Evidence map›Paper›PMID 18247107›Full record

ArticleJournal of genetic counseling2008

Consumer motivations for pursuing genetic testing and their preferences for the provision of genetic services for hearing loss.

Kara A Withrow, Sarah Burton, Kathleen S Arnos, Andrea Kalfoglou, Arti Pandya

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of genetic counseling, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Prevalence ofExperimental and therapeutic medicine · 2021
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  4. The value of diagnostic testing for parents of children with rare genetic diseases.Genetics in medicine : official journal of the American College of Medical Genetics · 2019
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  16. Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.Genetics in medicine : official journal of the American College of Medical Genetics · 2009
    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

5 authors at 3 institutions in 1 country.

Kara A WithrowDepartment of Human Genetics and Pediatrics, Medical College of Virginia at Virginia Commonwealth University, P.O. Box 980033, Richmond, VA 23298, USA.
Sarah Burton
Kathleen S Arnos
Andrea Kalfoglou
Arti Pandya
Gallaudet University · USVirginia Commonwealth University Medical Center · USUniversity of Maryland, Baltimore County · US

Funding

CREATION OF A DNA REPOSITORY TO IDENTIFY DEAFNESS GENESR01DC004293 · NIDCD · VIRGINIA COMMONWEALTH UNIVERSITY · PI NANCE, WALTER ELMORE · 2000 to 2004
$2.4M
NIDCD NIH HHS R01DC04293-01
6 · The paper itself

Abstract

Genetic services for deafness are being increasingly sought due to the introduction of early hearing detection and intervention programs, as well as the rapid progress in the identification of deafness genes. This study aimed to assess the motivations of consumers for pursuing genetic testing as well as their preferences for provision of these services. We conducted 5 focus groups consisting of hearing parents of deaf children, deaf parents, and unmarried deaf adults. Motivations for pursuing genetic testing included determining the etiology, helping to alleviate the guilt associated with the diagnosis of hearing loss in a child, and acquiring information to help them and other family members prepare for the future. Most participants thought that a genetic counselor/geneticist would be the most appropriate professional to provide genetics services. For culturally Deaf individuals, the communication method was seen as more important than the type of professional. Parents preferred that genetic evaluation, including testing, occur either immediately at or a few months after the audiologic diagnosis of hearing loss.

Indexed as

MotivationAdolescentAdultFemaleGenetic TestingHearing LossHumansMaleMiddle Aged

Identifiers

PMID18247107
OpenAlexW2058302816

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.