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

artículo científico publicado en 2012

Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutation

artículo científico publicado en 2007

Clinical utility of cancer family history collection in primary care

artículo científico publicado en 2009

Collection and use of cancer family history in primary care.

artículo científico publicado en 2007

Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study

artículo científico publicado en 2013

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

artículo científico publicado en 2013

Family history and improving health

scientific article published on August 2009

GenetiKit: a randomized controlled trial to enhance delivery of genetics services by family physicians

artículo científico publicado en 2011

Genetic education for primary care providers: improving attitudes, knowledge, and confidence

artículo científico publicado en 2009

Genetics: Newborn screening for sickle cell anemia

artículo científico publicado en 2009

Genetics: factor V Leiden.

artículo científico publicado en 2010

Genetics: hereditary hemochromatosis

artículo científico publicado en 2009

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

artículo científico publicado en 2011

Hereditary breast and ovarian cancers

artículo científico publicado en 2008

Implementation science as a leadership capability to improve patient outcomes and value in healthcare

scientific article published on 25 August 2019

Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources

scientific article published on 21 November 2019

Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changes

artículo científico publicado en 2013

Multigene panels in prostate cancer risk assessment

artículo científico publicado en 2012

Multigene panels in prostate cancer risk assessment: a systematic review

artículo científico

Primary care role in expanded newborn screening: After the heel prick test

artículo científico publicado en 2013

Psychosocial Factors of Health Professionals' Intention to Use a Decision Aid for Down Syndrome Screening: Cross-Sectional Quantitative Study.

artículo científico publicado en 2018

Public views on participating in newborn screening using genome sequencing

artículo científico publicado en 2014

Role of Psychosocial Factors and Health Literacy in Pregnant Women's Intention to Use a Decision Aid for Down Syndrome Screening: A Theory-Based Web Survey

artículo científico publicado en 2016

Supporting genetics in primary care: investigating how theory can inform professional education

artículo científico publicado en 2016

Systematic review: family history in risk assessment for common diseases

artículo científico publicado en 2009

The Gene Messenger Impact Project: An Innovative Genetics Continuing Education Strategy for Primary Care Providers

artículo científico publicado en 2016

The current state of cancer family history collection tools in primary care: a systematic review

artículo científico publicado en 2009

Understanding sickle cell carrier status identified through newborn screening: a qualitative study.

artículo científico publicado en 2009

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