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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

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 cas...

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Bibliographische Detailangaben
Hauptverfasser: Vijayakrishnan, Jayaram (VerfasserIn) , Rachakonda, P. Sivaramakrishna (VerfasserIn) , Köhler, Rolf (VerfasserIn) , Bartram, Claus R. (VerfasserIn) , Hemminki, Kari (VerfasserIn) , Kumar, Rajiv (VerfasserIn) , Brenner, Hermann (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2018
In: Nature Communications
Year: 2018, Jahrgang: 9
ISSN:2041-1723
DOI:10.1038/s41467-018-03178-z
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1038/s41467-018-03178-z
Volltext
Verfasserangaben:Jayaram Vijayakrishnan, James Studd, Peter Broderick, Ben Kinnersley, Amy Holroyd, Philip J. Law, Rajiv Kumar, James M. Allan, Christine J. Harrison, Anthony V. Moorman, Ajay Vora, Eve Roman, Sivaramakrishna Rachakonda, Sally E. Kinsey, Eamonn Sheridan, Pamela D. Thompson, Julie A. Irving, Rolf Koehler, Per Hoffmann, Markus M. Nöthen, Stefanie Heilmann-Heimbach, Karl-Heinz Jöckel, Douglas F. Easton, Paul D.P. Pharaoh, Alison M. Dunning, Julian Peto, Frederico Canzian, Anthony Swerdlow, Rosalind A. Eeles, ZSofia Kote-Jarai, Kenneth Muir, Nora Pashayan, the PRACTICAL consortium, Mel Greaves, Martin Zimmerman, Claus R. Bartram, Martin Schrappe, Martin Stanulla, Kari Hemminki & Richard S. Houlston
Beschreibung
Zusammenfassung: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.
Beschreibung:Gesehen am 07.03.2019
Hermann Brenner is a member of the PRACTICAL consortium
Beschreibung:Online Resource
ISSN:2041-1723
DOI:10.1038/s41467-018-03178-z

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