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PMID: 17015230 Published · ppublish English Journal Article Review

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders.

Neuron ·Vol. 52 ·No. 1 ·2006-10-05 ·Pages 103-21

Lee JA, Lupski JR

Abstract

Genomic disorders are a group of human genetic diseases caused by genomic rearrangements resulting in copy-number variation (CNV) affecting a dosage-sensitive gene or genes critical for normal development or maintenance. These disorders represent a wide range of clinically distinct entities but include many diseases affecting nervous system function. Herein, we review selected neurodevelopmental, neurodegenerative, and psychiatric disorders either known or suggested to be caused by genomic rearrangement and CNV. Further, we emphasize the cause-and-effect relationship between gene CNV and complex disease traits. We also discuss the prevalence and heritability of CNV, the correlation between CNV and higher-order genome architecture, and the heritability of personality, behavioral, and psychiatric traits. We speculate that CNV could underlie a significant proportion of normal human variation including differences in cognitive, behavioral, and psychological features.

MeSH Terms
Animals Chromosome Aberrations Chromosome Disorders/complications Chromosomes, Human Disease Models, Animal Gene Dosage/physiology Gene Rearrangement/physiology Genomics Humans Nervous System Diseases/etiology,genetics
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lee Jennifer A
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Lupski James R
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
2006-10-05
Pages
103-21
Language
English
Region
United States
NLM ID
8809320
Subset
IM
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