Population biobanks and returning individual research results: mission impossible or new directions?

The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies

(2011) Catherine A McCarty et al.   BMC Medical Genomics

A decade’s perspective on DNA sequencing technology

(2011) Elaine R. Mardis   NATURE

Communication of biobanks' research results: What do (potential) participants want?

(2010) Tineke M. Meulenkamp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Crime scene investigation (as seen on TV)

(2010) Evan W. Durnal   FORENSIC SCIENCE INTERNATIONAL

Direct-to-consumer personal genome testing: ethical and regulatory issues that arise from wanting to ‘know’ your DNA

(2010) G. N. Samuel et al.   INTERNAL MEDICINE JOURNAL

Genetic discrimination in private insurance: global perspectives

(2010) Yann Joly et al.   NEW GENETICS AND SOCIETY

Offering Individual Genetic Research Results: Context Matters

(2010) L. M. Beskow et al.   Science Translational Medicine

Personal genome research : what should the participant be told?

(2010) Amy L. McGuire et al.   TRENDS IN GENETICS

Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results

(2009) Joanna Stjernschantz Forsberg et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Direct-to-consumer genetic tests: beyond medical regulation?

(2009) David Magnus et al.   Genome Medicine

Public Expectations for Return of Results—Time to Stop Being Paternalistic?

(2008) Conrad Fernandez   AMERICAN JOURNAL OF BIOETHICS

Public Expectations for Return of Results from Large-Cohort Genetic Research

(2008) Juli Murphy et al.   AMERICAN JOURNAL OF BIOETHICS

The UK Biobank sample handling and storage protocol for the collection, processing and archiving of human blood and urine

(2008) P. Elliott et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY