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Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies

The Hastings Center report, 2018-07, Vol.48 (S2), p.S2-S6

2018

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Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

The Journal of law, medicine & ethics, 2008-06, Vol.36 (2), p.219-248

2008

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Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.70-87

2019

Volltextzugriff (PDF)

Have We Asked Too Much of Consent?

The Hastings Center report, 2014-07, Vol.44 (4), p.33-34

Koenig, Barbara A.

2014

Volltextzugriff (PDF)

Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.464-475

2015

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Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.486-501

2015

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Preference for secondary findings in prenatal and pediatric exome sequencing

Prenatal diagnosis, 2022-05, Vol.42 (6), p.753-761

2022

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Addiction science, meet translational genomics

Addiction (Abingdon, England), 2012-12, Vol.107 (12), p.2079-2080

Koenig, Barbara A.

2012

Volltextzugriff (PDF)

A Multicenter Comparison of Complementary and Alternative Medicine (CAM) Discussions in Oncology Care: The Role of Time, Patient‐Centeredness, and Practice Context

The oncologist (Dayton, Ohio), 2019-11, Vol.24 (11), p.e1180-e1189

2019

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Physician Perception of Pay Fairness and its Association with Work Satisfaction, Intent to Leave Practice, and Personal Health

Journal of general internal medicine : JGIM, 2018-06, Vol.33 (6), p.812-817

2018

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Characterizing the Biomedical Data-Sharing Landscape

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.21-30

2019

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Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.440-463

2015

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Framing Nicotine Addiction as a "Disease of the Brain": Social and Ethical Consequences

Social science quarterly, 2011-12, Vol.92 (5), p.1363-1388

2011

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Consumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience

The Milbank quarterly, 2017-06, Vol.95 (2), p.291-318

2017

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'To prove this is the industry's best hope': big tobacco's support of research on the genetics of nicotine addiction

Addiction (Abingdon, England), 2010-06, Vol.105 (6), p.974-983

2010

Volltextzugriff (PDF)

The Role of Participants in a Medical Information Commons

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.51-61

2019

Volltextzugriff (PDF)

Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.12-20

2019

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Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants

The Journal of law, medicine & ethics, 2018-03, Vol.46 (1), p.87-109

2018

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Participant Engagement in Translational Genomics Research: Respect for Persons—and Then Some

Ethics & human research, 2019-09, Vol.41 (5), p.2-15

2019

Volltextzugriff (PDF)

EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of California

Clinical and translational science, 2015-08, Vol.8 (4), p.362-366

2015

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Motivations for physician-assisted suicide: Patient and family voices

Journal of general internal medicine : JGIM, 2005-03, Vol.20 (3), p.234-239

2005

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World Health Organization (WHO) guideline on the complementary feeding of infants and young children aged 6−23 months 2023: A multisociety response

Journal of pediatric gastroenterology and nutrition, 2024-07, Vol.79 (1), p.181-188

2024

Volltextzugriff (PDF)

Return of individual results in epilepsy genomic research: A view from the field

Epilepsia (Copenhagen), 2018-09, Vol.59 (9), p.1635-1642

2018

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Another Voice: Have We Asked Too Much of Consent?

The Hastings Center report, 2014-07, Vol.44 (4), p.33-34

KOENIG, BARBARA A.

2014

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Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies

Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons

Have We Asked Too Much of Consent?

Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank

Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide

Preference for secondary findings in prenatal and pediatric exome sequencing

Addiction science, meet translational genomics

A Multicenter Comparison of Complementary and Alternative Medicine (CAM) Discussions in Oncology Care: The Role of Time, Patient‐Centeredness, and Practice Context

Physician Perception of Pay Fairness and its Association with Work Satisfaction, Intent to Leave Practice, and Personal Health

Characterizing the Biomedical Data-Sharing Landscape

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

Framing Nicotine Addiction as a "Disease of the Brain": Social and Ethical Consequences

Consumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience

'To prove this is the industry's best hope': big tobacco's support of research on the genetics of nicotine addiction

The Role of Participants in a Medical Information Commons

Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons

Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants

Participant Engagement in Translational Genomics Research: Respect for Persons—and Then Some

EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of California

Motivations for physician-assisted suicide: Patient and family voices

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience

World Health Organization (WHO) guideline on the complementary feeding of infants and young children aged 6−23 months 2023: A multisociety response

Return of individual results in epilepsy genomic research: A view from the field

Another Voice: Have We Asked Too Much of Consent?

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