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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 28544645)

  • 1. Germline INDELs and CNVs in a cohort of colorectal cancer patients: their characteristics, associations with relapse-free survival time, and potential time-varying effects on the risk of relapse.
    Werdyani S; Yu Y; Skardasi G; Xu J; Shestopaloff K; Xu W; Dicks E; Green J; Parfrey P; Yilmaz YE; Savas S
    Cancer Med; 2017 Jun; 6(6):1220-1232. PubMed ID: 28544645
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer.
    Yu Y; Werdyani S; Carey M; Parfrey P; Yilmaz YE; Savas S
    Mol Oncol; 2021 Dec; 15(12):3329-3347. PubMed ID: 34309201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two functional indel polymorphisms in the promoter region of the Brahma gene (BRM) and disease risk and progression-free survival in colorectal cancer.
    Yu Y; Cheng D; Parfrey P; Liu G; Savas S
    PLoS One; 2018; 13(6):e0198873. PubMed ID: 29894502
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Candidate predisposing germline copy number variants in early onset colorectal cancer patients.
    Brea-Fernandez AJ; Fernandez-Rozadilla C; Alvarez-Barona M; Azuara D; Ginesta MM; Clofent J; de Castro L; Gonzalez D; Andreu M; Bessa X; Llor X; Xicola R; Jover R; Castells A; Castellvi-Bel S; Capella G; Carracedo A; Ruiz-Ponte C
    Clin Transl Oncol; 2017 May; 19(5):625-632. PubMed ID: 27888432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
    Kim DS; Kim JH; Burt AA; Crosslin DR; Burnham N; Kim CE; McDonald-McGinn DM; Zackai EH; Nicolson SC; Spray TL; Stanaway IB; Nickerson DA; Heagerty PJ; Hakonarson H; Gaynor JW; Jarvik GP
    J Thorac Cardiovasc Surg; 2016 Apr; 151(4):1147-51.e4. PubMed ID: 26704054
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The long-term survival characteristics of a cohort of colorectal cancer patients and baseline variables associated with survival outcomes with or without time-varying effects.
    Yu Y; Carey M; Pollett W; Green J; Dicks E; Parfrey P; Yilmaz YE; Savas S
    BMC Med; 2019 Jul; 17(1):150. PubMed ID: 31352904
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A genome-wide assessment of rare copy number variants in colorectal cancer.
    Li Z; Yu D; Gan M; Shan Q; Yin X; Tang S; Zhang S; Shi Y; Zhu Y; Lai M; Zhang D
    Oncotarget; 2015 Sep; 6(28):26411-23. PubMed ID: 26315111
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.
    Yang R; Chen B; Pfütze K; Buch S; Steinke V; Holinski-Feder E; Stöcker S; von Schönfels W; Becker T; Schackert HK; Royer-Pokora B; Kloor M; Schmiegel WH; Büttner R; Engel C; Lascorz Puertolas J; Försti A; Kunkel N; Bugert P; Schreiber S; Krawczak M; Schafmayer C; Propping P; Hampe J; Hemminki K; Burwinkel B
    Carcinogenesis; 2014 Feb; 35(2):315-23. PubMed ID: 24127187
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancer.
    Bobyn A; Zarrei M; Zhu Y; Hoffman M; Brenner D; Resnick AC; Scherer SW; Gallo M
    BMC Med Genet; 2020 May; 21(1):92. PubMed ID: 32375678
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
    Degenhardt F; Priebe L; Herms S; Mattheisen M; Mühleisen TW; Meier S; Moebus S; Strohmaier J; Groß M; Breuer R; Lange C; Hoffmann P; Meyer-Lindenberg A; Heinz A; Walter H; Lucae S; Wolf C; Müller-Myhsok B; Holsboer F; Maier W; Rietschel M; Nöthen MM; Cichon S
    Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):263-73. PubMed ID: 22344817
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Family-Based Benchmarking of Copy Number Variation Detection Software.
    Nutsua ME; Fischer A; Nebel A; Hofmann S; Schreiber S; Krawczak M; Nothnagel M
    PLoS One; 2015; 10(7):e0133465. PubMed ID: 26197066
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comprehensive assessments of germline deletion structural variants reveal the association between prognostic MUC4 and CEP72 deletions and immune response gene expression in colorectal cancer patients.
    Lin PC; Chen HO; Lee CJ; Yeh YM; Shen MR; Chiang JH
    Hum Genomics; 2021 Jan; 15(1):3. PubMed ID: 33431054
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variations are progressively associated with the pathogenesis of colorectal cancer in ulcerative colitis.
    Shivakumar BM; Rotti H; Vasudevan TG; Balakrishnan A; Chakrabarty S; Bhat G; Rao L; Pai CG; Satyamoorthy K
    World J Gastroenterol; 2015 Jan; 21(2):616-22. PubMed ID: 25605985
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Breast cancer associated germline structural variants harboring small noncoding RNAs impact post-transcriptional gene regulation.
    Kumaran M; Krishnan P; Cass CE; Hubaux R; Lam W; Yasui Y; Damaraju S
    Sci Rep; 2018 May; 8(1):7529. PubMed ID: 29760470
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations.
    Deng L; Lou H; Zhang X; Thiruvahindrapuram B; Lu D; Marshall CR; Liu C; Xie B; Xu W; Wong LP; Yew CW; Farhang A; Ong RT; Hoque MZ; Thuhairah AR; Jong B; Phipps ME; Scherer SW; Teo YY; Kumar SV; Hoh BP; Xu S
    BMC Genomics; 2019 Nov; 20(1):842. PubMed ID: 31718558
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide association study identified copy number variants associated with sporadic colorectal cancer risk.
    Thean LF; Low YS; Lo M; Teo YY; Koh WP; Yuan JM; Chew MH; Tang CL; Cheah PY
    J Med Genet; 2018 Mar; 55(3):181-188. PubMed ID: 29079706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.