autism phenotype

Aliases

ASD, AUT, Autism Spectrum Disorder, Autism spectrum disorder, autism, autism risk, autism spectrum disorder, autism susceptibility, autistic, autistic adults, autistic child, autistic children, autistic disorder, autistic individuals, autistic phenotype, autistic population, autistic subject, autistic subjects, idiopathic autism, non-syndromic autism, nonsyndromic autism, simplex autism, sporadic autism

Related entities (3)

Mentioned in (55)

Papers in which this entity is mentioned.

• Single-cell exon deletion profiling reveals splicing events that shape gene expression and cell state dynamics. (2026)
• Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
• Normative modeling of brain MRI data identifies small subcortical volumes and associations with cognitive function in youth with fetal alcohol spectrum disorder (FASD). (2025)
• Identifying family environment profiles in families of children with prenatal alcohol exposure. (2025)
• Gastrulation-stage alcohol exposure induces similar rates of craniofacial malformations in male and female C57BL/6J mice. (2024)
• A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
• Adaptive, Externalizing, and Internalizing Behavior of Children with Prenatal Alcohol Exposure: A Comparison of Three Parent-Report Questionnaires. (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)
• Delayed cortical thinning in children and adolescents with prenatal alcohol exposure. (2023)
• Current considerations for fetal alcohol spectrum disorders: identification to intervention. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• mutations, genetic mosaicism and human disease. (2022)
• Stability and change in the interpretation of facial emotions in fetal alcohol spectrum disorders from childhood to adolescence. (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)
• SPOTlight: seeded NMF regression to deconvolute spatial transcriptomics spots with single-cell transcriptomes. (2021)
• Initial Feasibility of the "Families Moving Forward Connect" Mobile Health Intervention for Caregivers of Children With Fetal Alcohol Spectrum Disorders: Mixed Method Evaluation Within a Systematic User-Centered Design Approach. (2021)
• Best practices for variant calling in clinical sequencing. (2020)
• Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs. (2020)
• Kcnn2 blockade reverses learning deficits in a mouse model of fetal alcohol spectrum disorders. (2020)
• Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure. (2020)
• Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
• Clinical presentation, diagnosis, and management of fetal alcohol spectrum disorder. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE. (2018)
• Two-year cortical trajectories are abnormal in children and adolescents with prenatal alcohol exposure. (2018)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Functional connectivity abnormalities and associated cognitive deficits in fetal alcohol Spectrum disorders (FASD). (2017)
• Epigenetics studies of fetal alcohol spectrum disorder: where are we now? (2017)
• Longitudinal changes in pubertal maturation and white matter microstructure. (2017)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• Neurobehavioral Deficits Consistent Across Age and Sex in Youth with Prenatal Alcohol Exposure. (2016)
• Atypical cortical gyrification in adolescents with histories of heavy prenatal alcohol exposure. (2015)
• Anterior cingulate cortex surface area relates to behavioral inhibition in adolescents with and without heavy prenatal alcohol exposure. (2015)
• Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood. (2014)
• Automated cerebellar segmentation: Validation and application to detect smaller volumes in children prenatally exposed to alcohol. (2014)
• Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
• Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges. (2013)
• The effects of prenatal alcohol exposure and attention-deficit/hyperactivity disorder on psychopathology and behavior. (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)
• Adaptive behaviour in children and adolescents with foetal alcohol spectrum disorders: a comparison with specific learning disability and typical development. (2012)
• White matter microstructural alterations in children with prenatal methamphetamine/polydrug exposure. (2012)
• The quest for a neurobehavioral profile of heavy prenatal alcohol exposure. (2011)
• Magnetic resonance-based imaging in animal models of fetal alcohol spectrum disorder. (2011)
• Functional consequences of developmentally regulated alternative splicing. (2011)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (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)
• Differentiating prenatal exposure to methamphetamine and alcohol versus alcohol and not methamphetamine using tensor-based brain morphometry and discriminant analysis. (2010)
• Brain signatures of monetary loss and gain: outcome-related potentials in a single outcome gambling task. (2009)
• Copy-number-variation and copy-number-alteration region detection by cumulative plots. (2009)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)

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