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Genetic studies of neuropsychiatric disorders in Costa Rica:: a model for the use of isolated populations

期刊

PSYCHIATRIC GENETICS
卷 14, 期 1, 页码 13-23

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00041444-200403000-00003

关键词

genetics; neuropsychiatric disorders; bipolar disorder; Tourette Syndrome; genetic isolates; linkage disequilibrium; Costa Rica; review

资金

  1. NCRR NIH HHS [RR15533] Funding Source: Medline

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The importance of genetics in understanding the etiology of mental illness has become increasingly clear in recent years, as more evidence has mounted that almost all neuropsychiatric disorders have a genetic component. It has also become clear, however, that these disorders are etiologically complex, and multiple genetic and environmental factors contribute to their makeup. So far, traditional linkage mapping studies have not definitively identified specific disease genes for neuropsychiatric disorders, although some potential candidates have been identified via these methods (e.g. the dysbindin gene in schizophrenia; Straub et al, 2002; Schwab et al, 2003). For this reason, alternative approaches are being attempted, including studies in genetically isolated populations. Because isolated populations have a high degree of genetic homogeneity, their use may simplify the process of identifying disease genes in disorders where multiple genes may play a role. Several areas of Latin America contain genetically isolated populations that are well suited for the study of neuropsychiatric disorders. Genetic studies of several major psychiatric illnesses, including bipolar disorder, major depression, schizophrenia, Tourette Syndrome, alcohol dependence, attention deficit hyperactivity disorder, and obsessive-compulsive disorder, are currently underway in these regions. In this paper we highlight the studies currently being conducted by our groups in the Central Valley of Costa Rica to illustrate the potential advantages of this population for genetic studies. Psychiatr Genet 14:13-23 (C) 2004 Lippincoft Williams Wilkins.

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