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Article

Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia.

Leukemia - 1 Oct 2012

Enciso-Mora V, Hosking F J, Sheridan E, Kinsey S E, Lightfoot T, Roman E, Irving J A E, Tomlinson I P M, Allan J M, Taylor M, Greaves M, Houlston R S

Abstract excerpt

Recent genome-wide association studies (GWAS) have provided the first unambiguous evidence that common genetic variation influences the risk of childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL), identifying risk single-nucleotide polymorphisms (SNPs) localizing to 7p12.2, 9p21.3, 10q21.2 and 14q11.2. The testing of SNPs individually for an association in GWA studies necessitates the imposition of...

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PMID: 22456626
DOI: 10.1038/leu.2012.89

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

Source receipt: pubmed, retrieved 5 Sept 2026.

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