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SCI Abstract
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Harmonizing two measures of adaptive functioning using computational approaches: prediction of vineland adaptive behavior scales II (VABS-II) from the adaptive behavior assessment system II (ABAS-II) scores
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Behavioral decline in Shank3Δex4–22 mice during early adulthood parallels cerebellar granule cell glutamatergic synaptic changes
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Impact of chronic intranasal oxytocin administration on face expression processing in autistic children: a randomized controlled trial using fMRI
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Comparative profiling of white matter development in the human and mouse brain reveals volumetric deficits and delayed myelination in Angelman syndrome
Angelman syndrome (AS), a severe neurodevelopmental disorder resulting from the loss of the maternal UBE3A gene, is marked...
Molecular Autism
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Molecular architecture of the altered cortical complexity in autism
Autism spectrum disorder (ASD) is characterized by difficulties in social interaction, communication challenges, and repet...
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Is the association between mothers’ autistic traits and childhood autistic traits moderated by maternal pre-pregnancy body mass index?
Previous studies showed that there is a positive association between mothers’ and children’s autistic traits. ...
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Exploring the multidimensional nature of repetitive and restricted behaviors and interests (RRBI) in autism: neuroanatomical correlates and clinical implications
Repetitive and restricted behaviors and interests (RRBI) are core symptoms of autism with a complex entity and are commonl...
Molecular Autism
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Hyperthermia elevates brain temperature and improves behavioural signs in animal models of autism spectrum disorder
Autism spectrum disorders (ASD) are predominantly neurodevelopmental and largely genetically determined. However, there ar...
Molecular Autism
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Increased cerebral lactate levels in adults with autism spectrum disorders compared to non-autistic controls: a magnetic resonance spectroscopy study
Autism spectrum disorder (ASD) encompasses a heterogeneous group with varied phenotypes and etiologies. Identifying pathog...
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Effect of presentation rate on auditory processing in Rett syndrome: event-related potential study
Rett syndrome (RS) is a rare neurodevelopmental disorder characterized by mutations in the MECP2 gene. Patients with RS ha...
Molecular Autism
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Developmental prediction modeling based on diffusion tensor imaging uncovering age-dependent heterogeneity in early childhood autistic brain
There has been increasing evidence for atypical white matter (WM) microstructure in autistic people, but findings have bee...
Molecular Autism
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Tau reduction attenuates autism-like features in Fmr1 knockout mice
Fragile X syndrome (FXS) is a leading cause of autism spectrum disorder (ASD) and resulted from a loss of the FMR1-encoded...
Molecular Autism
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Translatome analysis of tuberous sclerosis complex 1 patient-derived neural progenitor cells reveals rapamycin-dependent and independent alterations
Tuberous sclerosis complex (TSC) is an inherited neurocutaneous disorder caused by mutations in the TSC1 or TSC2 genes, wi...
Molecular Autism
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Age-related changes in neural responses to sensory stimulation in autism: a cross-sectional study
Sensory over-responsivity (SOR) is an impairing sensory processing challenge in autism spectrum disorder (ASD) which shows...
Molecular Autism
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EEG functional connectivity in infants at elevated familial likelihood for autism spectrum disorder
Many studies have reported that autism spectrum disorder (ASD) is associated with atypical structural and functional conne...
Molecular Autism
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The neuroanatomical substrates of autism and ADHD and their link to putative genomic underpinnings
Autism spectrum disorders (ASD) are neurodevelopmental conditions accompanied by differences in brain development. Neuroan...
Molecular Autism
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Increased rates of chronic physical health conditions across all organ systems in autistic adolescents and adults
The poorer physical health of autistic adults compared to non-autistic adults has been highlighted by several epidemiologi...
Molecular Autism
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Cortex-restricted deletion of Foxp1 impairs barrel formation and induces aberrant tactile responses in a mouse model of autism
Many children and young people with autism spectrum disorder (ASD) display touch defensiveness or avoidance (hypersensitiv...
Molecular Autism
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Autistic adults benefit from and enjoy learning via social interaction as much as neurotypical adults do
Autistic people show poor processing of social signals (i.e. about the social world). But how do they learn via social int...
Molecular Autism
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Linking functional and structural brain organisation with behaviour in autism: a multimodal EU-AIMS Longitudinal European Autism Project (LEAP) study
Neuroimaging analyses of brain structure and function in autism have typically been conducted in isolation, missing the se...
Molecular Autism
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Examining the latent structure and correlates of sensory reactivity in autism: a multi-site integrative data analysis by the autism sensory research consortium
Differences in responding to sensory stimuli, including sensory hyperreactivity (HYPER), hyporeactivity (HYPO), and sensor...
Molecular Autism
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Sex-specific and sex-independent steroid-related biomarkers in early second trimester maternal serum associated with autism
Prenatal exposure to maternal metabolic conditions associated with inflammation and steroid dysregulation has previously b...
Molecular Autism
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Knockout of Tmlhe in mice is not associated with autism spectrum disorder phenotypes or motor dysfunction despite low carnitine levels
Deletion of exon 2 of the trimethyllysine hydroxylase epsilon (TMLHE) gene was identified in probands with autism spectrum...
Molecular Autism
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Shank3 deletion in PV neurons is associated with abnormal behaviors and neuronal functions that are rescued by increasing GABAergic signaling
Phelan–McDermid syndrome (PMS) is a neurodevelopmental disorder characterized by developmental delay, intellectual d...
Molecular Autism
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Personalized estimates of brain cortical structural variability in individuals with Autism spectrum disorder: the predictor of brain age and neurobiology relevance
Autism spectrum disorder (ASD) is a heritable condition related to brain development that affects a person’s percept...
Molecular Autism
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Neurodevelopmental impairments in children with septo-optic dysplasia spectrum conditions: a systematic review
Septo-optic dysplasia (SOD) is a rare condition diagnosed in children with two or more of the following: hypopituitarism, ...
Molecular Autism
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Rhesus macaque social functioning is paternally, but not maternally, inherited by sons: potential implications for autism
Quantitative autistic traits are common, heritable, and continuously distributed across the general human population. Patt...
Molecular Autism
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Correction: Understanding the relationship between cerebellar structure and social abilities
Sorbonne Université, UFR Médecine, 75005, Paris, FranceYannis ElandaloussiDepartment of Adult Psychiatry IMPACT-Mondor Uni...
Molecular Autism
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Autism-associated gene shank3 is necessary for social contagion in zebrafish
Animal models enable targeting autism-associated genes, such as the shank3 gene, to assess their impact on behavioural phe...
Molecular Autism
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Exploratory analysis of L1 retrotransposons expression in autism
Autism spectrum disorder (ASD) is a set of highly heterogeneous neurodevelopmental diseases whose genetic etiology is not ...
Molecular Autism
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