The clinical utility of whole-exome sequencing in the context of rare diseases - the changing tides of medical practice

FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project

(2014) Chandree L. Beaulieu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The usefulness of whole-exome sequencing in routine clinical practice

(2014) Alejandro Iglesias et al.   GENETICS IN MEDICINE

Genomics for clinical utility: the future is near

(2014) David Rossolatos et al.   Genome Medicine

Rare-disease genetics in the era of next-generation sequencing: discovery to translation

(2013) Kym M. Boycott et al.   NATURE REVIEWS GENETICS

Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders

(2013) Yaping Yang et al.   NEW ENGLAND JOURNAL OF MEDICINE

Exceptional know how? Possible pitfalls of routinising genetic services

(2010) D. Schmitz   JOURNAL OF MEDICAL ETHICS

Debating Clinical Utility

(2010) W. Burke et al.   Public Health Genomics

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