BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 23300798)

  • 1. 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]  

  • 2. 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]  

  • 3. Pleckstrin homology-like domain family B member 1 rs498872 polymorphism and glioma risk in Chinese Han population.
    Zhang JW; Liu ZH; Lin XH; Du YP; Guo HT
    Cell Mol Biol (Noisy-le-grand); 2017 Aug; 63(8):7-9. PubMed ID: 28886307
    [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. A PHLDB1 variant associated with the nonfunctional pituitary adenoma.
    Kim LH; Kim JH; Namgoong S; Cheong HS; Yoon SJ; Kim EH; Kim SH; Kim SH; Chang JH; Shin HD
    J Neurooncol; 2019 Apr; 142(2):223-229. PubMed ID: 30868356
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The PHLDB1 rs498872 (11q23.3) polymorphism and glioma risk: A meta-analysis.
    Gao X; Mi Y; Yan A; Sha B; Guo N; Hu Z; Zhang N; Jiang F; Gou X
    Asia Pac J Clin Oncol; 2015 Dec; 11(4):e13-21. PubMed ID: 24935770
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.
    Zhang J; Zhang Y; Yang J; Zhang L; Sun L; Pan HF; Hirankarn N; Ying D; Zeng S; Lee TL; Lau CS; Chan TM; Leung AM; Mok CC; Wong SN; Lee KW; Ho MH; Lee PP; Chung BH; Chong CY; Wong RW; Mok MY; Wong WH; Tong KL; Tse NK; Li XP; Avihingsanon Y; Rianthavorn P; Deekajorndej T; Suphapeetiporn K; Shotelersuk V; Ying SK; Fung SK; Lai WM; Garcia-Barceló MM; Cherny SS; Tam PK; Cui Y; Sham PC; Yang S; Ye DQ; Zhang XJ; Lau YL; Yang W
    Hum Mol Genet; 2014 Jan; 23(2):524-33. PubMed ID: 24001599
    [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. Assessment of glioma risk associated with an inherited variant at chromosome 11q23.
    Li Z; Wang Y; Guo X; Zhang L; Dong C; Zhang J
    Cell Biochem Biophys; 2015 Jan; 71(1):69-75. PubMed ID: 25182002
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 37(2):222-8. PubMed ID: 23280628
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer.
    Chung CC; Ciampa J; Yeager M; Jacobs KB; Berndt SI; Hayes RB; Gonzalez-Bosquet J; Kraft P; Wacholder S; Orr N; Yu K; Hutchinson A; Boland J; Chen Q; Feigelson HS; Thun MJ; Diver WR; Albanes D; Virtamo J; Weinstein S; Schumacher FR; Cancel-Tassin G; Cussenot O; Valeri A; Andriole GL; Crawford ED; Haiman CA; Henderson BE; Kolonel L; Le Marchand L; Siddiq A; Riboli E; Key TJ; Kaaks R; Isaacs WB; Isaacs SD; Grönberg H; Wiklund F; Xu J; Vatten LJ; Hveem K; Njolstad I; Gerhard DS; Tucker M; Hoover RN; Fraumeni JF; Hunter DJ; Thomas G; Chatterjee N; Chanock SJ
    Hum Mol Genet; 2011 Jul; 20(14):2869-78. PubMed ID: 21531787
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. RTEL1 tagging SNPs and haplotypes were associated with glioma development.
    Li G; Jin T; Liang H; Zhang Z; He S; Tu Y; Yang H; Geng T; Cui G; Chen C; Gao G
    Diagn Pathol; 2013 May; 8():83. PubMed ID: 23683922
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A Common Variant at 11q23.3 Is Associated with Susceptibility to Atopic Dermatitis in the Han Chinese Population.
    Li Y; Xiao FL; Cheng H; Liang B; Zhou FS; Li P; Zheng XD; Sun LD; Yang S; Zhang XJ
    Genet Test Mol Biomarkers; 2021 Oct; 25(10):638-645. PubMed ID: 34609929
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.