Neuroimaging has advanced the study of brain structure and function in schizophrenia. Magnetic resonance imaging provides measures of whole brain and regional anatomy and cerebrospinal fluid volume. Functional methods have included the Xenon-133 technique for measuring cerebral blood flow (CBF); positron emission tomography for assessing metabolism, CBF, and neuroreceptor functioning; and single photon emission computed tomography for studying CBF and neuroreceptors. Despite heterogeneity of patient samples, and studies which differed in the methodologies applied, there is converging evidence implicating three brain systems: frontal, temporolimbic, and basal ganglia. Current emphasis is aimed at probing specific regions across imaging modalities. Now these findings and research paradigms in neuroimaging must be integrated with phenomenological, neurobehavioral, and neuropathological investigations. The application of this technology is already helping to elucidate the neurobiology of schizophrenia, and further important advances can be anticipated.Neuroimaging methodology has been applied more to the study of schizophrenia than to any other psychiatric disorder. Investigators of brain function in schizophrenia have had to meet the challenge of using developing technology in a complex and heterogeneous disorder. In this article we will first summarize and review major issues and findings in the neurobiology of schizophrenia through the use of neuroimaging, emphasizing the last 5 years. We will then provide an integration across modalities, relating neuroimaging findings to neuropathological and neurobehavioral studies and focusing on brain systems likely to be involved in schizophrenia.Advances have been made in two related domains of neuroimaging research: structure and function. Structure is examined in neuroanatomic studies, which provide parameters of brain volume. Function is studied in neurophysiologic research, which provides measures of brain energy metabolism (glucose, oxygen) and blood flow; neurochemical research provides information on neuroreceptor density and affinity. Neuroimaging techniques have been able to both inform and advance hypotheses currently influencing schizophrenia research.Questions of the relation between functional and structural changes and symptom clusters are now easier to address. Dysfunction has been identified in neocortical association areas, temporolimbic regions, and basal ganglia (e.g., Buchsbaum 1990). In retrospect, our initial hypotheses regarding schizophrenia were simplistic. It is unlikely that a disorder as complex as schizophrenia is associated with a single structural or functional lesion in a single neuroanatomical location, and in fact, no such lesion has been identified. However, several findings have emerged consistently, and initial attempts have been made to link