| Literature DB >> 26106147 |
Patricia B Munroe1, Andrew Tinker2.
Abstract
The study of family pedigrees with rare monogenic cardiovascular disorders has revealed new molecular players in physiological processes. Genome-wide association studies of complex traits with a heritable component may afford a similar and potentially intellectually richer opportunity. In this review we focus on the interpretation of genetic associations and the issue of causality in relation to known and potentially new physiology. We mainly discuss cardiometabolic traits as it reflects our personal interests, but the issues pertain broadly in many other disciplines. We also describe some of the resources that are now available that may expedite follow up of genetic association signals into observations on causal mechanisms and pathophysiology.Entities:
Keywords: cardiometabolic traits; cardiovascular physiology; genome-wide association studies
Mesh:
Year: 2015 PMID: 26106147 PMCID: PMC4556941 DOI: 10.1152/physiolgenomics.00004.2015
Source DB: PubMed Journal: Physiol Genomics ISSN: 1094-8341 Impact factor: 3.107