Advanced search

Authors whose works are in public domain in at least one jurisdiction

List of works by Peter Szatmari

1-50 of 139 results

View this query on the Wikidata Query Service
Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article
Structural variation of chromosomes in autism spectrum disorder

scientific article
Synaptic, transcriptional and chromatin genes disrupted in autism

scientific article
Mapping autism risk loci using genetic linkage and chromosomal rearrangements

scientific article
Behavioral manifestations of autism in the first year of life

scientific article
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article
Contribution of SHANK3 mutations to autism spectrum disorder

scientific article
A genome-wide scan for common alleles affecting risk for autism

scientific journal article
Combining information from multiple sources in the diagnosis of autism spectrum disorders

scientific article published in September 2006
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing

scientific article published on 11 July 2013
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

scientific article
Whole-genome sequencing of quartet families with autism spectrum disorder

scientific article published on 26 January 2015
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

scientific article
SHANK1 Deletions in Males with Autism Spectrum Disorder

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

scientific article published on 6 March 2017
A prospective case series of high-risk infants who developed autism

scientific article published on 9 January 2007
Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

scientific article
Early language and communication development of infants later diagnosed with autism spectrum disorder

scientific article published in April 2006
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

scientific article published on September 2015
Challenges in evaluating psychosocial interventions for Autistic Spectrum Disorders

scientific article published in December 2005
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

scientific article
Rare deletions at the neurexin 3 locus in autism spectrum disorder

scientific article
Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority

scientific article published on June 13, 2015
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

scientific article
Investigating the structure of the restricted, repetitive behaviours and interests domain of autism

scientific article published in June 2006
Efficacy of family-based treatment for adolescents with eating disorders: a systematic review and meta-analysis

scientific article published on 23 July 2012
Autism spectrum disorders and epigenetics

scientific article published on 03 July 2010
Sex differences in repetitive stereotyped behaviors in autism: implications for genetic liability

scientific article published on 16 November 2011
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

scientific article published in November 2006
Human chromosome 7: DNA sequence and biology

scientific article
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

scientific article published on 14 October 2011
A discovery resource of rare copy number variations in individuals with autism spectrum disorder

scientific article
Temperament and its relationship to autistic symptoms in a high-risk infant sib cohort

scientific article published in January 2009
Investigating phenotypic heterogeneity in children with autism spectrum disorder: a factor mixture modeling approach

scientific article published in August 2012
Sex differences in children with autism spectrum disorder identified within a high-risk infant cohort

scientific article published in December 2012
Informative phenotypes for genetic studies of psychiatric disorders

scientific article published on July 2007
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

scientific article
Genome-wide characteristics of de novo mutations in autism

scientific article published on August 2016
Comorbidity of internalizing disorders in children with oppositional defiant disorder

scientific article published on 24 September 2007
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures

scientific article published on 7 February 2013
Stereotyped motor behaviors associated with autism in high-risk infants: a pilot videotape analysis of a sibling sample

scientific article published on 12 January 2007
A prospective study of autistic-like traits in unaffected siblings of probands with autism spectrum disorder

scientific article published in January 2013
Specifying PDD-NOS: a comparison of PDD-NOS, Asperger syndrome, and autism

scientific article
Developmental trajectories of symptom severity and adaptive functioning in an inception cohort of preschool children with autism spectrum disorder

scientific article published on March 2015
Genome-wide linkage analyses of quantitative and categorical autism subphenotypes

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

scientific article published on 30 December 2013
Quantifying and exploring camouflaging in men and women with autism

scientific article published on 29 November 2016
Structure of the autism symptom phenotype: A proposed multidimensional model

scientific article published in February 2007

Paulina is supported by:

About Paulina

Help