Connection

AMY MCGUIRE to Information Dissemination

This is a "connection" page, showing publications AMY MCGUIRE has written about Information Dissemination.
Connection Strength

7.303
  1. Data Sharing in the Context of Health-Related Citizen Science. J Law Med Ethics. 2020 03; 48(1_suppl):167-177.
    View in: PubMed
    Score: 0.559
  2. Introduction: Sharing Data in a Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):7-11.
    View in: PubMed
    Score: 0.522
  3. Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):12-20.
    View in: PubMed
    Score: 0.522
  4. Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons. J Law Med Ethics. 2019 03; 47(1):70-87.
    View in: PubMed
    Score: 0.522
  5. Who Owns the Data in a Medical Information Commons? J Law Med Ethics. 2019 03; 47(1):62-69.
    View in: PubMed
    Score: 0.522
  6. Creating a data resource: what will it take to build a medical information commons? Genome Med. 2017 09 22; 9(1):84.
    View in: PubMed
    Score: 0.472
  7. Sharing data under the 21st Century Cures Act. Genet Med. 2017 12; 19(12):1289-1294.
    View in: PubMed
    Score: 0.462
  8. Moving beyond Bermuda: sharing data to build a medical information commons. Genome Res. 2017 06; 27(6):897-901.
    View in: PubMed
    Score: 0.457
  9. Beyond Our Borders? Public Resistance to Global Genomic Data Sharing. PLoS Biol. 2016 Nov; 14(11):e2000206.
    View in: PubMed
    Score: 0.444
  10. Participants' recall and understanding of genomic research and large-scale data sharing. J Empir Res Hum Res Ethics. 2013 Oct; 8(4):42-52.
    View in: PubMed
    Score: 0.359
  11. Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives. Public Health Genomics. 2012; 15(2):106-14.
    View in: PubMed
    Score: 0.318
  12. To share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011 Nov; 13(11):948-55.
    View in: PubMed
    Score: 0.314
  13. Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience. Genome Res. 2011 Jul; 21(7):1001-7.
    View in: PubMed
    Score: 0.305
  14. Genetics. No longer de-identified. Science. 2006 Apr 21; 312(5772):370-1.
    View in: PubMed
    Score: 0.214
  15. The BRAIN Initiative data-sharing ecosystem: Characteristics, challenges, benefits, and opportunities. Elife. 2024 Nov 27; 13.
    View in: PubMed
    Score: 0.194
  16. "A Double-Edged Sword": A Brief History of Genomic Data Governance and Genetic Researcher Perspectives on Data Sharing. J Law Med Ethics. 2024; 52(2):399-411.
    View in: PubMed
    Score: 0.193
  17. "Extremely slow and capricious": A qualitative exploration of genetic researcher priorities in selecting shared data resources. Genet Med. 2023 01; 25(1):115-124.
    View in: PubMed
    Score: 0.169
  18. How NFTs could transform health information exchange. Science. 2022 02 04; 375(6580):500-502.
    View in: PubMed
    Score: 0.160
  19. Genomic Data-Sharing Practices. J Law Med Ethics. 2019 03; 47(1):31-40.
    View in: PubMed
    Score: 0.130
  20. What is a Medical Information Commons? J Law Med Ethics. 2019 03; 47(1):41-50.
    View in: PubMed
    Score: 0.130
  21. Characterizing the Biomedical Data-Sharing Landscape. J Law Med Ethics. 2019 03; 47(1):21-30.
    View in: PubMed
    Score: 0.130
  22. Pediatric data sharing in genomic research: attitudes and preferences of parents. Pediatrics. 2014 Apr; 133(4):690-7.
    View in: PubMed
    Score: 0.092
  23. Benefits of sharing neurophysiology data from the BRAIN Initiative Research Opportunities in Humans Consortium. Neuron. 2023 12 06; 111(23):3710-3715.
    View in: PubMed
    Score: 0.045
  24. An open access pilot freely sharing cancer genomic data from participants in Texas. Sci Data. 2016 Feb 16; 3:160010.
    View in: PubMed
    Score: 0.026
  25. Identifying personal genomes by surname inference. Science. 2013 Jan 18; 339(6117):321-4.
    View in: PubMed
    Score: 0.021
  26. Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium. Genet Med. 2010 Oct; 12(10):616-20.
    View in: PubMed
    Score: 0.018
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.