Co-Authors
This is a "connection" page, showing publications co-authored by AMY MCGUIRE and MARY MAJUMDER.
Connection Strength
9.013
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Large-scale genotype prediction from RNA sequence data necessitates a new ethical and policy framework. Nat Genet. 2024 Aug; 56(8):1537-1540.
Score: 0.988
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Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation. J Pers Med. 2021 Jul 08; 11(7).
Score: 0.799
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Direct-to-Consumer Genetic Testing: Value and Risk. Annu Rev Med. 2021 01 27; 72:151-166.
Score: 0.749
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Data Sharing in the Context of Health-Related Citizen Science. J Law Med Ethics. 2020 03; 48(1_suppl):167-177.
Score: 0.728
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Sharing data under the 21st Century Cures Act. Genet Med. 2017 12; 19(12):1289-1294.
Score: 0.601
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Beyond Our Borders? Public Resistance to Global Genomic Data Sharing. PLoS Biol. 2016 Nov; 14(11):e2000206.
Score: 0.578
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Two cheers for GINA? Genome Med. 2009 Jan 20; 1(1):6.
Score: 0.337
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Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi. J Law Biosci. 2023 Jul-Dec; 10(2):lsad022.
Score: 0.230
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Fresh takes on five health data sharing domains: Quality, privacy, equity, incentives, and sustainability. Front Big Data. 2023; 6:1095119.
Score: 0.223
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Family secrets: Experiences and outcomes of participating in direct-to-consumer genetic relative-finder services. Am J Hum Genet. 2022 03 03; 109(3):486-497.
Score: 0.209
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Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project. Genet Med. 2020 12; 22(12):2003-2010.
Score: 0.188
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Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs? BMC Med Ethics. 2019 11 21; 20(1):84.
Score: 0.178
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Learning Health System - Moving from Ethical Frameworks to Practical Implementation. J Law Med Ethics. 2019 09; 47(3):454-458.
Score: 0.176
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Introduction: Sharing Data in a Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):7-11.
Score: 0.170
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Genomic Data-Sharing Practices. J Law Med Ethics. 2019 03; 47(1):31-40.
Score: 0.170
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Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):12-20.
Score: 0.170
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Characterizing the Biomedical Data-Sharing Landscape. J Law Med Ethics. 2019 03; 47(1):21-30.
Score: 0.170
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Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):70-87.
Score: 0.170
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Citizen science, public policy. Science. 2018 07 13; 361(6398):134-136.
Score: 0.162
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Creating a data resource: what will it take to build a medical information commons? Genome Med. 2017 09 22; 9(1):84.
Score: 0.154
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Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions. Per Med. 2017; 14(4):339-354.
Score: 0.151
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Myriad take two: Can genomic databases remain secret? Science. 2017 05 12; 356(6338):586-587.
Score: 0.150
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The ethics of conducting molecular autopsies in cases of sudden death in the young. Genome Res. 2016 09; 26(9):1165-9.
Score: 0.141
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Ethical and Legal Challenges Associated with Public Molecular Autopsies. J Law Med Ethics. 2016 06; 44(2):309-18.
Score: 0.140
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Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel. Appl Transl Genom. 2016 Sep; 10:19-24.
Score: 0.140
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Developing context-specific next-generation sequencing policy. Nat Biotechnol. 2016 05 06; 34(5):466-70.
Score: 0.140
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Persistent confusion and controversy surrounding gene patents. Nat Biotechnol. 2016 Feb; 34(2):145-7.
Score: 0.137
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Cultivating Administrative Support for a Clinical Ethics Consultation Service. J Clin Ethics. 2016; 27(4):341-351.
Score: 0.136
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Legal Barriers to Adolescent Participation in Research About HIV and Other Sexually Transmitted Infections. Am J Public Health. 2016 Jan; 106(1):40-4.
Score: 0.135
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Taking DNA from the dead. Nat Rev Genet. 2010 May; 11(5):318.
Score: 0.091
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The ethics of lawyer-ethicists. J Law Med Ethics. 2005; 33(3):603-7.
Score: 0.064
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Genomic sequencing research in pediatric cancer care: Decision making, attitudes, and perceived utility among adolescents and young adults and their parents. Genet Med. 2024 Aug; 26(8):101168.
Score: 0.061
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Families' experiences accessing care after genomic sequencing in the pediatric cancer context: "It's just been a big juggle". J Genet Couns. 2024 Jan 15.
Score: 0.059
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Benefits of sharing neurophysiology data from the BRAIN Initiative Research Opportunities in Humans Consortium. Neuron. 2023 Dec 06; 111(23):3710-3715.
Score: 0.059
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Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research. J Adolesc Young Adult Oncol. 2023 10; 12(5):773-781.
Score: 0.055
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Neuroethics at 15: Keep the Kant but Add More Bacon. AJOB Neurosci. 2019 Jul-Sep; 10(3):97-100.
Score: 0.043
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What is a Medical Information Commons? J Law Med Ethics. 2019 03; 47(1):41-50.
Score: 0.042
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Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents. Patient Educ Couns. 2019 04; 102(4):680-686.
Score: 0.042
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Constraints on gene patent protection fuel secrecy concerns: a qualitative study. J Law Biosci. 2017 Dec; 4(3):542-564.
Score: 0.039
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Do privacy and security regulations need a status update? Perspectives from an intergenerational survey. PLoS One. 2017; 12(9):e0184525.
Score: 0.038