Denise Avard

Dados Biográficos

ID4256183
NOMEDenise Avard
PRENOMESDenise
SOBRENOMEAvard
ASSINATURAAVARD D
AFILIAÇÕESMcGill University
VERIFICADONão
TOTAL DE OBRAS6
TOTAL DE CITAÇÕES0
TOTAL COMO AUTOR6
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2005
ANO MAIS RECENTE DE PUBLICAÇÃO2015
ÍNDICE H0

  • Expectations and values about expanded newborn screening

    Open AccessRobin Z Hayeems, Fiona A Miller et al.ARTICLEHealth Expectations2015

    OBJECTIVES: Newborn bloodspot screening (NBS) panels have expanded to include conditions for which treatment effects are less certain, creating debate about population-based screening criteria. We investigated Canadian public expectations and values regarding the types of conditions that should be included in NBS and whether parents should provide consent. METHODS: Eight focus groups (FG; n = 60) included education, deliberative discussion and pr…

  • Public concerns regarding the storage and secondary uses of residual newborn bloodspots

    Open AccessShannon Cunningham, Kieran C O''Doherty et al.ARTICLEJournal of Community Genetics2014

  • Intrafamilial disclosure of risk for hereditary breast and ovarian cancer

    Open AccessLee Black, Kelly A McClellan et al.ARTICLEJournal of Community Genetics2012

    The primary goal of breast and ovarian cancer screening is to minimize the cases of advanced disease and therefore its mortality rate. For hereditary breast and ovarian cancer, one method to reach this goal is to disseminate genetic risk information among family members. However, experience tells us that this information does not always reach family members in a timely manner, if at all. There are many moving parts to a decision to disclose genet…

  • Public Health Genomics (PHG) and Public Participation

    Open AccessDenise Avard, Lucie M Bucci et al.ARTICLEJournal of Deliberative Democracy2009

    Large-scale population biobanks, which aim to collect biological tissues, personal health information, and genomic data, are being introduced worldwide with the promise of increasing knowledge on chronic diseases such as diabetes and heart disease. Experts recognize the need for public participation to address the many social, legal and ethical complexities raised by the introduction of biobanks for public health research. However many researcher…

  • Newborn Screening by Tandem Mass Spectrometry

    Open AccessDenise Avard, Hilary Vallance et al.ARTICLECanadian Journal of Public Health2007Referências: 11

  • La Protection De L’information Génétique Dans Le Domaine Médical Au Québec

    Open AccessEmmanuelle Lévesque, Bartha Maria Knoppers et al.ARTICLERevue de droit Université de…2005

    LA PROTECTION DE L’INFORMATION GÉNÉTIQUE DANS LE DOMAINE MÉDICAL AU QUÉBEC : PRINCIPE GÉNÉRAL DE CONFIDENTIALITÉ ET QUESTIONS SOULEVÉES PAR LES DISPOSITIONS D’EXCEPTION. Un article de la revue Revue de droit de l'Université de Sherbrooke (Volume 36, numéro 1-2, 2005–2006, p. 1-399) diffusée par la plateforme Érudit