These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
571 related articles for article (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 [TBL] [Abstract][Full Text] [Related]
2. Known glioma risk loci are associated with glioma with a family history of brain tumours -- a case-control gene association study. Melin B; Dahlin AM; Andersson U; Wang Z; Henriksson R; Hallmans G; Bondy ML; Johansen C; Feychting M; Ahlbom A; Kitahara CM; Wang SS; Ruder AM; Carreón T; Butler MA; Inskip PD; Purdue M; Hsing AW; Mechanic L; Gillanders E; Yeager M; Linet M; Chanock SJ; Hartge P; Rajaraman P Int J Cancer; 2013 May; 132(10):2464-8. PubMed ID: 23115063 [TBL] [Abstract][Full Text] [Related]
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; 25(7):1355-1365. PubMed ID: 36541697 [TBL] [Abstract][Full Text] [Related]
4. Replication of GWAS identifies RTEL1, CDKN2A/B, and PHLDB1 SNPs as risk factors in Portuguese gliomas patients. Viana-Pereira M; Moreno DA; Linhares P; Amorim J; Nabiço R; Costa S; Vaz R; Reis RM Mol Biol Rep; 2020 Feb; 47(2):877-886. PubMed ID: 31721021 [TBL] [Abstract][Full Text] [Related]
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; 173(8):915-22. PubMed ID: 21350045 [TBL] [Abstract][Full Text] [Related]
6. Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis. Walsh KM; Rice T; Decker PA; Kosel ML; Kollmeyer T; Hansen HM; Zheng S; McCoy LS; Bracci PM; Anderson E; Hsuang G; Wiemels JL; Pico AR; Smirnov I; Molinaro AM; Tihan T; Berger MS; Chang SM; Prados MD; Lachance DH; Sicotte H; Eckel-Passow JE; Wiencke JK; Jenkins RB; Wrensch MR Neuro Oncol; 2013 Aug; 15(8):1041-7. PubMed ID: 23733245 [TBL] [Abstract][Full Text] [Related]
7. Genome-wide association study identifies five susceptibility loci for glioma. Shete S; Hosking FJ; Robertson LB; Dobbins SE; Sanson M; Malmer B; Simon M; Marie Y; Boisselier B; Delattre JY; Hoang-Xuan K; El Hallani S; Idbaih A; Zelenika D; Andersson U; Henriksson R; Bergenheim AT; Feychting M; Lönn S; Ahlbom A; Schramm J; Linnebank M; Hemminki K; Kumar R; Hepworth SJ; Price A; Armstrong G; Liu Y; Gu X; Yu R; Lau C; Schoemaker M; Muir K; Swerdlow A; Lathrop M; Bondy M; Houlston RS Nat Genet; 2009 Aug; 41(8):899-904. PubMed ID: 19578367 [TBL] [Abstract][Full Text] [Related]
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; 36(8):876-82. PubMed ID: 26014354 [TBL] [Abstract][Full Text] [Related]
9. Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma. Ghasimi S; Wibom C; Dahlin AM; Brännström T; Golovleva I; Andersson U; Melin B J Neurooncol; 2016 May; 127(3):483-92. PubMed ID: 26839018 [TBL] [Abstract][Full Text] [Related]
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; 41(8):905-8. PubMed ID: 19578366 [TBL] [Abstract][Full Text] [Related]
12. Investigation of established genetic risk variants for glioma in prediagnostic samples from a population-based nested case-control study. Wibom C; Späth F; Dahlin AM; Langseth H; Hovig E; Rajaraman P; Johannesen TB; Andersson U; Melin B Cancer Epidemiol Biomarkers Prev; 2015 May; 24(5):810-6. PubMed ID: 25713050 [TBL] [Abstract][Full Text] [Related]
13. Genetic risk profiles identify different molecular etiologies for glioma. Simon M; Hosking FJ; Marie Y; Gousias K; Boisselier B; Carpentier C; Schramm J; Mokhtari K; Hoang-Xuan K; Idbaih A; Delattre JY; Lathrop M; Robertson LB; Houlston RS; Sanson M Clin Cancer Res; 2010 Nov; 16(21):5252-9. PubMed ID: 20847058 [TBL] [Abstract][Full Text] [Related]
14. Genetic causes of glioma: new leads in the labyrinth. Melin B Curr Opin Oncol; 2011 Nov; 23(6):643-7. PubMed ID: 21825990 [TBL] [Abstract][Full Text] [Related]
15. An Updated and Comprehensive Meta-Analysis of Association Between Seven Hot Loci Polymorphisms from Eight GWAS and Glioma Risk. Wu Q; Peng Y; Zhao X Mol Neurobiol; 2016 Sep; 53(7):4397-405. PubMed ID: 26243184 [TBL] [Abstract][Full Text] [Related]
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; 171(11):1165-73. PubMed ID: 20462933 [TBL] [Abstract][Full Text] [Related]
17. Cancer susceptibility variants and the risk of adult glioma in a US case-control study. Egan KM; Thompson RC; Nabors LB; Olson JJ; Brat DJ; Larocca RV; Brem S; Moots PL; Madden MH; Browning JE; Ann Chen Y J Neurooncol; 2011 Sep; 104(2):535-42. PubMed ID: 21203894 [TBL] [Abstract][Full Text] [Related]
19. Fine-mapping of a region of chromosome 5p15.33 (TERT-CLPTM1L) suggests a novel locus in TERT and a CLPTM1L haplotype are associated with glioma susceptibility in a Chinese population. Zhao Y; Chen G; Zhao Y; Song X; Chen H; Mao Y; Lu D Int J Cancer; 2012 Oct; 131(7):1569-76. PubMed ID: 22213090 [TBL] [Abstract][Full Text] [Related]
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; 11(10):e0163067. PubMed ID: 27780202 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]