epilepsy phenotype
Evidence from:
primary |
all sources
Related entities (11)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Alcoholic proband | associated_with | epilepsy | — | 1 |
| behavioral disorders | associated_with | epilepsy | — | 1 |
| beta oscillations | associated_with | epilepsy | — | 1 |
| beta power | risk_factor_for | epilepsy | — | 1 |
| beta power | associated_with | epilepsy | 0.014 | 1 |
| EEG | biomarker_for | epilepsy | — | 1 |
| EEG phenotypes | associated_with | epilepsy | — | 1 |
| GABA | targets | epilepsy | — | 1 |
| GABRA2 | associated_with | epilepsy | — | 1 |
| glutamate | associated_with | epilepsy | — | 1 |
| Kcnj6 | associated_with | epilepsy | — | 1 |
Mentioned in (82)
Papers in which this entity is mentioned.
- Regional cerebellum volume anomalies and associated cognitive function in children with fetal alcohol spectrum disorders. (2026)
- Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder. (2025)
- Intranasal Administration of KCNN2 Blocking Peptide Improves Deficits in Cognitive Flexibility in Mouse Model of Fetal Alcohol Spectrum Disorders. (2025)
- Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
- Regional hippocampal thinning and gyrification abnormalities and associated cognition in children with prenatal alcohol exposure. (2025)
- Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder. (2025)
- Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition. (2025)
- Parenting by individuals with fetal alcohol spectrum disorders and neurobehavioral outcomes in their offspring. (2024)
- Lower resting state functional connectivity partially mediates adverse effects of prenatal alcohol exposure on arithmetic performance in children. (2024)
- A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
- The Human Phenotype Ontology in 2024: phenotypes around the world. (2024)
- Larger-scale feasibility trial of the families moving forward (FMF) connect mobile health intervention for caregivers raising children with fetal alcohol spectrum disorders. (2024)
- My Health Coach: Community members' perspectives on a mobile health tool for adults with fetal alcohol spectrum disorders. (2024)
- Alcohol reverses the effects of KCNJ6 (GIRK2) noncoding variants on excitability of human glutamatergic neurons. (2023)
- Predicting Fetal Alcohol Spectrum Disorders Using Machine Learning Techniques: Multisite Retrospective Cohort Study. (2023)
- Gene-alcohol interactions in birth defects. (2023)
- Comparison of three systems for the diagnosis of fetal alcohol spectrum disorders in a community sample. (2023)
- Atypical developmental trajectories of white matter microstructure in prenatal alcohol exposure: Preliminary evidence from neurite orientation dispersion and density imaging. (2023)
- Delayed cortical thinning in children and adolescents with prenatal alcohol exposure. (2023)
- Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
- Compromised interhemispheric transfer of information partially mediates cognitive function deficits in adolescents with fetal alcohol syndrome. (2022)
- Stability and change in the interpretation of facial emotions in fetal alcohol spectrum disorders from childhood to adolescence. (2022)
- Evidence for long-lasting alterations in the fecal microbiota following prenatal alcohol exposure. (2022)
- Hippocampal subfield abnormalities and memory functioning in children with fetal alcohol Spectrum disorders. (2021)
- Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
- Nanopore sequencing technology, bioinformatics and applications. (2021)
- Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress. (2021)
- An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders. (2021)
- Effects of Prenatal Alcohol Exposure on the Volumes of the Lateral and Medial Walls of the Intraparietal Sulcus. (2021)
- Fetal Alcohol Exposure Alters BOLD Activation Patterns in Brain Regions Mediating the Interpretation of Facial Affect. (2021)
- Joint single-cell measurements of nuclear proteins and RNA in vivo. (2021)
- Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
- Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
- Validity of automated FreeSurfer segmentation compared to manual tracing in detecting prenatal alcohol exposure-related subcortical and corpus callosal alterations in 9- to 11-year-old children. (2020)
- Reduced Hippocampal Volumes Partially Mediate Effects of Prenatal Alcohol Exposure on Spatial Navigation on a Virtual Water Maze Task in Children. (2020)
- A Mobile Health Intervention for Fetal Alcohol Spectrum Disorders (Families Moving Forward Connect): Development and Qualitative Evaluation of Design and Functionalities. (2020)
