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Genetic variation in metabolic phenotypes: Study designs and applications.

Nat. Rev. Genet. 13, 759-769 (2012)
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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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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter GENOME-WIDE ASSOCIATION; HDL-CHOLESTEROL CONCENTRATIONS; CHRONIC KIDNEY-DISEASE; COMMON VARIANTS; SUSCEPTIBILITY LOCI; BILIRUBIN LEVELS; ACID INTAKE; METAANALYSIS; INDIVIDUALITY; INTERACTS
Sprache englisch
Veröffentlichungsjahr 2012
HGF-Berichtsjahr 2012
ISSN (print) / ISBN 1471-0056
e-ISSN 1471-0064
Quellenangaben Band: 13, Heft: 11, Seiten: 759-769 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Begutachtungsstatus Peer reviewed
POF Topic(s) 30505 - New Technologies for Biomedical Discoveries
30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
Forschungsfeld(er) Enabling and Novel Technologies
Genetics and Epidemiology
PSP-Element(e) G-503700-001
G-504100-001
PubMed ID 23032255
Scopus ID 84867744660
Erfassungsdatum 2012-10-31