Evidence map›Paper›PMID 30475858›Full record

ArticlePloS one2018

Thought leader perspectives on benefits and harms in precision medicine research.

Laura M Beskow, Catherine M Hammack, Kathleen M Brelsford

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Adults with Intellectual Disability and Consent to Precision Medicine Research: Using Supported Decision-Making to Facilitate First-Person Consent.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2026
    Article
  2. Risk management during times of health uncertainty in Spain: A qualitative analysis of ethical challenges.Risk analysis : an official publication of the Society for Risk Analysis · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. "Choice of law" in precision medicine research.American journal of human genetics · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Protecting Participants in Genomic Research: Understanding the "Web of Protections" Afforded by Federal and State Law.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2020
    Article
  12. Thought Leader Perspectives on Participant Protections in Precision Medicine Research.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Laura M BeskowCenter for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID 0000-0002-9314-1915
Catherine M HammackCenter for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Kathleen M BrelsfordCenter for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.

Funding

Beyond Data Security: Promoting Confidentiality and Advancing ScienceR01HG007733 · NHGRI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BESKOW, LAURA M. · 2014 to 2016
$1.3M
NHGRI NIH HHS R01 HG007733
6 · The paper itself

Abstract

Precision medicine research is underway to identify targeted approaches to improving health and preventing disease. However, such endeavors raise significant privacy and confidentiality concerns. The objective of this study was to elucidate the potential benefits and harms associated with precision medicine research through in-depth interviews with a diverse group of thought leaders, including primarily U.S.-based experts and scholars in the areas of ethics, genome research, health law, historically-disadvantaged populations, informatics, and participant-centric perspectives, as well as government officials and human subjects protections leaders. The results suggest the prospect of an array of individual and societal benefits, as well as physical, dignitary, group, economic, psychological, and legal harms. Relative to the way risks and harms are commonly described in consent forms for precision medicine research, the thought leaders we interviewed arguably emphasized a somewhat different set of issues. The return of individual research results, harm to socially-identifiable groups, the value-dependent nature of many benefits and harms, and the risks to the research enterprise itself emerged as important cross-cutting themes. Our findings highlight specific challenges that warrant concentrated care during the design, conduct, dissemination, and translation of precision medicine research and in the development of consent materials and processes.

Indexed as

Precision MedicineConfidentialityCost-Benefit AnalysisExpert TestimonyHumansInsurance, HealthInterviews as TopicStakeholder Participation

Identifiers

PMID30475858
PMCPMC6258115

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.