Literature DB >> 31173557

How Should Patients and Providers Interpret the US Food and Drug Administration's Regulatory Language for Direct-to-Consumer Genetic Tests?

Madison K Kilbride1, Susan M Domchek1, Angela R Bradbury1.   

Abstract

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Mesh：

Year:  2019        PMID： 31173557      PMCID： PMC7010426          DOI： 10.1200/JCO.18.01418

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN： 0732-183X            Impact factor:   44.544


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  4 in total

1.  NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.

Authors:  Mary B Daly; Robert Pilarski; Michael Berry; Saundra S Buys; Meagan Farmer; Susan Friedman; Judy E Garber; Noah D Kauff; Seema Khan; Catherine Klein; Wendy Kohlmann; Allison Kurian; Jennifer K Litton; Lisa Madlensky; Sofia D Merajver; Kenneth Offit; Tuya Pal; Gwen Reiser; Kristen Mahoney Shannon; Elizabeth Swisher; Shaveta Vinayak; Nicoleta C Voian; Jeffrey N Weitzel; Myra J Wick; Georgia L Wiesner; Mary Dwyer; Susan Darlow
Journal:  J Natl Compr Canc Netw       Date:  2017-01       Impact factor: 11.908

2.  Pervasive genetic testing.

Authors:  Paul T R Thiruchelvam; Carla S Fisher; Daniel R Leff; Susan M Domchek
Journal:  Lancet       Date:  2018-05-24       Impact factor: 79.321

3.  Direct-to-Consumer Genetic Testing: The Implications of the US FDA's First Marketing Authorization for BRCA Mutation Testing.

Authors:  Jennifer Gill; Adam J Obley; Vinay Prasad
Journal:  JAMA       Date:  2018-06-19       Impact factor: 56.272

4.  Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: U.S. Preventive Services Task Force recommendation statement.

Authors:  Virginia A Moyer
Journal:  Ann Intern Med       Date:  2014-02-18       Impact factor: 25.391
  4 in total
  1 in total

1.  Reply to Patel and McLeod.

Authors:  Madison K Kilbride; Susan M Domchek; Angela R Bradbury
Journal:  J Clin Oncol       Date:  2019-11-21       Impact factor: 44.544
  1 in total

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