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Anne Cambon‐thomsen

Dados Biográficos

ID4889035
NOMEAnne Cambon‐thomsen
PRENOMESAnne
SOBRENOMECambon‐thomsen
ASSINATURATHOMSEN A C
AFILIAÇÕESInserm
ORCID0000-0001-8793-3644
VERIFICADOSim
TOTAL DE OBRAS10
TOTAL DE CITAÇÕES2
TOTAL COMO AUTOR10
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2009
ANO MAIS RECENTE DE PUBLICAÇÃO2021
ÍNDICE H1
  • Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics

    Open Access•Michel Rosier, Myriam Guedj et al.•ARTICLE•Journal of Health Psychology•2021•Referências: 50

    Next-generation sequencing techniques enable unsolicited findings to be detected. This discovery raises ethical questions concerning the return of these findings. Our study aimed to highlight the views of the general public, patients under supervision and health professionals concerning the acceptability of disclosing unsolicited results to patients. In total, 449 participants assessed scenarios, consisted of all combinations of three factors (pa…

  • How to responsibly acknowledge research work in the era of big data and biobanks

    Open Access•Heidi Howard, Heidi Carmen Howard et al.•ARTICLE•Journal of Community Genetics•2017

    Currently, a great deal of biomedical research in fields such as epidemiology, clinical trials and genetics is reliant on vast amounts of biological and phenotypic information collected and assembled in biobanks. While many resources are being invested to ensure that comprehensive and well-organised biobanks are able to provide increased access to, and sharing of biomedical samples and information, many barriers and challenges remain to such resp…

  • From the arcane to the mundane

    Open Access•Alexandra Soulier, Samantha Leonard et al.•ARTICLE•New Genetics and Society•2016

    Genomic technologies are developing at a time when greater public involvement in research and clinical governance is sought. To this end, empirical bioethics studies, although conceptualized as academic endeavors, may draw on the inclusion of laypeople to justify informing policy. Doing so, they face similar concerns as those addressed to public consultations which cannot be termed democratic a priori and may reinforce the authority of experts. W…

  • Judging health risk as a function of risk factors and type of illness

    Open Access•Myriam Guedj, Etienne Mullet et al.•ARTICLE•Journal of Health Psychology•2016•Citada por: 1•Referências: 34

    We examined the extent to which lay people and health professionals are able to assess occurrence risks for multifactorial diseases. We asked 341 participants to assess the risk of developing lung cancer, coronary artery disease or rheumatoid arthritis in 16 scenarios, each featuring a combination of four factors (family history, daily alcohol intake, daily tobacco consumption and genetic test results). Participants considered all factors. Howeve…

  • Professionals’ Attitudes Regarding Large-Scale Genetic Information Generated Through Next Generation Sequencing in Research

    Open Access•Jane Miller, A Soulier et al.•ARTICLE•Journal of Empirical Research on…•2014

    Under the auspices of a multi-national European scientific project involving whole genome sequencing, GEUVADIS, we set out to investigate the attitudes of the participating scientists of having their own genome sequenced. The views of such researchers on this subject have not been fully explored before and we utilized questionnaires and discussion groups to elicit their opinions. Many said that it was the first time that they had an opportunity t…

  • Producing ‘Human Elements Based Medical Technologies’ in Biotech Companies

    Open Access•Virginie Tournay, Emmanuelle Rial-Sebbag et al.•ARTICLE•Science Technology and Society•2013

    This article is based on the findings of an EU-funded qualitative research project, entitled ‘From GMP to GBP: Fostering good bioethics practices [GBP] among the European biotechnology industry’, which seeks to improve the understanding of bioethical issues through the observation of the daily practices in European biotechnology companies and proposes a methodology approaching ethical issues. The comparative study was carried out in biotech compa…

  • Direct-to-consumer health genetic testing services

    Pascal Ducournau, Pierre-Antoine Gourraud et al.•ARTICLE•Health Sociology Review•2013•Citada por: 1•Referências: 4

