Hereditary Breast and Ovarian Cancer

Familial Investigations of Childhood Cancer Predisposition

Scalable Communication Modalities for Returning Genetic Research Results

Radical Fimbriectomy for Young BRCA Mutation Carriers

Cancer Genetics Hereditary Cancer Panel Testing

Sequential EHR Based Interventions to Increase Genetic Testing for Breast and Ovarian Cancer Predisposition

Triple Negative Breast Cancer and Germline Hereditary Breast and Ovarian Cancer Mutation Carrier Registry

CONTIGO - A Narrative Intervention to Enhance Genetic Counseling and Testing

Cascade Genetic Testing for Hereditary Breast/Ovarian Cancer and Lynch Syndrome in Switzerland

Investigation of Tumour Spectrum of Germline Mutations in Breast and Ovarian Cancer Genes.

Implementation of the Families Accelerating Cascade Testing Toolkit (FACTT) for Hereditary Breast and Ovarian Cancer and Lynch Syndrome

Feasibility of Lifestyle Intervention in BRCA1/2 Mutation Carriers

Efficacy of Lifestyle Intervention in BRCA1/2 Mutation Carriers

Multifactorial Risk Assessment for Breast & Ovarian Cancer Risk Detection

Study of Quality of Life Post Salpingo-oophorectomy in BRCA1/2 & PALB2 Mutation Carriers (BRCA-HRT)

Testing an Intelligent Tutoring System to Enhance Genetic Risk Assessment

Enhancing At-risk Latina Women's Use of Genetic Counseling for Hereditary Breast and Ovarian Cancer

Evaluation of the Adhesion to the GENEPY Network

Genetic Risk: Whether, When, and How to Tell Adolescents

Identification and Referral of Women at Risk for Hereditary Breast/Ovarian Cancer