Published in Nature on March 03, 2010
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A twin study of mitochondrial DNA polymorphisms shows that heteroplasmy at multiple sites is associated with mtDNA variant 16093 but not with zygosity. PLoS One (2011) 1.02
Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing. PLoS Genet (2014) 0.99
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Keeping mtDNA in shape between generations. PLoS Genet (2014) 0.98
Extensive tissue-related and allele-related mtDNA heteroplasmy suggests positive selection for somatic mutations. Proc Natl Acad Sci U S A (2015) 0.98
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Human skin carcinoma arising from kidney transplant-derived tumor cells. J Clin Invest (2013) 0.89
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Development and assessment of an optimized next-generation DNA sequencing approach for the mtgenome using the Illumina MiSeq. Forensic Sci Int Genet (2014) 0.89
A multi-parametric workflow for the prioritization of mitochondrial DNA variants of clinical interest. Hum Genet (2015) 0.89
Mechanism of homologous recombination and implications for aging-related deletions in mitochondrial DNA. Microbiol Mol Biol Rev (2013) 0.87
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The identification of mitochondrial DNA variants in glioblastoma multiforme. Acta Neuropathol Commun (2014) 0.87
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Physiology and pathophysiology of mitochondrial DNA. Adv Exp Med Biol (2012) 0.84
Mitochondrial genome instability resulting from SUV3 haploinsufficiency leads to tumorigenesis and shortened lifespan. Oncogene (2012) 0.84
Passenger mutations as a marker of clonal cell lineages in emerging neoplasia. Semin Cancer Biol (2010) 0.83
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Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma. PLoS One (2015) 0.83
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