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

Recurrent 16p11.2 microdeletions in autism.

Human molecular genetics - 15 Feb 2008

Kumar Ravinesh A, KaraMohamed Samer, Sudi Jyotsna, Conrad Donald F, Brune Camille, Badner Judith A, Gilliam T Conrad, Nowak Norma J, Cook Edwin H, Dobyns William B, Christian Susan L

Abstract excerpt

Autism is a childhood neurodevelopmental disorder with a strong genetic component, yet the identification of autism susceptibility loci remains elusive. We investigated 180 autism probands and 372 control subjects by array comparative genomic hybridization (aCGH) using a 19K whole-genome tiling path bacterial artificial chromosome microarray to identify submicroscopic chromosomal rearrangements specific to...

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 Chromosome Breakage

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosome Deletion

Share to Chromosomes, Artificial, Bacterial

Share to Chromosomes, Human, Pair 16

Share to DNA Primers

Share to In Situ Hybridization, Fluorescence

Share to Microsatellite Repeats

Source

Identifiers

PMID: 18156158
DOI: 10.1093/hmg/ddm376

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Recurrent 16p11.2 microdeletions in autism.PMID 18156158Read ↗

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.Semantic proximity Read ↗

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.Semantic proximity Read ↗

Association between microdeletion and microduplication at 16p11.2 and autism.Semantic proximity Read ↗

High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.Semantic proximity Read ↗

Structural variation of chromosomes in autism spectrum disorder.Semantic proximity Read ↗

A clinical study of patients with pericentromeric deletion and duplication within 16p12.2-p11.2.Semantic proximity Read ↗

Microdeletion and microduplication syndromes.Semantic proximity Read ↗

Association Between Microdeletion and Microduplication at 16p11.2 and AutismSemantic proximity Read ↗

Association and mutation analyses of 16p11.2 autism candidate genes.Semantic proximity Read ↗

Global increases in both common and rare copy number load associated with autismSemantic proximity Read ↗

Detection and characterization of copy number variation in autism spectrum disorder.Semantic proximity Read ↗

[16p11.2 Microdeletion: first report in Argentina].Semantic proximity Read ↗

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