Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Approach to the genetic evaluation of the child with autism.

Pediatric clinics of North America - 1 Feb 2012

Toriello Helga V

Abstract excerpt

Autism is a heterogeneous entity that clearly has a substantial genetic component to its cause. There is likely enough evidence to suggest that there are common genetic mechanisms that predispose to various psychiatric disorders. More recent studies have attempted to identify the specific genes i...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child Development Disorders, Pervasive
Share to Chromosome Aberrations
Share to Fragile X Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Metabolic Diseases

Share to Myotonic Dystrophy

Share to Neurofibromatoses

Share to Syndrome

Share to Tuberous Sclerosis

Source

Identifiers

PMID: 22284797
DOI: 10.1016/j.pcl.2011.10.014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22284797-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Approach to the genetic evaluation of the child with autism.PMID 22284797Read ↗

Syndromic autism: causes and pathogenetic pathways.Semantic proximity Read ↗

Neurometabolic disorders and dysfunction in autism spectrum disorders.Semantic proximity Read ↗

Genetic syndromes and co-mobidity with autism.Semantic proximity Read ↗

[Autism and metabolic disorders-a rational approach].Semantic proximity Read ↗

Specific genetic disorders and autism: clinical contribution towards their identification.Semantic proximity Read ↗

Mitochondrial dysfunction in autism spectrum disorders: cause or effect?Semantic proximity Read ↗

[Should a metabolic work-up be performed in autism?].Semantic proximity Read ↗

Inborn error metabolic screening in individuals with nonsyndromic autism spectrum disordersSemantic proximity Read ↗

Genetic advances in autism hinge on the method of measuring symptoms.Semantic proximity Read ↗

Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autismSemantic proximity Read ↗

Case report of a boy with autism spectrum disorder and lysinuric protein intolerance.Semantic proximity Read ↗

[Clinical heterogeneity of the autistic syndrome: a study of 60 families].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.