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

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.

Autism research : official journal of the International Society for Autism Research - 1 Aug 2011

Allen-Brady Kristina, Cai Guiqing, Cannon Dale, Robison Reid, McMahon William M, Coon Hilary, Buxbaum Joseph D

Abstract excerpt

Finding predisposition genes for Autism Spectrum Disorder (ASD) has proven challenging, and new methods are needed to aid the process. Using pedigree structure as a strategy to identify ASD predisposition genes, we previously performed a genome-wide linkage scan of 86 selected families from the Autism Resource Exchange (AGRE) that appeared to inherit ASD in a dominant manner. We identified a suggestive linkage...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child Development Disorders, Pervasive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Haplotypes

Share to Introns

Share to Linkage Disequilibrium

Share to Pedigree

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 21491612
DOI: 10.1002/aur.195

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.PMID 21491612Read ↗

Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD).Semantic proximity Read ↗

Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders.Semantic proximity Read ↗

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.Semantic proximity Read ↗

Replication of autism linkage: fine-mapping peak at 17q21.Semantic proximity Read ↗

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.Semantic proximity Read ↗

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.Semantic proximity Read ↗

A genomic screen of autism: evidence for a multilocus etiology.Semantic proximity Read ↗

IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.Semantic proximity Read ↗

Mutations in the calcium-related gene IL1RAPL1 are associated with autismSemantic proximity Read ↗

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.Semantic proximity Read ↗

Reelin gene alleles and susceptibility to autism spectrum disorders.Semantic proximity Read ↗

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree.Semantic proximity Read ↗

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