Author(s): Stessman HA, Bernier R, Eichler EE
Abstract Share this page
Abstract Medical genetics typically entails the detailed characterization of a patient's phenotypes followed by genotyping to discover the responsible gene or mutation. Here, we propose that the systematic discovery of genetic variants associated with complex diseases such as autism are progressing to a point where a reverse strategy may be fruitful in assigning the pathogenic effects of many different genes and in determining whether particular genotypes manifest as clinically recognizable phenotypes. This "genotype-first" approach for complex disease necessitates the development of large, highly integrated networks of researchers, clinicians, and patient families, with the promise of improved therapies for subsets of patients. Copyright © 2014 Elsevier Inc. All rights reserved.
This article was published in Cell
and referenced in Journal of Molecular and Genetic Medicine