29178651 26711421 24773317 26302600 29118898 29086656 28074382 29411211 32342788 27256128 24814192 25014338 32342793 - Search Results

Year	Number of Results
2014	3
2015	2
2016	2
2017	3
2018	1
2020	2
2023	0

1

Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry.

Laurino MY, Truitt AR, Tenney L, Fisher D, Lindor NM, Veenstra D, Jarvik GP, Newcomb PA, Fullerton SM. Laurino MY, et al. Mol Genet Genomic Med. 2017 Nov;5(6):700-708. doi: 10.1002/mgg3.328. Epub 2017 Aug 23. Mol Genet Genomic Med. 2017. PMID: 29178651 Free PMC article.

2

Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?

Prince AE, Conley JM, Davis AM, Lázaro-Muñoz G, Cadigan RJ. Prince AE, et al. J Law Med Ethics. 2015 Winter;43(4):827-42. doi: 10.1111/jlme.12323. J Law Med Ethics. 2015. PMID: 26711421 Free PMC article.

3

The Ethical, Legal, and Social Implications Program of the National Human Genome Research Institute: reflections on an ongoing experiment.

McEwen JE, Boyer JT, Sun KY, Rothenberg KH, Lockhart NC, Guyer MS. McEwen JE, et al. Annu Rev Genomics Hum Genet. 2014;15:481-505. doi: 10.1146/annurev-genom-090413-025327. Epub 2014 Apr 24. Annu Rev Genomics Hum Genet. 2014. PMID: 24773317 Review.

4

The Limits of FDA's Authority to Regulate Clinical Research Involving High-Throughput DNA Sequencing.

Evans BJ. Evans BJ. Food Drug Law J. 2015;70(2):259-87, ii. Food Drug Law J. 2015. PMID: 26302600 Free PMC article.

5

Power to the People: Data Citizens in the Age of Precision Medicine.

Evans BJ. Evans BJ. Vanderbilt J Entertain Technol Law. 2017 Winter;19(2):243-265. Vanderbilt J Entertain Technol Law. 2017. PMID: 29118898 Free PMC article.

6

Barbarians at the Gate: Consumer-Driven Health Data Commons and the Transformation of Citizen Science.

Evans BJ. Evans BJ. Am J Law Med. 2016 Nov;42(4):651-685. doi: 10.1177/0098858817700245. Am J Law Med. 2016. PMID: 29086656 Free PMC article.

7

Engaging Hmong adults in genomic and pharmacogenomic research: Toward reducing health disparities in genomic knowledge using a community-based participatory research approach.

Culhane-Pera KA, Straka RJ, Moua M, Roman Y, Vue P, Xiaaj K, Lo MX, Lor M. Culhane-Pera KA, et al. J Community Genet. 2017 Apr;8(2):117-125. doi: 10.1007/s12687-017-0292-x. Epub 2017 Jan 10. J Community Genet. 2017. PMID: 28074382 Free PMC article.

8

"Bridge to the Literature"? Third-Party Genetic Interpretation Tools and the Views of Tool Developers.

Nelson SC, Fullerton SM. Nelson SC, et al. J Genet Couns. 2018 Aug;27(4):770-781. doi: 10.1007/s10897-018-0217-9. Epub 2018 Feb 7. J Genet Couns. 2018. PMID: 29411211

9

Key Expert Stakeholder Perceptions of the Law of Genomics: Identified Problems and Potential Solutions.

Cheung FY, Clatch L, Wolf SM, Clayton EW, Lawrenz F. Cheung FY, et al. J Law Med Ethics. 2020 Mar;48(1):87-104. doi: 10.1177/1073110520916997. J Law Med Ethics. 2020. PMID: 32342788 Free PMC article.

10

Biobanking Research and Privacy Laws in the United States.

Harrell HL, Rothstein MA. Harrell HL, et al. J Law Med Ethics. 2016 Mar;44(1):106-27. doi: 10.1177/1073110516644203. J Law Med Ethics. 2016. PMID: 27256128

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