repetitive behaviors phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CHD8 | risk_factor_for | repetitive behaviors | — | 1 |
Mentioned in (9)
Papers in which this entity is mentioned.
- Altered dendritic morphology in dorsolateral prefrontal cortex of nonhuman primates prenatally exposed to maternal immune activation. (2023)
- Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring. (2020)
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. (2019)
- Hippocampal deficits in neurodevelopmental disorders. (2019)
- Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
- Effect of Neuroinflammation on Synaptic Organization and Function in the Developing Brain: Implications for Neurodevelopmental and Neurodegenerative Disorders. (2017)
- Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
Merged raw entities (1)
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 |
|---|---|---|---|
| repetitive behaviors | phenotype | 9 | 13 |