autism spectrum disorders phenotype
Evidence from:
primary |
all sources
Related entities (7)
Mentioned in (78)
Papers in which this entity is mentioned.
- Genome-wide association testing beyond SNPs. (2025)
- Single cell and spatial alternative splicing analysis with Nanopore long read sequencing. (2025)
- Machine learning approaches to the identification of children affected by prenatal alcohol exposure: A narrative review. (2024)
- A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
- Association of in utero HIV exposure with child brain structure and language development: a South African birth cohort study. (2024)
- An overview of DNA methylation-derived trait score methods and applications. (2023)
- Predicting Alcohol-Related Memory Problems in Older Adults: A Machine Learning Study with Multi-Domain Features. (2023)
- Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
- Chronic oligodendrocyte injury in central nervous system pathologies. (2022)
- Neurocognitive function and associations with mental health in adults born preterm with very low birthweight or small for gestational age at term. (2022)
- Newborn differential DNA methylation and subcortical brain volumes as early signs of severe neurodevelopmental delay in a South African Birth Cohort Study. (2022)
- Opportunities for increased reproducibility and replicability of developmental neuroimaging. (2021)
- Fetal Alcohol Exposure Alters BOLD Activation Patterns in Brain Regions Mediating the Interpretation of Facial Affect. (2021)
- Executive and Social Functioning Across Development in Children and Adolescents With Prenatal Alcohol Exposure. (2021)
- Neural correlates of polygenic risk score for autism spectrum disorders in general population. (2020)
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- Peripheral Biomarkers for First-Episode Psychosis-Opportunities from the Neuroinflammatory Hypothesis of Schizophrenia. (2019)
- Relation Between Oppositional/Conduct Behaviors and Executive Function Among Youth with Histories of Heavy Prenatal Alcohol Exposure. (2019)
- Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. (2019)
- Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders. (2019)
- Challenges in pediatric neuroimaging. (2019)
- Attention and corpus callosum volumes in individuals with mucopolysaccharidosis type I. (2019)
- Hippocampal deficits in neurodevelopmental disorders. (2019)
- What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics. (2018)
- The Predictive Value of Developmental Assessments at 1 and 2 for Intelligence Quotients at 6. (2018)
- Combined Face-Brain Morphology and Associated Neurocognitive Correlates in Fetal Alcohol Spectrum Disorders. (2018)
- Mental Illnesses-Associated Fxr1 and Its Negative Regulator Gsk3β Are Modulators of Anxiety and Glutamatergic Neurotransmission. (2018)
- Executive Functioning Correlates With Communication Ability in Youth With Histories of Heavy Prenatal Alcohol Exposure. (2018)
- Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
- Cerebral organoids reveal early cortical maldevelopment in schizophrenia-computational anatomy and genomics, role of FGFR1. (2017)
- Assembly of functionally integrated human forebrain spheroids. (2017)
- Environmental factors influencing the risk of autism. (2017)
- Autism with intellectual disability is associated with increased levels of maternal cytokines and chemokines during gestation. (2017)
- Fetal Alcohol Spectrum Disorders: A Case Study. (2017)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- A Decision Tree to Identify Children Affected by Prenatal Alcohol Exposure. (2016)
- Social cognition as an RDoC domain. (2016)
- Abnormal Eating Behaviors Are Common in Children with Fetal Alcohol Spectrum Disorder. (2016)
- Prenatal Exposure to Arsenic Impairs Behavioral Flexibility and Cortical Structure in Mice. (2016)
- Theory of Mind in Children with Fetal Alcohol Spectrum Disorders. (2016)
- Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
- Acute alcohol exposure during neurulation: Behavioral and brain structural consequences in adolescent C57BL/6J mice. (2016)
- Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. (2016)
- Antenatal depression, treatment with selective serotonin reuptake inhibitors, and neonatal brain structure: A propensity-matched cohort study. (2016)
- Aberrant development of post-movement beta rebound in adolescents and young adults with fetal alcohol spectrum disorders. (2015)
- Opposite effects on facial morphology due to gene dosage sensitivity. (2014)
- Adolescent brain maturation and cortical folding: evidence for reductions in gyrification. (2014)
- Prefrontal activation during inhibitory control measured by near-infrared spectroscopy for differentiating between autism spectrum disorders and attention deficit hyperactivity disorder in adults. (2014)
- Induced neuronal reprogramming. (2014)
- Common DNA methylation alterations in multiple brain regions in autism. (2014)
- Heritability and genomics of gene expression in peripheral blood. (2014)
- Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
- Face shape differs in phylogenetically related populations. (2014)
- The use of near-infrared spectroscopy in the study of typical and atypical development. (2014)
- Neonatal cytokines and chemokines and risk of Autism Spectrum Disorder: the Early Markers for Autism (EMA) study: a case-control study. (2014)
- Increased gyrification, but comparable surface area in adolescents with autism spectrum disorders. (2013)
- Longitudinal change in the neural bases of adolescent social self-evaluations: effects of age and pubertal development. (2013)
- Prenatal ethanol exposure disrupts intraneocortical circuitry, cortical gene expression, and behavior in a mouse model of FASD. (2013)
- Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. (2013)
- Gene expression in the human brain: the current state of the study of specificity and spatiotemporal dynamics. (2013)
- Aberrant expression of long noncoding RNAs in autistic brain. (2013)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Predicting developmental status from 12 to 24 months in infants at risk for Autism Spectrum Disorder: a preliminary report. (2012)
- Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. (2012)
- Functional magnetic resonance imaging study comparing rhythmic finger tapping in children and adults. (2012)
- Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. (2012)
- Plasma cytokine levels in children with autistic disorder and unrelated siblings. (2012)
- Sleep problems in children with fetal alcohol spectrum disorders. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Spatio-temporal transcriptome of the human brain. (2011)
- Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome. (2011)
- Risk factors for behavioural problems in foetal alcohol spectrum disorders. (2011)
- Dimensions and correlates of attention deficit/hyperactivity disorder and Sluggish Cognitive Tempo. (2010)
- Novel roles for immune molecules in neural development: implications for neurodevelopmental disorders. (2010)
- A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
- A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. (1998)
Merged raw entities (6)
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 |
|---|---|---|---|
| autism spectrum disorders | phenotype | 78 | 93 |
| icd-10 f84.0 | phenotype | — | — |
| icd-10 f84.1 | phenotype | — | — |
| icd-10 f84.5 | phenotype | — | — |
| icd-8 299,99 | phenotype | — | — |
| icd-9 2990 | phenotype | — | — |