Evidence map›Paper›PMID 41943275›Full record

ArticleJournal of Korean medical science2026

Perception of Family Genetic Testing for Hereditary Breast and Ovarian Cancer: A Survey of Patients and General Public.

Eun Jeong Lee, Ji Young Kim, Jiwoo An, Jeongjin Yun, Suhyun Jang, Minyoung Jung, Yeong Mi Jeong, Chanmi Cho, Tae-Dong Jeong, Jungmin Jo and 3 more

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Eun Jeong LeeDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0004-7811-9113
Ji Young KimDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0007-6358-3177
Jiwoo AnDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0002-4607-5748
Jeongjin YunDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0009-0355-5937
Suhyun JangDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0008-8163-9098
Minyoung JungDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0005-9315-9110
Yeong Mi JeongDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0002-4725-0237
Chanmi ChoDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0009-0007-8888-3547
Tae-Dong JeongDepartment of Laboratory Medicine, Ewha Womans University Seoul Hospital, Ewha Womans University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3873-3117
Jungmin JoDivision of Hematology-Oncology, Department of Internal Medicine, Ewha Womans University Mokdong Hospital, Ewha Womans University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9322-7540
Byung-In MoonCancer Center for Women, Ewha Womans University Mokdong Hospital, Ewha Womans University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7441-8472
Min-Kyung SoDepartment of Laboratory Medicine, Ewha Womans University Mokdong Hospital, Ewha Womans University College of Medicine, Seoul, Korea. mkso@ewha.ac.kr.ORCID https://orcid.org/0000-0001-9728-3008
Jungwon HuhDepartment of Genetic Counseling, Ewha Womans University College of Medicine Graduate School, Seoul, Korea.ORCID https://orcid.org/0000-0001-8758-9847

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFamily genetic testing facilitates early cancer diagnosis and prevention for relatives of individuals carrying Breast Cancer Susceptibility Genes 1 and 2 (

methodsA total of 186 participants (86 patients with cancer and 100 public controls) were educated on hereditary breast and ovarian cancer and family genetic testing via a presentation video accessed through QR codes or smartphone links. Afterward, participants completed a 10-question knowledge test, and perceptions were assessed using a questionnaire featuring a hypothetical

resultsPost-education, knowledge scores were significantly higher in the patient group than in the controls (median: 10 vs. 9,

conclusionPromoting family genetic testing requires effective communication and dissemination of accurate information. Developing systematic genetic counseling programs is essential to achieving these objectives.

Indexed as

Breast NeoplasmsGenetic TestingOvarian NeoplasmsAdultAgedBRCA1 ProteinBRCA2 ProteinFamilyFemaleGenetic CounselingGenetic Predisposition to DiseaseHealth Knowledge, Attitudes, PracticeHumansMiddle AgedSurveys and QuestionnairesBRCA1 ProteinBRCA2 ProteinBRCA1BRCA2Cancer PreventionFamilyFamily CommunicationGenetic CounselingGenetic TestingHereditary Breast and Ovarian Cancer SyndromeInherited Genetic VariantsSurveys and Questionnaires

Identifiers

PMID41943275
PMCPMC13036266

What OpenQuestion holds

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Registered trials

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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.