Lista de obras - Marc Woodbury-Smith - Dominio Público Uruguay

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.

artículo científico publicado en 2018

Adult Asperger Assessment

An nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)

Asperger Syndrome

artículo científico publicado en 2018

Asperger Syndrome

artículo científico publicado en 2013

Asperger Syndrome

scientific article from 2011

Asperger Syndrome Epidemiology

scholarly article published 2013

Asperger syndrome and criminal behaviour

Asperger?s Syndrome: A Comparison of Clinical Diagnoses and Those Made According to the ICD-10 and DSM-IV

artículo científico publicado en 2005

Autism spectrum conditions

scholarly article published June 2009

Autism spectrum disorder (ASD) and unlawful behaviour: where do we go from here?

artículo científico publicado en 2014

Autism spectrum disorder: advances in evidence-based practice

artículo científico publicado en 2014

Canada and Autism

article

Changing diagnostic practices: autism spectrum disorder

Circumscribed interests and ‘offenders’ with autism spectrum disorders: a case-control study

Clinical heterogeneity among people with high functioning autism spectrum conditions: evidence favouring a continuous severity gradient

artículo científico publicado en 2008

Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.

scientific article published on 13 February 2017

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

artículo científico publicado en 2013

Editorial: ASD and illegal behaviors

artículo científico publicado en 2014

Electronic Health Record Breaches as Social Indicators

article

Genome-wide association study of emotional empathy in children

artículo científico publicado en 2020

Genomic Context Analysis of de Novo STXBP1 Mutations Identifies Evidence of Splice Site DNA-Motif Associated Hotspots

artículo científico publicado en 2018

Germline and somatic mutations in STXBP1 with diverse neurodevelopmental phenotypes

artículo científico publicado en 2017

Improving the medical scale predictability by the pairwise comparisons method: evidence from a clinical data study

artículo científico publicado en 2011

Improving the uptake of health screening among individuals with intellectual disability

article

JBS Haldane: an evolutionary geneticist not without controversy

Legal System Involvement

Managing anxiety and depressive symptoms in adults with autism-spectrum disorders

artículo científico publicado en 2011

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

artículo científico publicado en 2015

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

artículo científico publicado en 2017

OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome

artículo científico publicado en 2018

Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder

artículo científico publicado en 2014

Progress in the genetics of autism spectrum disorder

artículo científico publicado en 2018

Rare Copy Number Variation In an Extremely Impulsively Violent Males

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

artículo científico publicado en 2020

Sex differences in repetitive stereotyped behaviors in autism: implications for genetic liability

artículo científico publicado en 2011

Simon Baron-Cohen

encyclopedia article

The Adult Asperger Assessment (AAA): a diagnostic method

artículo científico publicado en 2005

The Developmental Disabilities

The role of prenatal immune activation in the pathogenesis of autism and schizophrenia: A literature review

Unlawful Behaviors in Adolescents and Adults with Autism Spectrum Disorders

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

artículo científico publicado en 2014

Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes

artículo científico publicado en 2017

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

artículo científico publicado en 2017

Youth in transition: care, health and development

scientific article published on 01 November 2011

Lista de obras de Marc Woodbury-Smith

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.

Adult Asperger Assessment

An nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)

Asperger Syndrome

Asperger Syndrome

Asperger Syndrome

Asperger Syndrome Epidemiology

Asperger syndrome and criminal behaviour

Asperger?s Syndrome: A Comparison of Clinical Diagnoses and Those Made According to the ICD-10 and DSM-IV

Autism spectrum conditions

Autism spectrum disorder (ASD) and unlawful behaviour: where do we go from here?

Autism spectrum disorder: advances in evidence-based practice

Canada and Autism

Changing diagnostic practices: autism spectrum disorder

Circumscribed interests and ‘offenders’ with autism spectrum disorders: a case-control study

Clinical heterogeneity among people with high functioning autism spectrum conditions: evidence favouring a continuous severity gradient

Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

Editorial: ASD and illegal behaviors

Electronic Health Record Breaches as Social Indicators

Genome-wide association study of emotional empathy in children

Genomic Context Analysis of de Novo STXBP1 Mutations Identifies Evidence of Splice Site DNA-Motif Associated Hotspots

Germline and somatic mutations in STXBP1 with diverse neurodevelopmental phenotypes

Improving the medical scale predictability by the pairwise comparisons method: evidence from a clinical data study

Improving the uptake of health screening among individuals with intellectual disability

JBS Haldane: an evolutionary geneticist not without controversy

Legal System Involvement

Managing anxiety and depressive symptoms in adults with autism-spectrum disorders

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome

Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder

Progress in the genetics of autism spectrum disorder

Rare Copy Number Variation In an Extremely Impulsively Violent Males

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

Sex differences in repetitive stereotyped behaviors in autism: implications for genetic liability

Simon Baron-Cohen

The Adult Asperger Assessment (AAA): a diagnostic method

The Developmental Disabilities

The role of prenatal immune activation in the pathogenesis of autism and schizophrenia: A literature review

Unlawful Behaviors in Adolescents and Adults with Autism Spectrum Disorders

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

Youth in transition: care, health and development