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Genetic variation in metabolic phenotypes: Study designs and applications.

Nat. Rev. Genet. 13, 759-769 (2012)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Many complex disorders are linked to metabolic phenotypes. Revealing genetic influences on metabolic phenotypes is key to a systems-wide understanding of their interactions with environmental and lifestyle factors in their aetiology, and we can now explore the genetics of large panels of metabolic traits by coupling genome-wide association studies and metabolomics. These genome-wide association studies are beginning to unravel the genetic contribution to human metabolic individuality and to demonstrate its relevance for biomedical and pharmaceutical research. Adopting the most appropriate study designs and analytical tools is paramount to further refining the genotype-phenotype map and eventually identifying the part played by genetic influences on metabolic phenotypes. We discuss such design considerations and applications in this Review.
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Publication type Article: Journal article
Document type Review
Corresponding Author
Keywords GENOME-WIDE ASSOCIATION; HDL-CHOLESTEROL CONCENTRATIONS; CHRONIC KIDNEY-DISEASE; COMMON VARIANTS; SUSCEPTIBILITY LOCI; BILIRUBIN LEVELS; ACID INTAKE; METAANALYSIS; INDIVIDUALITY; INTERACTS
ISSN (print) / ISBN 1471-0056
e-ISSN 1471-0064
Quellenangaben Volume: 13, Issue: 11, Pages: 759-769 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Non-patent literature Publications
Reviewing status Peer reviewed