Evidence map›Paper›PMID 32382939›Full record

ArticleJournal of community genetics2020

Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals.

Anne E Reed-Weston, Aileen Espinal, Bianca Hasar, Codruta Chiuzan, Gabriel Lazarin, Chunhua Weng, Paul S Appelbaum, Wendy K Chung, Julia Wynn

Abstract read
In one paragraph

Article in Journal of community genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

9 authors at 3 institutions in 1 country.

Anne E Reed-WestonVagelos College of Physician & Surgeons, Columbia Irving University, New York, NY, USA.
Aileen EspinalDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Bianca HasarDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Codruta ChiuzanDepartment of Biostatistics, Columbia University Irving Medical Center, New York, NY, USA.
Gabriel LazarinDepartment of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
Chunhua WengMyriad Women's Health (Formerly Counsyl), South San Francisco, CA, USA.
Paul S AppelbaumDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Wendy K ChungDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Julia WynnDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA. jw2500@cumc.columbia.edu.ORCID http://orcid.org/0000-0002-5220-6022
Columbia University Irving Medical Center · USColumbia University · USMyriad Genetics · US

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
OMOP information model for eMERGE phenotypingU01HG008680 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wendy K Chung, GEORGE M HRIPCSAK · 2015 to 2026
$13.3M
NRSA Training CoreTL1TR001875 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SPANN, MARISA N, TAYLOR, JACQUELYN Y · 2016 to 2025
$8.9M
NCATS NIH HHS TL1 TR001875NCATS NIH HHS UL1 TR001873NCATS NIH HHS UL1TR001873NHGRI NIH HHS U01 HG008680NHGRI NIH HHS U01HG008680Office of Extramural Research, National Institutes of Health 5TL1TR001875-02
6 · The paper itself

Abstract

Genetic screening to inform personal risk has only recently become an option as the cost of sequencing decreases, and our ability to interpret sequence variants improves. Studies have demonstrated that people want to learn about their genetic information and do well after learning it, but minorities are underrepresented in these studies. We surveyed Ashkenazi Jewish (AJ) and Latino/a participants in a genetic screening study to solicit choices about genetic results to return, as well as their experience with learning these results and attitudes about genetic information secrecy and security. Participants had the option to proceed through the study self-guided, and few elected to have traditional pre-test genetic education and counseling. Despite this, the majority were satisfied with the process of selecting and receiving genetic results and felt that they understood their results. Concerns about privacy and confidentiality of genetic data were minimal, though some participants expressed modest concerns about keeping any potential results secret or the confidentiality of their genetic information. Our results support the feasibility of the option of self-guided genetic screening. Additional care will need to be taken when designing population-based screening studies to meet the needs of participants who come from communities with different experiences with genetics.

Identifiers

PMID32382939
PMCPMC7475159
OpenAlexW3023876564

What OpenQuestion holds

Textmetadata
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.