Search filters

List of works by Yvonne Bombard

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

scientific article published on 24 June 2024

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

scientific article published on 8 September 2016

An equity framework for health technology assessments

scientific article published on 7 November 2011

Assessing the impacts of citizen deliberations on the health technology process

scientific article published on 01 July 2013

Attitudes of Members of Genetics Professional Societies Toward Human Gene Editing

scientific article published on 01 October 2019

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

scientific article published on 06 September 2020

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

scientific article

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

scientific article published on January 23, 2013

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

scientific article published on 16 January 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

scientific article published in January 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

scientific article published on 08 March 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

scientific article published on 23 May 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

scientific article published on 23 March 2020

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

scientific article published on 26 April 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

scientific article published on February 2013

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

scientific article

Genetic testing and Huntington's disease: issues of employment

scientific article published in April 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?

scientific article published on 12 June 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

scientific article published on 21 August 2020

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

scientific article published on 9 November 2011

How digital tools can advance quality and equity in genomic medicine

scientific article published on 29 June 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

scientific article

Human Germline Genome Editing

scientific article

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

scientific article

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

scientific article

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.

scientific article published on 2 August 2016

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

scientific article

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

scientific article published on April 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

scientific article

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

scientific article published on 6 March 2017

Psychosocial effects of predictive testing for Huntington's disease.

scientific article

Public Perceptions of the Benefits and Risks of Newborn Screening

scientific article published on 13 July 2015

Public views on participating in newborn screening using genome sequencing

scientific article

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

scientific article published on 15 March 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

scientific article

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 ⬇️

scientific article published on February 29, 2012

Revealing the incidentalome when targeting the tumor genome

scientific article published on August 2013

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

The Genetic Discrimination Observatory: confronting novel issues in genetic discrimination

scientific article published in November 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

scientific article published in February 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

scientific article published on 23 July 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

scientific article

Translating genomics in cancer care

scientific article

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

scientific article published on 18 November 2015

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

scientific article

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

scientific article published on 01 October 2020

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

scientific article

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

scientific article published in November 2017

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

scientific article

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

scientific article published in 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

Paulina is supported by:

About Paulina

Help