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

Identification of Chromosomal Regions Linked to Autism-Spectrum Disorders: A Meta-Analysis of Genome-Wide Linkage Scans.

Genetic testing and molecular biomarkers - 1 Feb 2022

Mpoulimari Ioanna, Zintzaras Elias

Abstract excerpt

Background: Autism spectrum disorder (ASD) is a clinically and genetically heterogeneous group of pervasive neurodevelopmental disorders with a strong hereditary component. Although, genome-wide linkage scans (GWLS) and association studies (GWAS) have previously identified hundreds of ASD risk gene loci, the results remain inconclusive. Method: We performed a heterogeneity-based genome search meta-analysis...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes

Share to Genetic Linkage

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Source

Identifiers

PMID: 35225680
DOI: 10.1089/gtmb.2021.0236

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of Chromosomal Regions Linked to Autism-Spectrum Disorders: A Meta-Analysis of Genome-Wide Linkage Scans.PMID 35225680Read ↗

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.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 ↗

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.Semantic proximity Read ↗

Genome-wide linkage in Utah autism pedigrees.Semantic proximity Read ↗

Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders.Semantic proximity Read ↗

Copy number variation findings among 50 children and adolescents with autism spectrum disorder.Semantic proximity Read ↗

A heterogeneity-based genome search meta-analysis for autism-spectrum disordersSemantic proximity Read ↗

Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.Semantic proximity Read ↗

Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.Semantic proximity Read ↗

Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder.Semantic proximity Read ↗

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.Semantic proximity Read ↗

Clustering by phenotype and genome-wide association study in autismSemantic proximity Read ↗

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