Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Prediction of individual genetic risk of complex disease.

Current opinion in genetics & development - 1 Jun 2008

Wray Naomi R, Goddard Michael E, Visscher Peter M

Abstract excerpt

Most common diseases are caused by multiple genetic and environmental factors. In the last 2 years, genome-wide association studies (GWAS) have identified polymorphisms that are associated with risk to common disease, but the effect of any one risk allele is typically small. By combining information from many risk variants, will it be possible to predict accurately each individual person's genetic risk for a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Biomarkers
Share to Disease
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to Individuality

Share to Prognosis

Source

Identifiers

PMID: 18682292
DOI: 10.1016/j.gde.2008.07.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prediction of individual genetic risk of complex disease.PMID 18682292Read ↗

Prediction of individual genetic risk to disease from genome-wide association studies.Semantic proximity Read ↗

Genetic risk prediction in complex disease.Semantic proximity Read ↗

Genetic Risk Scores.Semantic proximity Read ↗

Genetic Risk Scores.Semantic proximity Read ↗

Genome-based prediction of common diseases: advances and prospects.Semantic proximity Read ↗

Discovery and implications of polygenicity of common diseases.Semantic proximity Read ↗

Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases.Semantic proximity Read ↗

Towards a complete resolution of the genetic architecture of disease.Semantic proximity Read ↗

Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data.Semantic proximity Read ↗

Genetic Epidemiology of Complex Phenotypes.Semantic proximity Read ↗

Genomic risk prediction of complex human disease and its clinical applicationSemantic proximity Read ↗

Contrasting the genetic architecture of 30 complex traits from summary association dataSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.