schizoaffective disorder phenotype
Evidence from:
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all sources
Related entities (6)
Mentioned in (26)
Papers in which this entity is mentioned.
- DNA methylation and brain structure and function across the life course: A systematic review. (2020)
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- A review on neuroimaging studies of genetic and environmental influences on early brain development. (2019)
- CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. (2019)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
- Social cognition as an RDoC domain. (2016)
- Comorbidity of severe psychotic disorders with measures of substance use. (2014)
- 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
- Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- DISC1 at 10: connecting psychiatric genetics and neuroscience. (2011)
- Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. (2011)
- Genome-wide association study identifies five new schizophrenia loci. (2011)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. (2011)
- Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. (2010)
- The contributions of disease and genetic factors towards regional cortical thinning in schizophrenia: the UCLA family study. (2010)
- MR diffusion tensor imaging: a window into white matter integrity of the working brain. (2010)
- A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder. (2009)
- Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10. (2009)
- Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. (2009)
- Association of psychiatric and substance use disorder comorbidity with cocaine dependence severity and treatment utilization in cocaine-dependent individuals. (2009)
- Large recurrent microdeletions associated with schizophrenia. (2008)
- Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
- Reduced N-acetyl-aspartate levels in schizophrenia patients with a younger onset age: a single-voxel 1H spectroscopy study. (2007)
- Site-specific role of catechol-O-methyltransferase in dopamine overflow within prefrontal cortex and dorsal striatum. (2007)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| schizoaffective disorder | phenotype | 26 | 35 |
| schizoaf | phenotype | — | — |
| schizoaffective | phenotype | — | — |
| schizoaffective concept | phenotype | — | — |