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Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical managementThe cognitive neuropsychological phenotype of carriers of the FMR1 premutation.Lifespan changes in working memory in fragile X premutation males.Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.Sleep in high-functioning children with autism: longitudinal developmental change and associations with behavior problems.Tracing syndrome-specific trajectories of attention across the lifespan.Development of static and dynamic perception for luminance-defined and texture-defined information.The relationship between sleep and behavior in autism spectrum disorder (ASD): a review.Selective executive markers of at-risk profiles associated with the fragile X premutation.Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women.Attention and language in fragile X.Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts.Attention deficits predict phenotypic outcomes in syndrome-specific and domain-specific ways.Charting the developmental trajectories of attention and executive function in Chinese school-aged children.Maternal predictors of anxiety risk in young males with fragile XDelineation of early attentional control difficulties in fragile X syndrome: focus on neurocomputational changes.β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles.The fragile X continuum: new advances and perspectives.Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females.Attention and Executive Function in Children Diagnosed with Attention Deficit Hyperactivity Disorder and Comorbid Disorders.Associating neural alterations and genotype in autism and fragile x syndrome: incorporating perceptual phenotypes in causal modeling.Fragile X syndrome and associated disorders.Gender differences in neurodevelopmental disorders: autism and fragile x syndrome.Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome.Understanding the neuropsychiatric phenotype of fragile X-associated tremor ataxia syndrome: a systematic review.Cognitive training as a resolution for early executive function difficulties in children with intellectual disabilities.Learning to read in Williams syndrome and Down syndrome: syndrome-specific precursors and developmental trajectories.Impact of Attention Training on Academic Achievement, Executive Functioning, and Behavior: A Randomized Controlled Trial.The developmental dynamics of gait maturation with a focus on spatiotemporal measures.Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responses.Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation.Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriers.Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation.White matter microstructure, cognition, and molecular markers in fragile X premutation females.Executive Dysfunction in Female FMR1 Premutation Carriers.Mechanisms of anxiety related attentional biases in children with autism spectrum disorder.Differential impact of the FMR1 gene on visual processing in fragile X syndrome.Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample.The interplay between executive control and motor functioning in Williams syndrome.Age-related changes in visual and auditory sustained attention in preschool-aged children.
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Kim M Cornish
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