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

A family genetic study of autism associated with profound mental retardation.

Journal of autism and developmental disorders - 1 Feb 2001

Starr E, Berument S K, Pickles A, Tomlins M, Bailey A, Papanikolaou K, Rutter M

Abstract excerpt

We sought to determine if the family loading for either the broader autism phenotype or for cognitive impairment differed according to whether or not autism was accompanied by severe mental retardation. The sample comprised 47 probands with autism meeting ICD-10 criteria, as assessed by the Autism Diagnostic Interview and the Autism Diagnostic Observation Schedule. Family history interview and findings were...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder
Share to Child, Preschool
Share to Down Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Educational Status

Share to Epilepsy

Share to Genetics, Population

Share to Intellectual Disability

Share to Intelligence

Source

Identifiers

PMID: 11439758
DOI: 10.1023/a:1005669915105

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A family genetic study of autism associated with profound mental retardation.PMID 11439758Read ↗

A case-control family history study of autism.Semantic proximity Read ↗

The broad autism phenotype: a complementary strategy for molecular genetic studies of autism.Semantic proximity Read ↗

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families.Semantic proximity Read ↗

Cognitive deficits in parents from multiple-incidence autism families.Semantic proximity Read ↗

Broader autistic phenotype in parents of children with autism: Autism Spectrum Quotient-Turkish version.Semantic proximity Read ↗

Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families.Semantic proximity Read ↗

Psychiatric disorders in parents of children with autism: a meta-analysis.Semantic proximity Read ↗

Neuropsychological profile of autism and the broad autism phenotype.Semantic proximity Read ↗

Broader autism phenotype in parents of autistic children: reality or myth?Semantic proximity Read ↗

A family history study of Asperger syndrome.Semantic proximity Read ↗

Variable expression of the autism broader phenotype: findings from extended pedigrees.Semantic proximity Read ↗

Psychiatric disorder and the broad autism phenotype: evidence from a family study of multiple-incidence autism families.Semantic proximity Read ↗

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