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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 Chromosomes, Human, Pair 15
Concept Sex Chromosome Aberrations
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Pair 16
Concept Chromosomes, Human, Pair 14
Concept Physical Chromosome Mapping
Concept Chromosomes, Human, Pair 11
Concept Chromosome Fragility
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 20
Concept Chromosomes
Concept Chromosomes, Human, Pair 4
Concept Chromosome Mapping
Concept Ring Chromosomes
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosome Inversion
Concept Chromosomes, Human, Pair 7
Concept Chromosomes, Human, Pair 2
Concept X Chromosome
Concept Chromosomes, Human, Pair 9
Concept Chromosome Disorders
Concept Chromosomes, Human, Pair 22
Concept Chromosome Fragile Sites
Academic Article Genetic and neurodevelopmental influences in autistic disorder.
Academic Article The search for autism disease genes.
Academic Article An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.
Academic Article Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
Academic Article Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Academic Article Contribution of SHANK3 mutations to autism spectrum disorder.
Academic Article Structural variation of chromosomes in autism spectrum disorder.
Academic Article Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.
Academic Article Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Academic Article Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.
Academic Article Autism spectrum disorders and epigenetics.
Academic Article Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Academic Article Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.
Academic Article Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Academic Article A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.
Academic Article Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
Academic 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.
Academic Article IQ and the genetics of autism.
Academic Article Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Academic Article Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Academic Article Possible similarities between the fragile X and Asperger's syndromes.
Academic Article Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.
Academic Article Effects of misclassification on estimates of relative risk in family history studies.
Academic Article Ring chromosome 22 and autism: report and review.
Academic Article Human chromosome 7: DNA sequence and biology.
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.

Search criteria
  • Chromosomes