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Full-Text Articles in Medicine and Health Sciences
Family-Focused Treatment For Adolescents And Young Adults At High Risk For Psychosis: Results Of A Randomized Trial, D. J. Miklowitz, M. P. O'Brien, D. A. Schlosser, J. Addington, K. A. Candan, B. C. Walsh, J. L. Zinberg, S. D. De Silva, M. Friedman-Yakoobian, T. D. Cannon, +2 Additional Authors
Family-Focused Treatment For Adolescents And Young Adults At High Risk For Psychosis: Results Of A Randomized Trial, D. J. Miklowitz, M. P. O'Brien, D. A. Schlosser, J. Addington, K. A. Candan, B. C. Walsh, J. L. Zinberg, S. D. De Silva, M. Friedman-Yakoobian, T. D. Cannon, +2 Additional Authors
Journal Articles
Objective: Longitudinal studies have begun to clarify the phenotypic characteristics of adolescents and young adults at clinical high risk for psychosis. This 8-site randomized trial examined whether a 6-month program of family psychoeducation was effective in reducing the severity of attenuated positive and negative psychotic symptoms and enhancing functioning among individuals at high risk. Method: Adolescents and young adults (mean age 17.4 +/- 4.1 years) with attenuated positive psychotic symptoms, brief and intermittent psychosis, or genetic risk with functional deterioration were randomly assigned to 18 sessions of family-focused therapy for individuals at clinical high risk (FFT-CHR) in 6 months or …
Copy Number Variation In Obsessive-Compulsive Disorder And Tourette Syndrome: A Cross-Disorder Study, L. M. Mcgrath, D. M. Yu, C. Marshall, L. K. Davis, B. Thiruvahindrapuram, B. B. Li, C. Cappi, R. D. Bruun, Cathy Budman, J. M. Scharf, +112 Additional Authors
Copy Number Variation In Obsessive-Compulsive Disorder And Tourette Syndrome: A Cross-Disorder Study, L. M. Mcgrath, D. M. Yu, C. Marshall, L. K. Davis, B. Thiruvahindrapuram, B. B. Li, C. Cappi, R. D. Bruun, Cathy Budman, J. M. Scharf, +112 Additional Authors
Journal Articles
Objective: Obsessive-compulsive disorder (OCD) and Tourette syndrome (TS) are heritable neurodevelopmental disorders with a partially shared genetic etiology. This study represents the first genome-wide investigation of large (>500 kb), rare (