BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 32681635)

  • 1. Tumor somatic mutations also existing as germline polymorphisms may help to identify functional SNPs from genome-wide association studies.
    Gorlov IP; Xia X; Tsavachidis S; Gorlova OY; Amos CI
    Carcinogenesis; 2020 Oct; 41(10):1353-1362. PubMed ID: 32681635
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Data-adaptive and pathway-based tests for association studies between somatic mutations and germline variations in human cancers.
    Chen Z; Liang H; Wei P
    Genet Epidemiol; 2023 Dec; 47(8):617-636. PubMed ID: 37822029
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal.
    Sun JX; He Y; Sanford E; Montesion M; Frampton GM; Vignot S; Soria JC; Ross JS; Miller VA; Stephens PJ; Lipson D; Yelensky R
    PLoS Comput Biol; 2018 Feb; 14(2):e1005965. PubMed ID: 29415044
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline and Somatic Genetic Variants in the p53 Pathway Interact to Affect Cancer Risk, Progression, and Drug Response.
    Zhang P; Kitchen-Smith I; Xiong L; Stracquadanio G; Brown K; Richter PH; Wallace MD; Bond E; Sahgal N; Moore S; Nornes S; De Val S; Surakhy M; Sims D; Wang X; Bell DA; Zeron-Medina J; Jiang Y; Ryan AJ; Selfe JL; Shipley J; Kar S; Pharoah PD; Loveday C; Jansen R; Grochola LF; Palles C; Protheroe A; Millar V; Ebner DV; Pagadala M; Blagden SP; Maughan TS; Domingo E; Tomlinson I; Turnbull C; Carter H; Bond GL
    Cancer Res; 2021 Apr; 81(7):1667-1680. PubMed ID: 33558336
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Multiethnic Germline-Somatic Association Database Deciphers Multilayered and Interconnected Genetic Mutations in Cancer.
    Xin J; Mo Z; Chai R; Hua W; Wang J
    Cancer Res; 2024 Feb; 84(3):364-371. PubMed ID: 38016109
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SNP eQTL status and eQTL density in the adjacent region of the SNP are associated with its statistical significance in GWA studies.
    Gorlov I; Xiao X; Mayes M; Gorlova O; Amos C
    BMC Genet; 2019 Nov; 20(1):85. PubMed ID: 31718536
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Relative effects of mutability and selection on single nucleotide polymorphisms in transcribed regions of the human genome.
    Gorlov IP; Gorlova OY; Amos CI
    BMC Genomics; 2008 Jun; 9():292. PubMed ID: 18559102
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples.
    Gorlov IP; Pikielny CW; Frost HR; Her SC; Cole MD; Strohbehn SD; Wallace-Bradley D; Kimmel M; Gorlova OY; Amos CI
    BMC Bioinformatics; 2018 Nov; 19(1):430. PubMed ID: 30453881
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas.
    Buckley AR; Ideker T; Carter H; Harismendy O; Schork NJ
    Genome Med; 2018 Sep; 10(1):69. PubMed ID: 30217226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identifying Putative Susceptibility Genes and Evaluating Their Associations with Somatic Mutations in Human Cancers.
    Chen Z; Wen W; Beeghly-Fadiel A; Shu XO; Díez-Obrero V; Long J; Bao J; Wang J; Liu Q; Cai Q; Moreno V; Zheng W; Guo X
    Am J Hum Genet; 2019 Sep; 105(3):477-492. PubMed ID: 31402092
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical significance of papillary thyroid cancer risk loci identified by genome-wide association studies.
    Wei WJ; Lu ZW; Wang Y; Zhu YX; Wang YL; Ji QH
    Cancer Genet; 2015 Mar; 208(3):68-75. PubMed ID: 25746573
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interaction analysis between germline susceptibility loci and somatic alterations in lung cancer.
    Wang Y; Wang C; Zhang J; Zhu M; Zhang X; Li Z; Dai J; Ma H; Hu Z; Jin G; Shen H
    Int J Cancer; 2018 Aug; 143(4):878-885. PubMed ID: 29492964
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The pattern of natural selection in somatic cancer mutations of human mtDNA.
    Stafford P; Chen-Quin EB
    J Hum Genet; 2010 Sep; 55(9):605-12. PubMed ID: 20613764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Single-Nucleotide Polymorphisms Sequencing Identifies Candidate Functional Variants at Prostate Cancer Risk Loci.
    Zhang P; Tillmans LS; Thibodeau SN; Wang L
    Genes (Basel); 2019 Jul; 10(7):. PubMed ID: 31323811
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of Germline versus Somatic BAP1 Mutations for Risk of Metastasis in Uveal Melanoma.
    Ewens KG; Lalonde E; Richards-Yutz J; Shields CL; Ganguly A
    BMC Cancer; 2018 Nov; 18(1):1172. PubMed ID: 30477459
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.
    Marouf C; Göhler S; Filho MI; Hajji O; Hemminki K; Nadifi S; Försti A
    BMC Cancer; 2016 Feb; 16():165. PubMed ID: 26920143
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Landscape of the Heritable Cancer Genome.
    Fanfani V; Citi L; Harris AL; Pezzella F; Stracquadanio G
    Cancer Res; 2021 May; 81(10):2588-2599. PubMed ID: 33731442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Integrative analysis of somatic mutations altering microRNA targeting in cancer genomes.
    Ziebarth JD; Bhattacharya A; Cui Y
    PLoS One; 2012; 7(10):e47137. PubMed ID: 23091610
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel and recurrent germline and somatic mutations in a cohort of 67 patients from 48 families with Brooke-Spiegler syndrome including the phenotypic variant of multiple familial trichoepitheliomas and correlation with the histopathologic findings in 379 biopsy specimens.
    Grossmann P; Vanecek T; Steiner P; Kacerovska D; Spagnolo DV; Cribier B; Rose C; Vazmitel M; Carlson JA; Emberger M; Martinek P; Pearce RL; Pearn J; Michal M; Kazakov DV
    Am J Dermatopathol; 2013 Feb; 35(1):34-44. PubMed ID: 23249834
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Combinations of single nucleotide polymorphisms identified in genome-wide association studies determine risk for colorectal cancer.
    Xin J; Du M; Gu D; Ge Y; Li S; Chu H; Meng Y; Shen H; Zhang Z; Wang M
    Int J Cancer; 2019 Nov; 145(10):2661-2669. PubMed ID: 30859566
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.