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Items: 1 to 20 of 21

1.

Legal and Ethical Implications of Data Sharing in International Biobanking Research: Toward a Global Response.

Tassé AM, Bledsoe MJ, Giepmans L, Rahimzadeh V.

Biopreserv Biobank. 2016 Jun;14(3):193-4. doi: 10.1089/bio.2016.29003.amt. Epub 2016 May 19. No abstract available.

PMID:
27195452
2.

A Comparative Analysis of the Legal and Bioethical Frameworks Governing the Secondary Use of Data for Research Purposes.

Tassé AM.

Biopreserv Biobank. 2016 Jun;14(3):207-16. doi: 10.1089/bio.2015.0121. Epub 2016 May 18.

PMID:
27192126
3.

Access Governance for Biobanks: The Case of the BioSHaRE-EU Cohorts.

Kaye J, Briceño Moraia L, Mitchell C, Bell J, Bovenberg JA, Tassé AM, Knoppers BM.

Biopreserv Biobank. 2016 Jun;14(3):201-6. doi: 10.1089/bio.2015.0124. Epub 2016 May 16.

PMID:
27183185
4.

Developing an Ethical and Legal Interoperability Assessment Process for Retrospective Studies.

Tassé AM, Kirby E, Fortier I.

Biopreserv Biobank. 2016 Jun;14(3):249-55. doi: 10.1089/bio.2015.0122. Epub 2016 Apr 26.

PMID:
27115199
5.

Data Safe Havens in health research and healthcare.

Burton PR, Murtagh MJ, Boyd A, Williams JB, Dove ES, Wallace SE, Tassé AM, Little J, Chisholm RL, Gaye A, Hveem K, Brookes AJ, Goodwin P, Fistein J, Bobrow M, Knoppers BM.

Bioinformatics. 2015 Oct 15;31(20):3241-8. doi: 10.1093/bioinformatics/btv279. Epub 2015 Jun 25. Review.

6.

What are some of the ELSI challenges of international collaborations involving biobanks, global sample collection, and genomic data sharing and how should they be addressed?

Dove ES, Tassé AM, Knoppers BM.

Biopreserv Biobank. 2014 Dec;12(6):363-4. doi: 10.1089/bio.2014.1263. No abstract available.

PMID:
25496146
7.

Genomic cloud computing: legal and ethical points to consider.

Dove ES, Joly Y, Tassé AM; Public Population Project in Genomics and Society (P3G) International Steering Committee; International Cancer Genome Consortium (ICGC) Ethics and Policy Committee, Knoppers BM.

Eur J Hum Genet. 2015 Oct;23(10):1271-8. doi: 10.1038/ejhg.2014.196. Epub 2014 Sep 24.

8.

P(3)G - 10 years of toolbuilding: From the population biobank to the clinic.

Ouellette S, Tassé AM.

Appl Transl Genom. 2014 Apr 13;3(2):36-40. doi: 10.1016/j.atg.2014.04.004. eCollection 2014 Jun 1.

9.

Data harmonization and federated analysis of population-based studies: the BioSHaRE project.

Doiron D, Burton P, Marcon Y, Gaye A, Wolffenbuttel BH, Perola M, Stolk RP, Foco L, Minelli C, Waldenberger M, Holle R, Kvaløy K, Hillege HL, Tassé AM, Ferretti V, Fortier I.

Emerg Themes Epidemiol. 2013 Nov 21;10(1):12. doi: 10.1186/1742-7622-10-12.

10.

Data sharing in large research consortia: experiences and recommendations from ENGAGE.

Budin-Ljøsne I, Isaeva J, Knoppers BM, Tassé AM, Shen HY, McCarthy MI, Harris JR; ENGAGE Consortium.

Eur J Hum Genet. 2014 Mar;22(3):317-21. doi: 10.1038/ejhg.2013.131. Epub 2013 Jun 19.

11.

Genotype-driven recruitment: a strategy whose time has come?

Budin-Ljøsne I, Soye KJ, Tassé AM, Knoppers BM, Harris JR.

BMC Med Genomics. 2013 May 23;6:19. doi: 10.1186/1755-8794-6-19.

12.

Population studies: return of research results and incidental findings Policy Statement.

Knoppers BM, Deschênes M, Zawati MH, Tassé AM.

Eur J Hum Genet. 2013 Mar;21(3):245-7. doi: 10.1038/ejhg.2012.152. Epub 2012 Jul 11.

13.

The return of results of deceased research participants.

Tassé AM.

J Law Med Ethics. 2011 Winter;39(4):621-30. doi: 10.1111/j.1748-720X.2011.00629.x.

PMID:
22084848
14.

Bridging consent: from toll bridges to lift bridges?

Budin-Ljøsne I, Tassé AM, Knoppers BM, Harris JR.

BMC Med Genomics. 2011 Oct 4;4:69. doi: 10.1186/1755-8794-4-69.

15.

Towards a data sharing Code of Conduct for international genomic research.

Knoppers BM, Harris JR, Tassé AM, Budin-Ljøsne I, Kaye J, Deschênes M, Zawati MH.

Genome Med. 2011 Jul 14;3(7):46. doi: 10.1186/gm262.

16.

Biobanking and deceased persons.

Tassé AM.

Hum Genet. 2011 Sep;130(3):415-23. doi: 10.1007/s00439-011-1049-y. Epub 2011 Jun 25. Review.

PMID:
21706182
17.

Asia-Pacific Health 2020 and Genomics without Borders: Co-Production of Knowledge by Science and Society Partnership for Global Personalized Medicine.

Ozdemir V, Muljono DH, Pang T, Ferguson LR, Manamperi A, Samper S, Someya T, Tassé AM, Tsai SJ, Zhou HH, Lee EJ.

Curr Pharmacogenomics Person Med. 2011 Mar 1;9(1):1-5. No abstract available.

18.

Regulatory approval for new pharmacogenomic tests: a comparative overview.

Joly Y, Koutrikas G, Tassé AM, Issa A, Carleton B, Hayden M, Rieder MJ, Ramos-Paque E, Avard D.

Food Drug Law J. 2011;66(1):1-24, i. Review.

PMID:
24505844
19.

Retrospective access to data: the ENGAGE consent experience.

Tassé AM, Budin-Ljøsne I, Knoppers BM, Harris JR.

Eur J Hum Genet. 2010 Jul;18(7):741-5. doi: 10.1038/ejhg.2010.30. Epub 2010 Mar 24.

20.

Differences in regulatory frameworks governing genetic laboratories in four countries.

Tassé AM, Petit E, Godard B.

J Law Med Ethics. 2009 Summer;37(2):351-7. doi: 10.1111/j.1748-720X.2009.00378.x.

PMID:
19493079
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