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 (122)

Mentioned in (326)

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)
• DNA methylation at birth and lateral ventricular volume in childhood: a neuroimaging epigenetics study. (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)
• Altered dendritic morphology in dorsolateral prefrontal cortex of nonhuman primates prenatally exposed to maternal immune activation. (2023)
• Delayed cortical thinning in children and adolescents with prenatal alcohol exposure. (2023)
• Current considerations for fetal alcohol spectrum disorders: identification to intervention. (2023)
• Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
• Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation. (2022)
• 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)
• Mapping brain asymmetry in health and disease through the ENIGMA consortium. (2022)
• Epigenetic profiling of social communication trajectories and co-occurring mental health problems: a prospective, methylome-wide association study. (2022)
• A methodological pipeline to generate an epigenetic marker of prenatal exposure to air pollution indicators. (2022)
• Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
• FXR1 regulation of parvalbumin interneurons in the prefrontal cortex is critical for schizophrenia-like behaviors. (2021)
• 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)
• Opportunities for increased reproducibility and replicability of developmental neuroimaging. (2021)
• Maternal Obesity during Pregnancy is Associated with Lower Cortical Thickness in the Neonate Brain. (2021)
• Placental genomic risk scores and early neurodevelopmental outcomes. (2021)
• SPOTlight: seeded NMF regression to deconvolute spatial transcriptomics spots with single-cell transcriptomes. (2021)
• Genetics of substance use disorders in the era of big data. (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)
• An enriched biosignature of gut microbiota-dependent metabolites characterizes maternal plasma in a mouse model of fetal alcohol spectrum disorder. (2021)
• Development of a high-throughput arrayed neural circuitry platform using human induced neurons for drug screening applications. (2020)
• Best practices for variant calling in clinical sequencing. (2020)
• Newborn amygdalar volumes are associated with maternal prenatal psychological distress in a sex-dependent way. (2020)
• Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs. (2020)
• Structural neuroimaging biomarkers for obsessive-compulsive disorder in the ENIGMA-OCD consortium: medication matters. (2020)
• Kcnn2 blockade reverses learning deficits in a mouse model of fetal alcohol spectrum disorders. (2020)
• Murine Models for the Study of Fetal Alcohol Spectrum Disorders: An Overview. (2020)
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
• PKA and Ube3a regulate SK2 channel trafficking to promote synaptic plasticity in hippocampus: Implications for Angelman Syndrome. (2020)
• Four-year follow-up of a randomized controlled trial of choline for neurodevelopment in fetal alcohol spectrum disorder. (2020)
• DNA methylation and brain structure and function across the life course: A systematic review. (2020)
• Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring. (2020)
• Relationship of prenatal maternal obesity and diabetes to offspring neurodevelopmental and psychiatric disorders: a narrative review. (2020)
• Para-limbic Structural Abnormalities Are Associated With Internalizing Symptoms in Children With Prenatal Alcohol Exposure. (2020)
• De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
• Multivariate models of brain volume for identification of children and adolescents with fetal alcohol spectrum disorder. (2020)
• Delineation of early brain development from fetuses to infants with diffusion MRI and beyond. (2019)
• "I'm Doing My Part, I Just Need Help From the Community": Intervention Implications of Foster and Adoptive Parents' Experiences Raising Children and Young Adults With FASD. (2019)
• Prenatal Developmental Origins of Future Psychopathology: Mechanisms and Pathways. (2019)
• Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
• In utero exposure to HIV and/or antiretroviral therapy: a systematic review of preclinical and clinical evidence of cognitive outcomes. (2019)
• A review on neuroimaging studies of genetic and environmental influences on early brain development. (2019)
• Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
• 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)
• Global DNA Methylation and Histone Posttranslational Modifications in Human and Nonhuman Primate Brain in Association with Prenatal Alcohol Exposure. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Growth and Neurodevelopment of HIV-Exposed Uninfected Children: a Conceptual Framework. (2019)
