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Jessica Bytautas

University of Toronto

H指数:21

被引数:1,134

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Differing Conceptualizations of the Goals of Care Discussion: A Critical Discourse Analysis

护理讨论目标的不同概念化: 批判性话语分析

JOURNAL OF PAIN AND SYMPTOM MANAGEMENT

IF3.5

2022-04-015

PRE

Modes of coordination for health technology adoption: Health Technology Assessment agencies and Group Procurement Organizations in a polycentric regulatory regime

卫生技术采用的协调模式: 多中心监管制度中的卫生技术评估机构和团体采购组织

SOCIAL SCIENCE & MEDICINE

IF5

2020-11-014

PREAI

Interoperable Electronic Health Records and Health Information Exchanges: Systematic Review

可互操作的电子健康记录和健康信息交换: 系统评价

JMIR MEDICAL INFORMATICS

IF3.8

2019-06-0624

OAAI

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

OSTEOARTHRITIS AND CARTILAGE

IF9

2017-07-015

PREAI

Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

JOURNAL OF PEDIATRICS

IF3.5

2017-05-0132

PREAI

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

IF6.4

2016-09-0129

OAAI

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

BMJ QUALITY & SAFETY

IF6.5

2016-04-206

PREAI

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

OSTEOARTHRITIS AND CARTILAGE

IF9

2015-06-0136

OAAI

Genomic Testing in Cancer Patient Knowledge, Attitudes, and Expectations

癌症患者知识，态度和期望的基因组测试

IF5.1

2014-06-2468

OAAI

CHALLENGES TO PARTICIPATION IN ACTIVITY FOLLOWING TOTAL JOINT REPLACEMENT: THE PERSON, THEIR HEALTH AND THEIR SOCIO-CULTURAL CONTEXT

OSTEOARTHRITIS AND CARTILAGE

IF9

2014-04-010

OA

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

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2013-07-1789

OA

Do Canadian Researchers and the Lay Public Prioritize Biomedical Research Outcomes Equally? A Choice Experiment

加拿大研究人员和公众是否平等地优先考虑生物医学研究成果？选择实验

ACADEMIC MEDICINE

IF5.2

2013-04-0115

OAAI

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

HEALTH EXPECTATIONS

IF3.2

2013-02-0128

OAAI

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

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2012-02-1516

OAAI

Citizens' Values Regarding Research With Stored Samples From Newborn Screening in Canada

IF6.4

2012-02-0141

PREAI

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

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2011-11-0918

OAAI

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

JOURNAL OF MEDICAL ETHICS

IF3.4

2011-06-1623

PREAI

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

并非如此简单: 研究人员如何裁定遗传研究结果的准实验研究

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2011-03-1623

OAAI

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

什么是有意义的结果？向研究参与者披露自闭症基因组研究的结果

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2010-03-1755

OAAI

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

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2009-10-0727

OAAI