We have updated our privacy policy. If you have any question, contact us at privacy@scicrunch.org. Dismiss and don't show again

Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

An integrative genomics approach to infer causal associations between gene expression and disease.

Nature genetics | Jul 1, 2005

A key goal of biomedical research is to elucidate the complex network of gene interactions underlying complex traits such as common human diseases. Here we detail a multistep procedure for identifying potential key drivers of complex traits that integrates DNA-variation and gene-expression data with other complex trait data in segregating mouse populations. Ordering gene expression traits relative to one another and relative to other complex traits is achieved by systematically testing whether variations in DNA that lead to variations in relative transcript abundances statistically support an independent, causative or reactive function relative to the complex traits under consideration. We show that this approach can predict transcriptional responses to single gene-perturbation experiments using gene-expression data in the context of a segregating mouse population. We also demonstrate the utility of this approach by identifying and experimentally validating the involvement of three new genes in susceptibility to obesity.

Pubmed ID: 15965475 RIS Download

Mesh terms: 11-beta-Hydroxysteroid Dehydrogenase Type 1 | Animals | DNA-Binding Proteins | Female | Gene Expression | Gene Expression Profiling | Genetic Predisposition to Disease | Genome | Male | Membrane Proteins | Mice | Mice, Inbred C57BL | Mice, Inbred DBA | Models, Genetic | Obesity | Quantitative Trait Loci | Receptors, Complement | Repressor Proteins | Transforming Growth Factor beta | Transforming Growth Factor beta2

Research resources used in this publication

None found

Research tools detected in this publication

None found

Data used in this publication

Associated grants

  • Agency: NHLBI NIH HHS, Id: P01 HL030568-220011
  • Agency: NHLBI NIH HHS, Id: R01 HL094322
  • Agency: NHLBI NIH HHS, Id: P01 HL028481-21A10010
  • Agency: NHLBI NIH HHS, Id: P01 HL028481
  • Agency: NHLBI NIH HHS, Id: P01 HL030568
  • Agency: NHLBI NIH HHS, Id: P01 HL030568-220009
  • Agency: NHLBI NIH HHS, Id: P01 HL028481-21A1

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

We have not found any resources mentioned in this publication.