Rare germline genetic variation in PAX8 transcription factor binding sites and susceptibility to epithelial ovarian cancer.
Ezquina SAM; Jones M; Dicks E; de Vries A; Peng PC; Lawrenson K; Corona RI; Tyrer J · 2025 · American journal of epidemiology
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)
Common genetic variation throughout the genome and rare coding variants identified to date explain about half of the inherited genetic component of epithelial ovarian cancer risk. It is likely that rare variation in the noncoding genome…
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Metadata source: Europe PMC · DOI 10.1093/aje/kwae301