Provider Discussions of Genetic Tests With U.S. Women at Risk for a BRCA Mutation.

doi:10.1016/j.amepre.2017.10.015

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Provider Discussions of Genetic Tests With U.S. Women at Risk for a BRCA Mutation.

American journal of preventive medicine - 1 Feb 2018

Hull Leland E, Haas Jennifer S, Simon Steven R

Abstract excerpt

INTRODUCTION: The U.S. Preventive Services Task Force recommends that primary care providers screen unaffected women with a family history of BRCA mutation-associated cancers, but without a personal history of BRCA-related cancer, for referral to genetic counseling and potential genetic testing. METHODS: The 2015 National Health Interview Survey was analyzed in January 2017 to determine the rates at which...

Topics

Adult
Age Factors
Aged
BRCA1 Protein
BRCA2 Protein
Breast Neoplasms
Early Detection of Cancer
Female
Genetic Counseling
Genetic Predisposition to Disease
Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Health Surveys

Humans

Middle Aged

Mutation

Ovarian Neoplasms

Referral and Consultation

Risk Factors

Source

Open in PubMed

Identifiers

PMID: 29241717
DOI: 10.1016/j.amepre.2017.10.015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Provider Discussions of Genetic Tests With U.S. Women at Risk for a BRCA Mutation.PMID 29241717Read ↗

Exploring Predictors of Genetic Counseling and Testing for Hereditary Breast and Ovarian Cancer: Findings from the 2015 U.S. National Health Interview SurveySemantic proximity Read ↗

BRCA1 and BRCA2 Mutation Testing in Young Women With Breast Cancer.Semantic proximity Read ↗

Perceptions and care Recommendations from Previvors: Qualitative analysis of female BRCA1/2 mutation Carriers’ experience with genetic testing and counselingSemantic proximity Read ↗

Communication of BRCA results and family testing in 1,103 high-risk women.Semantic proximity Read ↗

Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast CancerSemantic proximity Read ↗

Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.Semantic proximity Read ↗

Gaps in Receipt of Clinically Indicated Genetic Counseling After Diagnosis of Breast Cancer.Semantic proximity Read ↗

National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.Semantic proximity Read ↗

Genetic Counseling, Testing, and Family Communication Into Survivorship After Diagnosis of Breast CancerSemantic proximity Read ↗

Genetic Counselors' Experiences Regarding Communication of Reproductive Risks with Autosomal Recessive Conditions found on Cancer Panels.Semantic proximity Read ↗

Uptake of genetic counseling and multi-gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing.Semantic proximity Read ↗

Family communication of BRCA1/2 results and family uptake of BRCA1/2 testing in a diverse population of BRCA1/2 carriers.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.