    Online availability of direct-to-consumer health genetic testing services for various diseases and behavioural traits appears to have created a business dynamic since its beginning around the turn of the millennium. What are the marketing strategies implemented by the companies commercialising these tests and the social expectations they feed on? From a quantitative and qualitative analysis of the websites offering such tests for health, it appea…

  • Direct-to-consumerhealth genetic testing services

    Pascal Ducournau, P-A Gourraud et al.•ARTICLE•Health Sociology Review•2013

    Online availability of direct-to-consumer health genetic testing services for various diseases and behavioural traits appears to have created a business dynamic since its beginning around the turn of the millennium. What are the marketing strategies implemented by the companies commercialising these tests and the social expectations they feed on? From a quantitative and qualitative analysis of the websites offering such tests for health, it appea…

  • The Emergence of Biobanks in the Legal Landscape

    Open Access•Emmanuelle Rial‐Sebbag, Anne Cambon‐thomsen•ARTICLE•Journal of Law and Society•2012

    Biobanks are increasingly seen as new tools for medical research. Their main purpose is to collect, store, and distribute human body materials. These activities are regulated by legal instruments which are heterogeneous in source (national and international), and in form (binding and non‐binding). We analyse these to underline the need for a new model of governance for modern biobanks. The protection initially ensured by respect for fundamental r…

  • Public Health Genomics (PHG) and Public Participation

    Open Access•Denise Avard, Lucie M Bucci et al.•ARTICLE•Journal of Deliberative Democracy•2009

    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…

  • Judging health risk as a function of risk factors and type of illness

    Open Access•Myriam Guedj, Etienne Mullet et al.•ARTICLE•Journal of Health Psychology•2016•Citada por: 1•Referências: 34

    We examined the extent to which lay people and health professionals are able to assess occurrence risks for multifactorial diseases. We asked 341 participants to assess the risk of developing lung cancer, coronary artery disease or rheumatoid arthritis in 16 scenarios, each featuring a combination of four factors (family history, daily alcohol intake, daily tobacco consumption and genetic test results). Participants considered all factors. Howeve…

  • Direct-to-consumer health genetic testing services

    Pascal Ducournau, Pierre-Antoine Gourraud et al.•ARTICLE•Health Sociology Review•2013•Citada por: 1•Referências: 4

    Online availability of direct-to-consumer health genetic testing services for various diseases and behavioural traits appears to have created a business dynamic since its beginning around the turn of the millennium. What are the marketing strategies implemented by the companies commercialising these tests and the social expectations they feed on? From a quantitative and qualitative analysis of the websites offering such tests for health, it appea…

  • Public Health Genomics (PHG) and Public Participation

    Open Access•Denise Avard, Lucie M Bucci et al.•ARTICLE•Journal of Deliberative Democracy•2009

    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…

  • The Emergence of Biobanks in the Legal Landscape

    Open Access•Emmanuelle Rial‐Sebbag, Anne Cambon‐thomsen•ARTICLE•Journal of Law and Society•2012

    Biobanks are increasingly seen as new tools for medical research. Their main purpose is to collect, store, and distribute human body materials. These activities are regulated by legal instruments which are heterogeneous in source (national and international), and in form (binding and non‐binding). We analyse these to underline the need for a new model of governance for modern biobanks. The protection initially ensured by respect for fundamental r…

  • Producing ‘Human Elements Based Medical Technologies’ in Biotech Companies

    Open Access•Virginie Tournay, Emmanuelle Rial-Sebbag et al.•ARTICLE•Science Technology and Society•2013

    This article is based on the findings of an EU-funded qualitative research project, entitled ‘From GMP to GBP: Fostering good bioethics practices [GBP] among the European biotechnology industry’, which seeks to improve the understanding of bioethical issues through the observation of the daily practices in European biotechnology companies and proposes a methodology approaching ethical issues. The comparative study was carried out in biotech compa…

  • Direct-to-consumer health genetic testing services

    Pascal Ducournau, Pierre-Antoine Gourraud et al.•ARTICLE•Health Sociology Review•2013•Citada por: 1•Referências: 4

