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

Potential clinical applications of advanced genomic analysis in cerebral palsy.

EBioMedicine - 1 Aug 2024

Lewis Sara A, Ruttenberg Andrew, Iyiyol Tuğçe, Kong Nahyun, Jin Sheng Chih, Kruer Michael C

Abstract excerpt

Cerebral palsy (CP) has historically been attributed to acquired insults, but emerging research suggests that genetic variations are also important causes of CP. While microarray and whole-exome sequencing based studies have been the primary methods for establishing new CP-gene relationships and providing a genetic etiology for individual patients, the cause of their condition remains unknown for many patients...

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 Exome Sequencing
Share to CP gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genetic Variation

Share to Genome, Human

Share to Genomics

Share to Transcriptome

Source

Open in PubMed Open full text

Identifiers

PMID: 38970919
DOI: 10.1016/j.ebiom.2024.105229
PMCID: PMC11282942

Genes

CP

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

Potential clinical applications of advanced genomic analysis in cerebral palsy.PMID 38970919Read ↗

Insights From Genetic Studies of Cerebral PalsySemantic proximity Read ↗

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

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

Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies.Semantic proximity Read ↗

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

Genomics in Cerebral Palsy phenotype across the lifespan: Comparison of diagnostic yield between children and adult population.Semantic proximity Read ↗

The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study.Semantic proximity Read ↗

Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral PalsySemantic proximity Read ↗

Genetics of Cerebral Palsy: Diagnosis, Differential Diagnosis, and BeyondSemantic proximity Read ↗

Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing.Semantic proximity Read ↗

Mendelian etiologies identified with whole exome sequencing in cerebral palsy.Semantic proximity Read ↗

Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.Semantic proximity Read ↗

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