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Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders

Journal of autism and developmental disorders, 2012-07, Vol.42 (7), p.1459-1469

2012

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Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind

Developmental science, 2012-03, Vol.15 (2), p.272-280

2012

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Population- and Family-Based Studies Associate the MTHFR Gene with Idiopathic Autism in Simplex Families

Journal of autism and developmental disorders, 2011-07, Vol.41 (7), p.938-944

2011

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Development and Initial Validation of a Parent Report Measure of the Behavioral Development of Infants at Risk for Autism Spectrum Disorders

Journal of autism and developmental disorders, 2012, Vol.42 (1), p.13-22

2012

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Trends in Autism Prevalence: Diagnostic Substitution Revisited

Journal of autism and developmental disorders, 2008-07, Vol.38 (6), p.1036-1046

2008

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Brief Report: Telephone Administration of the Autism Diagnostic Interview—Revised: Reliability and Suitability for Use in Research

Journal of autism and developmental disorders, 2010-10, Vol.40 (10), p.1285-1290

2010

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A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-07, Vol.147B (5), p.628-636

2008

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Differential impact of the FMR1 gene on visual processing in fragile X syndrome

Brain (London, England : 1878), 2004-03, Vol.127 (3), p.591-601

2004

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

European journal of human genetics : EJHG, 2009-02, Vol.17 (2), p.228-235

2009

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Understanding the impact of 1q21.1 copy number variant

Orphanet journal of rare diseases, 2011-08, Vol.6 (1), p.54-54, Article 54

2011

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DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families

Behavioral and brain functions, 2012-05, Vol.8 (1), p.19-19, Article 19

2012

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Developmental Trajectories in Syndromes with Intellectual Disability, with a Focus on Wolf-Hirschhorn and Its Cognitive-Behavioral Profile

American journal on intellectual and developmental disabilities, 2012-03, Vol.117 (2), p.167

2012

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The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of gender

American journal of medical genetics. Part A, 2010-06, Vol.152A (6), p.1498-1509

2010

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Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders

American journal of medical genetics. Part A, 2007-10, Vol.143A (20), p.2478-2489

2007

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Trends in Special Education Code Assignment for Autism: Implications for Prevalence Estimates

Journal of autism and developmental disorders, 2007-11, Vol.37 (10), p.1941-1948

2007

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Age at Diagnosis of Autism Spectrum Disorders in Four Regions of Canada

Canadian journal of public health, 2009-07, Vol.100 (4), p.268-273

2009

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Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis

BMC genomics, 2007-06, Vol.8 (1), p.167-167, Article 167

2007

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2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

European journal of human genetics : EJHG, 2011-12, Vol.19 (12), p.1264-1270

2011

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Association of MAOA, 5-HTT, and NET promoter polymorphisms with gene expression and protein activity in human placentas

Physiological genomics, 2010-06, Vol.42 (1), p.85-92

2010

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Addressing Health Disparities Through Promoting Equity for Individuals with Intellectual Disability

Canadian journal of public health, 2005-03, Vol.96 (S2), p.S8-S22

2005

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Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene: ATL1, FMRb, and Microsatellite Haplotypes Differ from Those Found in Common-Size FMR1 Alleles

Human biology, 2005-02, Vol.77 (1), p.137-151

2005

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XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

BMC medical genetics, 2005-04, Vol.6 (1), p.16-16, Article 16

2005

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Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

Molecular cytogenetics, 2008-11, Vol.1 (1), p.23-23, Article 23

2008

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Behavioral Relationship between Autism and Fragile X Syndrome

American journal of mental retardation, 2003-09, Vol.108 (5), p.314

2003

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Prevalence of Pervasive Developmental Disorders in Two Canadian Provinces

Journal of policy and practice in intellectual disabilities, 2006-09, Vol.3 (3), p.164-172

2006

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Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders

Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind

Population- and Family-Based Studies Associate the MTHFR Gene with Idiopathic Autism in Simplex Families

Development and Initial Validation of a Parent Report Measure of the Behavioral Development of Infants at Risk for Autism Spectrum Disorders

Trends in Autism Prevalence: Diagnostic Substitution Revisited

Brief Report: Telephone Administration of the Autism Diagnostic Interview—Revised: Reliability and Suitability for Use in Research

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families

Differential impact of the FMR1 gene on visual processing in fragile X syndrome

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

Understanding the impact of 1q21.1 copy number variant

DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families

Developmental Trajectories in Syndromes with Intellectual Disability, with a Focus on Wolf-Hirschhorn and Its Cognitive-Behavioral Profile

The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of gender

Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders

Trends in Special Education Code Assignment for Autism: Implications for Prevalence Estimates

Age at Diagnosis of Autism Spectrum Disorders in Four Regions of Canada

Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

Association of MAOA, 5-HTT, and NET promoter polymorphisms with gene expression and protein activity in human placentas

Addressing Health Disparities Through Promoting Equity for Individuals with Intellectual Disability

Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene: ATL1, FMRb, and Microsatellite Haplotypes Differ from Those Found in Common-Size FMR1 Alleles

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

Behavioral Relationship between Autism and Fragile X Syndrome

Prevalence of Pervasive Developmental Disorders in Two Canadian Provinces

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