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

The genetics of lissencephaly.

American journal of medical genetics. Part C, Seminars in medical genetics - 1 Jun 2014

Fry Andrew E, Cushion Thomas D, Pilz Daniela T

Abstract excerpt

Lissencephaly is a spectrum of severe brain malformations caused by the failure of migrating neurons to reach optimal positions in the developing cerebral cortex. Several syndromes associated with lissencephaly have been characterized in recent years. Identification of the genetic basis of these disorders has brought fascinating insights into the mechanisms of brain development, as well as benefits to patients...

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
Share to Genetic Heterogeneity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lissencephaly

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Neurogenesis and neuroplasticity mechanisms

Share to Neuroimaging

Share to Phenotype

Source

Identifiers

PMID: 24862549
DOI: 10.1002/ajmg.c.31402

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

The genetics of lissencephaly.PMID 24862549Read ↗

Lissencephaly: Update on diagnostics and clinical management.Semantic proximity Read ↗

Lissencephaly and the molecular basis of neuronal migration.Semantic proximity Read ↗

Lissencephaly and Other Malformations of Cortical Development: 1995 UpdateSemantic proximity Read ↗

Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.Semantic proximity Read ↗

Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.Semantic proximity Read ↗

The clinical patterns and molecular genetics of lissencephaly and subcortical band heterotopiaSemantic proximity Read ↗

Lissencephaly: Expanded imaging and clinical classification.Semantic proximity Read ↗

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13Semantic proximity Read ↗

Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasiasSemantic proximity Read ↗

Malformations of cortical development.Semantic proximity Read ↗

[Molecular genetics of lissencephaly and microcephaly].Semantic proximity Read ↗

Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly.Semantic proximity Read ↗

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