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Search Results to Peter Szatmari

This is a "connection" page, showing the details of why an item matched the keywords from your search.


One or more keywords matched the following items that are connected to Szatmari, Peter

Item TypeName
Concept Mothers
Concept Schools
Concept Genome, Human
Concept Social Support
Concept Genome-Wide Association Study
Concept Genome
Academic Article Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.
Academic Article Functional impact of global rare copy number variation in autism spectrum disorders.
Academic Article A genome-wide scan for common alleles affecting risk for autism.
Academic Article Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Academic Article Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.
Academic Article Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.
Academic Article A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Academic Article Sex differences in repetitive stereotyped behaviors in autism: implications for genetic liability.
Academic Article Individual common variants exert weak effects on the risk for autism spectrum disorders.
Academic Article Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Academic Article Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Academic Article Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Academic Article Whole-genome sequencing of quartet families with autism spectrum disorder.
Academic Article Genome-wide characteristics of de novo mutations in autism.
Academic Article Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Academic Article Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.
Academic Article Cost-effectiveness of Genome and Exome Sequencing in Children Diagnosed with Autism Spectrum Disorder.
Academic Article A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Academic Article A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.
Academic Article Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Academic Article Genome-wide association study of emotional empathy in children.
Academic Article Genome-wide detection of tandem DNA repeats that are expanded in autism.

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