- Neurodevelopment in adolescents and adults with fetal alcohol spectrum disorders (FASD): A magnetic resonance region of interest analysis. (2020)
- Prenatal Alcohol Exposure Alters Error Detection During Simple Arithmetic Processing: An Electroencephalography Study. (2020)
- Patterns of Prenatal Alcohol Exposure and Alcohol-Related Dysmorphic Features. (2020)
- Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure. (2020)
- Linking genes, circuits, and behavior: network connectivity as a novel endophenotype of externalizing. (2019)
- Clinical presentation, diagnosis, and management of fetal alcohol spectrum disorder. (2019)
- Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
- Two-year cortical trajectories are abnormal in children and adolescents with prenatal alcohol exposure. (2018)
- GAVIN: Gene-Aware Variant INterpretation for medical sequencing. (2017)
- Cortical gyrification is abnormal in children with prenatal alcohol exposure. (2017)
- The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
- Genetic correlates of the development of theta event related oscillations in adolescents and young adults. (2017)
- Heavy Prenatal Alcohol Exposure is Related to Smaller Corpus Callosum in Newborn MRI Scans. (2017)
- Fetal Alcohol Spectrum Disorders: A Case Study. (2017)
- Functional connectivity abnormalities and associated cognitive deficits in fetal alcohol Spectrum disorders (FASD). (2017)
- Reductions in Corpus Callosum Volume Partially Mediate Effects of Prenatal Alcohol Exposure on IQ. (2017)
- Longitudinal changes in pubertal maturation and white matter microstructure. (2017)
- Prospective Memory Impairment in Children with Prenatal Alcohol Exposure. (2016)
- New insights into the generation and role of de novo mutations in health and disease. (2016)
- Theory of Mind in Children with Fetal Alcohol Spectrum Disorders. (2016)
- Verbal learning and memory impairment in children with fetal alcohol spectrum disorders. (2015)
- Gender modulates the development of theta event related oscillations in adolescents and young adults. (2015)
- Neural correlates of cerebellar-mediated timing during finger tapping in children with fetal alcohol spectrum disorders. (2015)
- An in vivo 1H magnetic resonance spectroscopy study of the deep cerebellar nuclei in children with fetal alcohol spectrum disorders. (2014)
- A tensor-based morphometry analysis of regional differences in brain volume in relation to prenatal alcohol exposure. (2014)
- Infant emotional withdrawal: a precursor of affective and cognitive disturbance in fetal alcohol spectrum disorders. (2014)
- The clinical utility and specificity of parent report of executive function among children with prenatal alcohol exposure. (2014)
- Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges. (2013)
- Effect of predictive cuing on response inhibition in children with heavy prenatal alcohol exposure. (2013)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- Large-scale objective phenotyping of 3D facial morphology. (2012)
- Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
- Alcohol delays the emergence of the fetal elicited startle response, but only transiently. (2012)
- Magnetic resonance-based imaging in animal models of fetal alcohol spectrum disorder. (2011)
- Functional consequences of developmentally regulated alternative splicing. (2011)
- The effects of a single memantine treatment on behavioral alterations associated with binge alcohol exposure in neonatal rats. (2011)
- Focus on: magnetic resonance-based studies of fetal alcohol spectrum disorders in animal models. (2011)
- Ventromedian forebrain dysgenesis follows early prenatal ethanol exposure in mice. (2011)
- Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
- Obesity, smoking, and frontal brain dysfunction. (2010)
- Infant Symbolic Play as an Early Indicator of Fetal Alcohol-Related Deficit. (2010)
- Cingulate gyrus morphology in children and adolescents with fetal alcohol spectrum disorders. (2010)
- Magnetic resonance microscopy defines ethanol-induced brain abnormalities in prenatal mice: effects of acute insult on gestational day 7. (2010)
- Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence. (2009)
- Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)
Merged raw entities (10)
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 |
|---|---|---|---|
| epilepsy | phenotype | 190 | 348 |
| seizures | phenotype | 125 | 186 |
| seizure | phenotype | 24 | 48 |
| seizure disorder | phenotype | 19 | 22 |
| epileptic seizures | phenotype | 7 | 9 |
| idiopathic epilepsy | phenotype | 3 | 4 |
| generalized epilepsy | phenotype | 2 | 4 |
| epileptic seizure | phenotype | 1 | 1 |
| epileptic | phenotype | — | — |
| epileptic focus | phenotype | — | — |