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Characterizing biobank organizations in the U.S.: results from a national survey

Genome medicine, 2013-01, Vol.5 (1), p.3-3

2013

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Attitudes About Analytic Treatment Interruption (ATI) in HIV Remission Trials with Different Antiretroviral Therapy (ART) Resumption Criteria

AIDS and behavior, 2022-05, Vol.26 (5), p.1504-1516

2022

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Public participation in human genome editing research governance: what do scientists think?

Journal of community genetics, 2024-02, Vol.15 (3), p.249-257

2024

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Development and validation of a measure of comprehension of genomic screening-negative results (CoG-NR)

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1394-1402

2020

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The View from the Benches: Scientists' Perspectives on the Uses and Governance of Human Gene-Editing Research

CRISPR journal, 2021-08, Vol.4 (4), p.609

2021

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Decision making for invasive and non-invasive optional procedures within an acute HIV research cohort in Bangkok

Contemporary clinical trials communications, 2023-02, Vol.31, p.101054-101054, Article 101054

2023

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"Forward-Thinking" in U.S. Biobanking

Genetic testing and molecular biomarkers, 2017-03, Vol.21 (3), p.148

2017

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Understanding Breastfeeding Initiation and Continuation in Rural Communities: A Combined Qualitative/Quantitative Approach

Maternal and child health journal, 2008-05, Vol.12 (3), p.402-414

2008

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Neglected ethical issues in biobank management: Results from a U.S. study

Life sciences, society and policy, 2013-12, Vol.9 (1), p.1-1, Article 1

2013

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Professionalism and Ethics: A Standardized Patient Observed Standardized Clinical Examination to Assess ACGME Pediatric Professionalism Milestones

MedEdPORTAL, 2020-01, Vol.16, p.10873-10873

2020

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Hospital Policies During COVID-19: An Analysis of Visitor Restrictions

Journal of public health management and practice, 2022-01, Vol.28 (1), p.E299

2022

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Am I a control?: Genotype-driven research recruitment and self-understandings of study participants

Genetics in medicine, 2012-12, Vol.14 (12), p.983-989

2012

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Community perceptions of genomic research: implications for addressing health disparities

North Carolina medical journal (Durham, N.C.), 2013-11, Vol.74 (6), p.470-476

2013

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Parallel but connected: Nuances of conducting behavioral and social science research alongside ethically challenging HIV remission trials

Contemporary clinical trials communications, 2020-09, Vol.19, p.100594-100594, Article 100594

2020

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The Promise and Reality of Public Engagement in the Governance of Human Genome Editing Research

American journal of bioethics, 2023-07, Vol.23 (7), p.9-16

2023

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Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review

Pharmacogenomics and personalized medicine, 2017-01, Vol.10, p.49-60

2017

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Reflections on ‘common’ genetic medical history questions: Time to examine the what, why, and how

Patient education and counseling, 2024-05, Vol.122, p.108190, Article 108190

2024

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Scientists' Views on Scientific Self-Governance for Human Genome Editing Research

Human gene therapy, 2022-11, Vol.33 (21-22), p.1157

2022

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The Meaning of Genetic Research Results: Reflections from Individuals With and Without a Known Genetic Disorder

Journal of empirical research on human research ethics, 2011-12, Vol.6 (4), p.30-40

2011

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"If It's Ethical During a Pandemic...": Lessons from COVID-19 for Post-Pandemic Biobanking

American journal of bioethics, 2021-12, Vol.21 (12), p.34-36

2021

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Returning negative results to individuals in a genomic screening program: lessons learned

Genetics in medicine, 2019-02, Vol.21 (2), p.409-416

2019

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Underutilization of specimens in biobanks: an ethical as well as a practical concern?

Genetics in medicine, 2014-10, Vol.16 (10), p.738-740

2014

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Advancing HIV research with pregnant women: navigating challenges and opportunities

AIDS (London), 2016-09, Vol.30 (15), p.2261-2265

2016

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Prepared patients: Internet information seeking by new rheumatology patients

Arthritis and rheumatism, 2008-04, Vol.59 (4), p.575-582

2008

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Symptoms of depression and their management among low-income African-American and White mothers in the rural South

Ethnicity & health, 2015-05, Vol.20 (3), p.293-308

2015

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Characterizing biobank organizations in the U.S.: results from a national survey

Attitudes About Analytic Treatment Interruption (ATI) in HIV Remission Trials with Different Antiretroviral Therapy (ART) Resumption Criteria

Public participation in human genome editing research governance: what do scientists think?

Development and validation of a measure of comprehension of genomic screening-negative results (CoG-NR)

The View from the Benches: Scientists' Perspectives on the Uses and Governance of Human Gene-Editing Research

Decision making for invasive and non-invasive optional procedures within an acute HIV research cohort in Bangkok

"Forward-Thinking" in U.S. Biobanking

Understanding Breastfeeding Initiation and Continuation in Rural Communities: A Combined Qualitative/Quantitative Approach

Neglected ethical issues in biobank management: Results from a U.S. study

Professionalism and Ethics: A Standardized Patient Observed Standardized Clinical Examination to Assess ACGME Pediatric Professionalism Milestones

Hospital Policies During COVID-19: An Analysis of Visitor Restrictions

Am I a control?: Genotype-driven research recruitment and self-understandings of study participants

Community perceptions of genomic research: implications for addressing health disparities

Parallel but connected: Nuances of conducting behavioral and social science research alongside ethically challenging HIV remission trials

The Promise and Reality of Public Engagement in the Governance of Human Genome Editing Research

Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review

Reflections on ‘common’ genetic medical history questions: Time to examine the what, why, and how

Scientists' Views on Scientific Self-Governance for Human Genome Editing Research

The Meaning of Genetic Research Results: Reflections from Individuals With and Without a Known Genetic Disorder

"If It's Ethical During a Pandemic...": Lessons from COVID-19 for Post-Pandemic Biobanking

Returning negative results to individuals in a genomic screening program: lessons learned

Underutilization of specimens in biobanks: an ethical as well as a practical concern?

Advancing HIV research with pregnant women: navigating challenges and opportunities

Prepared patients: Internet information seeking by new rheumatology patients

Symptoms of depression and their management among low-income African-American and White mothers in the rural South

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