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Article

Identifying rarer genetic variants for common complex diseases: diseased versus neutral discovery panels.

Annals of human genetics - 1 Jan 2009

Curtin K, Iles M M, Camp N J

Abstract excerpt

The power of genetic association studies to identify disease susceptibility alleles fundamentally relies on the variants studied. The standard approach is to determine a set of tagging-SNPs (tSNPs) that capture the majority of genomic variation in regions of interest by exploiting local correlation structures. Typically, tSNPs are selected from neutral discovery panels - collections of individuals comprehensively...

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Identifiers

PMID: 19132978
DOI: 10.1111/j.1469-1809.2008.00483.x
PMCID: PMC2705828

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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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