Evidence map›Paper›PMID 28983318›Full record

ArticleFrontiers in genetics2017

Breast Cancer Risk Estimation and Personal Insurance: A Qualitative Study Presenting Perspectives from Canadian Patients and Decision Makers.

Gratien Dalpé, Ida Ngueng Feze, Shahad Salman, Yann Joly, Julie Hagan, Emmanuelle Lévesque, Véronique Dorval, Jolyane Blouin-Bougie, Nabil Amara, Michel Dorval and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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  9. MicroRNA-216b targetsInternational journal of biological sciences · 2021
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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

11 authors at 3 institutions in 1 country.

Gratien DalpéDepartment of Human Genetics, Faculty of Medicine, Centre of Genomics and Policy, McGill UniversityMontreal, QC, Canada.
Ida Ngueng FezeDepartment of Human Genetics, Faculty of Medicine, Centre of Genomics and Policy, McGill UniversityMontreal, QC, Canada.
Shahad SalmanDepartment of Human Genetics, Faculty of Medicine, Centre of Genomics and Policy, McGill UniversityMontreal, QC, Canada.
Yann JolyDepartment of Human Genetics, Faculty of Medicine, Centre of Genomics and Policy, McGill UniversityMontreal, QC, Canada.
Julie HaganDepartment of Human Genetics, Faculty of Medicine, Centre of Genomics and Policy, McGill UniversityMontreal, QC, Canada.
Emmanuelle LévesqueDepartment of Human Genetics, Faculty of Medicine, Centre of Genomics and Policy, McGill UniversityMontreal, QC, Canada.
Véronique DorvalCentre de Recherche du CHU de Quebec, Laval UniversityQuebec, QC, Canada.
Jolyane Blouin-BougieFaculty of Science of Administration, Laval UniversityQuebec, QC, Canada.
Nabil AmaraFaculty of Science of Administration, Laval UniversityQuebec, QC, Canada.
Michel DorvalCentre de Recherche du CHU de Quebec, Laval UniversityQuebec, QC, Canada.
Jacques SimardCentre de Recherche du CHU de Quebec, Laval UniversityQuebec, QC, Canada.
McGill University · CAUniversité Laval · CACentre hospitalier de l'Université Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic stratification approaches in personalized medicine may considerably improve our ability to predict breast cancer risk for women at higher risk of developing breast cancer. Notwithstanding these advantages, concerns have been raised about the use of the genetic information derived in these processes, outside of the research and medical health care settings, by third parties such as insurers. Indeed, insurance applicants are asked to consent to insurers accessing their medical information (implicitly including genetic) to verify or determine their insurability level, or eligibility to certain insurance products. This use of genetic information may result in the differential treatment of individuals based on their genetic information, which could lead to higher premium, exclusionary clauses or even the denial of coverage. This phenomenon has been commonly referred to as "Genetic Discrimination" (GD). In the Canadian context, where federal Bill S-201,

Indexed as

breast cancerCanadagenetic discriminationgenetic testinginformed consentinsurabilitypersonal insurancerisk

Identifiers

PMID28983318
PMCPMC5613157
OpenAlexW2757063603

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.