Lista de obras -

A proposal for an inclusive working definition of genetic discrimination to promote a more coherent debate

artículo científico publicado en 2024

A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis

artículo científico publicado en 2016

An equity framework for health technology assessments

artículo científico publicado en 2011

Assessing the impacts of citizen deliberations on the health technology process

artículo científico publicado en 2013

Attitudes of Members of Genetics Professional Societies Toward Human Gene Editing

artículo científico publicado en 2019

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings

artículo científico publicado en 2020

Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease

artículo científico publicado en 2012

Citizens' perspectives on personalized medicine: a qualitative public deliberation study

artículo científico publicado en 2013

Citizens' values regarding research with stored samples from newborn screening in Canada

artículo científico publicado en 2012

Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis

scientific article published on 14 September 2020

Confronting New Issues in Genetic Discrimination

artículo científico publicado en 2021

Correction: Variant classification changes over time in BRCA1 and BRCA2

scientific article published on 01 October 2019

Development of patient "profiles" to tailor counseling for incidental genomic sequencing results

artículo científico publicado en 2019

Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

scientific article published on 11 December 2019

Eliciting ethical and social values in health technology assessment: A participatory approach

artículo científico publicado en 2011

Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease ⬇️

scientific article published on 24 October 2007

Engaging patients to improve quality of care: a systematic review

scholarly article by Yvonne Bombard et al published 26 July 2018 in Implementation Science

Establishing the International Genetic Discrimination Observatory

artículo científico publicado en 2020

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.

artículo científico publicado en 2018

Evaluation of the impact of patient involvement in health technology assessments: A scoping review

scientific article published on 08 May 2020

Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study

scientific article published on 24 June 2020

Expectations and values about expanded newborn screening: a public engagement study

artículo científico publicado en 2013

Factors associated with experiences of genetic discrimination among individuals at risk for Huntington disease

artículo científico publicado en 2010

Genetic testing and Huntington's disease: issues of employment

artículo científico publicado en 2004

Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing

scholarly article

Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?

artículo científico publicado en 2018

Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial

scientific article published on 07 October 2019

Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment

artículo científico publicado en 2020

Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

artículo científico publicado en 2011

How digital tools can advance quality and equity in genomic medicine

artículo científico publicado en 2020

How do women trade-off benefits and risks in chemotherapy treatment decisions based on gene expression profiling for early-stage breast cancer? A discrete choice experiment

artículo científico publicado en 2016

Human Germline Genome Editing

artículo científico publicado en 2017

Implementation of serological and molecular tools to inform COVID-19 patient management: protocol for the GENCOV prospective cohort study

publication published on 30 September 2021

In their own words: reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND-HD study

artículo científico publicado en 2010

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

artículo científico publicado en 2015

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

article

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

Parent Experience With False-Positive Newborn Screening Results for Cystic Fibrosis.

artículo científico publicado en 2016

Perception, experience, and response to genetic discrimination in Huntington disease: the international RESPOND-HD study

artículo científico publicado en 2010

Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease

artículo científico publicado en 2008

Perceptions of genetic discrimination among people at risk for Huntington's disease: a cross sectional survey

scientific article published on 09 June 2009

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

artículo científico publicado en 2015

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

article published in 2015

Primary care provider perspectives on using genomic sequencing in the care of healthy children

scientific article published on 05 December 2019

Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

artículo científico publicado en 2017

Psychosocial effects of predictive testing for Huntington's disease.

artículo científico publicado en 2005

Public Perceptions of the Benefits and Risks of Newborn Screening

artículo científico publicado en 2015

Public views on participating in newborn screening using genome sequencing

artículo científico publicado en 2014

Q-SEA - a tool for quality assessment of ethics analyses conducted as part of health technology assessments.

artículo científico publicado en 2017

Quality of life drives patients' preferences for secondary findings from genomic sequencing

scientific article published on 18 May 2020

Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening

artículo científico publicado en 2010

Recontacting clinical genetics patients with reclassified results: equity and policy challenges

scientific article published on 01 April 2019

Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics

artículo científico publicado en 2012

Revealing the incidentalome when targeting the tumor genome

artículo científico publicado en 2013

Risks to Relatives in Genomic Research: A Duty to Warn?