• Sex differences in the developing brain: insights from multimodal neuroimaging. (2019)
• Longitudinal associations between white matter maturation and cognitive development across early childhood. (2019)
• SK Channel Modulates Synaptic Plasticity by Tuning CaMKIIα/β Dynamics. (2019)
• Identification of common genetic risk variants for autism spectrum disorder. (2019)
• Prenatal Environment That Affects Neuronal Migration. (2019)
• Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue. (2019)
• Hippocampal deficits in neurodevelopmental disorders. (2019)
• Longitudinally Mapping Childhood Socioeconomic Status Associations with Cortical and Subcortical Morphology. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
• Epigenetic mechanisms in alcohol- and adversity-induced developmental origins of neurobehavioral functioning. (2018)
• What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics. (2018)
• Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE. (2018)
• Cerebrospinal fluid and the early brain development of autism. (2018)
• Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
• Imaging structural and functional brain development in early childhood. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
• Prenatal Alcohol Exposure: Profiling Developmental DNA Methylation Patterns in Central and Peripheral Tissues. (2018)
• Two-year cortical trajectories are abnormal in children and adolescents with prenatal alcohol exposure. (2018)
• Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
• Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. (2018)
• Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014. (2018)
• Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium. (2018)
• Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. (2018)
• Altered brain morphometry in 7-year old HIV-infected children on early ART. (2018)
• Developmental Connectomics from Infancy through Early Childhood. (2017)
• Satellite-like cells contribute to pax7-dependent skeletal muscle repair in adult zebrafish. (2017)
• Cerebral organoids reveal early cortical maldevelopment in schizophrenia-computational anatomy and genomics, role of FGFR1. (2017)
• Functional Connectivity of the Infant Human Brain: Plastic and Modifiable. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Machine learning shows association between genetic variability in and cerebral connectivity in preterm infants. (2017)
• Environmental factors influencing the risk of autism. (2017)
• Quantifying cortical development in typically developing toddlers and young children, 1-6 years of age. (2017)
• BECon: a tool for interpreting DNA methylation findings from blood in the context of brain. (2017)
• Sex differences in DNA methylation of the cord blood are related to sex-bias psychiatric diseases. (2017)
• Parent-Mediated Intervention Training Delivered Remotely for Children With Autism Spectrum Disorder Living Outside of Urban Areas: Systematic Review. (2017)
• Early childhood development coming of age: science through the life course. (2017)
• Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants. (2017)
• Sexual dimorphism of volume reduction but not cognitive deficit in fetal alcohol spectrum disorders: A combined diffusion tensor imaging, cortical thickness and brain volume study. (2017)
• ApoE, ApoE Receptors, and the Synapse in Alzheimer's Disease. (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)
• Effect of Neuroinflammation on Synaptic Organization and Function in the Developing Brain: Implications for Neurodevelopmental and Neurodegenerative Disorders. (2017)
• Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential. (2017)
• Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature. (2017)
• Dysregulation of Cortical Neuron DNA Methylation Profile in Autism Spectrum Disorder. (2017)
• Single-Cell Profiling of an In Vitro Model of Human Interneuron Development Reveals Temporal Dynamics of Cell Type Production and Maturation. (2017)
• Neural correlates of language variability in preschool-aged boys with autism spectrum disorder. (2017)
• Evidence for an immune signature of prenatal alcohol exposure in female rats. (2016)
• Translating genome-wide association findings into new therapeutics for psychiatry. (2016)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• Efficient derivation of microglia-like cells from human pluripotent stem cells. (2016)
• De novo variants in sporadic cases of childhood onset schizophrenia. (2016)
• Abnormal Eating Behaviors Are Common in Children with Fetal Alcohol Spectrum Disorder. (2016)
• Neurobehavioral Deficits Consistent Across Age and Sex in Youth with Prenatal Alcohol Exposure. (2016)
