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Lista de obras de Jessica P Bytautas

A prospective cohort study examining medical and social factors associated with engagement in life activities following total hip replacement.

artículo científico publicado en 2017

A scoping review of medical education research in family medicine

artículo científico publicado en 2015

A scoping review of online repositories of quality improvement projects, interventions and initiatives in healthcare

artículo científico publicado en 2016

Approaching a collaborative research agenda for health systems performance in circumpolar regions

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screening

article

Consent for newborn screening: the attitudes of health care providers.

artículo científico publicado en 2009

Do canadian researchers and the lay public prioritize biomedical research outcomes equally? A choice experiment

artículo científico publicado en 2013

Does a duty of disclosure foster special treatment of genetic research participants?

artículo científico publicado en 2013

Does the person's context influence engagement in life activities following primary knee replacement? Results from a Canadian prospective cohort study

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Genomic testing in cancer: patient knowledge, attitudes, and expectations

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Interoperable Electronic Health Records and Health Information Exchanges: Systematic Review

scientific article published on 06 June 2019

Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results

artículo científico publicado en 2011

One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants ⬇️

artículo científico publicado el 15 de febrero de 2012

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

artículo científico publicado en 2017

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care

artículo científico publicado en 2013

The primary care physician role in cancer genetics: a qualitative study of patient experience

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Understanding why people do or do not engage in activities following total joint replacement: a longitudinal qualitative study.

artículo científico publicado en 2015

What does 'respect for persons' require? Attitudes and reported practices of genetics researchers in informing research participants about research

artículo científico publicado en 2011

What is a meaningful result? Disclosing the results of genomic research in autism to research participants

artículo científico publicado en 2010

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