| Literature DB >> 29906445 |
Naomi R Wray1, Cisca Wijmenga2, Patrick F Sullivan3, Jian Yang4, Peter M Visscher4.
Abstract
The evidence that most adult-onset common diseases have a polygenic genetic architecture fully consistent with robust biological systems supported by multiple back-up mechanisms is now overwhelming. In this context, we consider the recent "omnigenic" or "core genes" model. A key assumption of the model is that there is a relatively small number of core genes relevant to any disease. While intuitively appealing, this model may underestimate the biological complexity of common disease, and therefore, the goal to discover core genes should not guide experimental design. We consider other implications of polygenicity, concluding that a focus on patient stratification is needed to achieve the goals of precision medicine.Entities:
Mesh:
Year: 2018 PMID: 29906445 DOI: 10.1016/j.cell.2018.05.051
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582