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A Content Analysis of 100 Qualitative Health Research Articles to Examine Researcher-Participant Relationships and Implications for Data Sharing

International journal of qualitative methods, 2022-05, Vol.21, p.160940692211050

2022

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Barriers and facilitators to qualitative data sharing in the United States: A survey of qualitative researchers

PloS one, 2021-12, Vol.16 (12), p.e0261719-e0261719

2021

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Core Functions of Communication in Pediatric Medicine: an Exploratory Analysis of Parent and Patient Narratives

Journal of cancer education, 2020-04, Vol.35 (2), p.256-263

2020

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Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?

Genome medicine, 2014-12, Vol.6 (12), p.121-121, Article 121

2014

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Results of Annual Screening in Phase I of the United Kingdom Familial Ovarian Cancer Screening Study Highlight the Need for Strict Adherence to Screening Schedule

Journal of clinical oncology, 2013-01, Vol.31 (1), p.49-57

2013

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Potentially Identifying Variables Reported in 100 Qualitative Health Research Articles: Implications for Data Sharing and Secondary Analysis

Forum, qualitative social research, 2023-05, Vol.24 (2), p.1-22

2023

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How do clinical research coordinators learn Good Clinical Practice? A mixed-methods study of factors that predict uptake of knowledge

Clinical trials (London, England), 2020-04, Vol.17 (2), p.166-175

2020

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Risky Genes: Genetics, Breast Cancer and Jewish Identity

Mozersky, Jessica

1, 2013

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Understanding the Use of Optimal Formatting and Plain Language When Presenting Key Information in Clinical Trials

Journal of empirical research on human research ethics, 2022-02, Vol.17 (1-2), p.177-192

2022

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Assessing clinical research coordinator knowledge of good clinical practice: An evaluation of the state of the art and a test validation study

Journal of clinical and translational science, 2020-04, Vol.4 (2), p.141-145

2020

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Responding to Sexual Abuse in Health Care: Development of a Guide for Patients

Journal of patient-centered research and reviews, 2022-01, Vol.9 (2), p.117-121

2022

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Seeing Beyond the Margins: Challenges to Informed Inclusion of Vulnerable Populations in Research

The Journal of law, medicine & ethics, 2018-03, Vol.46 (1), p.30-43

2018

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Validating curricular competencies in innovation and entrepreneurship for biomedical research trainees: A modified Delphi approach

Journal of clinical and translational science, 2019-08, Vol.3 (4), p.165-183

2019

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Attitudes toward genomics and precision medicine

Journal of clinical and translational science, 2021, Vol.5 (1), p.e120-e120, Article e120

2021

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“Use it or lose it” as an alternative approach to protect genetic privacy in personalized medicine

Urologic oncology, 2014-02, Vol.32 (2), p.198-201

2014

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Breast Cancer Gene Research and Medical Practices: Transnational Perspectives in the Time of BRCA

1, 2014

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How are US institutions implementing the new key information requirement?

Journal of clinical and translational science, 2020-08, Vol.4 (4), p.365-369

2020

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A randomized implementation trial to increase adoption of evidence-informed consent practices

Journal of clinical and translational science, 2023, Vol.7 (1), p.e28-e28, Article e28

2023

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4484 The Entrepreneurship for Biomedicine (E4B) Training Program

Journal of clinical and translational science, 2020-06, Vol.4 (s1), p.68-68

2020

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Comprehension of an Elevated Amyloid Positron Emission Tomography Biomarker Result by Cognitively Normal Older Adults

JAMA neurology, 2018-01, Vol.75 (1), p.44

2018

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Perceived barriers to assessing understanding and appreciation of informed consent in clinical trials: A mixed-method study

Journal of clinical and translational science, 2021, Vol.5 (1), p.e164-e164, Article e164

2021

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Who’s to blame? Accounts of genetic responsibility and blame among Ashkenazi Jewish women at risk of BRCA breast cancer

Sociology of health & illness, 2012-06, Vol.34 (5), p.776-790

Mozersky, Jessica

2012

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Are we ready to share qualitative research data? Knowledge and preparedness among qualitative researchers, IRB Members, and data repository curators

IASSIST quarterly, 2020-01, Vol.43 (4), p.1-23

2020

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Risky genes: genetics, breast cancer, and Jewish identity

Mozersky, Jessica

2013

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A Content Analysis of 100 Qualitative Health Research Articles to Examine Researcher-Participant Relationships and Implications for Data Sharing

Barriers and facilitators to qualitative data sharing in the United States: A survey of qualitative researchers

Core Functions of Communication in Pediatric Medicine: an Exploratory Analysis of Parent and Patient Narratives

Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?

Results of Annual Screening in Phase I of the United Kingdom Familial Ovarian Cancer Screening Study Highlight the Need for Strict Adherence to Screening Schedule

Potentially Identifying Variables Reported in 100 Qualitative Health Research Articles: Implications for Data Sharing and Secondary Analysis

How do clinical research coordinators learn Good Clinical Practice? A mixed-methods study of factors that predict uptake of knowledge

Risky Genes: Genetics, Breast Cancer and Jewish Identity

Understanding the Use of Optimal Formatting and Plain Language When Presenting Key Information in Clinical Trials

Assessing clinical research coordinator knowledge of good clinical practice: An evaluation of the state of the art and a test validation study

Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents

Responding to Sexual Abuse in Health Care: Development of a Guide for Patients

Seeing Beyond the Margins: Challenges to Informed Inclusion of Vulnerable Populations in Research

Validating curricular competencies in innovation and entrepreneurship for biomedical research trainees: A modified Delphi approach

Attitudes toward genomics and precision medicine

“Use it or lose it” as an alternative approach to protect genetic privacy in personalized medicine

Breast Cancer Gene Research and Medical Practices: Transnational Perspectives in the Time of BRCA

How are US institutions implementing the new key information requirement?

A randomized implementation trial to increase adoption of evidence-informed consent practices

4484 The Entrepreneurship for Biomedicine (E4B) Training Program

Comprehension of an Elevated Amyloid Positron Emission Tomography Biomarker Result by Cognitively Normal Older Adults

Perceived barriers to assessing understanding and appreciation of informed consent in clinical trials: A mixed-method study

Who’s to blame? Accounts of genetic responsibility and blame among Ashkenazi Jewish women at risk of BRCA breast cancer

Are we ready to share qualitative research data? Knowledge and preparedness among qualitative researchers, IRB Members, and data repository curators

Risky genes: genetics, breast cancer, and Jewish identity

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