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Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders

Proceedings of the National Academy of Sciences - PNAS, 2011-12, Vol.108 (50), p.20195-20200

2011

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Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome

PloS one, 2014-08, Vol.9 (8), p.e103884

2014

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Real-time cognitive performance metrics derived from a digital therapeutic for inattention predict ADHD-related clinical outcomes: Replication across three independent trials of AKL-T01

Translational psychiatry, 2024-08, Vol.14 (1), p.328-8, Article 328

2024

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22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

Nature reviews. Neuroscience, 2010-06, Vol.11 (6), p.402-416

2010

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The development of cognitive control in children with chromosome 22q11.2 deletion syndrome

Frontiers in psychology, 2014-06, Vol.5, p.566-566

2014

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Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task

Frontiers in human neuroscience, 2011, Vol.5, p.63-63

2011

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The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety

Journal of psychiatry & neuroscience, 2016-05, Vol.41 (3), p.203-213

2016

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Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome

Journal of neurodevelopmental disorders, 2019-12, Vol.11 (1), p.40-40, Article 40

2019

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Assessment of the Prodromal Questionnaire-Brief Child Version for Measurement of Self-reported Psychoticlike Experiences in Childhood

JAMA psychiatry (Chicago, Ill.), 2018-08, Vol.75 (8), p.853

2018

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Eye Movements Reveal Impaired Inhibitory Control in Adult Male Fragile X Premutation Carriers Asymptomatic for FXTAS

Neuropsychology, 2014-07, Vol.28 (4), p.571-584

2014

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Abnormal Trajectories in Cerebellum and Brainstem Volumes in Carriers of the Fragile X Premutation

Neurobiology of aging, 2017-07, Vol.55, p.11-19

2017

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Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome

The Journal of biological chemistry, 2015-09, Vol.290 (38), p.23240-23253

2015

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Bullying and psychosis: The impact of chronic traumatic stress on psychosis risk in 22q11.2 deletion syndrome - a uniquely vulnerable population

Journal of psychiatric research, 2019-07, Vol.114, p.99-104

2019

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A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome

Frontiers in psychiatry, 2013, Vol.4, p.81-81

2013

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Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

Behavioral and brain functions, 2007-10, Vol.3 (1), p.54-54

2007

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Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?

Journal of autism and developmental disorders, 2014-04, Vol.44 (4), p.739-746

2014

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Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls

Frontiers in human neuroscience, 2015-02, Vol.9, p.37-37

2015

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Cognitive Characteristics of Children with Genetic Syndromes

Child and adolescent psychiatric clinics of North America, 2007-07, Vol.16 (3), p.599-616

Simon, Tony J., PhD

2007

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Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.456-468

2020

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Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness

The American journal of psychiatry, 2020-07, Vol.177 (7), p.589-600

2020

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Structure-specific statistical mapping of white matter tracts

NeuroImage (Orlando, Fla.), 2008-06, Vol.41 (2), p.448-461

2008

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Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome

Brain research, 2007-02, Vol.1131 (1), p.197-210

2007

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Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome

Schizophrenia research, 2010-05, Vol.118 (1), p.118-121

2010

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Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

Journal of neurodevelopmental disorders, 2012-04, Vol.4 (1), p.6-6, Article 6

2012

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White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging

NeuroImage (Orlando, Fla.), 2013-11, Vol.81, p.441-454

2013

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Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders

Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome

Real-time cognitive performance metrics derived from a digital therapeutic for inattention predict ADHD-related clinical outcomes: Replication across three independent trials of AKL-T01

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome

Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task

The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety

Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome

Assessment of the Prodromal Questionnaire-Brief Child Version for Measurement of Self-reported Psychoticlike Experiences in Childhood

Eye Movements Reveal Impaired Inhibitory Control in Adult Male Fragile X Premutation Carriers Asymptomatic for FXTAS

Abnormal Trajectories in Cerebellum and Brainstem Volumes in Carriers of the Fragile X Premutation

Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome

Bullying and psychosis: The impact of chronic traumatic stress on psychosis risk in 22q11.2 deletion syndrome - a uniquely vulnerable population

A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome

Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?

Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls

Cognitive Characteristics of Children with Genetic Syndromes

Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis

Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness

Structure-specific statistical mapping of white matter tracts

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome

Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging

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