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Items: 1 to 20 of 106

1.

Copy number variants are produced in response to low-dose ionizing radiation in cultured cells.

Arlt MF, Rajendran S, Birkeland SR, Wilson TE, Glover TW.

Environ Mol Mutagen. 2014 Mar;55(2):103-13. doi: 10.1002/em.21840. Epub 2013 Dec 10.

2.

Hydroxyurea induces de novo copy number variants in human cells.

Arlt MF, Ozdemir AC, Birkeland SR, Wilson TE, Glover TW.

Proc Natl Acad Sci U S A. 2011 Oct 18;108(42):17360-5. doi: 10.1073/pnas.1109272108. Epub 2011 Oct 10.

3.

Replication stress and mechanisms of CNV formation.

Arlt MF, Wilson TE, Glover TW.

Curr Opin Genet Dev. 2012 Jun;22(3):204-10. doi: 10.1016/j.gde.2012.01.009. Epub 2012 Feb 23. Review.

4.

De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining.

Arlt MF, Rajendran S, Birkeland SR, Wilson TE, Glover TW.

PLoS Genet. 2012 Sep;8(9):e1002981. doi: 10.1371/journal.pgen.1002981. Epub 2012 Sep 20.

5.

Origins and breakpoint analyses of copy number variations: up close and personal.

van Binsbergen E.

Cytogenet Genome Res. 2011;135(3-4):271-6. doi: 10.1159/000330267. Epub 2011 Aug 12. Review.

PMID:
21846967
6.

Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing.

Cardoso-Moreira M, Arguello JR, Clark AG.

Genome Biol. 2012 Dec 22;13(12):R119. doi: 10.1186/gb-2012-13-12-r119.

7.

Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.

Arlt MF, Mulle JG, Schaibley VM, Ragland RL, Durkin SG, Warren ST, Glover TW.

Am J Hum Genet. 2009 Mar;84(3):339-50. doi: 10.1016/j.ajhg.2009.01.024. Epub 2009 Feb 19.

8.

Large transcription units unify copy number variants and common fragile sites arising under replication stress.

Wilson TE, Arlt MF, Park SH, Rajendran S, Paulsen M, Ljungman M, Glover TW.

Genome Res. 2015 Feb;25(2):189-200. doi: 10.1101/gr.177121.114. Epub 2014 Nov 4.

9.

Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencing.

Arlt MF, Ozdemir AC, Birkeland SR, Lyons RH Jr, Glover TW, Wilson TE.

Genetics. 2011 Mar;187(3):675-83. doi: 10.1534/genetics.110.124776. Epub 2011 Jan 6.

10.

Contrasting mechanisms of de novo copy number mutagenesis suggest the existence of different classes of environmental copy number mutagens.

Conover HN, Argueso JL.

Environ Mol Mutagen. 2016 Jan;57(1):3-9. doi: 10.1002/em.21967. Epub 2015 Aug 6. Review.

PMID:
26247157
11.

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.

Vissers LE, Bhatt SS, Janssen IM, Xia Z, Lalani SR, Pfundt R, Derwinska K, de Vries BB, Gilissen C, Hoischen A, Nesteruk M, Wisniowiecka-Kowalnik B, Smyk M, Brunner HG, Cheung SW, van Kessel AG, Veltman JA, Stankiewicz P.

Hum Mol Genet. 2009 Oct 1;18(19):3579-93. doi: 10.1093/hmg/ddp306. Epub 2009 Jul 3.

PMID:
19578123
12.
13.

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.

Saadati HR, Wittig M, Helbig I, Häsler R, Anderson CA, Mathew CG, Kupcinskas L, Parkes M, Karlsen TH, Rosenstiel P, Schreiber S, Franke A.

BMC Med Genet. 2016 Apr 1;17:26. doi: 10.1186/s12881-016-0289-z.

14.

Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array.

Molin AM, Berglund J, Webster MT, Lindblad-Toh K.

BMC Genomics. 2014 Mar 19;15:210. doi: 10.1186/1471-2164-15-210.

15.

H2AX foci in late S/G2- and M-phase cells after hydroxyurea- and aphidicolin-induced DNA replication stress in Vicia.

Rybaczek D, Bodys A, Maszewski J.

Histochem Cell Biol. 2007 Sep;128(3):227-41. Epub 2007 Jul 18.

PMID:
17636317
16.

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.

Conrad DF, Bird C, Blackburne B, Lindsay S, Mamanova L, Lee C, Turner DJ, Hurles ME.

Nat Genet. 2010 May;42(5):385-91. doi: 10.1038/ng.564. Epub 2010 Apr 4.

17.

The genome-wide effects of ionizing radiation on mutation induction in the mammalian germline.

Adewoye AB, Lindsay SJ, Dubrova YE, Hurles ME.

Nat Commun. 2015 Mar 26;6:6684. doi: 10.1038/ncomms7684.

18.

CNV Concordance in 1,097 MZ Twin Pairs.

Abdellaoui A, Ehli EA, Hottenga JJ, Weber Z, Mbarek H, Willemsen G, van Beijsterveldt T, Brooks A, Hudziak JJ, Sullivan PF, de Geus EJ, Davies GE, Boomsma DI.

Twin Res Hum Genet. 2015 Feb;18(1):1-12. doi: 10.1017/thg.2014.86. Epub 2015 Jan 12.

PMID:
25578775
19.

Elevated variant density around SV breakpoints in germline lineage lends support to error-prone replication hypothesis.

Dhokarh D, Abyzov A.

Genome Res. 2016 Jul;26(7):874-81. doi: 10.1101/gr.205484.116. Epub 2016 May 23.

20.

Population-genetic nature of copy number variations in the human genome.

Kato M, Kawaguchi T, Ishikawa S, Umeda T, Nakamichi R, Shapero MH, Jones KW, Nakamura Y, Aburatani H, Tsunoda T.

Hum Mol Genet. 2010 Mar 1;19(5):761-73. doi: 10.1093/hmg/ddp541. Epub 2009 Dec 5.

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