intellectual disability phenotype
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Related entities (32)
Mentioned in (157)
Papers in which this entity is mentioned.
- Single cell and spatial alternative splicing analysis with Nanopore long read sequencing. (2025)
- Gastrulation-stage alcohol exposure induces similar rates of craniofacial malformations in male and female C57BL/6J mice. (2024)
- Reduction of APOE accounts for neurobehavioral deficits in fetal alcohol spectrum disorders. (2024)
- CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
- A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
- Associations among prenatal exposure to gestational diabetes mellitus, brain structure, and child adiposity markers. (2023)
- Adverse childhood experiences in children with fetal alcohol spectrum disorders and their effects on behavior. (2023)
- Effect of schizophrenia common variants on infant brain volumes: cross-sectional study in 207 term neonates in developing Human Connectome Project. (2023)
- Spiral drawing deficits in children with prenatal alcohol exposure. (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)
- mutations, genetic mosaicism and human disease. (2022)
- The effects of gestational choline supplementation on cerebellar Purkinje cell number in the sheep model of binge alcohol exposure during the first trimester-equivalent. (2022)
- A methodological pipeline to generate an epigenetic marker of prenatal exposure to air pollution indicators. (2022)
- Newborn differential DNA methylation and subcortical brain volumes as early signs of severe neurodevelopmental delay in a South African Birth Cohort Study. (2022)
- Fetal Alcohol Spectrum Disorders: Awareness to Insight in Just 50 Years. (2022)
- DNA methylation in relation to gestational age and brain dysmaturation in preterm infants. (2022)
- FXR1 regulation of parvalbumin interneurons in the prefrontal cortex is critical for schizophrenia-like behaviors. (2021)
- Validity and Reliability of Executive Function Measures in Children With Heavy Prenatal Alcohol Exposure: Correspondence Between Multiple Raters and Laboratory Measures. (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)
- Alternative splicing: Human disease and quantitative analysis from high-throughput sequencing. (2021)
- Effects of Prenatal Alcohol Exposure on the Volumes of the Lateral and Medial Walls of the Intraparietal Sulcus. (2021)
- Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
- Ethanol modulation of hippocampal neuroinflammation, myelination, and neurodevelopment in a postnatal mouse model of fetal alcohol spectrum disorders. (2021)
- Best practices for variant calling in clinical sequencing. (2020)
- Childhood Obesity, Cortical Structure, and Executive Function in Healthy Children. (2020)
- Tead transcription factors differentially regulate cortical development. (2020)
- Neural correlates of polygenic risk score for autism spectrum disorders in general population. (2020)
- Prenatal drug exposure and neurodevelopmental programming of glucocorticoid signalling. (2020)
- Kcnn2 blockade reverses learning deficits in a mouse model of fetal alcohol spectrum disorders. (2020)
- Choline, Neurological Development and Brain Function: A Systematic Review Focusing on the First 1000 Days. (2020)
- Neurodevelopment in adolescents and adults with fetal alcohol spectrum disorders (FASD): A magnetic resonance region of interest analysis. (2020)
- Murine Models for the Study of Fetal Alcohol Spectrum Disorders: An Overview. (2020)
- Trends in Alcohol Use Among Pregnant Women in the U.S., 2011-2018. (2020)
- The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
- The Relationship Between Socioeconomic Status and Brain Volume in Children and Adolescents With Prenatal Alcohol Exposure. (2020)
- Relationship of prenatal maternal obesity and diabetes to offspring neurodevelopmental and psychiatric disorders: a narrative review. (2020)
- Modification of stem cell states by alcohol and acetaldehyde. (2020)
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- Long-term spatial tracking of cells affected by environmental insults. (2020)
- Association Between Prenatal Exposure to Alcohol and Tobacco and Neonatal Brain Activity: Results From the Safe Passage Study. (2020)
- Construct and factorial validity of Neurobehavioral Disorder associated with Prenatal Alcohol Exposure (ND-PAE). (2020)
- Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
- A review on neuroimaging studies of genetic and environmental influences on early brain development. (2019)
- Alcohol Use in Pregnancy. (2019)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. (2019)
- Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders. (2019)
- Structural variant calling: the long and the short of it. (2019)
- Identification of common genetic risk variants for autism spectrum disorder. (2019)
- Hippocampal deficits in neurodevelopmental disorders. (2019)
- Psychiatric Genomics: An Update and an Agenda. (2018)
- What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics. (2018)
- Implications of altered maternal cytokine concentrations on infant outcomes in children with prenatal alcohol exposure. (2018)
- Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
- Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
- Activity-dependent Signaling and Epigenetic Abnormalities in Mice Exposed to Postnatal Ethanol. (2018)
- Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014. (2018)
- Identification of novel candidate disease genes from de novo exonic copy number variants. (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)
- Evidence that increased Kcnj6 gene dose is necessary for deficits in behavior and dentate gyrus synaptic plasticity in the Ts65Dn mouse model of Down syndrome. (2017)
- Genome-wide association analysis identifies common variants influencing infant brain volumes. (2017)
- Mapping and phasing of structural variation in patient genomes using nanopore sequencing. (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)
- 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)
- Epigenetic profiling of ADHD symptoms trajectories: a prospective, methylome-wide study. (2017)
- Prefrontal cortical responses in children with prenatal alcohol-related neurodevelopmental impairment: A functional near-infrared spectroscopy study. (2017)
- Translating genome-wide association findings into new therapeutics for psychiatry. (2016)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
- Nuclear organization and 3D chromatin architecture in cognition and neuropsychiatric disorders. (2016)
- New insights into the generation and role of de novo mutations in health and disease. (2016)
- Social cognition as an RDoC domain. (2016)
- De novo variants in sporadic cases of childhood onset schizophrenia. (2016)
- Fetal alcohol spectrum disorders: Clinical phenotype among a high-risk group of children and adolescents in Korea. (2016)
