Home > Publications database > Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. > print |
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024 | 7 | _ | |a 10.1038/s41467-018-03178-z |2 doi |
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037 | _ | _ | |a DKFZ-2018-00511 |
041 | _ | _ | |a eng |
082 | _ | _ | |a 500 |
100 | 1 | _ | |a Vijayakrishnan, Jayaram |b 0 |
245 | _ | _ | |a Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. |
260 | _ | _ | |a London |c 2018 |b Nature Publishing Group |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1525866246_16254 |2 PUB:(DE-HGF) |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
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336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
520 | _ | _ | |a Genome-wide association studies (GWAS) have advanced our understanding of susceptibility to B-cell precursor acute lymphoblastic leukemia (BCP-ALL); however, much of the heritable risk remains unidentified. Here, we perform a GWAS and conduct a meta-analysis with two existing GWAS, totaling 2442 cases and 14,609 controls. We identify risk loci for BCP-ALL at 8q24.21 (rs28665337, P = 3.86 × 10-9, odds ratio (OR) = 1.34) and for ETV6-RUNX1 fusion-positive BCP-ALL at 2q22.3 (rs17481869, P = 3.20 × 10-8, OR = 2.14). Our findings provide further insights into genetic susceptibility to ALL and its biology. |
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700 | 1 | _ | |a Roman, Eve |b 11 |
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700 | 1 | _ | |a Pharaoh, Paul D P |0 0000-0001-8494-732X |b 23 |
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700 | 1 | _ | |a De Ruyck, Kim |b 85 |
700 | 1 | _ | |a Razack, Azad |b 86 |
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773 | _ | _ | |a 10.1038/s41467-018-03178-z |g Vol. 9, no. 1, p. 1340 |0 PERI:(DE-600)2553671-0 |n 1 |p 1340 |t Nature Communications |v 9 |y 2018 |x 2041-1723 |
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