The implications of de novo coding mutations in simplex autism families.

doi:10.1111/cge.12582

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

Community

Back to search

Article

The implications of de novo coding mutations in simplex autism families.

Clinical genetics - 1 May 2015

Utami K H

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Child Development Disorders, Pervasive
Share to Genetic Predisposition to Disease
Share to Mutation
Share to Open Reading Frames

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed

Identifiers

PMID: 25753786
DOI: 10.1111/cge.12582

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The implications of de novo coding mutations in simplex autism families.PMID 25753786Read ↗

The contribution of de novo coding mutations to autism spectrum disorder.Semantic proximity Read ↗

Genomic Patterns of De Novo Mutation in Simplex Autism.Semantic proximity Read ↗

The role of de novo mutations in the genetics of autism spectrum disorders.Semantic proximity Read ↗

Recurrent de novo mutations implicate novel genes underlying simplex autism risk.Semantic proximity Read ↗

Linking newly occurring mutations to autism.Semantic proximity Read ↗

Genetics. Insights into the pathogenesis of autism.Semantic proximity Read ↗

De Novo Variants Predominate in Autism Spectrum DisorderSemantic proximity Read ↗

Postzygotic single nucleotide mosaicisms and autism risk.Semantic proximity Read ↗

A surprising METamorphosis: autism genetics finds a common functional variant.Semantic proximity Read ↗

Autism: the difficult hunt for disease genes.Semantic proximity Read ↗

SnapShot: genetics of autism.Semantic proximity Read ↗

Rates of contributory de novo mutation in high and low-risk autism families.Semantic proximity Read ↗

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