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Article

New Genome-Wide Methods for Elucidation of Candidate Copy Number Variations (CNVs) Contributing to Alzheimer's Disease Heritability.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2016

Szigeti Kinga

Abstract excerpt

The complexity of human genetic variation has been extended by the observation of abundant and widespread variation in the copy number of submicroscopic DNA segments. The discovery of this novel level of genome organization opened new possibilities concerning the genetic variation that may confer susceptibility to or cause disease. Copy number variants (CNVs) influence gene expression, phenotypic variation and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 26235076
DOI: 10.1007/978-1-4939-2627-5_19

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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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