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

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.

Human genetics - 1 Jan 2011

Chapman Nicola H, Estes Annette, Munson Jeff, Bernier Raphael, Webb Sara J, Rothstein Joseph H, Minshew Nancy J, Dawson Geraldine, Schellenberg Gerard D, Wijsman Ellen M

Abstract excerpt

Performance IQ (PIQ) greater than verbal IQ (VIQ) is often observed in studies of the cognitive abilities of autistic individuals. This characteristic is correlated with social and communication impairments, key parts of the autism diagnosis. We present the first genetic analyses of IQ discrepanc...

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 Cadherins
Share to Chromosomes, Human, Pair 10

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 16

Share to Genetic Loci

Share to Intelligence

Share to Microsatellite Repeats

Share to Verbal Behavior

Source

Open in PubMed Open full text

Identifiers

PMID: 20963441
DOI: 10.1007/s00439-010-0899-z
PMCID: PMC3082447

Genes

CDH13

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20963441-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.PMID 20963441Read ↗

Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16pSemantic proximity Read ↗

Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.Semantic proximity Read ↗

Clinical Insights into the Neurodevelopmental Impact of 16p CNVs in an Italian Clinical Cohort.Semantic proximity Read ↗

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.Semantic proximity Read ↗

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.Semantic proximity Read ↗

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.Semantic proximity Read ↗

Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders.Semantic proximity Read ↗

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.Semantic proximity Read ↗

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.Semantic proximity Read ↗

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.Semantic proximity Read ↗

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.Semantic proximity Read ↗

Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p.Semantic proximity Read ↗

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