Connection

AMY MCGUIRE to Decision Making

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

1.647
  1. Beyond shared decision making: an expanded typology of medical decisions. Med Decis Making. 2008 Sep-Oct; 28(5):699-705.
    View in: PubMed
    Score: 0.206
  2. Missed expectations? Physicians' views of patients' participation in medical decision-making. Med Care. 2005 May; 43(5):466-70.
    View in: PubMed
    Score: 0.166
  3. 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.
    View in: PubMed
    Score: 0.155
  4. Deciding with Others: Interdependent Decision-Making. Hastings Cent Rep. 2022 11; 52(6):23-32.
    View in: PubMed
    Score: 0.139
  5. Responsibility, culpability, and parental views on genomic testing for seriously ill children. Genet Med. 2019 12; 21(12):2791-2797.
    View in: PubMed
    Score: 0.110
  6. 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: 0.094
  7. Overcoming the reimbursement barriers for clinical sequencing. JAMA. 2014 Nov 12; 312(18):1857-8.
    View in: PubMed
    Score: 0.080
  8. 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: 0.076
  9. 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: 0.074
  10. The indispensable role of professional judgment in genomic medicine. JAMA. 2013 Apr 10; 309(14):1465-6.
    View in: PubMed
    Score: 0.072
  11. Currents in contemporary bioethics. Identifying consanguinity through routine genomic analysis: reporting requirements. J Law Med Ethics. 2012; 40(4):1040-6.
    View in: PubMed
    Score: 0.066
  12. Shaping patients' decisions. Chest. 2011 Feb; 139(2):424-429.
    View in: PubMed
    Score: 0.062
  13. The right to ignore genetic status of late onset genetic disease in the genomic era; Prenatal testing for Huntington disease as a paradigm. Am J Med Genet A. 2010 Jul; 152A(7):1774-80.
    View in: PubMed
    Score: 0.059
  14. Beneficent persuasion: techniques and ethical guidelines to improve patients' decisions. Ann Fam Med. 2010 May-Jun; 8(3):260-4.
    View in: PubMed
    Score: 0.059
  15. A typology of shared decision making, informed consent, and simple consent. Ann Intern Med. 2004 Jan 06; 140(1):54-9.
    View in: PubMed
    Score: 0.038
  16. 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.
    View in: PubMed
    Score: 0.035
  17. Parents' decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project. Genet Med. 2023 03; 25(3):100002.
    View in: PubMed
    Score: 0.035
  18. 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.
    View in: PubMed
    Score: 0.026
  19. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019 05; 21(5):1100-1110.
    View in: PubMed
    Score: 0.026
  20. Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project. Genet Med. 2018 09; 20(9):1069-1076.
    View in: PubMed
    Score: 0.025
  21. Consumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience. Milbank Q. 2017 06; 95(2):291-318.
    View in: PubMed
    Score: 0.024
  22. Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group. Genet Med. 2014 Oct; 16(10):727-35.
    View in: PubMed
    Score: 0.019
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.