Related references
Note: Only part of the references are listed.An informatics approach to analyzing the incidentalome
Jonathan S. Berg et al.
GENETICS IN MEDICINE (2013)
Implementing genomic medicine in the clinic: the future is here
Teri A. Manolio et al.
GENETICS IN MEDICINE (2013)
Deleterious- and Disease-Allele Prevalence in Healthy Individuals: Insights from Current Predictions, Mutation Databases, and Population-Scale Resequencing
Yali Xue et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes
Jennifer J. Johnston et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Human Genome Sequencing in Health and Disease
Claudia Gonzaga-Jauregui et al.
ANNUAL REVIEW OF MEDICINE, VOL 63 (2012)
VarSifter: Visualizing and analyzing exome-scale sequence variation data on a desktop computer
Jamie K. Teer et al.
BIOINFORMATICS (2012)
Exploring concordance and discordance for return of incidental findings from clinical sequencing
Robert C. Green et al.
GENETICS IN MEDICINE (2012)
Incidental Medical Information in Whole-Exome Sequencing
Benjamin D. Solomon et al.
PEDIATRICS (2012)
A public resource facilitating clinical use of genomes
Madeleine P. Ball et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Applying Genomic Analysis to Newborn Screening
B. D. Solomon et al.
MOLECULAR SYNDROMOLOGY (2012)
Direct-to-Consumer Genetic Testing: Reliable or Risky?
David H. Spencer et al.
CLINICAL CHEMISTRY (2011)
Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time
Jonathan S. Berg et al.
GENETICS IN MEDICINE (2011)
Next-Generation DNA Sequencing, Regulation, and the Limits of Paternalism The Next Challenge
James P. Evans et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2011)
Personalized genomic medicine: Lessons from the exome
Benjamin D. Solomon et al.
MOLECULAR GENETICS AND METABOLISM (2011)
Exome sequencing as a tool for Mendelian disease gene discovery
Michael J. Bamshad et al.
NATURE REVIEWS GENETICS (2011)
Whole-Genome Sequencing for Optimized Patient Management
Matthew N. Bainbridge et al.
SCIENCE TRANSLATIONAL MEDICINE (2011)
Exome sequencing: the expert view
Leslie G. Biesecker et al.
GENOME BIOLOGY (2011)
Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy.
James R. Lupski et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Sequencing and analysis of an Irish human genome
Pin Tong et al.
GENOME BIOLOGY (2010)
Genome sequencing reveals Charcot-Marie-Tooth disease mutation
[Anonymous]
FUTURE NEUROLOGY (2010)
Screening for the Lynch syndrome (Hereditary nonpolyposis colorectal cancer).
H Hampel et al.
NEW ENGLAND JOURNAL OF MEDICINE (2005)
Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway
U Schwarze et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Share Paper
