| Literature DB >> 24132899 |
Matthew Schreiber1, Michael Dorschner, Debby Tsuang.
Abstract
Schizophrenia is a debilitating lifelong illness that lacks a cure and poses a worldwide public health burden. The disease is characterized by a heterogeneous clinical and genetic presentation that complicates research efforts to identify causative genetic variations. This review examines the potential of current findings in schizophrenia and in other related neuropsychiatric disorders for application in next-generation technologies, particularly whole-exome sequencing (WES) and whole-genome sequencing (WGS). These approaches may lead to the discovery of underlying genetic factors for schizophrenia and may thereby identify and target novel therapeutic targets for this devastating disorder.Entities:
Keywords: autism; genetics; schizophrenia; sequencing; whole exome
Mesh:
Year: 2013 PMID: 24132899 DOI: 10.1002/ajmg.b.32156
Source DB: PubMed Journal: Am J Med Genet B Neuropsychiatr Genet ISSN: 1552-4841 Impact factor: 3.568