Lista de obras -

"Maybe they have found something new" participants' views on returning cohort psychosocial survey results

artículo científico publicado en 2014

"They should take time": Disclosure of clinical trial results as part of a social relationship

artículo científico publicado en 2012

Assessment of care by breast cancer patients participating or not participating in a randomized controlled trial: a report with the Patients' Committee for Clinical Trials of the Ligue Nationale Contre le Cancer

Awareness of acute myeloid leukaemia risk induced by diagnosis of a myelodysplastic syndrome

artículo científico publicado en 2016

BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis

artículo científico publicado en 2012

Behavioral and economic impact of a familial history of cancers.

artículo científico publicado en 2005

Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec

artículo científico publicado en 2011

Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilities

artículo científico publicado en 2013

Cancer risk management strategies and perceptions of unaffected women 5 years after predictive genetic testing for BRCA1/2 mutations ⬇️

artículo científico publicado el 26 de enero de 2011

Cancer survivors: familial risk perception and management advice given to their relatives.

artículo científico publicado en 2011

Cigarette smoking in women after BRCA1/2 genetic test disclosure: a 5-year follow-up study of the GENEPSO PS cohort

artículo científico publicado en 2014

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.

artículo científico publicado en 2010

Congress report of the seventh international meeting on psychosocial aspects of genetic testing for hereditary breast and/or ovarian cancer (HBOC) and hereditary non-polyposis colorectal cancer (HNPCC).

artículo científico publicado en 2002

Consent for biobanking: assessing the understanding and views of cancer patients

artículo científico publicado en 2010

Contributing to research via biobanks: what it means to cancer patients

artículo científico publicado en 2012

Cross-cultural validation of the Decisional Conflict Scale in a sample of French patients

artículo científico publicado en 2006

Development of a scale for assessing respondents' perceptions of health research questionnaires (the REP-HQ Scale).

artículo científico publicado en 2012

Diffusion of information about genetic risk within families.

artículo científico publicado en 1993

Disclosure of research results: a randomized study on GENEPSO-PS cohort participants

artículo científico publicado en 2015

Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden

artículo científico publicado en 2008

Effects of genetic consultation on perception of a family risk of breast/ovarian cancer and determinants of inaccurate perception after the consultation

scientific article published on 01 July 2002

France: genetics education for non-genetics health care providers

artículo científico publicado en 2006

General Practitioners and Breast Surgeons in France, Germany, Netherlands and the UK show variable breast cancer risk communication profiles

artículo científico publicado en 2015

General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers' practices

artículo científico publicado en 2010

Genetic education and nongenetic health professionals: educational providers and curricula in Europe

artículo científico publicado en 2005

Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany

artículo científico publicado en 2011

How to share results of clinical trials with study participants?

artículo científico publicado en 2012

Impact of BRCA1/2 mutation on young women's 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort).

artículo científico publicado en 2015

Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

artículo científico publicado en 2006

Impact of gene patents on the cost-effective delivery of care: the case of BRCA1 genetic testing

artículo científico publicado en 2003

International perspectives on genetic counseling and testing for breast cancer risk

artículo científico publicado en 2006

Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

artículo científico publicado en 2013

Parental disclosure of positive BRCA1/2 mutation status to children 10 years after genetic testing

artículo científico publicado en 2019

Patients' Non-Medical Characteristics Contribute to Collective Medical Decision-Making at Multidisciplinary Oncological Team Meetings.

artículo científico publicado en 2016

Patients' characteristics and rate of Internet use to obtain cancer information

artículo científico publicado en 2006

Patients' regrets after participating in a randomized controlled trials depended on their involvement in the decision making

artículo científico publicado en 2012

Professionals assess the acceptability of preimplantation genetic diagnosis and prenatal diagnosis for managing inherited predisposition to cancer

artículo científico publicado en 2009

Psychometric properties of a French version of a Dutch scale for assessing breast and body image (BBIS) in healthy women

artículo científico publicado en 2013

Risk communication strategies: state of the art and effectiveness in the context of cancer genetic services ⬇️

artículo científico publicado el 1 de octubre de 2003

Spontaneous disclosure of BRCA1/2 genetic test results to employers: a French prospective study ⬇️

artículo científico publicado el 29 de febrero de 2012

Testing for BRCA1 mutations: a cost-effectiveness analysis

artículo científico publicado en 2002

Testing participation in BRCA1/2-positive families: initiator role of index cases

artículo científico publicado en 2003

Testing the children: do non-genetic health-care providers differ in their decision to advise genetic presymptomatic testing on minors? A cross-sectional study in five countries in the European Union.