- Developmental ethanol exposure-induced sleep fragmentation predicts adult cognitive impairment. (2016)
- Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
- Plasma miRNA Profiles in Pregnant Women Predict Infant Outcomes following Prenatal Alcohol Exposure. (2016)
- Genome-wide association study identifies 74 loci associated with educational attainment. (2016)
- The association between parental attributions of misbehavior and parenting practices in caregivers raising children with prenatal alcohol exposure: A mixed-methods study. (2016)
- Dietary Nutrient Intake in School-Aged Children With Heavy Prenatal Alcohol Exposure. (2016)
- Maternal iron deficiency worsens the associative learning deficits and hippocampal and cerebellar losses in a rat model of fetal alcohol spectrum disorders. (2015)
- Fetal Alcohol Spectrum Disorders: An Overview from the Glia Perspective. (2015)
- Atypical cortical gyrification in adolescents with histories of heavy prenatal alcohol exposure. (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)
- Aberrant development of post-movement beta rebound in adolescents and young adults with fetal alcohol spectrum disorders. (2015)
- The discovery of integrated gene networks for autism and related disorders. (2015)
- Prenatal alcohol exposure alters steady-state and activated gene expression in the adult rat brain. (2015)
- Genetics and genomics of psychiatric disease. (2015)
- Neurobehavioral Disorder Associated with Prenatal Alcohol Exposure (ND-PAE): Review of Evidence and Guidelines for Assessment. (2015)
- The Effects of Arsenic Exposure on Neurological and Cognitive Dysfunction in Human and Rodent Studies: A Review. (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)
- Pre-administration of G9a/GLP inhibitor during synaptogenesis prevents postnatal ethanol-induced LTP deficits and neurobehavioral abnormalities in adult mice. (2014)
- Specific learning disorder: prevalence and gender differences. (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)
- Gene-ethanol interactions underlying fetal alcohol spectrum disorders. (2014)
- The clinical utility and specificity of parent report of executive function among children with prenatal alcohol exposure. (2014)
- A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. (2014)
- Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
- Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
- A comparison of the different animal models of fetal alcohol spectrum disorders and their use in studying complex behaviors. (2014)
- Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome. (2014)
- Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. (2013)
- Prevalence of amblyopia or strabismus in asian and non-Hispanic white preschool children: multi-ethnic pediatric eye disease study. (2013)
- Low dose prenatal ethanol exposure induces anxiety-like behaviour and alters dendritic morphology in the basolateral amygdala of rat offspring. (2013)
- Inadequate intake of nutrients essential for neurodevelopment in children with fetal alcohol spectrum disorders (FASD). (2013)
- Clinical whole-exome sequencing for the diagnosis of mendelian disorders. (2013)
- G9a-mediated histone methylation regulates ethanol-induced neurodegeneration in the neonatal mouse brain. (2013)
- Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013)
- Distribution of disease-associated copy number variants across distinct disorders of cognitive development. (2013)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Children with heavy prenatal alcohol exposure experience reduced control of isotonic force. (2013)
- Adequacy of maternal iron status protects against behavioral, neuroanatomical, and growth deficits in fetal alcohol spectrum disorders. (2012)
- Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
- Comparing the Effectiveness of On-Line versus In-Person Caregiver Education and Training for Behavioral Regulation in Families of Children with FASD. (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)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. (2012)
- A longitudinal study of the long-term consequences of drinking during pregnancy: heavy in utero alcohol exposure disrupts the normal processes of brain development. (2012)
- 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)
- Epilepsy genetics--past, present, and future. (2011)
- Spatio-temporal transcriptome of the human brain. (2011)
- Fetal alcohol spectrum disorders: neuropsychological and behavioral features. (2011)
- Human aggression across the lifespan: genetic propensities and environmental moderators. (2011)
- Down syndrome: searching for the genetic culprits. (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)
- 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)
- Early pharmacotherapy restores neurogenesis and cognitive performance in the Ts65Dn mouse model for Down syndrome. (2010)
- Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. (2010)
- A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
- Histone methylation regulates memory formation. (2010)
- The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. (2010)
- Prenatal Maternal Stress Associated with ADHD and Autistic Traits in early Childhood. (2010)
- Reduced cortical folding in mental retardation. (2010)
- Prenatal exposure to drugs: effects on brain development and implications for policy and education. (2009)
- The enrichment study of the Minnesota twin family study: increasing the yield of twin families at high risk for externalizing psychopathology. (2009)
- Mapping white matter integrity and neurobehavioral correlates in children with fetal alcohol spectrum disorders. (2008)
- Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
- PIASx is a MEF2 SUMO E3 ligase that promotes postsynaptic dendritic morphogenesis. (2007)
- Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis. (2005)
- Genetic contributions to human gyrification: sulcal morphometry in Williams syndrome. (2005)
- Origins of cortical interneuron subtypes. (2004)
- Relationship between availability of NMDA receptor subunits and their expression at the synapse. (2002)
- Effect of enriched environment rearing on impairments in cortical excitability and plasticity after prenatal alcohol exposure. (1999)
- Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. (1998)
- MRI and Prenatal Alcohol Exposure: Images Provide Insight Into FAS. (1994)
- A Long-Term Perspective of FAS. (1994)
Merged raw entities (7)
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 |
|---|---|---|---|
| intellectual disability | phenotype | 157 | 292 |
| icd-10 f7 | phenotype | — | — |
| icd-8 311-315 | phenotype | — | — |
| icd-9 317-319 | phenotype | — | — |
| non-familial id | phenotype | — | — |
| non-syndromic intellectual disability | phenotype | — | — |
| syndromic intellectual disability | phenotype | — | — |