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

Genetic testing in individuals with cerebral palsy.

Developmental medicine and child neurology - 1 Dec 2021

May Halie J, Fasheun Jennifer A, Bain Jennifer M, Baugh Evan H, Bier Louise E, Revah-Politi Anya, Roye David P, Goldstein David B, Carmel Jason B

Abstract excerpt

AIM To determine which patients with cerebral palsy (CP) should undergo genetic testing, we compared the rate of likely causative genetic variants from whole-exome sequencing in individuals with and without environmental risk factors. METHOD Patients were part of a convenience and physician-referred cohort recruited from a single medical center, and research whole-exome sequencing was completed. Participants were...

Read the complete abstract on PubMed

Topics

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

Share to Cerebral Palsy
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exome Sequencing

Share to Genetic Testing

Share to Infant

Share to Infant, Newborn

Share to Premature Birth

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 34114234
DOI: 10.1111/dmcn.14948
PMCID: PMC9277698

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Genetic testing in individuals with cerebral palsy.PMID 34114234Read ↗

Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.Semantic proximity Read ↗

Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencingSemantic proximity Read ↗

Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing GuidelinesSemantic proximity Read ↗

Cerebral palsy: causes, pathways, and the role of genetic variants.Semantic proximity Read ↗

Genetic and Genomic Insights Into Cerebral Palsy: Relevance for Precision Diagnosis and Personalised OutcomesSemantic proximity Read ↗

Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy.Semantic proximity Read ↗

The emerging genetic landscape of cerebral palsy.Semantic proximity Read ↗

Insights From Genetic Studies of Cerebral PalsySemantic proximity Read ↗

Potential clinical applications of advanced genomic analysis in cerebral palsy.Semantic proximity Read ↗

Genetic testing and genetic findings in Korean children with cerebral palsySemantic proximity Read ↗

Clinical actionability of genetic findings in cerebral palsySemantic proximity Read ↗

Clinical Actionability of Genetic Findings in Cerebral PalsySemantic proximity Read ↗

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