BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 28026089)

  • 1. Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications.
    Soussi T; Taschner PE; Samuels Y
    Hum Mutat; 2017 Apr; 38(4):339-342. PubMed ID: 28026089
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inferring Potential Cancer Driving Synonymous Variants.
    Zeng Z; Bromberg Y
    Genes (Basel); 2022 Apr; 13(5):. PubMed ID: 35627162
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An Ensemble Approach to Predict the Pathogenicity of Synonymous Variants.
    Ranganathan Ganakammal S; Alexov E
    Genes (Basel); 2020 Sep; 11(9):. PubMed ID: 32967157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Computational identification of deleterious synonymous variants in human genomes using a feature-based approach.
    Shi F; Yao Y; Bin Y; Zheng CH; Xia J
    BMC Med Genomics; 2019 Jan; 12(Suppl 1):12. PubMed ID: 30704475
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synonymous Variants: Necessary Nuance in Our Understanding of Cancer Drivers and Treatment Outcomes.
    Kaissarian NM; Meyer D; Kimchi-Sarfaty C
    J Natl Cancer Inst; 2022 Aug; 114(8):1072-1094. PubMed ID: 35477782
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein.
    Kim A; Le Douce J; Diab F; Ferovova M; Dubourg C; Odent S; Dupé V; David V; Diambra L; Watrin E; de Tayrac M
    Brain; 2020 Jul; 143(7):2027-2038. PubMed ID: 32542401
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Discovery of Cancer Driver Long Noncoding RNAs across 1112 Tumour Genomes: New Candidates and Distinguishing Features.
    Lanzós A; Carlevaro-Fita J; Mularoni L; Reverter F; Palumbo E; Guigó R; Johnson R
    Sci Rep; 2017 Jan; 7():41544. PubMed ID: 28128360
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational landscape of MCPyV-positive and MCPyV-negative Merkel cell carcinomas with implications for immunotherapy.
    Goh G; Walradt T; Markarov V; Blom A; Riaz N; Doumani R; Stafstrom K; Moshiri A; Yelistratova L; Levinsohn J; Chan TA; Nghiem P; Lifton RP; Choi J
    Oncotarget; 2016 Jan; 7(3):3403-15. PubMed ID: 26655088
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The FABRIC Cancer Portal: A Ranked Catalogue of Gene Selection in Tumors Over the Human Coding Genome.
    Kelman G; Brandes N; Linial M
    Cancer Res; 2021 Feb; 81(4):1178-1185. PubMed ID: 33277365
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of coding and non-coding mutational hotspots in cancer genomes.
    Piraino SW; Furney SJ
    BMC Genomics; 2017 Jan; 18(1):17. PubMed ID: 28056774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synonymous mutations frequently act as driver mutations in human cancers.
    Supek F; Miñana B; Valcárcel J; Gabaldón T; Lehner B
    Cell; 2014 Mar; 156(6):1324-1335. PubMed ID: 24630730
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Discovery and clinical application of mutations in the cancer genome].
    Mano H
    Nihon Rinsho; 2015 Aug; 73(8):1251-5. PubMed ID: 26281674
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cancer regulatory variation.
    Hennessey RC; Brown KM
    Curr Opin Genet Dev; 2021 Feb; 66():41-49. PubMed ID: 33422949
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers.
    Zheng CX; Gu ZH; Han B; Zhang RX; Pan CM; Xiang Y; Rong XJ; Chen X; Li QY; Wan HY
    Int J Oncol; 2013 Sep; 43(3):755-64. PubMed ID: 23799614
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide mutational spectra analysis reveals significant cancer-specific heterogeneity.
    Tan H; Bao J; Zhou X
    Sci Rep; 2015 Jul; 5():12566. PubMed ID: 26212640
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers.
    Wang Q; Jia P; Li F; Chen H; Ji H; Hucks D; Dahlman KB; Pao W; Zhao Z
    Genome Med; 2013; 5(10):91. PubMed ID: 24112718
    [TBL] [Abstract][Full Text] [Related]  

  • 17. In silico whole-genome screening for cancer-related single-nucleotide polymorphisms located in human mRNA untranslated regions.
    Aouacheria A; Navratil V; López-Pérez R; Gutiérrez NC; Churkin A; Barash D; Mouchiroud D; Gautier C
    BMC Genomics; 2007 Jan; 8():2. PubMed ID: 17201911
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Gene polymorphisms].
    Robert J
    Bull Cancer; 2010 Nov; 97(11):1253-64. PubMed ID: 21115419
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms.
    Hoang PH; Dobbins SE; Cornish AJ; Chubb D; Law PJ; Kaiser M; Houlston RS
    Leukemia; 2018 Nov; 32(11):2459-2470. PubMed ID: 29654271
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.
    Fu W; O'Connor TD; Jun G; Kang HM; Abecasis G; Leal SM; Gabriel S; Rieder MJ; Altshuler D; Shendure J; Nickerson DA; Bamshad MJ; ; Akey JM
    Nature; 2013 Jan; 493(7431):216-20. PubMed ID: 23201682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.