• The diffusion tensor imaging (DTI) component of the NIH MRI study of normal brain development (PedsDTI). (2016)
• The placenta and neurodevelopment: sex differences in prenatal vulnerability. (2016)
• Delayed match-to-sample in working memory: A BrainMap meta-analysis. (2016)
• Sustained synchronized neuronal network activity in a human astrocyte co-culture system. (2016)
• The Placenta as a Mediator of Stress Effects on Neurodevelopmental Reprogramming. (2016)
• Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
• DNA methylation signature of human fetal alcohol spectrum disorder. (2016)
• Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. (2016)
• The association between parental attributions of misbehavior and parenting practices in caregivers raising children with prenatal alcohol exposure: A mixed-methods study. (2016)
• The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort. (2016)
• Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure. (2015)
• Fetal Alcohol Spectrum Disorders: An Overview from the Glia Perspective. (2015)
• Functional and structural brain correlates of risk for major depression in children with familial depression. (2015)
• Early maternal alcohol consumption alters hippocampal DNA methylation, gene expression and volume in a mouse model. (2015)
• Executive functioning deficits in preschool children with Fetal Alcohol Spectrum Disorders. (2015)
• Recent genetic findings in schizophrenia and their therapeutic relevance. (2015)
• Child psychiatry branch of the National Institute of Mental Health longitudinal structural magnetic resonance imaging study of human brain development. (2015)
• Atypical cortical gyrification in adolescents with histories of heavy prenatal alcohol exposure. (2015)
• A review of the nonpressor and nonantidiuretic actions of the hormone vasopressin. (2015)
• An introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disorders. (2015)
• Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model. (2015)
• Annual research review: Growth connectomics--the organization and reorganization of brain networks during normal and abnormal development. (2015)
• The potential of infant fMRI research and the study of early life stress as a promising exemplar. (2015)
• Cortical maturation and myelination in healthy toddlers and young children. (2015)
• ERBB4 polymorphism and family history of psychiatric disorders on age-related cortical changes in healthy children. (2015)
• Long Noncoding RNA-Directed Epigenetic Regulation of Gene Expression Is Associated With Anxiety-like Behavior in Mice. (2015)
• Development of the uncinate fasciculus: Implications for theory and developmental disorders. (2015)
• Impact of prenatal environmental stress on cortical development. (2015)
• Early-life exposure to the SSRI paroxetine exacerbates depression-like behavior in anxiety/depression-prone rats. (2015)
• Evaluating historical candidate genes for schizophrenia. (2015)
• Methylomic trajectories across human fetal brain development. (2015)
• Use of resting-state functional MRI to study brain development and injury in neonates. (2015)
• The discovery of integrated gene networks for autism and related disorders. (2015)
• Anterior cingulate cortex surface area relates to behavioral inhibition in adolescents with and without heavy prenatal alcohol exposure. (2015)
• The neurobiology of childhood structural brain development: conception through adulthood. (2014)
• Developmental stages and sex differences of white matter and behavioral development through adolescence: a longitudinal diffusion tensor imaging (DTI) study. (2014)
• Moderator effects of working memory on the stability of ADHD symptoms by dopamine receptor gene polymorphisms during development. (2014)
• White matter development and early cognition in babies and toddlers. (2014)
• Multi-atlas segmentation of subcortical brain structures via the AutoSeg software pipeline. (2014)
• High resolution magnetic resonance imaging for characterization of the neuroligin-3 knock-in mouse model associated with autism spectrum disorder. (2014)
• The role of BAF (mSWI/SNF) complexes in mammalian neural development. (2014)
• Guidelines for investigating causality of sequence variants in human disease. (2014)
• Pre-administration of G9a/GLP inhibitor during synaptogenesis prevents postnatal ethanol-induced LTP deficits and neurobehavioral abnormalities in adult mice. (2014)
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
• Pediatric neuroimaging using magnetic resonance imaging during non-sedated sleep. (2014)
• Programming of neural cells by (endo)cannabinoids: from physiological rules to emerging therapies. (2014)
• Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood. (2014)
• Common DNA methylation alterations in multiple brain regions in autism. (2014)
