Pathways to understanding psychosis through rare – 22q11.2DS - and common variants
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference41 articles.
1. 22q.2 deletion syndrome;McDonald-McGinn;Nat Rev Dis Prim,2015
2. Rare genome-wide copy number variation and expression of schizophrenia in 22q.2 deletion syndrome;Bassett;Am J Psychiatry,2017
3. The psychosis spectrum in 22q.2 deletion syndrome is comparable to that of nondeleted youths;Tang;Biol Psychiatry,2017
4. A neurogenetic model for the study of schizophrenia spectrum disorders: the international 22q.2 deletion syndrome brain behavior consortium;Gur;Mol Psychiatry,2017
5. Using common genetic variation to examine phenotypic expression and risk prediction in 22q.2 deletion syndrome;Davies;Nat Med,2020
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1. The Genesis of Schizophrenia: An Origin Story;American Journal of Psychiatry;2024-06-01
2. The copy number variant architecture of psychopathology and cognitive development in the ABCD®study;2024-05-15
3. Neuropsychological Profile of 25 Brazilian Patients with 22q11.2 Deletion Syndrome: Effects of Clinical and Socioeconomic Variables;Genes;2024-05-08
4. Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort;JAMA Psychiatry;2022-07-01
5. Considering alternatives to the schizophrenia construct;Schizophrenia Research;2022-04
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