Clinical and personal utility of genomic high-throughput technologies: perspectives of medical professionals and affected persons

Personal utility is inherent to direct-to-consumer genomic testing

(2016) Matthew Wai Heng Chung et al.   JOURNAL OF MEDICAL ETHICS

Are physicians prepared for whole genome sequencing? a qualitative analysis

(2015) K.D. Christensen et al.   CLINICAL GENETICS

‘Someday it will be the norm’: physician perspectives on the utility of genome sequencing for patient care in the MedSeqProject

(2015) Jason L Vassy et al.   Personalized Medicine

Parent and Public Interest in Whole-Genome Sequencing

(2015) Daniel S. Dodson et al.   Public Health Genomics

Multiplex genetic testing: reconsidering utility and informed consent in the era of next-generation sequencing

(2014) Angela R. Bradbury et al.   GENETICS IN MEDICINE

Personal utility in genomic testing: is there such a thing?

(2014) Eline M Bunnik et al.   JOURNAL OF MEDICAL ETHICS

Next Generation Sequencing in der diagnostischen Praxis

(2014) T. Bettecken et al.   Medizinische Genetik

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

(2013) Zoe Lohn et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

‘Information is information’: a public perspective on incidental findings in clinical and research genome-based testing

(2013) S Daack-Hirsch et al.   CLINICAL GENETICS

Disclosing incidental findings in genetics contexts: A review of the empirical ethical research

(2013) Gabrielle M. Christenhusz et al.   European Journal of Medical Genetics

Genomic sequencing for psychiatric disorders: promise and challenge

(2013) Barbara Bowles Biesecker et al.   INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY

A Closer Look at the Recommended Criteria for Disclosing Genetic Results: Perspectives of Medical Genetic Specialists, Genomic Researchers, and Institutional Review Board Chairs

(2013) Debra S. Brandt et al.   Journal of Genetic Counseling

Genetics patients’ perspectives on clinical genomic testing

(2013) Michelle L McGowan et al.   Personalized Medicine

P4 medicine: how systems medicine will transform the healthcare sector and society

(2013) Mauricio Flores et al.   Personalized Medicine

Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms

(2012) Holly K. Tabor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study

(2012) AA Lemke et al.   CLINICAL GENETICS

Consuming genomes: scientific and social innovation in direct-to-consumer genetic testing

(2012) Margaret Curnutte et al.   NEW GENETICS AND SOCIETY

What Research Participants Want to Know About Genetic Research Results: The Impact of “Genetic Exceptionalism”

(2011) Miguel Ruiz-Canela et al.   Journal of Empirical Research on Human Research Ethics

Health outcomes in economic evaluation: the QALY and utilities

(2010) S. J. Whitehead et al.   BRITISH MEDICAL BULLETIN

Personalized genomic information: preparing for the future of genetic medicine

(2010) Alan E. Guttmacher et al.   NATURE REVIEWS GENETICS

Personal utility and genomic information: Look before you leap

(2009) Scott D Grosse et al.   GENETICS IN MEDICINE

Evaluating the utility of personal genomic information

(2009) Morris W Foster et al.   GENETICS IN MEDICINE

Letting the Genome out of the Bottle — Will We Get Our Wish?

(2008) David J. Hunter et al.   NEW ENGLAND JOURNAL OF MEDICINE