Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study

Although most participants communicated results with family members and healthcare providers in accordance with their risk level, questions remain about how to adequately prepare individuals to receive pathogenic results, ensure timely and accessible follow-up care, and facilitate genetic counseling and cascade testing of at-risk relatives in the setting of population risk-based screening.

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Publication Details

Journal
Public Health Genomics
Published
2024-09-20
DOI
https://doi.org/10.1159/000540680
Citations
2
Primary Topic
BRCA gene mutations in cancer
Type
article
Field-Weighted Citation Impact
1.10

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article

Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study

Leah Sabacan, Leslie Riddle, Diane Heditsian, Galen Joseph et al.
2 citations
Public Health Genomics
BRCA gene mutations in cancer
1.10
article

Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study

Leah Sabacan, Leslie Riddle, Diane Heditsian, Galen Joseph, Jennifer E. James, Barry Tong, Katherine Ross, Barbara A. Koenig, Arash Naeim, Martin Eklund, Neil S. Wenger, Diana De Rosa, Lisa Madlensky, Allison Stover Fiscalini, Susie Brain
article en
2 citations

Abstract

Although most participants communicated results with family members and healthcare providers in accordance with their risk level, questions remain about how to adequately prepare individuals to receive pathogenic results, ensure timely and accessible follow-up care, and facilitate genetic counseling and cascade testing of at-risk relatives in the setting of population risk-based screening.

Public Health GenomicsVol. 27(1)
Cancer Prevention Institute of California (US), University of California, Los Angeles (US), University of California, San Francisco (US), UCLA Health (US), Karolinska Institutet (SE), Institute on Aging (US), Cancer Genetics (United States) (US)
National Cancer Institute
Openalex Percentile: Top 19%
BRCA gene mutations in cancer
1.10
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