Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families

Author:

Vicuña Belinda,Delaney Harold D.,Flores Kristina G.,Ballinger Lori,Royce Melanie,Dayao Zoneddy,Pal Tuya,Kinney Anita Y.

Funder

National Cancer Institute at the National Institutes of Health

University of New Mexico Comprehensive Cancer Center Support Grant: Development Funds

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Public Health, Environmental and Occupational Health,Epidemiology

Reference65 articles.

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2. Armstrong J, Toscano M, Kotchko N, Friedman S, Schwartz MD, Virgo KS et al (2015) Utilization and outcomes of BRCA genetic testing and counseling in a national commercially insured population: the ABOUT Study. JAMA Oncology 1(9):1251–1260

3. Armstrong K, Weiner J, Weber B, Asch DA (2003) Early adoption of BRCA 1/2 testing: who and why. Genetics in Medicine 5(2):92–98. doi: 10.1097/01.GIM.0000056829.76915.2A

4. Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P (2003) International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc 195(9131/03):3508–1381

5. Bradbury AR, Patrick-Miller L, Domchek S (2015) Multiplex genetic testing: Reconsidering utility and informed consent in the era of next-generation sequencing. Genetics in Medicine 17(2):97–98. doi: 10.1038/Gim.2014.85

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