Parkinson’s disease phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| WDR6 | associated_with | Parkinson’s disease | — | 1 |
Mentioned in (14)
Papers in which this entity is mentioned.
- Single-cell exon deletion profiling reveals splicing events that shape gene expression and cell state dynamics. (2026)
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- High-Parameter Spatial Multi-Omics through Histology-Anchored Integration (2025)
- Human 3D brain organoids: steering the demolecularization of brain and neurological diseases. (2023)
- Nanopore sequencing technology, bioinformatics and applications. (2021)
- Application of third-generation sequencing in cancer research. (2021)
- HSP70 and HSP90 in neurodegenerative diseases. (2020)
- The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
- Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure. (2020)
- Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. (2019)
- Advances in Diagnosis and Treatment of Fetal Alcohol Spectrum Disorders: From Animal Models to Human Studies. (2015)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
- Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. (2011)
- Abnormal brain activation during working memory in children with prenatal exposure to drugs of abuse: the effects of methamphetamine, alcohol, and polydrug exposure. (2011)
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 |
|---|---|---|---|
| parkinson’s disease | phenotype | 64 | 111 |