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For: Hill KA, Wang J, Farwell KD, Scaringe WA, Sommer SS. Spontaneous multiple mutations show both proximal spacing consistent with chronocoordinate events and alterations with p53-deficiency. Mutat Res 2004;554:223-40. [PMID: 15450421 DOI: 10.1016/j.mrfmmm.2004.05.005] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 1.1] [Reference Citation Analysis]
Number Citing Articles
1 Hashimoto K, Rogozin IB, Panchenko AR. Oncogenic potential is related to activating effect of cancer single and double somatic mutations in receptor tyrosine kinases. Hum Mutat 2012;33:1566-75. [PMID: 22753356 DOI: 10.1002/humu.22145] [Cited by in Crossref: 25] [Cited by in F6Publishing: 23] [Article Influence: 2.5] [Reference Citation Analysis]
2 Lawing AM, McCoy M, Reinke BA, Sarkar SK, Smith FA, Wright D. A Framework for Investigating Rules of Life by Establishing Zones of Influence. Integr Comp Biol 2021:icab169. [PMID: 34297089 DOI: 10.1093/icb/icab169] [Reference Citation Analysis]
3 Drake JW. Too many mutants with multiple mutations. Crit Rev Biochem Mol Biol 2007;42:247-58. [PMID: 17687667 DOI: 10.1080/10409230701495631] [Cited by in Crossref: 58] [Cited by in F6Publishing: 54] [Article Influence: 3.9] [Reference Citation Analysis]
4 Nikitaki Z, Hellweg CE, Georgakilas AG, Ravanat JL. Stress-induced DNA damage biomarkers: applications and limitations. Front Chem 2015;3:35. [PMID: 26082923 DOI: 10.3389/fchem.2015.00035] [Cited by in Crossref: 79] [Cited by in F6Publishing: 68] [Article Influence: 11.3] [Reference Citation Analysis]
5 Chan K, Gordenin DA. Clusters of Multiple Mutations: Incidence and Molecular Mechanisms. Annu Rev Genet 2015;49:243-67. [PMID: 26631512 DOI: 10.1146/annurev-genet-112414-054714] [Cited by in Crossref: 76] [Cited by in F6Publishing: 60] [Article Influence: 12.7] [Reference Citation Analysis]
6 Chen JM, Férec C, Cooper DN. Transient hypermutability, chromothripsis and replication-based mechanisms in the generation of concurrent clustered mutations. Mutat Res 2012;750:52-9. [PMID: 22100908 DOI: 10.1016/j.mrrev.2011.10.002] [Cited by in Crossref: 22] [Cited by in F6Publishing: 19] [Article Influence: 2.2] [Reference Citation Analysis]
7 Balin SJ, Cascalho M. The rate of mutation of a single gene. Nucleic Acids Res 2010;38:1575-82. [PMID: 20007603 DOI: 10.1093/nar/gkp1119] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
8 Alexander HK, Mayer SI, Bonhoeffer S. Population Heterogeneity in Mutation Rate Increases the Frequency of Higher-Order Mutants and Reduces Long-Term Mutational Load. Mol Biol Evol 2017;34:419-36. [PMID: 27836985 DOI: 10.1093/molbev/msw244] [Cited by in Crossref: 3] [Cited by in F6Publishing: 11] [Article Influence: 0.6] [Reference Citation Analysis]
9 Crabbe RA, Prtenjaca A, Tarnowski HE, Hill KA. A novel germline mutation in Big Blue® mice. Environ Mol Mutagen 2009;50:114-20. [DOI: 10.1002/em.20442] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
10 Gu D, Scaringe WA, Li K, Saldivar JS, Hill KA, Chen Z, Gonzalez KD, Sommer SS. Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature. Hum Mutat 2007;28:760-70. [PMID: 17429853 DOI: 10.1002/humu.20512] [Cited by in Crossref: 37] [Cited by in F6Publishing: 34] [Article Influence: 2.5] [Reference Citation Analysis]
