Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.

doi:10.1038/jhg.2010.97

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Article

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.

Journal of human genetics - 1 Nov 2010

Bae Joon Seol, Cheong Hyun Sub, Park Byung Lae, Kim Lyoung Hyo, Park Tae Joon, Kim Jason Yongha, Pasaje Charisse Flerida A, Lee Jin Sol, Cui Tailin, Inoue Ituro, Shin Hyoung Doo

Abstract excerpt

Subarachnoid aneurysmal hemorrhage (SAH) due to cerebral aneurysm rupture is a very serious disease resulting in high mortality rate. It has been known that genetic factors are involved in the risk of SAH. A recent breakthrough in genomic variation called copy number variation (CNV) has been revealed to be involved in risks of human diseases. In this study, we hypothesized that CNVs can predict the risk of SAH....

Topics

Adult
Aged
Aged, 80 and over
Asian People
DNA Copy Number Variations
Databases, Genetic
Gene Dosage
Genome, Human
Genome-Wide Association Study
Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Humans

Japan

Middle Aged

Oligonucleotide Array Sequence Analysis

Polymorphism, Single Nucleotide

Subarachnoid Hemorrhage

Source

Open in PubMed

Identifiers

PMID: 20703242
DOI: 10.1038/jhg.2010.97

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-20703242-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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