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Updated: Aug 18, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Genetics of schizophrenia: implications for treatment
Abbegail Northup1, Vishwajit L Nimgaonkar
1Department of Psychiatry, University of Pittsburgh, School of Medicine and Graduate School of Public Health, WPIC, Room 443, 3811 O'Hara Street, Pittsburgh, PA 15213, USA. northupaj2@upmc.edu
Abstract:
Schizophrenia is a common, debilitating illness for which treatment is empirical and unsatisfactory. Intense efforts to identify etiological factors have been launched in order to facilitate rational therapy. Such efforts have included gene-mapping studies since a significant heritability has been proved. In common with other polygenic/multifactorial disorders, mapping efforts for schizophrenia pose daunting challenges. Faced with such complexities, attempts to detect genetic associations with pharmacological response have been initiated. Although intriguing associations have been reported, formal replication is required. Suggestions for the design of replicate studies are proposed. This review is restricted to studies that investigated response to clozapine (Clozaril, Novartis) and other novel antipsychotic medications.
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