164 related articles for article (PubMed ID: 22688887)
1. Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma.
Liu Y; Melin BS; Rajaraman P; Wang Z; Linet M; Shete S; Amos CI; Lau CC; Scheurer ME; Tsavachidis S; Armstrong GN; Houlston RS; Hosking FJ; Claus EB; Barnholtz-Sloan J; Lai R; Il'yasova D; Schildkraut J; Sadetzki S; Johansen C; Bernstein JL; Olson SH; Jenkins RB; LaChance D; Vick NA; Wrensch M; Davis F; McCarthy BJ; Andersson U; Thompson PA; Chanock S; ; Bondy ML
Hum Genet; 2012 Sep; 131(9):1507-17. PubMed ID: 22688887
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium.
Shete S; Lau CC; Houlston RS; Claus EB; Barnholtz-Sloan J; Lai R; Il'yasova D; Schildkraut J; Sadetzki S; Johansen C; Bernstein JL; Olson SH; Jenkins RB; Yang P; Vick NA; Wrensch M; Davis FG; McCarthy BJ; Leung EH; Davis C; Cheng R; Hosking FJ; Armstrong GN; Liu Y; Yu RK; Henriksson R; ; Melin BS; Bondy ML
Cancer Res; 2011 Dec; 71(24):7568-75. PubMed ID: 22037877
[TBL] [Abstract][Full Text] [Related]
3. Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.
Song X; Zhou K; Zhao Y; Huai C; Zhao Y; Yu H; Chen Y; Chen G; Chen H; Fan W; Mao Y; Lu D
Carcinogenesis; 2012 May; 33(5):1065-71. PubMed ID: 22387365
[TBL] [Abstract][Full Text] [Related]
4. A novel low-penetrance locus for familial glioma at 15q23-q26.3.
Paunu N; Lahermo P; Onkamo P; Ollikainen V; Rantala I; Helén P; Simola KO; Kere J; Haapasalo H
Cancer Res; 2002 Jul; 62(13):3798-802. PubMed ID: 12097292
[TBL] [Abstract][Full Text] [Related]
5. Fine mapping of a region of chromosome 11q23.3 reveals independent locus associated with risk of glioma.
Chen H; Sun B; Zhao Y; Song X; Fan W; Zhou K; Zhou L; Mao Y; Lu D
PLoS One; 2012; 7(12):e52864. PubMed ID: 23300798
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Association of genetic variants in the retinoblastoma binding protein 6 gene with the risk of glioma: a case-control study in a Chinese Han population.
Hu D; Zhang S; Zhao Y; Wang S; Wang Q; Song X; Lu D; Mao Y; Chen H
J Neurosurg; 2014 Nov; 121(5):1209-18. PubMed ID: 25127414
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. GLIOGENE an International Consortium to Understand Familial Glioma.
Malmer B; Adatto P; Armstrong G; Barnholtz-Sloan J; Bernstein JL; Claus E; Davis F; Houlston R; Il'yasova D; Jenkins R; Johansen C; Lai R; Lau C; McCarthy B; Nielsen H; Olson SH; Sadetzki S; Shete S; Wiklund F; Wrensch M; Yang P; Bondy M
Cancer Epidemiol Biomarkers Prev; 2007 Sep; 16(9):1730-4. PubMed ID: 17855690
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Functional variants of 17q12-21 are associated with allergic asthma but not allergic rhinitis.
Andiappan AK; Sio YY; Lee B; Suri BK; Matta SA; Lum J; Foo S; Koh G; Liu J; Zolezzi F; Poidinger M; Wang de Y; Rotzschke O; Chew FT
J Allergy Clin Immunol; 2016 Mar; 137(3):758-66.e3. PubMed ID: 26483175
[TBL] [Abstract][Full Text] [Related]
12. Genetic variations in the homologous recombination repair pathway genes modify risk of glioma.
Zhang H; Liu Y; Zhou K; Zhou C; Zhou R; Cheng C; Wei Q; Lu D; Zhou L
J Neurooncol; 2016 Jan; 126(1):11-17. PubMed ID: 26514363
[TBL] [Abstract][Full Text] [Related]
13. Genetic variants in inflammation pathway genes and asthma in glioma susceptibility.
Amirian E; Liu Y; Scheurer ME; El-Zein R; Gilbert MR; Bondy ML
Neuro Oncol; 2010 May; 12(5):444-52. PubMed ID: 20406895
[TBL] [Abstract][Full Text] [Related]
14. Association and interactions between DNA repair gene polymorphisms and adult glioma.
Liu Y; Scheurer ME; El-Zein R; Cao Y; Do KA; Gilbert M; Aldape KD; Wei Q; Etzel C; Bondy ML
Cancer Epidemiol Biomarkers Prev; 2009 Jan; 18(1):204-14. PubMed ID: 19124499
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Functional analysis of the 11q23.3 glioma susceptibility locus implicates PHLDB1 and DDX6 in glioma susceptibility.
Baskin R; Woods NT; Mendoza-Fandiño G; Forsyth P; Egan KM; Monteiro AN
Sci Rep; 2015 Nov; 5():17367. PubMed ID: 26610392
[TBL] [Abstract][Full Text] [Related]
17. Possible association between genetic variants in the H2AFX promoter region and risk of adult glioma in a Chinese Han population.
Fan W; Zhou K; Zhao Y; Wu W; Chen H; Jin L; Chen G; Shi J; Wei Q; Zhang T; Du G; Mao Y; Lu D; Zhou L
J Neurooncol; 2011 Nov; 105(2):211-8. PubMed ID: 21512825
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A comprehensive study of the association between the EGFR and ERBB2 genes and glioma risk.
Andersson U; Schwartzbaum J; Wiklund F; Sjöström S; Liu Y; Tsavachidis S; Ahlbom A; Auvinen A; Collatz-Laier H; Feychting M; Johansen C; Kiuru A; Lönn S; Schoemaker MJ; Swerdlow AJ; Henriksson R; Bondy M; Melin B
Acta Oncol; 2010 Aug; 49(6):767-75. PubMed ID: 20446891
[TBL] [Abstract][Full Text] [Related]
20. 1p34.2 rs621559 and 14q21 rs398652 leukocyte telomere length-related genetic variants contribute to glioma susceptibility.
Chen YD; Lu C; Wei J; Han S; Wang H; Jiang T; Qiu XG; Yang M
J Neurooncol; 2014 Aug; 119(1):71-8. PubMed ID: 24844311
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
