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Article

Informed genome-wide association analysis with family history as a secondary phenotype identifies novel loci of lung cancer.

Genetic epidemiology - 1 Mar 2015

Poirier Julia G, Brennan Paul, McKay James D, Spitz Margaret R, Bickeböller Heike, Risch Angela, Liu Geoffrey, Le Marchand Loic, Tworoger Shelley, McLaughlin John, Rosenberger Albert, Heinrich Joachim, Brüske Irene, Muley Thomas, Henderson Brian E, Wilkens Lynne R, Zong Xuchen, Li Yafang, Hao Ke, Timens Wim, Bossé Yohan, Sin Don D, Obeidat Ma'en, Amos Christopher I, Hung Rayjean J

Abstract excerpt

Lung cancer is the leading cause of cancer death worldwide. Although several genetic variants associated with lung cancer have been identified in the past, stringent selection criteria of genome-wide association studies (GWAS) can lead to missed variants. The objective of this study was to uncove...

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Identifiers

PMID: 25644374
DOI: 10.1002/gepi.21882
PMCID: PMC4554719

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FFAR4
KCNIP4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-25644374-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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