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@ARTICLE{Vijayakrishnan:132868,
author = {J. Vijayakrishnan and J. Studd and P. Broderick and B.
Kinnersley and A. Holroyd and P. J. Law and R. Kumar$^*$ and
J. M. Allan and C. J. Harrison and A. V. Moorman and A. Vora
and E. Roman and S. Rachakonda$^*$ and S. E. Kinsey and E.
Sheridan and P. D. Thompson and J. A. Irving and R. Koehler
and P. Hoffmann and M. M. Nöthen and S. Heilmann-Heimbach
and K.-H. Jöckel and D. F. Easton and P. D. P. Pharaoh and
A. M. Dunning and J. Peto and F. Canzian$^*$ and A. Swerdlow
and R. A. Eeles and Z. Kote-Jarai and K. Muir and N.
Pashayan and M. Greaves and M. Zimmerman and C. R. Bartram
and M. Schrappe and M. Stanulla and K. Hemminki$^*$ and R.
S. Houlston and B. E. Henderson and C. A. Haiman and S.
Benlloch and F. R. Schumacher and A. A. A. Olama and S. I.
Berndt and D. V. Conti and F. Wiklund and S. Chanock and V.
L. Stevens and C. M. Tangen and J. Batra and J. Clements and
H. Gronberg and J. Schleutker and D. Albanes and S.
Weinstein and A. Wolk and C. West and L. Mucci and G.
Cancel-Tassin and S. Koutros and K. D. Sorensen and L.
Maehle and D. E. Neal and R. C. Travis and R. J. Hamilton
and S. A. Ingles and B. Rosenstein and Y.-J. Lu and G. G.
Giles and A. S. Kibel and A. Vega and M. Kogevinas and K. L.
Penney and J. Y. Park and J. L. Stanford and C. Cybulski and
B. G. Nordestgaard and H. Brenner$^*$ and C. Maier and J.
Kim and E. M. John and M. R. Teixeira and S. L. Neuhausen
and K. De Ruyck and A. Razack and L. F. Newcomb and D.
Lessel and R. Kaneva and N. Usmani and F. Claessens and P.
A. Townsend and M. G. Dominguez and M. J. Roobol and F.
Menegaux},
collaboration = {P. Consortium},
title = {{G}enome-wide association study identifies susceptibility
loci for {B}-cell childhood acute lymphoblastic leukemia.},
journal = {Nature Communications},
volume = {9},
number = {1},
issn = {2041-1723},
address = {London},
publisher = {Nature Publishing Group},
reportid = {DKFZ-2018-00511},
pages = {1340},
year = {2018},
abstract = {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.},
cin = {C050 / C055 / C070 / G110},
ddc = {500},
cid = {I:(DE-He78)C050-20160331 / I:(DE-He78)C055-20160331 /
I:(DE-He78)C070-20160331 / I:(DE-He78)G110-20160331},
pnm = {317 - Translational cancer research (POF3-317)},
pid = {G:(DE-HGF)POF3-317},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:29632299},
pmc = {pmc:PMC5890276},
doi = {10.1038/s41467-018-03178-z},
url = {https://inrepo02.dkfz.de/record/132868},
}