Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study. Read more about Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study.
Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study. Read more about Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study.
Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results. Read more about Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.
Validation of an Efficient Screening Tool to Identify Low-Income Women at High Risk for Hereditary Breast Cancer. Read more about Validation of an Efficient Screening Tool to Identify Low-Income Women at High Risk for Hereditary Breast Cancer.
Efficient identification and referral of low-income women at high risk for hereditary breast cancer: a practice-based approach. Read more about Efficient identification and referral of low-income women at high risk for hereditary breast cancer: a practice-based approach.
A health services research agenda for cellular, molecular and genomic technologies in cancer care. Read more about A health services research agenda for cellular, molecular and genomic technologies in cancer care.
