Parkinson’s disease phenotype
Evidence from:
primary |
all sources
Related entities (32)
Mentioned in (64)
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)
- An overview of DNA methylation-derived trait score methods and applications. (2023)
- Human 3D brain organoids: steering the demolecularization of brain and neurological diseases. (2023)
- A systematic review of neuroimaging epigenetic research: calling for an increased focus on development. (2023)
- Newborn differential DNA methylation and subcortical brain volumes as early signs of severe neurodevelopmental delay in a South African Birth Cohort Study. (2022)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
- Nanopore sequencing technology, bioinformatics and applications. (2021)
- Application of third-generation sequencing in cancer research. (2021)
- Transcriptional and anatomical diversity of medium spiny neurons in the primate striatum. (2021)
- Cotinine: Pharmacologically Active Metabolite of Nicotine and Neural Mechanisms for Its Actions. (2021)
- Choline Kinase: An Unexpected Journey for a Precision Medicine Strategy in Human Diseases. (2021)
- An enriched biosignature of gut microbiota-dependent metabolites characterizes maternal plasma in a mouse model of fetal alcohol spectrum disorder. (2021)
- HSP70 and HSP90 in neurodegenerative diseases. (2020)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
- The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
- ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (2020)
- Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure. (2020)
- CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. (2019)
- Transient Potassium Channels: Therapeutic Targets for Brain Disorders. (2019)
- Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. (2019)
- Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. (2019)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
- Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
- Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. (2018)
- Neurotrophins in the Brain: Interaction With Alcohol Exposure During Development. (2017)
- Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants. (2017)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
- Neural activation patterns of successful episodic encoding: Reorganization during childhood, maintenance in old age. (2016)
- Neuroanatomical substrates of executive functions: Beyond prefrontal structures. (2016)
- Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. (2015)
- Genetic absence of nNOS worsens fetal alcohol effects in mice. II: microencephaly and neuronal losses. (2015)
- Functional Connectivity Disruption in Neonates with Prenatal Marijuana Exposure. (2015)
- Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer. (2015)
- Advances in Diagnosis and Treatment of Fetal Alcohol Spectrum Disorders: From Animal Models to Human Studies. (2015)
- Induced neuronal reprogramming. (2014)
- Integrated Laplacian-based phase unwrapping and background phase removal for quantitative susceptibility mapping. (2014)
- Genetic variability in the regulation of gene expression in ten regions of the human brain. (2014)
- PolymiRTS Database 3.0: linking polymorphisms in microRNAs and their target sites with human diseases and biological pathways. (2014)
- Brain Imaging Analysis. (2014)
- A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
- Gene expression in the human brain: the current state of the study of specificity and spatiotemporal dynamics. (2013)
- The "Reading the Mind in the Eyes" test: systematic review of psychometric properties and a validation study in Italy. (2013)
- A large scale (N=102) functional neuroimaging study of response inhibition in a Go/NoGo task. (2013)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
- Whole brain susceptibility mapping using compressed sensing. (2012)
- Pilot study of iPS-derived neural cells to examine biologic effects of alcohol on human neurons in vitro. (2012)
- Acetylcholine as a neuromodulator: cholinergic signaling shapes nervous system function and behavior. (2012)
- Emerging role of non-coding RNA in neural plasticity, cognitive function, and neuropsychiatric disorders. (2012)
- Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. (2011)
- Role of ubiquitin-proteasome-mediated proteolysis in nervous system disease. (2011)
- Associations between cortical thickness and verbal fluency in childhood, adolescence, and young adulthood. (2011)
- Postmortem interval effect on RNA and gene expression in human brain tissue. (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)
- Pharmacological treatment of cannabis dependence. (2011)
- Motor response programming and movement time in children with heavy prenatal alcohol exposure. (2010)
- Meta-analysis in genome-wide association studies. (2009)
- Genome-wide association studies in ADHD. (2009)
- Neurotoxic effects and biomarkers of lead exposure: a review. (2009)
- Persistent deficits in heart rate response habituation following neonatal binge ethanol exposure. (2009)
- The error-related negativity (ERN) and psychopathology: toward an endophenotype. (2008)
- Mechanism of alcohol-induced oxidative stress and neuronal injury. (2008)
- Reduced striatal dopamine transporter density in abstinent methamphetamine and methcathinone users: evidence from positron emission tomography studies with [11C]WIN-35,428. (1998)
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 |