11 Chen JM, Férec C, Cooper DN. Gene conversion in human genetic disease. Genes (Basel) 2010;1:550-63. [PMID: 24710102 DOI: 10.3390/genes1030550] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis]
12 Luo B, Edge AK, Tolg C, Turley EA, Dean CB, Hill KA, Kulperger RJ. Spatial statistical tools for genome-wide mutation cluster detection under a microarray probe sampling system. PLoS One 2018;13:e0204156. [PMID: 30252889 DOI: 10.1371/journal.pone.0204156] [Reference Citation Analysis]
13 van den Boogaard ML, Lemmers RJ, Camaño P, van der Vliet PJ, Voermans N, van Engelen BG, Lopez de Munain A, Tapscott SJ, van der Stoep N, Tawil R, van der Maarel SM. Double SMCHD1 variants in FSHD2: the synergistic effect of two SMCHD1 variants on D4Z4 hypomethylation and disease penetrance in FSHD2. Eur J Hum Genet 2016;24:78-85. [PMID: 25782668 DOI: 10.1038/ejhg.2015.55] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 2.3] [Reference Citation Analysis]
14 Hill KA, Gonzalez KD, Scaringe WA, Wang JC, Sommer SS. Preferential occurrence of 1-2 microindels. Hum Mutat 2006;27:55-61. [PMID: 16281281 DOI: 10.1002/humu.20260] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
15 Wang J, Gonzalez KD, Scaringe WA, Tsai K, Liu N, Gu D, Li W, Hill KA, Sommer SS. Evidence for mutation showers. Proc Natl Acad Sci U S A 2007;104:8403-8. [PMID: 17485671 DOI: 10.1073/pnas.0610902104] [Cited by in Crossref: 61] [Cited by in F6Publishing: 54] [Article Influence: 4.1] [Reference Citation Analysis]
16 Chen Z, Feng J, Buzin CH, Sommer SS. Epidemiology of doublet/multiplet mutations in lung cancers: evidence that a subset arises by chronocoordinate events. PLoS One 2008;3:e3714. [PMID: 19005564 DOI: 10.1371/journal.pone.0003714] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 1.4] [Reference Citation Analysis]
17 Gonzalez KD, Hill KA, Li K, Li W, Scaringe WA, Wang JC, Gu D, Sommer SS. Somatic microindels: analysis in mouse soma and comparison with the human germline. Hum Mutat 2007;28:69-80. [PMID: 16977595 DOI: 10.1002/humu.20416] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 0.8] [Reference Citation Analysis]
18 Chen Z, Feng J, Saldivar JS, Gu D, Bockholt A, Sommer SS. EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acids. Oncogene 2008;27:4336-43. [PMID: 18372921 DOI: 10.1038/onc.2008.71] [Cited by in Crossref: 51] [Cited by in F6Publishing: 52] [Article Influence: 3.6] [Reference Citation Analysis]
19 Drake JW, Bebenek A, Kissling GE, Peddada S. Clusters of mutations from transient hypermutability. Proc Natl Acad Sci U S A 2005;102:12849-54. [PMID: 16118275 DOI: 10.1073/pnas.0503009102] [Cited by in Crossref: 59] [Cited by in F6Publishing: 53] [Article Influence: 3.5] [Reference Citation Analysis]
20 Chen JM, Férec C, Cooper DN. Closely spaced multiple mutations as potential signatures of transient hypermutability in human genes. Hum Mutat 2009;30:1435-48. [PMID: 19685533 DOI: 10.1002/humu.21088] [Cited by in Crossref: 42] [Cited by in F6Publishing: 39] [Article Influence: 3.2] [Reference Citation Analysis]
21 Bergeron F, Auvré F, Radicella JP, Ravanat JL. HO* radicals induce an unexpected high proportion of tandem base lesions refractory to repair by DNA glycosylases. Proc Natl Acad Sci U S A 2010;107:5528-33. [PMID: 20212167 DOI: 10.1073/pnas.1000193107] [Cited by in Crossref: 99] [Cited by in F6Publishing: 88] [Article Influence: 8.3] [Reference Citation Analysis]