Lista de obras -

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

artículo científico publicado en 2016

Academic family health teams: Part 1: patient perceptions of core primary care domains

artículo científico publicado en 2016

Academic family health teams: Part 2: patient perceptions of access

artículo científico publicado en 2016

Assessing family history of chronic disease in primary care: Prevalence, documentation, and appropriate screening

artículo científico publicado en 2017

Canadian Nursing in the Genomic Era: A Call for Leadership

article

Canadian nursing in the genomic era: a call for leadership

artículo científico publicado en 2005

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

artículo científico publicado en 2012

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

Educating women about breast cancer. An intervention for women with a family history of breast cancer.

artículo científico publicado en 2003

Effectiveness of screening with annual magnetic resonance imaging and mammography: results of the initial screen from the ontario high risk breast screening program

artículo científico publicado en 2014

Effectiveness of the Antenatal Psychosocial Health Assessment (ALPHA) form in detecting psychosocial concerns: a randomized controlled trial

artículo científico publicado en 2005

Establishing roles in genetic nursing: interviews with Canadian nurses.

artículo científico publicado en 2005

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 assessment wait time indicators in the High Risk Ontario Breast Screening Program

artículo científico publicado en 2018

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

artículo científico publicado en 2009

Genetic susceptibility to cancer. Family physicians' experience.

artículo científico publicado en 2003

Genetics: Alzheimer disease

artículo científico publicado en 2009

Genetics: Codeine metabolism.

artículo científico publicado en 2009

Genetics: Hypertrophic cardiomyopathy

artículo científico publicado en 2009

Genetics: Newborn screening for sickle cell anemia

artículo científico publicado en 2009

Genetics: Preimplantation genetic diagnosis

artículo científico publicado en 2010

Genetics: factor V Leiden.

artículo científico publicado en 2010

Genetics: familial melanoma.

artículo científico publicado en 2010

Genetics: hereditary hemochromatosis

artículo científico publicado en 2009

Genetics: newborn screening for MCAD deficiency.

artículo científico publicado en 2009

Genetics: prostate cancer

artículo científico publicado en 2009

Genetics: schizophrenia

artículo científico publicado en 2009

Genetics: type 2 diabetes

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

Hereditary colorectal cancer screening: A 10-year longitudinal cohort study following an educational intervention

artículo científico publicado en 2020

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

scientific article published on 21 November 2019

Interactive genetic counseling role-play: a novel educational strategy for family physicians.

artículo científico publicado en 2008

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

artículo científico publicado en 2013

Nursing and genetics

article

Pilot study of an information aid for women with a family history of breast cancer.

artículo científico publicado en 1999

Primary care providers' experiences with and perceptions of personalized genomic medicine

artículo científico publicado en 2016

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

artículo científico publicado en 2013

Public views on participating in newborn screening using genome sequencing

artículo científico publicado en 2014

Screening for asymptomatic bacteriuria in pregnancy

artículo científico publicado en 2005

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 Educational Needs and Professional Roles of Canadian Physicians and Nurses regarding Genetic Testing and Adult Onset Hereditary Disease

article

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

artículo científico publicado en 2016

The Use of the Antenatal Psychosocial Health Assessment (ALPHA) Tool in the Detection of Psychosocial Risk Factors for Postpartum Depression: A Randomized Controlled Trial

article

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

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

artículo científico publicado en 2016

Lista de obras de

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

Academic family health teams: Part 1: patient perceptions of core primary care domains

Academic family health teams: Part 2: patient perceptions of access

Assessing family history of chronic disease in primary care: Prevalence, documentation, and appropriate screening

Canadian Nursing in the Genomic Era: A Call for Leadership

Canadian nursing in the genomic era: a call for leadership

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

Clinical utility of cancer family history collection in primary care

Collection and use of cancer family history in primary care.

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

Educating women about breast cancer. An intervention for women with a family history of breast cancer.

Effectiveness of screening with annual magnetic resonance imaging and mammography: results of the initial screen from the ontario high risk breast screening program

Effectiveness of the Antenatal Psychosocial Health Assessment (ALPHA) form in detecting psychosocial concerns: a randomized controlled trial

Establishing roles in genetic nursing: interviews with Canadian nurses.

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

Family history and improving health

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

Genetic assessment wait time indicators in the High Risk Ontario Breast Screening Program

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

Genetic susceptibility to cancer. Family physicians' experience.

Genetics: Alzheimer disease

Genetics: Codeine metabolism.

Genetics: Hypertrophic cardiomyopathy

Genetics: Newborn screening for sickle cell anemia

Genetics: Preimplantation genetic diagnosis

Genetics: factor V Leiden.

Genetics: familial melanoma.

Genetics: hereditary hemochromatosis

Genetics: newborn screening for MCAD deficiency.

Genetics: prostate cancer

Genetics: schizophrenia

Genetics: type 2 diabetes

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

Hereditary breast and ovarian cancers

Hereditary colorectal cancer screening: A 10-year longitudinal cohort study following an educational intervention

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

Interactive genetic counseling role-play: a novel educational strategy for family physicians.

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

Nursing and genetics

Pilot study of an information aid for women with a family history of breast cancer.

Primary care providers' experiences with and perceptions of personalized genomic medicine

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

Public views on participating in newborn screening using genome sequencing

Screening for asymptomatic bacteriuria in pregnancy

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

Systematic review: family history in risk assessment for common diseases

The Educational Needs and Professional Roles of Canadian Physicians and Nurses regarding Genetic Testing and Adult Onset Hereditary Disease

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

The Use of the Antenatal Psychosocial Health Assessment (ALPHA) Tool in the Detection of Psychosocial Risk Factors for Postpartum Depression: A Randomized Controlled Trial

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

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

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