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SCI Abstract
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Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletion
16p11.2 deletion syndrome (16p11.2DS) is a recurrent CNV that occurs de novo in approximately 70% of cases and confers ris...
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Pathways to autism diagnosis in adulthood
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Diffusivity alterations related to cognitive performance and phenylalanine levels in early-treated adults with phenylketonuria
Altered white matter (WM) is consistently reported in patients with phenylketonuria (PKU). However, the knowledge about WM...
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Novel ANKRD17 variants implicate synaptic and mitochondrial disruptions in intellectual disability and autism spectrum disorder
ANKRD17 has recently been implicated in intellectual disability (ID) and autism spectrum disorder (ASD); however, the unde...
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Assessing receptive verb knowledge in late talkers and autistic children: advances and cautionary tales
Using eye-tracking, we assessed the receptive verb vocabularies of age-matched late talkers and typically developing child...
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Degraded inferior colliculus responses to complex sounds in prenatally exposed VPA rats
Individuals with autism spectrum disorders (ASD) often exhibit altered sensory processing and deficits in language develop...
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White matter microstructure of children with sensory over-responsivity is associated with affective behavior
Sensory processing dysfunction (SPD) is linked to altered white matter (WM) microstructure in school-age children. Sensory...
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Assessing the integrity of auditory sensory memory processing in CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): an auditory evoked potential study of the duration-evoked mismatch negativity (MMN)
We interrogated auditory sensory memory capabilities in individuals with CLN3 disease (juvenile neuronal ceroid lipofuscin...
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The association between cardiovascular health and cognition in adults with Down syndrome
Evidence in the general population suggests that predictors of cardiovascular health such as moderate to vigorous physical...
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The use of eye-tracking technology as a tool to evaluate social cognition in people with an intellectual disability: a systematic review and meta-analysis
Relatively little is known about social cognition in people with intellectual disability (ID), and how this may support un...
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Endophenotype trait domains for advancing gene discovery in autism spectrum disorder
Autism spectrum disorder (ASD) is associated with a diverse range of etiological processes, including both genetic and non...
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Neural oscillatory activity and connectivity in children who stutter during a non-speech motor task
Neural motor control rests on the dynamic interaction of cortical and subcortical regions, which is reflected in the modul...
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Autism through midlife: trajectories of symptoms, behavioral functioning, and health
This study describes change in autism symptoms, behavioral functioning, and health measured prospectively over 22 ...
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Age of diagnosis for children with chromosome 15q syndromes
The objective of this study was to identify the age of diagnosis for children with one of three neurogenetic conditions re...
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Correction: The diagnostic journey of genetically defined neurodevelopmental disorders
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, whi...
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A mouse model of ATRX deficiency with cognitive deficits and autistic traits
ATRX is an ATP-dependent chromatin remodeling protein with essential roles in safeguarding genome integrity and modulating...
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Hypovitaminosis D in persons with Down syndrome and autism spectrum disorder
Plasma levels of vitamin D have been reported to be low in persons with Down syndrome (DS) and existing data is limited to...
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The microstructural change of the brain and its clinical severity association in pediatric Tourette syndrome patients
Gilles de la Tourette syndrome (GTS) is a prevalent pediatric neurological disorder. Most studies point to abnormalities i...
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Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study
Recent advances in the understanding of neurodevelopmental disorders such as Rett syndrome (RTT) have enabled the discover...
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International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)
Tuberous sclerosis complex (TSC) is associated with a wide range of physical manifestations for which international clinic...
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Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, whi...
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Neurogenetic mechanisms of risk for ADHD: Examining associations of polygenic scores and brain volumes in a population cohort
ADHD polygenic scores (PGSs) have been previously shown to predict ADHD outcomes in several studies. However, ADHD PGSs ar...
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Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
Williams syndrome (WS), a rare neurodevelopmental disorder caused by hemizygous deletion of ~ 25 genes from ch...
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Why are only some children with autism spectrum disorder misclassified by the social communication questionnaire? An empirical investigation of individual differences in sensitivity and specificity in a clinic-referred sample
The Social Communication Questionnaire (SCQ) is a checklist for autism spectrum disorder (ASD) commonly used in research a...
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Intelligence, motoric and psychological outcomes in children from different ART treatments: a systematic review and meta-analysis
Subtle abnormalities in children’s intelligence, motor skills, and psychology from various assisted reproductive tre...
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Properties of white matter tract diffusivity in children with developmental dyslexia and comorbid attention deficit/hyperactivity disorder
Developmental dyslexia (DD) and attention deficit/hyperactivity disorder (ADHD) are highly comorbid neurodevelopmental dis...
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Clinical characteristics and long-term neurodevelopmental outcomes of leukomalacia in preterm infants and term infants: a cohort study
Leukomalacia is a serious form of neonatal brain injury that often leads to neurodevelopmental impairment, and studies on ...
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Enabling endpoint development for interventional clinical trials in individuals with Angelman syndrome: a prospective, longitudinal, observational clinical study (FREESIAS)
Angelman syndrome (AS) is a rare neurodevelopmental disorder characterized by the absence of a functional UBE3A gene, whic...
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Developmental delays in cortical auditory temporal processing in a mouse model of Fragile X syndrome
Autism spectrum disorders (ASD) encompass a wide array of debilitating symptoms, including sensory dysfunction and delayed...
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Sleep disturbances are associated with irritability in ASD children with sensory sensitivities
Parent reports suggest that 44–84% of children with ASD exhibit sleep disturbances that are of clinical concern. Pre...
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