research With Stored Samples From Newborn Screening in Canada

Y. Bombard, J. Little, J. Allanson, 2012, Pediatrics.

Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities

D. Secko, D. Avard, K. Sénécal, 2015, Journal of Community Genetics.

Public Health Genomics (PHG) and Public Participation: Points to Consider

A. Cambon-Thomsen, J. Kaye, D. Avard, 2009 .

BEST PRACTICES FOR HEALTH RESEARCH INVOLVING CHILDREN AND ADOLESCENTS

B. Knoppers, D. Avard, G. Griener, 2011 .

Emerging issues in paediatric health research consent forms in Canada: working towards best practices

B. Knoppers, D. Avard, E. Dove, 2013, BMC medical ethics.

Physician Recruitment of Patients to Non-Therapeutic Oncology Clinical Trials: Ethics Revisited

B. Knoppers, G. Batist, D. Avard, 2013, Front. Pharmacol..

Birth patterns: are the Chinese in Guangzhou City different?

D. Avard, T. Abernathy, C. Nimrod, 1988, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

SOCIO-ETHICAL ISSUES IN PERSONALIZED MEDICINE: A SYSTEMATIC REVIEW OF ENGLISH LANGUAGE HEALTH TECHNOLOGY ASSESSMENTS OF GENE EXPRESSION PROFILING TESTS FOR BREAST CANCER PROGNOSIS

M. Hallett, D. Avard, N. Palmour, 2015, International Journal of Technology Assessment in Health Care.

Breast-feeding policies and practices in Canadian hospitals providing maternity care.

D. Avard, L. Hanvey, G. Chance, 1996, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

A new twist on an old problem: primary care physicians and results from direct-to-consumer genetic testing.

B. Knoppers, G. Bartlett, D. Avard, 2013, Personalized Medicine.

Disclosure of incidental findings in cancer genomic research: investigators' perceptions on obligations and barriers

G. Sauvageau, D. Avard, E. Kleiderman, 2015, Clinical genetics.

Funding considerations for the disclosure of genetic incidental findings in biobank research

B. Knoppers, G. Sauvageau, D. Avard, 2013, Clinical genetics.

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting

C. Strahlendorf, P. Sorensen, B. Knoppers, 2013, Genetics in Medicine.