Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project

GINA, Genetic Discrimination, and Genomic Medicine

(2015) Robert C. Green et al.   NEW ENGLAND JOURNAL OF MEDICINE

Attitudes of research participants and the general public towards genomic data sharing: a systematic literature review

(2014) Mahsa Shabani et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

(2014) Yaping Yang et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Resistance to Therapy in Acute Promyelocytic Leukemia

(2014) Jacqueline Lehmann-Che et al.   NEW ENGLAND JOURNAL OF MEDICINE

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine

(2014) Jason L Vassy et al.   Trials

Research participants’ attitudes towards the confidentiality of genomic sequence information

(2013) Leila Jamal et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Personalized Medicine vs Guideline-Based Medicine

(2013) Jeffrey J. Goldberger et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Personalized genomic disease risk of volunteers

(2013) M. L. Gonzalez-Garay et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genomics in Clinical Practice: Lessons from the Front Lines

(2013) H. J. Jacob et al.   Science Translational Medicine

Genome sequencing for healthy individuals

(2013) Saskia C. Sanderson   TRENDS IN GENETICS

Reflections on the Cost of "Low-Cost" Whole Genome Sequencing: Framing the Health Policy Debate

(2013) Timothy Caulfield et al.   PLOS BIOLOGY

Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research

(2012) Flavia M Facio et al.   BMC Medical Genomics

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

(2012) Flavia M Facio et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Tilting at windmills no longer: a data-driven discussion of DTC DNA ancestry tests

(2012) Jennifer K. Wagner et al.   GENETICS IN MEDICINE

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

(2012) Juli Murphy Bollinger et al.   GENETICS IN MEDICINE

Experiences of Early Users of Direct-to-Consumer Genomics in Switzerland: An Exploratory Study

(2012) E. Vayena et al.   Public Health Genomics

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research

(2011) Flavia M Facio et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Public Perspectives Regarding Data-Sharing Practices in Genomics Research

(2011) S.B. Haga et al.   Public Health Genomics

Motivations and Perceptions of Early Adopters of Personalized Genomics: Perspectives from Research Participants

(2011) S.E. Gollust et al.   Public Health Genomics

Balancing the Risks and Benefits of Genomic Data Sharing: Genome Research Participants’ Perspectives

(2011) J.M. Oliver et al.   Public Health Genomics

Genomic research and wide data sharing: Views of prospective participants

(2010) Susan Brown Trinidad et al.   GENETICS IN MEDICINE

Consumer perceptions of direct-to-consumer personalized genomic risk assessments

(2010) Cinnamon S Bloss et al.   GENETICS IN MEDICINE

Clinical assessment incorporating a personal genome

(2010) Euan A Ashley et al.   LANCET

Subjects matter: a survey of public opinions about a large genetic cohort study

(2008) David Kaufman et al.   GENETICS IN MEDICINE