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Times Cited: 15
Times Cited: 15
Times Cited
Times Co-cited
Similarity
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The role of microhomology in genomic structural variation.
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The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.
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The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.
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A microhomology-mediated break-induced replication model for the origin of human copy number variation.
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Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication.
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Replicative mechanisms for CNV formation are error prone.
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Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability.
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DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakage.
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Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching.
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Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
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Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome.
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Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females.
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Somatic mosaicism: implications for disease and transmission genetics.
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Migrating bubble during break-induced replication drives conservative DNA synthesis.
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DNA polymerases ζ and Rev1 mediate error-prone bypass of non-B DNA structures.
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Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.
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Absence of heterozygosity due to template switching during replicative rearrangements.
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Inverted low-copy repeats and genome instability--a genome-wide analysis.
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Chromosome rearrangements via template switching between diverged repeated sequences.
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Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions.
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Mechanisms for recurrent and complex human genomic rearrangements.
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On the mechanism of gene amplification induced under stress in Escherichia coli.
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Break-induced replication repair of damaged forks induces genomic duplications in human cells.
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Characterization of two unusual truncating PMM2 mutations in two CDG-Ia patients.
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A novel complex deletion-insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency.
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A comprehensive map of mobile element insertion polymorphisms in humans.
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MFN2 deletion of exons 7 and 8: founder mutation in the UK population.
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Motor chip: a comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders.
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Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.