Search Results - "Avard, Denise"

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    Pharmacogenetics of opioids for the treatment of acute maternal pain during pregnancy and lactation by Madadi, Parvaz, Avard, Denise, Koren, Gideon

    Published in Current drug metabolism (01-07-2012)
    “…There have been an increasing number of clinical studies investigating the relationship between interindividual genetic variability and the safety and efficacy…”
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    Journal Article
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    Citizens' Values Regarding Research With Stored Samples From Newborn Screening in Canada by BOMBARD, Yvonne, MILLER, Fiona A, GIGUERE, Yves, CHAKRABORTY, Pranesh, HAYEEMS, Robin Z, CARROLL, June C, AVARD, Denise I, WILSON, Brenda J, LITTLE, Julian, BYTAUTAS, Jessica P, ALLANSON, Judith, AXLER, Renata

    Published in Pediatrics (Evanston) (01-02-2012)
    “…Newborn screening (NBS) programs may store bloodspot samples and use them for secondary purposes. Recent public controversies and lawsuits over storage and…”
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    Emerging issues in paediatric health research consent forms in Canada: working towards best practices by Dove, Edward S, Avard, Denise, Black, Lee, Knoppers, Bartha M

    Published in BMC medical ethics (30-01-2013)
    “…Obtaining a research participant's voluntary and informed consent is the bedrock of sound ethics practice. Greater inclusion of children in research has led to…”
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    Recruiting terminally ill patients into non-therapeutic oncology studies: views of health professionals by Kleiderman, Erika, Avard, Denise, Black, Lee, Diaz, Zuanel, Rousseau, Caroline, Knoppers, Bartha Maria

    Published in BMC medical ethics (05-12-2012)
    “…Non-therapeutic trials in which terminally ill cancer patients are asked to undergo procedures such as biopsies or venipunctures for research purposes, have…”
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    Whole-genome sequencing in newborn screening programs by Knoppers, Bartha M, Sénécal, Karine, Borry, Pascal, Avard, Denise

    Published in Science translational medicine (26-03-2014)
    “…The availability of whole-genome sequencing (WGS) is likely to change the practice of population screening programs such as newborn screening (NBS). This…”
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    Ethical dimensions of genetics in pediatric neurology: a look into the future by Avard, Denise M, Knoppers, Bartha M

    Published in Seminars in pediatric neurology (01-03-2002)
    “…Health care providers and families with children who participate in genetic research or who need specialized genetic services, including genetic testing, will…”
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    Public Health Genomics (PHG) and Public Participation: Points to Consider by Catherine Heeney, Denise Avard, Jane Kaye, Lucie M. Bucci, Michael M. Burgess, Tarik Sabry, Yanick Farmer

    Published in Journal of deliberative democracy (15-05-2009)
    “…Large-scale population biobanks, which aim to collect biological tissues, personal health information, and genomic data, are being introduced worldwide with…”
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    Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases by Kleiderman, Erika, Knoppers, Bartha Maria, Fernandez, Conrad V, Boycott, Kym M, Ouellette, Gail, Wong-Rieger, Durhane, Adam, Shelin, Richer, Julie, Avard, Denise

    Published in Journal of medical ethics (01-10-2014)
    “…Purpose To explore parental perceptions and experiences regarding the return of genomic incidental research findings in children with rare diseases. Methods…”
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    Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information by NYCUM, Gillian, AVARD, Denise, KNOPPERS, Bartha M

    Published in European journal of human genetics : EJHG (01-07-2009)
    “…What factors influence intrafamilial communication of hereditary breast and ovarian cancer (HBOC) genetic risk information? Such information can have health…”
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    Attitudes of parents toward the return of targeted and incidental genomic research findings in children by Fernandez, Conrad V., Bouffet, Eric, Malkin, David, Jabado, Nada, O’Connell, Colleen, Avard, Denise, Knoppers, Bartha M., Ferguson, Meghan, Boycott, Kym M., Sorensen, Poul H., Orr, Andrew C., Robitaille, Johane M., McMaster, Christopher R.

    Published in Genetics in medicine (01-08-2014)
    “…Purpose: We describe parental attitudes toward the return of targeted and incidental genomic research results in the setting of high-risk pediatric cancer and…”
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    Personalized medicine and access to health care: potential for inequitable access? by McClellan, Kelly A, Avard, Denise, Simard, Jacques, Knoppers, Bartha M

    Published in European journal of human genetics : EJHG (01-02-2013)
    “…Personalized medicine promises that an individual's genetic information will be increasingly used to prioritize access to health care. Use of genetic…”
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    Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms? by HOWARD, Heidi Carmen, AVARD, Denise, BORRY, Pascal

    Published in European journal of human genetics : EJHG (01-11-2011)
    “…The genetic testing of minors within the direct-to-consumer (DTC) genetic testing (GT) context has been given relatively little attention. The issue of testing…”
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    To disclose, or not to disclose? Context matters by Rahimzadeh, Vasiliki, Avard, Denise, Sénécal, Karine, Knoppers, Bartha Maria, Sinnett, Daniel

    Published in European journal of human genetics : EJHG (01-03-2015)
    “…Progress in understanding childhood disease using next-generation sequencing (NGS) portends vast improvements in the nature and quality of patient care…”
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