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Journal Abstract Search

572 related items for PubMed ID: 22886559

  • 1. Genome-wide association study of glioma and meta-analysis.
    Rajaraman P, Melin BS, Wang Z, McKean-Cowdin R, Michaud DS, Wang SS, Bondy M, Houlston R, Jenkins RB, Wrensch M, Yeager M, Ahlbom A, Albanes D, Andersson U, Freeman LE, Buring JE, Butler MA, Braganza M, Carreon T, Feychting M, Fleming SJ, Gapstur SM, Gaziano JM, Giles GG, Hallmans G, Henriksson R, Hoffman-Bolton J, Inskip PD, Johansen C, Kitahara CM, Lathrop M, Liu C, Le Marchand L, Linet MS, Lonn S, Peters U, Purdue MP, Rothman N, Ruder AM, Sanson M, Sesso HD, Severi G, Shu XO, Simon M, Stampfer M, Stevens VL, Visvanathan K, White E, Wolk A, Zeleniuch-Jacquotte A, Zheng W, Decker P, Enciso-Mora V, Fridley B, Gao YT, Kosel M, Lachance DH, Lau C, Rice T, Swerdlow A, Wiemels JL, Wiencke JK, Shete S, Xiang YB, Xiao Y, Hoover RN, Fraumeni JF, Chatterjee N, Hartge P, Chanock SJ.
    Hum Genet; 2012 Dec; 131(12):1877-88. PubMed ID: 22886559
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  • 3. Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26.
    Alpen K, Vajdic CM, MacInnis RJ, Milne RL, Koh ES, Hovey E, Harrup R, Bruinsma F, Nguyen TL, Li S, Joseph D, Benke G, Dugué PA, Southey MC, Giles GG, Rosenthal M, Drummond KJ, Nowak AK, Hopper JL, Kapuscinski M, Makalic E.
    Neuro Oncol; 2023 Jul 06; 25(7):1355-1365. PubMed ID: 36541697
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  • 5. Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population.
    Chen H, Chen Y, Zhao Y, Fan W, Zhou K, Liu Y, Zhou L, Mao Y, Wei Q, Xu J, Lu D.
    Am J Epidemiol; 2011 Apr 15; 173(8):915-22. PubMed ID: 21350045
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  • 8. CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility.
    Adel Fahmideh M, Lavebratt C, Schüz J, Röösli M, Tynes T, Grotzer MA, Johansen C, Kuehni CE, Lannering B, Prochazka M, Schmidt LS, Feychting M.
    Carcinogenesis; 2015 Aug 15; 36(8):876-82. PubMed ID: 26014354
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  • 10. Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
    Wrensch M, Jenkins RB, Chang JS, Yeh RF, Xiao Y, Decker PA, Ballman KV, Berger M, Buckner JC, Chang S, Giannini C, Halder C, Kollmeyer TM, Kosel ML, LaChance DH, McCoy L, O'Neill BP, Patoka J, Pico AR, Prados M, Quesenberry C, Rice T, Rynearson AL, Smirnov I, Tihan T, Wiemels J, Yang P, Wiencke JK.
    Nat Genet; 2009 Aug 15; 41(8):905-8. PubMed ID: 19578366
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  • 14. Genetic causes of glioma: new leads in the labyrinth.
    Melin B.
    Curr Opin Oncol; 2011 Nov 15; 23(6):643-7. PubMed ID: 21825990
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  • 16. Interaction between 5 genetic variants and allergy in glioma risk.
    Schoemaker MJ, Robertson L, Wigertz A, Jones ME, Hosking FJ, Feychting M, Lönn S, McKinney PA, Hepworth SJ, Muir KR, Auvinen A, Salminen T, Kiuru A, Johansen C, Houlston RS, Swerdlow AJ.
    Am J Epidemiol; 2010 Jun 01; 171(11):1165-73. PubMed ID: 20462933
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  • 18. Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies.
    Walsh KM, Anderson E, Hansen HM, Decker PA, Kosel ML, Kollmeyer T, Rice T, Zheng S, Xiao Y, Chang JS, McCoy LS, Bracci PM, Wiemels JL, Pico AR, Smirnov I, Lachance DH, Sicotte H, Eckel-Passow JE, Wiencke JK, Jenkins RB, Wrensch MR.
    Genet Epidemiol; 2013 Feb 01; 37(2):222-8. PubMed ID: 23280628
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  • 20. Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor.
    Dahlin AM, Wibom C, Ghasimi S, Brännström T, Andersson U, Melin B.
    PLoS One; 2016 Feb 01; 11(10):e0163067. PubMed ID: 27780202
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