• Roles of heat shock factor 1 in neuronal response to fetal environmental risks and its relevance to brain disorders. (2014)
• Effects of Acute Prenatal Exposure to Ethanol on microRNA Expression are Ameliorated by Social Enrichment. (2014)
• Pattern classification of response inhibition in ADHD: toward the development of neurobiological markers for ADHD. (2014)
• Heritability and genomics of gene expression in peripheral blood. (2014)
• Cortical morphology in children with alcohol-related neurodevelopmental disorder. (2014)
• Ethanol exposure induces neonatal neurodegeneration by enhancing CB1R Exon1 histone H4K8 acetylation and up-regulating CB1R function causing neurobehavioral abnormalities in adult mice. (2014)
• Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
• Prevention of secondary conditions in fetal alcohol spectrum disorders: identification of systems-level barriers. (2014)
• Genome-wide association discoveries of alcohol dependence. (2014)
• Automated cerebellar segmentation: Validation and application to detect smaller volumes in children prenatally exposed to alcohol. (2014)
• In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (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)
• Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
• Development of thalamocortical connectivity during infancy and its cognitive correlations. (2014)
• Identification of cell-specific patterns of reference gene stability in quantitative reverse-transcriptase polymerase chain reaction studies of embryonic, placental and neural stem models of prenatal ethanol exposure. (2013)
• Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges. (2013)
• Modeling transformations of neurodevelopmental sequences across mammalian species. (2013)
• Topological properties of large-scale structural brain networks in children with familial risk for reading difficulties. (2013)
• Candidate gene association studies: a comprehensive guide to useful in silico tools. (2013)
• Glycine receptors and brain development. (2013)
• Longitudinal change in the neural bases of adolescent social self-evaluations: effects of age and pubertal development. (2013)
• Inadequate intake of nutrients essential for neurodevelopment in children with fetal alcohol spectrum disorders (FASD). (2013)
• A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
• Prenatal ethanol exposure disrupts intraneocortical circuitry, cortical gene expression, and behavior in a mouse model of FASD. (2013)
• Global functional connectivity abnormalities in children with fetal alcohol spectrum disorders. (2013)
• Functional brain imaging across development. (2013)
• Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. (2013)
• Distribution of disease-associated copy number variants across distinct disorders of cognitive development. (2013)
• Gait analysis of teenagers and young adults diagnosed with autism and severe verbal communication disorders. (2013)
• The effects of prenatal alcohol exposure and attention-deficit/hyperactivity disorder on psychopathology and behavior. (2013)
• A developmental study of the feedback-related negativity from 10-17 years: age and sex effects for reward versus non-reward. (2013)
• Long-lasting neural circuit dysfunction following developmental ethanol exposure. (2013)
• Coordinated cell type-specific epigenetic remodeling in prefrontal cortex begins before birth and continues into early adulthood. (2013)
• Aberrant expression of long noncoding RNAs in autistic brain. (2013)
• Topological organization of functional brain networks in healthy children: differences in relation to age, sex, and intelligence. (2013)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
• The "Reading the Mind in the Eyes" test: systematic review of psychometric properties and a validation study in Italy. (2013)
• Cognition assessment using the NIH Toolbox. (2013)
• Topological organization of functional brain networks in healthy children: differences in relation to age, sex, and intelligence. (2013)
• Development of cortical surface area and gyrification in attention-deficit/hyperactivity disorder. (2012)
• Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
• Large-scale objective phenotyping of 3D facial morphology. (2012)
• HDAC1 regulates fear extinction in mice. (2012)
• Neuroanatomical assessment of biological maturity. (2012)
• Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
• Predicting developmental status from 12 to 24 months in infants at risk for Autism Spectrum Disorder: a preliminary report. (2012)
• Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. (2012)
• Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum. (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)
• Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. (2012)
• CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
• Plasma cytokine levels in children with autistic disorder and unrelated siblings. (2012)
• Pathway analysis of genomic data: concepts, methods, and prospects for future development. (2012)
• Asymmetric bias in user guided segmentations of brain structures. (2012)
• The genetic basis of addictive disorders. (2012)
• Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. (2012)
• Maternal immune activation yields offspring displaying mouse versions of the three core symptoms of autism. (2012)
• The neural effects of psychotropic medications in children and adolescents. (2012)
• Chronic intermittent ethanol exposure and its removal induce a different miRNA expression pattern in primary cortical neuronal cultures. (2012)
• Emerging role of non-coding RNA in neural plasticity, cognitive function, and neuropsychiatric disorders. (2012)
• Maternal immune activation by LPS selectively alters specific gene expression profiles of interneuron migration and oxidative stress in the fetus without triggering a fetal immune response. (2012)
• Exploration and modulation of brain network interactions with noninvasive brain stimulation in combination with neuroimaging. (2012)
• The quest for a neurobehavioral profile of heavy prenatal alcohol exposure. (2011)
• High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
• Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
• DISC1 at 10: connecting psychiatric genetics and neuroscience. (2011)
• Epilepsy genetics--past, present, and future. (2011)
• Mapping infant brain myelination with magnetic resonance imaging. (2011)
• Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes. (2011)
• Relating MEG measured motor cortical oscillations to resting γ-aminobutyric acid (GABA) concentration. (2011)
• Teratogenic effects of thalidomide: molecular mechanisms. (2011)
• Early childhood exposure to anesthesia and risk of developmental and behavioral disorders in a sibling birth cohort. (2011)
• Developmental trajectories during adolescence in males and females: a cross-species understanding of underlying brain changes. (2011)
• Magnetic resonance-based imaging in animal models of fetal alcohol spectrum disorder. (2011)
• Classification of neurocognitive disorders in DSM-5: a work in progress. (2011)
• Functional connectivity MRI in infants: exploration of the functional organization of the developing brain. (2011)
• Functional consequences of developmentally regulated alternative splicing. (2011)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• How does your cortex grow? (2011)
• Characterization of the corpus callosum in very preterm and full-term infants utilizing MRI. (2011)
• Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. (2011)
• MicroRNA expression aberration as potential peripheral blood biomarkers for schizophrenia. (2011)
• Thirty years and counting: finding meaning in the N400 component of the event-related brain potential (ERP). (2011)
• Inter-hemispheric functional connectivity disruption in children with prenatal alcohol exposure. (2011)
• Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
• Expanding the range of ZNF804A variants conferring risk of psychosis. (2011)
• Basal forebrain involvement in low-functioning autistic children: a voxel-based morphometry study. (2011)
• Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. (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)
• Increased midgestational IFN-γ, IL-4 and IL-5 in women bearing a child with autism: A case-control study. (2011)
• Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions. (2011)
• Brain growth across the life span in autism: age-specific changes in anatomical pathology. (2011)
• From genotype to EEG endophenotype: a route for post-genomic understanding of complex psychiatric disease? (2010)
• Genetics of psychiatric disorders methods: molecular approaches. (2010)
• Prenatal alcohol exposure alters biobehavioral reactivity to pain in newborns. (2010)
• Genetic control over the resting brain. (2010)
• "CRASH"ing with the worm: insights into L1CAM functions and mechanisms. (2010)
• Motor response programming and movement time in children with heavy prenatal alcohol exposure. (2010)
• A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
• Does childhood executive function predict adolescent functional outcomes in girls with ADHD? (2010)
• Normal development of brain circuits. (2010)
• Genetic and epigenetic insights into fetal alcohol spectrum disorders. (2010)
• Structural MRI of pediatric brain development: what have we learned and where are we going? (2010)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. (2010)
• The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. (2010)
