BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 23275252)

  • 1. Germline copy number variations associated with breast cancer susceptibility in a Japanese population.
    Suehiro Y; Okada T; Shikamoto N; Zhan Y; Sakai K; Okayama N; Nishioka M; Furuya T; Oga A; Kawauchi S; Maeda N; Tamesa M; Nagashima Y; Yamamoto S; Oka M; Hinoda Y; Sasaki K
    Tumour Biol; 2013 Apr; 34(2):947-52. PubMed ID: 23275252
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.
    Walker LC; Pearson JF; Wiggins GA; Giles GG; Hopper JL; Southey MC
    Breast Cancer Res; 2017 Mar; 19(1):30. PubMed ID: 28302160
    [TBL] [Abstract][Full Text] [Related]  

  • 3. E2F1 copy number variations in germline and breast cancer: a retrospective study of 222 Italian women.
    Rocca MS; Benna C; Goldin E; Di Nisio A; De Toni L; Cosci I; Marchet A; Nitti D; Foresta C
    Mol Med; 2021 Mar; 27(1):26. PubMed ID: 33691613
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline copy number variations are associated with breast cancer risk and prognosis.
    Kumaran M; Cass CE; Graham K; Mackey JR; Hubaux R; Lam W; Yasui Y; Damaraju S
    Sci Rep; 2017 Nov; 7(1):14621. PubMed ID: 29116104
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variations of DNA repair genes and the age-related cataract: Jiangsu Eye Study.
    Jiang J; Zhou J; Yao Y; Zhu R; Liang C; Jiang S; Yang M; Lu Y; Xing Q; Guan H
    Invest Ophthalmol Vis Sci; 2013 Feb; 54(2):932-8. PubMed ID: 23329665
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Germline DNA copy number variation in familial and early-onset breast cancer.
    Krepischi AC; Achatz MI; Santos EM; Costa SS; Lisboa BC; Brentani H; Santos TM; Gonçalves A; Nóbrega AF; Pearson PL; Vianna-Morgante AM; Carraro DM; Brentani RR; Rosenberg C
    Breast Cancer Res; 2012 Feb; 14(1):R24. PubMed ID: 22314128
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copy number variations of HLA-DRB5 is associated with systemic lupus erythematosus risk in Chinese Han population.
    Wu L; Guo S; Yang D; Ma Y; Ji H; Chen Y; Zhang J; Wang Y; Jin L; Wang J; Liu J
    Acta Biochim Biophys Sin (Shanghai); 2014 Feb; 46(2):155-60. PubMed ID: 24366815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copy Number Variation in
    Wang Y; Li L; Yang Y; Feng J; Wang L; Zhang H
    Genet Test Mol Biomarkers; 2020 Apr; 24(4):173-180. PubMed ID: 32208937
    [No Abstract]   [Full Text] [Related]  

  • 9. A copy number variation in PKD1L2 is associated with colorectal cancer predisposition in korean population.
    Park C; Kim JI; Hong SN; Jung HM; Kim TJ; Lee S; Kim SJ; Kim HC; Kim DH; Cho B; Park JH; Sung J; Lee DS; Kang M; Son HJ; Kim YH
    Int J Cancer; 2017 Jan; 140(1):86-94. PubMed ID: 27605020
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large germline copy number variations as predisposing factor in childhood neoplasms.
    Krepischi AC; Capelli LP; Silva AG; de Araújo ÉS; Pearson PL; Heck B; da Costa CM; de Camargo B; Rosenberg C
    Future Oncol; 2014; 10(9):1627-33. PubMed ID: 25145432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A common deletion in the APOBEC3 genes and breast cancer risk.
    Long J; Delahanty RJ; Li G; Gao YT; Lu W; Cai Q; Xiang YB; Li C; Ji BT; Zheng Y; Ali S; Shu XO; Zheng W
    J Natl Cancer Inst; 2013 Apr; 105(8):573-9. PubMed ID: 23411593
    [TBL] [Abstract][Full Text] [Related]  

  • 12. E2F1 germline copy number variations and melanoma susceptibility.
    Rocca MS; Benna C; Mocellin S; Rossi CR; Msaki A; Di Nisio A; Opocher G; Foresta C
    J Transl Med; 2019 May; 17(1):181. PubMed ID: 31142321
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.
    Bae JS; Cheong HS; Park BL; Kim LH; Park TJ; Kim JY; Pasaje CF; Lee JS; Cui T; Inoue I; Shin HD
    J Hum Genet; 2010 Nov; 55(11):726-30. PubMed ID: 20703242
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Genome-Wide Association Study to Identify Potential Germline Copy Number Variants for Sporadic Breast Cancer Susceptibility.
    Sapkota Y; Narasimhan A; Kumaran M; Sehrawat BS; Damaraju S
    Cytogenet Genome Res; 2016; 149(3):156-164. PubMed ID: 27668787
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia.
    Higashiyama R; Ohnuma T; Takebayashi Y; Hanzawa R; Shibata N; Yamamori H; Yasuda Y; Kushima I; Aleksic B; Kondo K; Ikeda M; Hashimoto R; Iwata N; Ozaki N; Arai H
    Am J Med Genet B Neuropsychiatr Genet; 2016 Apr; 171B(3):447-57. PubMed ID: 26852906
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA copy number is associated with breast cancer risk.
    Thyagarajan B; Wang R; Nelson H; Barcelo H; Koh WP; Yuan JM
    PLoS One; 2013; 8(6):e65968. PubMed ID: 23776581
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
    Uebe S; Ehrlicher M; Ekici AB; Behrens F; Böhm B; Homuth G; Schurmann C; Völker U; Jünger M; Nauck M; Völzke H; Traupe H; Krawczak M; Burkhardt H; Reis A; Hüffmeier U
    BMC Med Genet; 2017 Aug; 18(1):92. PubMed ID: 28835222
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Germline copy number variants are not associated with globally acquired copy number changes in familial breast tumours.
    Walker LC; Krause L; ; Spurdle AB; Waddell N
    Breast Cancer Res Treat; 2012 Aug; 134(3):1005-11. PubMed ID: 22434526
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma.
    Shi J; Zhou W; Zhu B; Hyland PL; Bennett H; Xiao Y; Zhang X; Burke LS; Song L; Hsu CH; Yan C; Chen Q; Meerzaman D; Dagnall CL; Burdette L; Hicks B; Freedman ND; Chanock SJ; Yeager M; Tucker MA; Goldstein AM; Yang XR
    J Invest Dermatol; 2016 Dec; 136(12):2436-2443. PubMed ID: 27476724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.
    Poniah P; Mohd Zain S; Abdul Razack AH; Kuppusamy S; Karuppayah S; Sian Eng H; Mohamed Z
    Urol Oncol; 2017 Sep; 35(9):545.e1-545.e11. PubMed ID: 28527622
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.