Illustrating Cancer Risk: Patient Risk Communication Preferences and Interest regarding a Novel <b><i>BRCA1/2</i></b> Genetic Risk Modifier Test-Reference-Cited by-同舟云学术

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Illustrating Cancer Risk: Patient Risk Communication Preferences and Interest regarding a Novel BRCA1/2 Genetic Risk Modifier Test

Published:2020 Issue:1-2 Volume:23 Page:6-19
ISSN:1662-4246
Container-title:Public Health Genomics
language:en
Short-container-title:Public Health Genomics

Author:

Hamilton Jada G.,Genoff Garzon Margaux,Shah Ibrahim H.,Cadet Kechna,Shuk Elyse,Westerman Joy S.,Hay Jennifer L.,Offit Kenneth,Robson Mark E.

Publisher

S. Karger AG

Subject

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

Reference60 articles.

1. Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, et al. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet. 2003 May;72(5):1117–30.

2. Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, et al.; The Breast Cancer Linkage Consortium. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet. 1998 Mar;62(3):676–89.

3. Robson M, Offit K. Clinical practice. Management of an inherited predisposition to breast cancer. N Engl J Med. 2007 Jul;357(2):154–62.

4. Kamenova K, Reshef A, Caulfield T. Angelina Jolie’s faulty gene: newspaper coverage of a celebrity’s preventive bilateral mastectomy in Canada, the United States, and the United Kingdom. Genet Med. 2014 Jul;16(7):522–8.

5. Borzekowski DL, Guan Y, Smith KC, Erby LH, Roter DL. The Angelina effect: immediate reach, grasp, and impact of going public. Genet Med. 2014 Jul;16(7):516–21.

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