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 *

455 related articles for article (PubMed ID: 25985141)

  • 21. Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.
    Carlson J; Locke AE; Flickinger M; Zawistowski M; Levy S; Myers RM; Boehnke M; Kang HM; Scott LJ; Li JZ; Zöllner S;
    Nat Commun; 2018 Sep; 9(1):3753. PubMed ID: 30218074
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. A genome-wide analysis of CpG dinucleotides in the human genome distinguishes two distinct classes of promoters.
    Saxonov S; Berg P; Brutlag DL
    Proc Natl Acad Sci U S A; 2006 Jan; 103(5):1412-7. PubMed ID: 16432200
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Why do human diversity levels vary at a megabase scale?
    Hellmann I; Prüfer K; Ji H; Zody MC; Pääbo S; Ptak SE
    Genome Res; 2005 Sep; 15(9):1222-31. PubMed ID: 16140990
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multi-nucleotide de novo Mutations in Humans.
    Besenbacher S; Sulem P; Helgason A; Helgason H; Kristjansson H; Jonasdottir A; Jonasdottir A; Magnusson OT; Thorsteinsdottir U; Masson G; Kong A; Gudbjartsson DF; Stefansson K
    PLoS Genet; 2016 Nov; 12(11):e1006315. PubMed ID: 27846220
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Higher intensity of purifying selection on >90% of the human genes revealed by the intrinsic replacement mutation rates.
    Subramanian S; Kumar S
    Mol Biol Evol; 2006 Dec; 23(12):2283-7. PubMed ID: 16982819
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Nucleosome positioning stability is a modulator of germline mutation rate variation across the human genome.
    Li C; Luscombe NM
    Nat Commun; 2020 Mar; 11(1):1363. PubMed ID: 32170069
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Direct estimate of the spontaneous germ line mutation rate in African green monkeys.
    Pfeifer SP
    Evolution; 2017 Dec; 71(12):2858-2870. PubMed ID: 29068052
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence.
    Goldmann JM; Seplyarskiy VB; Wong WSW; Vilboux T; Neerincx PB; Bodian DL; Solomon BD; Veltman JA; Deeken JF; Gilissen C; Niederhuber JE
    Nat Genet; 2018 Apr; 50(4):487-492. PubMed ID: 29507425
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Context dependence, ancestral misidentification, and spurious signatures of natural selection.
    Hernandez RD; Williamson SH; Bustamante CD
    Mol Biol Evol; 2007 Aug; 24(8):1792-800. PubMed ID: 17545186
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Short template switch events explain mutation clusters in the human genome.
    Löytynoja A; Goldman N
    Genome Res; 2017 Jun; 27(6):1039-1049. PubMed ID: 28385709
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Timing, rates and spectra of human germline mutation.
    Rahbari R; Wuster A; Lindsay SJ; Hardwick RJ; Alexandrov LB; Turki SA; Dominiczak A; Morris A; Porteous D; Smith B; Stratton MR; ; Hurles ME
    Nat Genet; 2016 Feb; 48(2):126-133. PubMed ID: 26656846
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Point mutations as a source of de novo genetic disease.
    de Ligt J; Veltman JA; Vissers LE
    Curr Opin Genet Dev; 2013 Jun; 23(3):257-63. PubMed ID: 23453690
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Paternal age in rhesus macaques is positively associated with germline mutation accumulation but not with measures of offspring sociability.
    Wang RJ; Thomas GWC; Raveendran M; Harris RA; Doddapaneni H; Muzny DM; Capitanio JP; Radivojac P; Rogers J; Hahn MW
    Genome Res; 2020 Jun; 30(6):826-834. PubMed ID: 32461224
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Context-dependent mutation rates may cause spurious signatures of a fixation bias favoring higher GC-content in humans.
    Hernandez RD; Williamson SH; Zhu L; Bustamante CD
    Mol Biol Evol; 2007 Oct; 24(10):2196-202. PubMed ID: 17656634
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutational spectrum in the recent human genome inferred by single nucleotide polymorphisms.
    Jiang C; Zhao Z
    Genomics; 2006 Nov; 88(5):527-34. PubMed ID: 16860534
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Impact of replication timing on non-CpG and CpG substitution rates in mammalian genomes.
    Chen CL; Rappailles A; Duquenne L; Huvet M; Guilbaud G; Farinelli L; Audit B; d'Aubenton-Carafa Y; Arneodo A; Hyrien O; Thermes C
    Genome Res; 2010 Apr; 20(4):447-57. PubMed ID: 20103589
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rate of de novo mutations and the importance of father's age to disease risk.
    Kong A; Frigge ML; Masson G; Besenbacher S; Sulem P; Magnusson G; Gudjonsson SA; Sigurdsson A; Jonasdottir A; Jonasdottir A; Wong WS; Sigurdsson G; Walters GB; Steinberg S; Helgason H; Thorleifsson G; Gudbjartsson DF; Helgason A; Magnusson OT; Thorsteinsdottir U; Stefansson K
    Nature; 2012 Aug; 488(7412):471-5. PubMed ID: 22914163
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Properties and rates of germline mutations in humans.
    Campbell CD; Eichler EE
    Trends Genet; 2013 Oct; 29(10):575-84. PubMed ID: 23684843
    [TBL] [Abstract][Full Text] [Related]  

  • 40. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
    Kessler MD; Loesch DP; Perry JA; Heard-Costa NL; Taliun D; Cade BE; Wang H; Daya M; Ziniti J; Datta S; Celedón JC; Soto-Quiros ME; Avila L; Weiss ST; Barnes K; Redline SS; Vasan RS; Johnson AD; Mathias RA; Hernandez R; Wilson JG; Nickerson DA; Abecasis G; Browning SR; Zöllner S; O'Connell JR; Mitchell BD; ; ; O'Connor TD
    Proc Natl Acad Sci U S A; 2020 Feb; 117(5):2560-2569. PubMed ID: 31964835
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.