242 related articles for article (PubMed ID: 19681141)
1. Nervecenter: consumer gene tests face uncertain legal, regulatory future.
Ann Neurol; 2009 Jul; 66(1):A10-5. PubMed ID: 19681141
[No Abstract] [Full Text] [Related]
2. The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues.
Hogarth S; Javitt G; Melzer D
Annu Rev Genomics Hum Genet; 2008; 9():161-82. PubMed ID: 18767961
[TBL] [Abstract][Full Text] [Related]
3. A conceptual framework for genetic policy: comparing the medical, public health, and fundamental rights models.
Andrews LB
Wash Univ Law Q; 2001; 79(152):221-85. PubMed ID: 16211786
[No Abstract] [Full Text] [Related]
4. Health savings accounts face an uncertain future.
Carroll J
Manag Care; 2006 Nov; 15(11):11-2. PubMed ID: 17168065
[No Abstract] [Full Text] [Related]
5. The allocation of genetic services: economics, expectations, ethics and the law.
Caulfield TA
Health Law J; 1995; 3():213-34. PubMed ID: 10569877
[No Abstract] [Full Text] [Related]
6. Ethical, legal, and social issues in genetic testing for complex genetic diseases.
Andrews L; Zuiker ES
Valparaiso Univ Law Rev; 2003; 37(3):793-829. PubMed ID: 15378818
[No Abstract] [Full Text] [Related]
7. Who speaks for the health consumer?
Fox MH
J Health Care Poor Underserved; 2008 Aug; 19(3):671-6. PubMed ID: 18677063
[TBL] [Abstract][Full Text] [Related]
8. Worth waiting for.
Nature; 2010 Nov; 468(7321):134. PubMed ID: 21068784
[No Abstract] [Full Text] [Related]
9. Regulation: The FDA is overcautious on consumer genomics.
Green RC; Farahany NA
Nature; 2014 Jan; 505(7483):286-7. PubMed ID: 24436984
[No Abstract] [Full Text] [Related]
10. Genes and disability: questions at the crossroads.
Crossley M; Shepherd L
Fla State Univ Law Rev; 2003; 30(2):xi-xxiii. PubMed ID: 15083827
[No Abstract] [Full Text] [Related]
11. Essentially Yours: The Protection of Human Genetic Information in Australia--the impact on clinical practice and the 'new genetics'.
Trent RJ
Univ N S W Law J; 2003; 26(3):807-12. PubMed ID: 16617535
[No Abstract] [Full Text] [Related]
12. American society of human genetics updates guidance on genetic testing in children: Group addresses predictive genetic testing, use of secondary findings from genomic sequencing tests.
Am J Med Genet A; 2015 Oct; 167A(10):viii-ix. PubMed ID: 26355290
[No Abstract] [Full Text] [Related]
13. Consumer alert: ethical issues raised by the sale of genetic tests directly to consumers.
Wasson K
Am J Bioeth; 2008 Jun; 8(6):16-8. PubMed ID: 18726774
[No Abstract] [Full Text] [Related]
14. Scientific rationality, uncertainty and the governance of human genetics: an interview study with researchers at deCODE genetics.
Hjörleifsson S; Schei E
Eur J Hum Genet; 2006 Jul; 14(7):802-8. PubMed ID: 16622446
[TBL] [Abstract][Full Text] [Related]
15. Survey confirms fears about licensing of genetic tests.
Schissel A; Merz JF; Cho MK
Nature; 1999 Nov; 402(6758):118. PubMed ID: 10646997
[No Abstract] [Full Text] [Related]
16. Enhancing medical care in the United States via health savings accounts.
Faria MA
Surg Neurol; 2005 Sep; 64(3):276-7. PubMed ID: 16099266
[No Abstract] [Full Text] [Related]
17. Genetic services in Spain.
Ramos-Arroyo MA; Benitez J; Estivill J
Eur J Hum Genet; 1997; 5 Suppl 2():163-8. PubMed ID: 9450217
[No Abstract] [Full Text] [Related]
18. The spectre of coercion: is public health genetics the route to policies of enforced disease prevention?
van den Daele W
Community Genet; 2006; 9(1):40-9. PubMed ID: 16490958
[TBL] [Abstract][Full Text] [Related]
19. Regulators weigh risks of consumer genetic tests.
Schmidt C
Nat Biotechnol; 2008 Feb; 26(2):145-6. PubMed ID: 18259159
[No Abstract] [Full Text] [Related]
20. Genetic services in France.
Aymé S; Briard ML; Mattei JF
Eur J Hum Genet; 1997; 5 Suppl 2():76-80. PubMed ID: 9450200
[No Abstract] [Full Text] [Related]
[Next] [New Search]