The Genetic Discrimination Observatory: confronting novel issues in genetic discrimination

artículo científico publicado en 2021

The Genetic Non-Discrimination Act: critical for promoting health and science in Canada

scientific article published on 01 May 2018

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

artículo científico publicado en 2018

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results

scientific article published on 01 April 2019

The clinical application of gene editing: ethical and social issues

artículo científico publicado en 2019

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

The influence of gene expression profiling on decisional conflict in decision making for early-stage breast cancer chemotherapy

article

The value of personalizing medicine: medical oncologists' views on gene expression profiling in breast cancer treatment

artículo científico publicado en 2015

Translating genomics in cancer care

artículo científico publicado en 2013

Translating personalized genomic medicine into clinical practice: evidence, values, and health policy

artículo científico publicado en 2015

Universal tumor screening for Lynch syndrome: health-care providers' perspectives.

artículo científico publicado en 2016

Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders' perspectives

artículo científico publicado en 2020

Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options

artículo científico publicado en 2016

Variant classification changes over time in BRCA1 and BRCA2

scientific article published on 11 April 2019

What do we do now?: Responding to claims of germline gene editing in humans

scientific article published on 27 March 2019

What's Involved with Wanting to Be Involved? Comparing Expectations for Public Engagement in Health Policy across Research and Care Contexts

artículo científico publicado en 2017

When they hear what we say: ethical challenges in presenting research findings to the Huntington disease community

artículo científico publicado en 2011

eP392: A comprehensive genomic test reporting structure for communicating cancer and incidental findings

artículo científico publicado en 2022

“I don’t need any more unknowns hanging over my head”: Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing

Lista de obras de

A proposal for an inclusive working definition of genetic discrimination to promote a more coherent debate

A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis

An equity framework for health technology assessments

Assessing the impacts of citizen deliberations on the health technology process

Attitudes of Members of Genetics Professional Societies Toward Human Gene Editing

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings

Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease

Citizens' perspectives on personalized medicine: a qualitative public deliberation study

Citizens' values regarding research with stored samples from newborn screening in Canada

Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis

Confronting New Issues in Genetic Discrimination

Correction: Variant classification changes over time in BRCA1 and BRCA2

Development of patient "profiles" to tailor counseling for incidental genomic sequencing results

Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

Eliciting ethical and social values in health technology assessment: A participatory approach

Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease ⬇️

Engaging patients to improve quality of care: a systematic review

Establishing the International Genetic Discrimination Observatory

Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.

Evaluation of the impact of patient involvement in health technology assessments: A scoping review

Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study

Expectations and values about expanded newborn screening: a public engagement study

Factors associated with experiences of genetic discrimination among individuals at risk for Huntington disease

Genetic testing and Huntington's disease: issues of employment

Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing

Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?

Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial

Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment

Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

How digital tools can advance quality and equity in genomic medicine

How do women trade-off benefits and risks in chemotherapy treatment decisions based on gene expression profiling for early-stage breast cancer? A discrete choice experiment

Human Germline Genome Editing

Implementation of serological and molecular tools to inform COVID-19 patient management: protocol for the GENCOV prospective cohort study

In their own words: reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND-HD study

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

Parent Experience With False-Positive Newborn Screening Results for Cystic Fibrosis.

Perception, experience, and response to genetic discrimination in Huntington disease: the international RESPOND-HD study

Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease

Perceptions of genetic discrimination among people at risk for Huntington's disease: a cross sectional survey

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

Primary care provider perspectives on using genomic sequencing in the care of healthy children

Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

Psychosocial effects of predictive testing for Huntington's disease.

Public Perceptions of the Benefits and Risks of Newborn Screening

Public views on participating in newborn screening using genome sequencing

Q-SEA - a tool for quality assessment of ethics analyses conducted as part of health technology assessments.

Quality of life drives patients' preferences for secondary findings from genomic sequencing

Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening

Recontacting clinical genetics patients with reclassified results: equity and policy challenges

Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics

Revealing the incidentalome when targeting the tumor genome

Risks to Relatives in Genomic Research: A Duty to Warn?

The Genetic Discrimination Observatory: confronting novel issues in genetic discrimination

The Genetic Non-Discrimination Act: critical for promoting health and science in Canada

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results

The clinical application of gene editing: ethical and social issues

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

The influence of gene expression profiling on decisional conflict in decision making for early-stage breast cancer chemotherapy

The value of personalizing medicine: medical oncologists' views on gene expression profiling in breast cancer treatment

Translating genomics in cancer care

Translating personalized genomic medicine into clinical practice: evidence, values, and health policy

Universal tumor screening for Lynch syndrome: health-care providers' perspectives.

Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders' perspectives

Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options

Variant classification changes over time in BRCA1 and BRCA2

What do we do now?: Responding to claims of germline gene editing in humans

What's Involved with Wanting to Be Involved? Comparing Expectations for Public Engagement in Health Policy across Research and Care Contexts

When they hear what we say: ethical challenges in presenting research findings to the Huntington disease community

eP392: A comprehensive genomic test reporting structure for communicating cancer and incidental findings

“I don’t need any more unknowns hanging over my head”: Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing