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Jacques Simard

Biographic Data

ID4115927
NAMEJacques Simard
GIVEN NAMESJacques
FAMILY NAMESimard
SIGNATURESIMARD J
AFFILIATIONSUniversité Laval
ORCID0000-0001-6906-3390
VERIFIEDYes
TOTAL WORKS4
TOTAL CITATIONS0
AUTHOR COUNT4
EDITOR COUNT0
FIRST PUBLICATION YEAR2006
LATEST PUBLICATION YEAR2024
H-INDEX0
  • General Medical Practitioners Acting as Geneticists, a Risky Business

    Open Access•Aurélie Dauge, Yann Joly et al.•ARTICLE•Lex Electronica•2024•References: 38

    The availability of precision medicine tools and approaches has increased considerably over the past decades, propelled by rapid scientific advances in genomics and the popularity of direct-to-consumer genetic testing. Genetic specialists working within public healthcare systems are struggling to meet the growing demand for clinical genetic services. Some experts have suggested that doctors who are not specialized in genetics could take on some o…

  • Survey of primary care physicians’ views about breast and ovarian cancer screening for true BRCA1/2 non-carriers

    Open Access•S Pelletier, Geneviève Larouche et al.•ARTICLE•Journal of Community Genetics•2019

  • Organizational challenges to equity in the delivery of services within a new personalized risk-based approach to breast cancer screening

    Open Access•Emmanuelle Lévesque, Julie Hagan et al.•ARTICLE•New Genetics and Society•2018

    Emerging evidence opens new possibilities to improve current breast cancer mammography screening programs. One promising avenue is to tailor mammography screening according to individual risk. However, some factors could challenge the implementation of such approach, specifically its potential impact on the equitable delivery of services. This study aims to identify the barriers and facilitators to the equitable delivery of services within a futu…

  • Using the Impact of Event Scale to Evaluate Distress in the Context of Genetic Testing for Breast Cancer Susceptibility

    Open Access•Michel Dorval, Mélanie Drolet et al.•ARTICLE•Psychological Reports•2006

    The data obtained with two forms of the Impact of Event Scale were compared, one referring to a BRCA1/2 test result (IES-T) and another to cancer (IES-C). The sample consisted of 272 women with a family history suggestive of a BRCA1/2 mutation who underwent genetic testing and received results: noncarrier, carrier, or inconclusive. Globally, mean scores on the IES-C form were higher than those obtained on the IES-T form. Among carriers of a BRCA1…

No prominent works on this page.

  • Using the Impact of Event Scale to Evaluate Distress in the Context of Genetic Testing for Breast Cancer Susceptibility

    Open Access•Michel Dorval, Mélanie Drolet et al.•ARTICLE•Psychological Reports•2006

    The data obtained with two forms of the Impact of Event Scale were compared, one referring to a BRCA1/2 test result (IES-T) and another to cancer (IES-C). The sample consisted of 272 women with a family history suggestive of a BRCA1/2 mutation who underwent genetic testing and received results: noncarrier, carrier, or inconclusive. Globally, mean scores on the IES-C form were higher than those obtained on the IES-T form. Among carriers of a BRCA1…

  • Organizational challenges to equity in the delivery of services within a new personalized risk-based approach to breast cancer screening

    Open Access•Emmanuelle Lévesque, Julie Hagan et al.•ARTICLE•New Genetics and Society•2018

    Emerging evidence opens new possibilities to improve current breast cancer mammography screening programs. One promising avenue is to tailor mammography screening according to individual risk. However, some factors could challenge the implementation of such approach, specifically its potential impact on the equitable delivery of services. This study aims to identify the barriers and facilitators to the equitable delivery of services within a futu…

  • Survey of primary care physicians’ views about breast and ovarian cancer screening for true BRCA1/2 non-carriers

    Open Access•S Pelletier, Geneviève Larouche et al.•ARTICLE•Journal of Community Genetics•2019

  • General Medical Practitioners Acting as Geneticists, a Risky Business

    Open Access•Aurélie Dauge, Yann Joly et al.•ARTICLE•Lex Electronica•2024•References: 38

    The availability of precision medicine tools and approaches has increased considerably over the past decades, propelled by rapid scientific advances in genomics and the popularity of direct-to-consumer genetic testing. Genetic specialists working within public healthcare systems are struggling to meet the growing demand for clinical genetic services. Some experts have suggested that doctors who are not specialized in genetics could take on some o…

BRCA gene mutations in cancer (3 works) · Breast cancer (3 works) · Cancer (3 works) · Medicine (3 works) · Psychology (3 works) · Business (2 works) · Global Cancer Incidence and Screening (2 works) · Internal Medicine (2 works) · Oncology (2 works) · Biology (1 works)

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