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Topic: Genetic Basis and Treatment of Psychiatric Disorders



           Special Issue Introduction:
           The etiology of psychiatric disease remains elusive. Although many psychiatric symptoms and diseases appear to
           cluster within families, the genetic basis of psychiatric disease remains complex and elusive. There is little support for
           classical Mendelian inheritance of psychiatric disorders. Many non-Mendelian inheritance models may account for the
           genetic influence on psychiatric disorders; these include, but are not limited to: (1) complex interactions between genetic
           predisposition and environmental factors including social-economic, nutritional, infectious and other factors; (2) polygenetic
           and  oligogenetic  inheritance;  (3)  methylation  and  imprinting;  and  (4)  mitochondrial  inheritance.  Still  the  manners  in
           which psychiatric disorders are defined and sub-classified have also influenced the results of the outcomes of genetic
           studies. Advances in understanding neurobiology have started to provide insight as to the underlying biological nature
           of behaviorally-defined conditions. Understanding perturbations in genes involved in specific pathways and mechanisms
           such as channelopathies, neurotransmitters, cell signaling, energy metabolism, amino acid metabolism, circadian rhythm,
           synaptic plasticity, and synaptic structure have provided insights into the underlying biology. Using innovative techniques
           to understand genetic mechanisms has provided advances in the field. Through a better understanding of the genetic
           basis of psychiatric disease, we can look forward to the management and prevention of psychiatric disease through a
           precise, personalized medicine approach. This Special Issue will highlight innovative studies examining the underlying
           genetic basis of psychiatric disease, especially with respect to genetic alternation and variations which may impact optimal
           treatments.


           Guest Editor

                                             Prof. Richard E. Frye

                                             Prof. Richard E. Frye is a Child Neurologist specializing in neurodevelopmental
                                             and neurometabolic disorders. He earned his MD and PhD in Physiology and
                                             Biophysics  from  Georgetown  University.  His  extensive  training  includes  a
                                             Pediatrics residency at the University of Miami, a Child Neurology residency
                                             and a Fellowship in Behavioral Neurology and Learning Disabilities at Harvard
                                             University/Children’s Hospital Boston, as well as a Fellowship in Psychology
                                             at Boston University. Additionally, he holds a Master’s degree in Biomedical
                                             Science and Biostatistics from Drexel University. Prof. Frye is board-certified
                                             in  Pediatrics  and  Neurology  with  Special  Competence  in  Child  Neurology.
                                             With over 300 publications and book chapters, Prof. Frye also serves on several
                                             Editorial Boards.






















                       Journal of Translational Genetics and Genomics                                        I
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