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Stakeholder engagement in policy development: challenges and opportunities for human genomics

Genetics in medicine, 2015-12, Vol.17 (12), p.949-957

2015

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Digital health-enabled genomics: Opportunities and challenges

American journal of human genetics, 2022-07, Vol.109 (7), p.1190-1198

2022

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Perceived benefits and barriers to implementing precision preventive care: Results of a national physician survey

European journal of human genetics : EJHG, 2023-11, Vol.31 (11), p.1309-1316

2023

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Addressing underrepresentation in genomics research through community engagement

American journal of human genetics, 2022-09, Vol.109 (9), p.1563-1571

2022

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Primary care physician use of patient race and polygenic risk scores in medical decision-making

Genetics in medicine, 2023-04, Vol.25 (4), p.100800-100800, Article 100800

2023

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Biobank participation and returning research results: Perspectives from a deliberative engagement in South Side Chicago

American journal of medical genetics. Part A, 2012-05, Vol.158A (5), p.1029-1037

2012

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Implementing Primary Care Mediated Population Genetic Screening Within an Integrated Health System

Journal of the American Board of Family Medicine, 2021-07, Vol.34 (4), p.861-865

2021

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Patient perspectives following pharmacogenomics results disclosure in an integrated health system

Pharmacogenomics, 2018-03, Vol.19 (4), p.321-331

2018

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Collaborative Counseling Considerations for Pharmacogenomic Tests

Pharmacotherapy, 2017-09, Vol.37 (9), p.990-999

2017

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Patient-Reported Outcomes and Experiences with Population Genetic Testing Offered Through a Primary Care Network

Genetic testing and molecular biomarkers, 2021-02, Vol.25 (2), p.152-160

2021

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Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population

Genetics in medicine, 2009-11, Vol.11 (11), p.783-789

2009

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Assessing Vietnamese American patient perspectives on population genetic testing in primary care: A community-engaged approach

HGG advances, 2022-10, Vol.3 (4), p.100134-100134, Article 100134

2022

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Data from a national survey of United States primary care physicians on genetic risk scores for common disease prevention

Data in brief, 2024-02, Vol.52, p.109930-109930, Article 109930

2024

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“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation

Public health genomics, 2022-05, Vol.25 (3-4), p.98-107

2022

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Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment

Journal of community genetics, 2020-07, Vol.11 (3), p.339-350

2020

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Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment

Journal of personalized medicine, 2020-10, Vol.10 (4), p.165

2020

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Primary care physician experiences with integrated pharmacogenomic testing in a community health system

Personalized medicine, 2017-09, Vol.14 (5), p.389-400

2017

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Ethical and Legal Issues Surrounding Genetic Testing in the NICU

Neoreviews (Elk Grove Village, Ill.), 2024-03, Vol.25 (3), p.e127-e138

2024

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Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

Genetics in medicine, 2010-10, Vol.12 (10), p.616-620

2010

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Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit

Ethics & human research, 2024-01, Vol.46 (1), p.43-48

2024

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Genetics researchers’ and IRB professionals’ attitudes toward genetic research review: a comparative analysis

Genetics in medicine, 2012-02, Vol.14 (2), p.236-242

2012

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Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit

Journal of personalized medicine, 2023-06, Vol.13 (7), p.1026

2023

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Sources of Intergenerational Conflict in Chinese Immigrant Families in the United States

Journal of family issues, 2022-09, Vol.43 (9), p.2275-2294

2022

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Patient Care Situations Benefiting from Pharmacogenomic Testing

Current genetic medicine reports, 2018-06, Vol.6 (2), p.43-51

2018

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Attitudes Toward Genetic Research Review: Results from a National Survey of Professionals Involved in Human Subjects Protection

Journal of empirical research on human research ethics, 2010-03, Vol.5 (1), p.83-92

2010

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Stakeholder engagement in policy development: challenges and opportunities for human genomics

Digital health-enabled genomics: Opportunities and challenges

Perceived benefits and barriers to implementing precision preventive care: Results of a national physician survey

Addressing underrepresentation in genomics research through community engagement

Primary care physician use of patient race and polygenic risk scores in medical decision-making

Biobank participation and returning research results: Perspectives from a deliberative engagement in South Side Chicago

Implementing Primary Care Mediated Population Genetic Screening Within an Integrated Health System

Patient perspectives following pharmacogenomics results disclosure in an integrated health system

Collaborative Counseling Considerations for Pharmacogenomic Tests

Patient-Reported Outcomes and Experiences with Population Genetic Testing Offered Through a Primary Care Network

Evaluation of a breast/ovarian cancer genetics referral screening tool in a mammography population

Assessing Vietnamese American patient perspectives on population genetic testing in primary care: A community-engaged approach

Data from a national survey of United States primary care physicians on genetic risk scores for common disease prevention

“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation

Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment

Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment

Primary care physician experiences with integrated pharmacogenomic testing in a community health system

Ethical and Legal Issues Surrounding Genetic Testing in the NICU

Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit

Genetics researchers’ and IRB professionals’ attitudes toward genetic research review: a comparative analysis

Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit

Sources of Intergenerational Conflict in Chinese Immigrant Families in the United States

Patient Care Situations Benefiting from Pharmacogenomic Testing

Attitudes Toward Genetic Research Review: Results from a National Survey of Professionals Involved in Human Subjects Protection

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