A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk
Jade Chapman; Elliott Rees; Denise Harold; Dobril Ivanov; Amy Gerrish; Rebecca Sims; Paul Hollingworth; Alexandra Stretton · 2012 · Human Molecular Genetics
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
We assessed the role of rare copy number variants (CNVs) in Alzheimer's disease (AD) using intensity data from 3260 AD cases and 1290 age-matched controls from the genome-wide association study (GWAS) conducted by the Genetic and…
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Metadata source: OpenAlex · DOI 10.1093/hmg/dds476