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]