• Associations between IQ, total and regional brain volumes, and demography in a large normative sample of healthy children and adolescents. (2010)
• Neuroimaging study designs, computational analyses and data provenance using the LONI pipeline. (2010)
• Novel roles for immune molecules in neural development: implications for neurodevelopmental disorders. (2010)
• Contribution of callosal connections to the interhemispheric integration of visuomotor and cognitive processes. (2010)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• MR diffusion tensor imaging: a window into white matter integrity of the working brain. (2010)
• Cortical gyrification in autistic and Asperger disorders: a preliminary magnetic resonance imaging study. (2010)
• Externalizing and internalizing behaviors in ASD. (2010)
• Prenatal Maternal Stress Associated with ADHD and Autistic Traits in early Childhood. (2010)
• Differentiating prenatal exposure to methamphetamine and alcohol versus alcohol and not methamphetamine using tensor-based brain morphometry and discriminant analysis. (2010)
• Total brain volume and corpus callosum size in medication-naïve adolescents and young adults with autism spectrum disorder. (2009)
• The epigenetics of sex differences in the brain. (2009)
• Altering cortical connectivity: remediation-induced changes in the white matter of poor readers. (2009)
• Classification in DTI using shapes of white matter tracts. (2009)
• A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
• Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
• A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder. (2009)
• Group analysis of DTI fiber tract statistics with application to neurodevelopment. (2009)
• Neurocognitive profile in children with fetal alcohol spectrum disorders. (2009)
• Brain signatures of monetary loss and gain: outcome-related potentials in a single outcome gambling task. (2009)
• A comprehensive volumetric analysis of the cerebellum in children and adolescents with autism spectrum disorder. (2009)
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
• Genome-wide association studies in ADHD. (2009)
• Microstructural corpus callosum anomalies in children with prenatal alcohol exposure: an extension of previous diffusion tensor imaging findings. (2009)
• Cerebellar vermal volumes and behavioral correlates in children with autism spectrum disorder. (2009)
• Neuroimaging of children following prenatal drug exposure. (2009)
• New insights into the genetics of addiction. (2009)
• Neuroimaging of children following prenatal drug exposure. (2009)
• Copy-number-variation and copy-number-alteration region detection by cumulative plots. (2009)
• Impact of maternal stress, depression and anxiety on fetal neurobehavioral development. (2009)
• Effects of prenatal methamphetamine exposure on verbal memory revealed with functional magnetic resonance imaging. (2009)
• Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. (2009)
• Evolution of the neocortex: a perspective from developmental biology. (2009)
• Efficient, Distributed and Interactive Neuroimaging Data Analysis Using the LONI Pipeline. (2009)
• Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
• Characterization of white matter microstructure in fetal alcohol spectrum disorders. (2009)
• A structural MRI study of human brain development from birth to 2 years. (2008)
• The relationship of 5HTT (SLC6A4) methylation and genotype on mRNA expression and liability to major depression and alcohol dependence in subjects from the Iowa Adoption Studies. (2008)
• Measuring brain connectivity: diffusion tensor imaging validates resting state temporal correlations. (2008)
• Structural insights into aberrant topological patterns of large-scale cortical networks in Alzheimer's disease. (2008)
• The changing impact of genes and environment on brain development during childhood and adolescence: initial findings from a neuroimaging study of pediatric twins. (2008)
• Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
• The new neurobiology of autism: cortex, connectivity, and neuronal organization. (2007)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
• Triangulating a cognitive control network using diffusion-weighted magnetic resonance imaging (MRI) and functional MRI. (2007)
• Season of birth and dopamine receptor gene associations with impulsivity, sensation seeking and reproductive behaviors. (2007)
• Maternal immune activation alters fetal brain development through interleukin-6. (2007)
• Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience. (2006)
• Dynamic mapping of human cortical development during childhood through early adulthood. (2004)
• Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. (2000)
• Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. (1998)

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