Sökning: onr:"swepub:oai:DiVA.org:umu-135267" > Genome-wide associa...
Fältnamn | Indikatorer | Metadata |
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000 | 05158naa a2201045 4500 | |
001 | oai:DiVA.org:umu-135267 | |
003 | SwePub | |
008 | 170526s2017 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1352672 URI |
024 | 7 | a https://doi.org/10.1038/ng.38232 DOI |
040 | a (SwePub)umu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Melin, Beatrice S.u Umeå universitet,Institutionen för strålningsvetenskaper4 aut0 (Swepub:umu)bema0010 |
245 | 1 0 | a Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors |
264 | c 2017-03-27 | |
264 | 1 | b Springer Science and Business Media LLC,c 2017 |
338 | a print2 rdacarrier | |
520 | a Genome-wide association studies (GWAS) have transformed our understanding of glioma susceptibility, but individual studies have had limited power to identify risk loci. We performed a meta-analysis of existing GWAS and two new GWAS, which totaled 12,496 cases and 18,190 controls. We identified five new loci for glioblastoma (GBM) at 1p31.3 (rs12752552; P = 2.04 x 10(-9), odds ratio (OR) = 1.22), 11q14.1 (rs11233250; P = 9.95 x 10(-10), OR = 1.24), 16p13.3 (rs2562152; P = 1.93 x 10-8, OR = 1.21), 16q12.1 (rs10852606; P = 1.29 x 10(-11), OR = 1.18) and 22q13.1 (rs2235573; P = 1.76 x 10(-10), OR = 1.15), as well as eight loci for non-GBM tumors at 1q32.1 (rs4252707; P = 3.34 x 10(-9), OR = 1.19), 1q44 (rs12076373; P = 2.63 x 10(-10), OR = 1.23), 2q33.3 (rs7572263; P = 2.18 x 10(-10), OR = 1.20), 3p14.1 (rs11706832; P = 7.66 x 10(-9), OR = 1.15), 10q24.33 (rs11598018; P = 3.39 x 10-8, OR = 1.14), 11q21 (rs7107785; P = 3.87 x 10(-10), OR = 1.16), 14q12 (rs10131032; P = 5.07 x 10(-11), OR = 1.33) and 16p13.3 (rs3751667; P = 2.61 x 10(-9), OR = 1.18). These data substantiate that genetic susceptibility to GBM and non-GBM tumors are highly distinct, which likely reflects different etiology. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Medicinsk genetik0 (SwePub)301072 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Medical Genetics0 (SwePub)301072 hsv//eng |
700 | 1 | a Barnholtz-Sloan, Jill S.4 aut |
700 | 1 | a Wrensch, Margaret R.4 aut |
700 | 1 | a Johansen, Christoffer4 aut |
700 | 1 | a Il'yasova, Dora4 aut |
700 | 1 | a Kinnersley, Ben4 aut |
700 | 1 | a Ostrom, Quinn T.4 aut |
700 | 1 | a Labreche, Karim4 aut |
700 | 1 | a Chen, Yanwen4 aut |
700 | 1 | a Armstrong, Georgina4 aut |
700 | 1 | a Liu, Yanhong4 aut |
700 | 1 | a Eckel-Passow, Jeanette E.4 aut |
700 | 1 | a Decker, Paul A.4 aut |
700 | 1 | a Labussiere, Marianne4 aut |
700 | 1 | a Idbaih, Ahmed4 aut |
700 | 1 | a Hoang-Xuan, Khe4 aut |
700 | 1 | a Di Stefano, Anna-Luisa4 aut |
700 | 1 | a Mokhtari, Karima4 aut |
700 | 1 | a Delattre, Jean-Yves4 aut |
700 | 1 | a Broderick, Peter4 aut |
700 | 1 | a Galan, Pilar4 aut |
700 | 1 | a Gousias, Konstantinos4 aut |
700 | 1 | a Schramm, Johannes4 aut |
700 | 1 | a Schoemaker, Minouk J.4 aut |
700 | 1 | a Fleming, Sarah J.4 aut |
700 | 1 | a Herms, Stefan4 aut |
700 | 1 | a Heilmann, Stefanie4 aut |
700 | 1 | a Noethen, Markus M.4 aut |
700 | 1 | a Wichmann, Heinz-Erich4 aut |
700 | 1 | a Schreiber, Stefan4 aut |
700 | 1 | a Swerdlow, Anthony4 aut |
700 | 1 | a Lathrop, Mark4 aut |
700 | 1 | a Simon, Matthias4 aut |
700 | 1 | a Sanson, Marc4 aut |
700 | 1 | a Andersson, Ulrikau Umeå universitet,Institutionen för strålningsvetenskaper4 aut0 (Swepub:umu)ulan0002 |
700 | 1 | a Rajaraman, Preetha4 aut |
700 | 1 | a Chanock, Stephen4 aut |
700 | 1 | a Linet, Martha4 aut |
700 | 1 | a Wang, Zhaoming4 aut |
700 | 1 | a Yeager, Meredith4 aut |
700 | 1 | a Wiencke, John K.4 aut |
700 | 1 | a Hansen, Helen4 aut |
700 | 1 | a Mccoy, Lucie4 aut |
700 | 1 | a Rice, Terri4 aut |
700 | 1 | a Kosel, Matthew L.4 aut |
700 | 1 | a Sicotte, Hugues4 aut |
700 | 1 | a Amos, Christopher I.4 aut |
700 | 1 | a Bernstein, Jonine L.4 aut |
700 | 1 | a Davis, Faith4 aut |
700 | 1 | a Lachance, Dan4 aut |
700 | 1 | a Lau, Ching4 aut |
700 | 1 | a Merrell, Ryan T.4 aut |
700 | 1 | a Shildkraut, Joellen4 aut |
700 | 1 | a Ali-Osman, Francis4 aut |
700 | 1 | a Sadetzki, Siegal4 aut |
700 | 1 | a Scheurer, Michael4 aut |
700 | 1 | a Shete, Sanjay4 aut |
700 | 1 | a Lai, Rose K.4 aut |
700 | 1 | a Claus, Elizabeth B.4 aut |
700 | 1 | a Olson, Sara H.4 aut |
700 | 1 | a Jenkins, Robert B.4 aut |
700 | 1 | a Houlston, Richard S.4 aut |
700 | 1 | a Bondy, Melissa L.4 aut |
710 | 2 | a Umeå universitetb Institutionen för strålningsvetenskaper4 org |
773 | 0 | t Nature Geneticsd : Springer Science and Business Media LLCg 49:5, s. 789-794q 49:5<789-794x 1061-4036x 1546-1718 |
856 | 4 | u https://europepmc.org/articles/pmc5558246?pdf=render |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-135267 |
856 | 4 8 | u https://doi.org/10.1038/ng.3823 |
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