Prediction of psychosis in youth at high clinical risk: a multisite longitudinal study in North America.
By Tyrone D. Cannon, K. Cadenhead, B. Cornblatt, S. Woods, J. Addington, E. Walker, Larry J. Seidman, D. Perkins, M. Tsuang, Thomas H. McGlashan and 1 more. Archives of General Psychiatry, 2008
1,301 citations recorded by the source corpus.
Subfields: Psychiatry and Mental health, Philosophy
View Paper: https://www.semanticscholar.org/paper/1507137ee277b7abb6bfbcf67efc705e1c785d06
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Citations in the corpus
- Predicting Psychosis: Meta-analysis of Transition Outcomes in Individuals at High Clinical Risk (2013, result): “Although these values must be interpreted with caution because they were derived by pooling data from different samples rather than by using data from a single prospective sample, they are consistent with recent evidence that some HR patients develop psychosis after the first 24 months following pre”
- Schizophrenia, "just the facts" 4. Clinical features and conceptualization. (2009, neutral): “(2009), doi:10.1016/j.schres.2009.03.005 sixth to one-half go on to develop schizophrenia depending on the population studied and criteria utilized (Yung et al., 2003; Cannon et al., 2008; Yung et al., 2008).”
- Elevated striatal dopamine function linked to prodromal signs of schizophrenia. (2009, methodology): “The mean times to onset of psychotic illness in these studies were 223 days(19) and 276 days.(18) We investigated the striatal dopaminergic system in a group of patients meeting operationalized criteria for ARMS using (18)F-dopa PET imaging, comparing them with patients with schizophrenia and with h”
- The dopamine hypothesis of schizophrenia: version III--the final common pathway. (2009, neutral): “Individuals meeting clinical criteria for a high risk of psychosis, eg, have an approximate 400-fold increased risk of developing of psychotic illnesses, predominantly schizophrenia, within the following few years.(115,116) They show elevated striatal [(18)F]-dopa accumulation, which is positively a”