Whole genome sequencing in support of wellness and health maintenance
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Whole genome sequencing in support of wellness and health maintenance
Authors
Keywords
genetic prediction, risk assessment, preventive medicine, clinical profiling
Journal
Genome Medicine
Volume 5, Issue 6, Pages 58
Publisher
Springer Nature
Online
2013-06-28
DOI
10.1186/gm462
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genetic risk prediction in a small cohort of healthy adults in Atlanta
- (2013) JING ZHAO et al. Genetics Research
- Comprehensive Characterization of Human Genome Variation by High Coverage Whole-Genome Sequencing of Forty Four Caucasians
- (2013) Hui Shen et al. PLoS One
- Five Years of GWAS Discovery
- (2012) Peter M. Visscher et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Sequencing and analysis of a South Asian-Indian personal genome
- (2012) Ravi Gupta et al. BMC GENOMICS
- Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes
- (2012) Rui Chen et al. CELL
- Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies
- (2012) Janet Chou et al. Current Opinion in Allergy and Clinical Immunology
- Exploring concordance and discordance for return of incidental findings from clinical sequencing
- (2012) Robert C. Green et al. GENETICS IN MEDICINE
- Risk estimation and risk prediction using machine-learning methods
- (2012) Jochen Kruppa et al. HUMAN GENETICS
- Clinical application of exome sequencing in undiagnosed genetic conditions
- (2012) Anna C Need et al. JOURNAL OF MEDICAL GENETICS
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- (2012) Stephan J. Sanders et al. NATURE
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- Comparison of Family History and SNPs for Predicting Risk of Complex Disease
- (2012) Chuong B. Do et al. PLoS Genetics
- Type 2 Diabetes Risk Alleles Demonstrate Extreme Directional Differentiation among Human Populations, Compared to Other Diseases
- (2012) Rong Chen et al. PLoS Genetics
- Integrating Comparative Effectiveness Research Programs Into Predictive Health: A Unique Role for Academic Health Centers
- (2011) Kimberly J. Rask et al. ACADEMIC MEDICINE
- Whole exome and whole genome sequencing
- (2011) David Bick et al. CURRENT OPINION IN PEDIATRICS
- Array-Based Sequence Capture and Next-Generation Sequencing for the Identification of Primary Immunodeficiencies
- (2011) S. Ghosh et al. SCANDINAVIAN JOURNAL OF IMMUNOLOGY
- Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence
- (2011) Frederick E. Dewey et al. PLoS Genetics
- The pursuit of genome-wide association studies: where are we now?
- (2010) Chee Seng Ku et al. JOURNAL OF HUMAN GENETICS
- Clinical assessment incorporating a personal genome
- (2010) Euan A Ashley et al. LANCET
- Hundreds of variants clustered in genomic loci and biological pathways affect human height
- (2010) Hana Lango Allen et al. NATURE
- Genomic Medicine — An Updated Primer
- (2010) W. Gregory Feero et al. NEW ENGLAND JOURNAL OF MEDICINE
- Likelihood ratios for genome medicine
- (2010) Alexander A Morgan et al. Genome Medicine
- The Characterization of Twenty Sequenced Human Genomes
- (2010) Kimberly Pelak et al. PLoS Genetics
- The Genetic Interpretation of Area under the ROC Curve in Genomic Profiling
- (2010) Naomi R. Wray et al. PLoS Genetics
- Overview of the Symposium on Public Health Significance of Genomics and Eco-Genetics
- (2009) Gilbert S. Omenn Annual Review of Public Health
- Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk
- (2009) David M. Evans et al. HUMAN MOLECULAR GENETICS
- The Health and Cost Benefits of Work Site Health-Promotion Programs
- (2008) Ron Z. Goetzel et al. Annual Review of Public Health
- General Cardiovascular Risk Profile for Use in Primary Care
- (2008) Ralph B. D’Agostino et al. CIRCULATION
- Prediction of individual genetic risk of complex disease
- (2008) Naomi R Wray et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Genotype Score in Addition to Common Risk Factors for Prediction of Type 2 Diabetes
- (2008) James B. Meigs et al. NEW ENGLAND JOURNAL OF MEDICINE
- Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes
- (2008) Valeriya Lyssenko et al. NEW ENGLAND JOURNAL OF MEDICINE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now