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Article

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.

Genome medicine - 25 Oct 2019

Chow Julie, Jensen Matthew, Amini Hajar, Hormozdiari Farhad, Penn Osnat, Shifman Sagiv, Girirajan Santhosh, Hormozdiari Fereydoun

Abstract excerpt

BACKGROUND: Neurodevelopmental disorders (NDDs) such as autism spectrum disorder, intellectual disability, developmental disability, and epilepsy are characterized by abnormal brain development that may affect cognition, learning, behavior, and motor skills. High co-occurrence (comorbidity) of NDDs indicates a shared, underlying biological mechanism. The genetic heterogeneity and overlap observed in NDDs make it...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 31653223
DOI: 10.1186/s13073-019-0678-y
PMCID: PMC6815046

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.

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