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Article

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population.

Biochemical and biophysical research communications - 5 Sept 2008

Bae Joon Seol, Cheong Hyun Sub, Kim Ji-On, Lee Soo Ok, Kim Eun Mi, Lee Hye Won, Kim Sangsoo, Kim Ji-woong, Cui Tailin, Inoue Ituro, Shin Hyoung Doo

Abstract excerpt

Copy number variation (CNV) is emerging as a new tool for understanding human genomic variation, but its relationship with human disease is not yet fully understood. The data for a total of 317,503 genotypes were collected for a genome-wide association study of subarachnoid aneurismal hemorrhage (SAH) in a Japanese population (cases and controls, n=497) using Illumina HumanHap300 BeadChip. To identify...

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PMID: 18601904
DOI: 10.1016/j.bbrc.2008.06.083

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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