Connection

AMY MCGUIRE to Genetic Research

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

3.405
  1. Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs? BMC Med Ethics. 2019 11 21; 20(1):84.
    View in: PubMed
    Score: 0.647
  2. 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: 0.422
  3. 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: 0.374
  4. Informed consent in genomics and genetic research. Annu Rev Genomics Hum Genet. 2010; 11:361-81.
    View in: PubMed
    Score: 0.326
  5. Identifiability of DNA data: the need for consistent federal policy. Am J Bioeth. 2008 Oct; 8(10):75-6.
    View in: PubMed
    Score: 0.299
  6. Genetics. No longer de-identified. Science. 2006 Apr 21; 312(5772):370-1.
    View in: PubMed
    Score: 0.252
  7. Meeting the growing demands of genetic research. J Law Med Ethics. 2006; 34(4):809-12.
    View in: PubMed
    Score: 0.247
  8. "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: 0.227
  9. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. AJOB Empir Bioeth. 2017 Apr-Jun; 8(2):82-88.
    View in: PubMed
    Score: 0.133
  10. Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject. J Law Med Ethics. 2015; 43(3):529-37.
    View in: PubMed
    Score: 0.115
  11. Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board. Genet Med. 2014 Jul; 16(7):547-52.
    View in: PubMed
    Score: 0.108
  12. Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group. Circ Cardiovasc Genet. 2010 Dec; 3(6):574-80.
    View in: PubMed
    Score: 0.087
  13. 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: 0.086
  14. Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017 Feb; 139(2).
    View in: PubMed
    Score: 0.033
  15. Experiences and attitudes of genome investigators regarding return of individual genetic test results. Genet Med. 2013 Nov; 15(11):882-7.
    View in: PubMed
    Score: 0.026
  16. Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility. Genome Res. 2012 Mar; 22(3):421-8.
    View in: PubMed
    Score: 0.023
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.