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HmtDB, a genomic resource for mitochondrion-based human variability studies.
Rubino F, Piredda R, Calabrese FM, Simone D, Lang M, Calabrese C, Petruzzella V, Tommaseo-Ponzetta M, Gasparre G, Attimonelli M. Rubino F, et al. Among authors: attimonelli m. Nucleic Acids Res. 2012 Jan;40(Database issue):D1150-9. doi: 10.1093/nar/gkr1086. Epub 2011 Dec 1. Nucleic Acids Res. 2012. PMID: 22139932 Free PMC article.
Polymorphic NumtS trace human population relationships.
Lang M, Sazzini M, Calabrese FM, Simone D, Boattini A, Romeo G, Luiselli D, Attimonelli M, Gasparre G. Lang M, et al. Among authors: attimonelli m. Hum Genet. 2012 May;131(5):757-71. doi: 10.1007/s00439-011-1125-3. Epub 2011 Dec 8. Hum Genet. 2012. PMID: 22160368
Primates and mouse NumtS in the UCSC Genome Browser.
Calabrese FM, Simone D, Attimonelli M. Calabrese FM, et al. Among authors: attimonelli m. BMC Bioinformatics. 2012 Mar 28;13 Suppl 4(Suppl 4):S15. doi: 10.1186/1471-2105-13-S4-S15. BMC Bioinformatics. 2012. PMID: 22536961 Free PMC article.
Deep sequencing unearths nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants.
Petruzzella V, Carrozzo R, Calabrese C, Dell'Aglio R, Trentadue R, Piredda R, Artuso L, Rizza T, Bianchi M, Porcelli AM, Guerriero S, Gasparre G, Attimonelli M. Petruzzella V, et al. Among authors: attimonelli m. Hum Mol Genet. 2012 Sep 1;21(17):3753-64. doi: 10.1093/hmg/dds182. Epub 2012 May 15. Hum Mol Genet. 2012. PMID: 22589247
MToolBox: a highly automated pipeline for heteroplasmy annotation and prioritization analysis of human mitochondrial variants in high-throughput sequencing.
Calabrese C, Simone D, Diroma MA, Santorsola M, Guttà C, Gasparre G, Picardi E, Pesole G, Attimonelli M. Calabrese C, et al. Among authors: attimonelli m. Bioinformatics. 2014 Nov 1;30(21):3115-7. doi: 10.1093/bioinformatics/btu483. Epub 2014 Jul 14. Bioinformatics. 2014. PMID: 25028726 Free PMC article.
75 results