artículo científico publicado en 2009

The supply of breast/ovarian cancer genetic susceptibility tests in France

artículo científico publicado en 2004

Transparency in the presentation of trial results may not increase patients' trust in medical researchers.

artículo científico publicado en 2011

Uptake of genetic counseling among adult children of BRCA1/2 mutation carriers in France

scientific article published on 17 July 2019

Validation of a scale for assessing attitudes towards outcomes of genetic cancer testing among primary care providers and breast specialists

artículo científico publicado en 2017

What makes decision-making difficult for oncologists faced with critical situations? The socio-affective side of the physician-patient relationship

artículo científico publicado en 2018

Which factors predict proposal and uptake of psychological counselling after BRCA1/2 test result disclosure?

artículo científico publicado en 2013

Women's perceptions and experience of adjuvant tamoxifen therapy account for their adherence: breast cancer patients' point of view

artículo científico publicado en 2010

Lista de obras de

"Maybe they have found something new" participants' views on returning cohort psychosocial survey results

"They should take time": Disclosure of clinical trial results as part of a social relationship

Assessment of care by breast cancer patients participating or not participating in a randomized controlled trial: a report with the Patients' Committee for Clinical Trials of the Ligue Nationale Contre le Cancer

Awareness of acute myeloid leukaemia risk induced by diagnosis of a myelodysplastic syndrome

BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis

Behavioral and economic impact of a familial history of cancers.

Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec

Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilities

Cancer risk management strategies and perceptions of unaffected women 5 years after predictive genetic testing for BRCA1/2 mutations ⬇️

Cancer survivors: familial risk perception and management advice given to their relatives.

Cigarette smoking in women after BRCA1/2 genetic test disclosure: a 5-year follow-up study of the GENEPSO PS cohort

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.

Congress report of the seventh international meeting on psychosocial aspects of genetic testing for hereditary breast and/or ovarian cancer (HBOC) and hereditary non-polyposis colorectal cancer (HNPCC).

Consent for biobanking: assessing the understanding and views of cancer patients

Contributing to research via biobanks: what it means to cancer patients

Cross-cultural validation of the Decisional Conflict Scale in a sample of French patients

Development of a scale for assessing respondents' perceptions of health research questionnaires (the REP-HQ Scale).

Diffusion of information about genetic risk within families.

Disclosure of research results: a randomized study on GENEPSO-PS cohort participants

Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden

Effects of genetic consultation on perception of a family risk of breast/ovarian cancer and determinants of inaccurate perception after the consultation

France: genetics education for non-genetics health care providers

General Practitioners and Breast Surgeons in France, Germany, Netherlands and the UK show variable breast cancer risk communication profiles

General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers' practices

Genetic education and nongenetic health professionals: educational providers and curricula in Europe

Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany

How to share results of clinical trials with study participants?

Impact of BRCA1/2 mutation on young women's 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort).

Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

Impact of gene patents on the cost-effective delivery of care: the case of BRCA1 genetic testing

International perspectives on genetic counseling and testing for breast cancer risk

Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

Parental disclosure of positive BRCA1/2 mutation status to children 10 years after genetic testing

Patients' Non-Medical Characteristics Contribute to Collective Medical Decision-Making at Multidisciplinary Oncological Team Meetings.

Patients' characteristics and rate of Internet use to obtain cancer information

Patients' regrets after participating in a randomized controlled trials depended on their involvement in the decision making

Professionals assess the acceptability of preimplantation genetic diagnosis and prenatal diagnosis for managing inherited predisposition to cancer

Psychometric properties of a French version of a Dutch scale for assessing breast and body image (BBIS) in healthy women

Risk communication strategies: state of the art and effectiveness in the context of cancer genetic services ⬇️

Spontaneous disclosure of BRCA1/2 genetic test results to employers: a French prospective study ⬇️

Testing for BRCA1 mutations: a cost-effectiveness analysis

Testing participation in BRCA1/2-positive families: initiator role of index cases

Testing the children: do non-genetic health-care providers differ in their decision to advise genetic presymptomatic testing on minors? A cross-sectional study in five countries in the European Union.

The supply of breast/ovarian cancer genetic susceptibility tests in France

Transparency in the presentation of trial results may not increase patients' trust in medical researchers.

Uptake of genetic counseling among adult children of BRCA1/2 mutation carriers in France

Validation of a scale for assessing attitudes towards outcomes of genetic cancer testing among primary care providers and breast specialists

What makes decision-making difficult for oncologists faced with critical situations? The socio-affective side of the physician-patient relationship

Which factors predict proposal and uptake of psychological counselling after BRCA1/2 test result disclosure?

Women's perceptions and experience of adjuvant tamoxifen therapy account for their adherence: breast cancer patients' point of view