    Online availability of direct-to-consumer health genetic testing services for various diseases and behavioural traits appears to have created a business dynamic since its beginning around the turn of the millennium. What are the marketing strategies implemented by the companies commercialising these tests and the social expectations they feed on? From a quantitative and qualitative analysis of the websites offering such tests for health, it appea…

  • Direct-to-consumerhealth genetic testing services

    Pascal Ducournau, P-A Gourraud et al.•ARTICLE•Health Sociology Review•2013

    Online availability of direct-to-consumer health genetic testing services for various diseases and behavioural traits appears to have created a business dynamic since its beginning around the turn of the millennium. What are the marketing strategies implemented by the companies commercialising these tests and the social expectations they feed on? From a quantitative and qualitative analysis of the websites offering such tests for health, it appea…

  • Professionals’ Attitudes Regarding Large-Scale Genetic Information Generated Through Next Generation Sequencing in Research

    Open Access•Jane Miller, A Soulier et al.•ARTICLE•Journal of Empirical Research on…•2014

    Under the auspices of a multi-national European scientific project involving whole genome sequencing, GEUVADIS, we set out to investigate the attitudes of the participating scientists of having their own genome sequenced. The views of such researchers on this subject have not been fully explored before and we utilized questionnaires and discussion groups to elicit their opinions. Many said that it was the first time that they had an opportunity t…

  • From the arcane to the mundane

    Open Access•Alexandra Soulier, Samantha Leonard et al.•ARTICLE•New Genetics and Society•2016

    Genomic technologies are developing at a time when greater public involvement in research and clinical governance is sought. To this end, empirical bioethics studies, although conceptualized as academic endeavors, may draw on the inclusion of laypeople to justify informing policy. Doing so, they face similar concerns as those addressed to public consultations which cannot be termed democratic a priori and may reinforce the authority of experts. W…

  • Judging health risk as a function of risk factors and type of illness

    Open Access•Myriam Guedj, Etienne Mullet et al.•ARTICLE•Journal of Health Psychology•2016•Citada por: 1•Referências: 34

    We examined the extent to which lay people and health professionals are able to assess occurrence risks for multifactorial diseases. We asked 341 participants to assess the risk of developing lung cancer, coronary artery disease or rheumatoid arthritis in 16 scenarios, each featuring a combination of four factors (family history, daily alcohol intake, daily tobacco consumption and genetic test results). Participants considered all factors. Howeve…

  • How to responsibly acknowledge research work in the era of big data and biobanks

    Open Access•Heidi Howard, Heidi Carmen Howard et al.•ARTICLE•Journal of Community Genetics•2017

    Currently, a great deal of biomedical research in fields such as epidemiology, clinical trials and genetics is reliant on vast amounts of biological and phenotypic information collected and assembled in biobanks. While many resources are being invested to ensure that comprehensive and well-organised biobanks are able to provide increased access to, and sharing of biomedical samples and information, many barriers and challenges remain to such resp…

  • Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics

    Open Access•Michel Rosier, Myriam Guedj et al.•ARTICLE•Journal of Health Psychology•2021•Referências: 50

    Next-generation sequencing techniques enable unsolicited findings to be detected. This discovery raises ethical questions concerning the return of these findings. Our study aimed to highlight the views of the general public, patients under supervision and health professionals concerning the acceptability of disclosing unsolicited results to patients. In total, 449 participants assessed scenarios, consisted of all combinations of three factors (pa…

Biomedical Ethics and Regulation (8 obras) · Political science (8 obras) · Ethics in Clinical Research (7 obras) · Biology (6 obras) · Medicine (6 obras) · Law (5 obras) · Business (4 obras) · Engineering (4 obras) · Engineering ethics (4 obras) · Public relations (4 obras)

Ethnos_APP • Projeto Open Source • Licença MIT • Frontend v2.0.0 • Privacidade e Cookies • Documentação da API: api.ethnos.app/docs • Código da API: GitHub • DOI: 10.5281/zenodo.17049435 • Código do Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae