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 *

272 related articles for article (PubMed ID: 30218074)

  • 21. Local Determinants of the Mutational Landscape of the Human Genome.
    Gonzalez-Perez A; Sabarinathan R; Lopez-Bigas N
    Cell; 2019 Mar; 177(1):101-114. PubMed ID: 30901533
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The large-scale distribution of somatic mutations in cancer genomes.
    Hodgkinson A; Chen Y; Eyre-Walker A
    Hum Mutat; 2012 Jan; 33(1):136-43. PubMed ID: 21953857
    [TBL] [Abstract][Full Text] [Related]  

  • 23. HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination.
    Sigurdsson MI; Smith AV; Bjornsson HT; Jonsson JJ
    Genome Res; 2009 Apr; 19(4):581-9. PubMed ID: 19158364
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Limited role of generation time changes in driving the evolution of the mutation spectrum in humans.
    Gao Z; Zhang Y; Cramer N; Przeworski M; Moorjani P
    Elife; 2023 Feb; 12():. PubMed ID: 36779395
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria.
    Wang S; Pitt JJ; Zheng Y; Yoshimatsu TF; Gao G; Sanni A; Oluwasola O; Ajani M; Fitzgerald D; Odetunde A; Khramtsova G; Hurley I; Popoola A; Falusi A; Ogundiran T; Obafunwa J; Ojengbede O; Ibrahim N; Barretina J; White KP; Huo D; Olopade OI
    Int J Cancer; 2019 Dec; 145(12):3321-3333. PubMed ID: 31173346
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The rate of CpG mutation in Alu repetitive elements within the p53 tumor suppressor gene in the primate germline.
    Yang AS; Gonzalgo ML; Zingg JM; Millar RP; Buckley JD; Jones PA
    J Mol Biol; 1996 May; 258(2):240-50. PubMed ID: 8627622
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic and chemotherapeutic influences on germline hypermutation.
    Kaplanis J; Ide B; Sanghvi R; Neville M; Danecek P; Coorens T; Prigmore E; Short P; Gallone G; McRae J; ; Carmichael J; Barnicoat A; Firth H; O'Brien P; Rahbari R; Hurles M
    Nature; 2022 May; 605(7910):503-508. PubMed ID: 35545669
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sequence context at human single nucleotide polymorphisms: overrepresentation of CpG dinucleotide at polymorphic sites and suppression of variation in CpG islands.
    Tomso DJ; Bell DA
    J Mol Biol; 2003 Mar; 327(2):303-8. PubMed ID: 12628237
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Origins and characterization of variants shared between databases of somatic and germline human mutations.
    Meyerson W; Leisman J; Navarro FCP; Gerstein M
    BMC Bioinformatics; 2020 Jun; 21(1):227. PubMed ID: 32498674
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Contrasting Determinants of Mutation Rates in Germline and Soma.
    Chen C; Qi H; Shen Y; Pickrell J; Przeworski M
    Genetics; 2017 Sep; 207(1):255-267. PubMed ID: 28733365
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome-Wide Estimates of Mutation Rates and Spectrum in Schizosaccharomyces pombe Indicate CpG Sites are Highly Mutagenic Despite the Absence of DNA Methylation.
    Behringer MG; Hall DW
    G3 (Bethesda); 2015 Nov; 6(1):149-60. PubMed ID: 26564949
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Population sequencing data reveal a compendium of mutational processes in the human germ line.
    Seplyarskiy VB; Soldatov RA; Koch E; McGinty RJ; Goldmann JM; Hernandez RD; Barnes K; Correa A; Burchard EG; Ellinor PT; McGarvey ST; Mitchell BD; Vasan RS; Redline S; Silverman E; Weiss ST; Arnett DK; Blangero J; Boerwinkle E; He J; Montgomery C; Rao DC; Rotter JI; Taylor KD; Brody JA; Chen YI; de Las Fuentes L; Hwu CM; Rich SS; Manichaikul AW; Mychaleckyj JC; Palmer ND; Smith JA; Kardia SLR; Peyser PA; Bielak LF; O'Connor TD; Emery LS; ; ; Gilissen C; Wong WSW; Kharchenko PV; Sunyaev S
    Science; 2021 Aug; 373(6558):1030-1035. PubMed ID: 34385354
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The genomic distribution and local context of coincident SNPs in human and chimpanzee.
    Hodgkinson A; Eyre-Walker A
    Genome Biol Evol; 2010; 2():547-57. PubMed ID: 20675616
    [TBL] [Abstract][Full Text] [Related]  

  • 34. How much of the variation in the mutation rate along the human genome can be explained?
    Eyre-Walker A; Eyre-Walker YC
    G3 (Bethesda); 2014 Jul; 4(9):1667-70. PubMed ID: 24996580
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Preservation of methylated CpG dinucleotides in human CpG islands.
    Panchin AY; Makeev VJ; Medvedeva YA
    Biol Direct; 2016 Mar; 11(1):11. PubMed ID: 27005429
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fine-tuning germline mutation rates across evolution.
    Bush SJ; Goriely A
    Trends Genet; 2023 Aug; 39(8):598-599. PubMed ID: 37244758
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation dynamics of CpG dinucleotides during a recent event of vertebrate diversification.
    Pértille F; Da Silva VH; Johansson AM; Lindström T; Wright D; Coutinho LL; Jensen P; Guerrero-Bosagna C
    Epigenetics; 2019 Jul; 14(7):685-707. PubMed ID: 31070073
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel method distinguishes between mutation rates and fixation biases in patterns of single-nucleotide substitution.
    Lipatov M; Arndt PF; Hwa T; Petrov DA
    J Mol Evol; 2006 Feb; 62(2):168-75. PubMed ID: 16362483
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Whole-genome bisulfite sequencing in systemic sclerosis provides novel targets to understand disease pathogenesis.
    Lu T; Klein KO; Colmegna I; Lora M; Greenwood CMT; Hudson M
    BMC Med Genomics; 2019 Oct; 12(1):144. PubMed ID: 31651337
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.
    Bodian DL; McCutcheon JN; Kothiyal P; Huddleston KC; Iyer RK; Vockley JG; Niederhuber JE
    PLoS One; 2014; 9(4):e94554. PubMed ID: 24728327
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.