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The international Genome sample resource (IGSR): A worldwide collection of genome variation incorporating the 1000 Genomes Project data

Nucleic acids research, 2017-01, Vol.45 (D1), p.D854-D859

2017

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Genomic cloud computing: legal and ethical points to consider

European journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1271-1278

2015

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

European journal of human genetics : EJHG, 2013-03, Vol.21 (3), p.245-247

2013

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Biobanking and deceased persons

Human genetics, 2011-09, Vol.130 (3), p.415-423

Tasse, Anne Marie

2011

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Is written informed consent outdated?

European journal of public health, 2017-04, Vol.27 (2), p.195-196

2017

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

European journal of human genetics : EJHG, 2014-03, Vol.22 (3), p.317-321

2014

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

Emerging themes in epidemiology, 2013-11, Vol.10 (1), p.12-12, Article 12

2013

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The Return of Results of Deceased Research Participants

The Journal of law, medicine & ethics, 2011-12, Vol.39 (4), p.621-630

Tasse, Anne Marie

2011

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

Biopreservation and biobanking, 2016-06, Vol.14 (3), p.207-216

Tassé, Anne-Marie

2016

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Consent Processes for Mobile App Mediated Research: Systematic Review

JMIR mHealth and uHealth, 2017-08, Vol.5 (8), p.e126-e126

2017

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Model consent clauses for rare disease research

BMC medical ethics, 2019-08, Vol.20 (1), p.55-55, Article 55

2019

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Barriers and Opportunities in Consent and Access Procedures in Low- and Middle-Income Country Biobanks: Meeting Notes from the BCNet Training and General Assembly

Biopreservation and biobanking, 2018-06, Vol.16 (3), p.171-178

2018

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From ICH to IBH in Biobanking? A Legal Perspective on Harmonization, Standardization and Unification

Studies in Ethics, Law, and Technology, 2013-12, Vol.7 (1)

Tassé, Anne-Marie

2013

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Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M)

Npj genomic medicine, 2018-07, Vol.3 (1), p.17-6, Article 17

2018

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

Biopreservation and biobanking, 2016-06, Vol.14 (3), p.201-206

2016

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Next-Generation Sequencing and the Return of Results

Cold Spring Harbor perspectives in medicine, 2016-10, Vol.6 (10), p.a026724

2016

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Developing an Ethical and Legal Interoperability Assessment Process for Retrospective Studies

Biopreservation and biobanking, 2016-06, Vol.14 (3), p.249-255

2016

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Retrospective access to data: the ENGAGE consent experience

European journal of human genetics : EJHG, 2010-07, Vol.18 (7), p.741-745

2010

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

Biopreservation and biobanking, 2016-06, Vol.14 (3), p.193-194

2016

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European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

European journal of human genetics : EJHG, 2019-12, Vol.27 (12), p.1763-1773

2019

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

Applied & translational genomics, 2014-06, Vol.3 (2), p.36-40

2014

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International Biobanking Summit V: Harmonizing Privacy Laws to Enable International Biobank Research

Biopreservation and biobanking, 2016-10, Vol.14 (5), p.452-453

2016

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Epigenome-based cancer risk prediction: rationale, opportunities and challenges

Nature reviews. Clinical oncology, 2018-05, Vol.15 (5), p.292-309

2018

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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?

Biopreservation and biobanking, 2014-12, Vol.12 (6), p.363-364

2014

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Data Safe Havens in health research and healthcare

Bioinformatics, 2015-10, Vol.31 (20), p.3241-3248

2015

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The international Genome sample resource (IGSR): A worldwide collection of genome variation incorporating the 1000 Genomes Project data

Genomic cloud computing: legal and ethical points to consider

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

Biobanking and deceased persons

Is written informed consent outdated?

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

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

The Return of Results of Deceased Research Participants

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

Consent Processes for Mobile App Mediated Research: Systematic Review

Model consent clauses for rare disease research

Barriers and Opportunities in Consent and Access Procedures in Low- and Middle-Income Country Biobanks: Meeting Notes from the BCNet Training and General Assembly

From ICH to IBH in Biobanking? A Legal Perspective on Harmonization, Standardization and Unification

Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M)

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

Next-Generation Sequencing and the Return of Results

Developing an Ethical and Legal Interoperability Assessment Process for Retrospective Studies

Retrospective access to data: the ENGAGE consent experience

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

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

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

International Biobanking Summit V: Harmonizing Privacy Laws to Enable International Biobank Research

Epigenome-based cancer risk prediction: rationale, opportunities and challenges

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?

Data Safe Havens in health research and healthcare

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