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Page 1
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder.
Caporali L, Fiorini C, Palombo F, Romagnoli M, Baccari F, Zenesini C, Visconti P, Posar A, Scaduto MC, Ormanbekova D, Battaglia A, Tancredi R, Cameli C, Viggiano M, Olivieri A, Torroni A, Maestrini E, Rochat MJ, Bacchelli E, Carelli V, Maresca A. Caporali L, et al. Among authors: torroni a. Front Genet. 2022 Nov 7;13:953762. doi: 10.3389/fgene.2022.953762. eCollection 2022. Front Genet. 2022. PMID: 36419830 Free PMC article.
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy.
Caporali L, Iommarini L, La Morgia C, Olivieri A, Achilli A, Maresca A, Valentino ML, Capristo M, Tagliavini F, Del Dotto V, Zanna C, Liguori R, Barboni P, Carbonelli M, Cocetta V, Montopoli M, Martinuzzi A, Cenacchi G, De Michele G, Testa F, Nesti A, Simonelli F, Porcelli AM, Torroni A, Carelli V. Caporali L, et al. Among authors: torroni a. PLoS Genet. 2018 Feb 14;14(2):e1007210. doi: 10.1371/journal.pgen.1007210. eCollection 2018 Feb. PLoS Genet. 2018. PMID: 29444077 Free PMC article.
The role of mtDNA haplogroups on metabolic features in narcolepsy type 1.
Caporali L, Moresco M, Pizza F, La Morgia C, Fiorini C, Strobbe D, Zenesini C, Hooshiar Kashani B, Torroni A, Pagotto U, Carelli V, Plazzi G. Caporali L, et al. Among authors: torroni a. Mitochondrion. 2022 Mar;63:37-42. doi: 10.1016/j.mito.2022.01.005. Epub 2022 Jan 17. Mitochondrion. 2022. PMID: 35051655
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.
Carelli V, Achilli A, Valentino ML, Rengo C, Semino O, Pala M, Olivieri A, Mattiazzi M, Pallotti F, Carrara F, Zeviani M, Leuzzi V, Carducci C, Valle G, Simionati B, Mendieta L, Salomao S, Belfort R Jr, Sadun AA, Torroni A. Carelli V, et al. Among authors: torroni a. Am J Hum Genet. 2006 Apr;78(4):564-74. doi: 10.1086/501236. Epub 2006 Jan 27. Am J Hum Genet. 2006. PMID: 16532388 Free PMC article.
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance.
Carossa V, Ghelli A, Tropeano CV, Valentino ML, Iommarini L, Maresca A, Caporali L, La Morgia C, Liguori R, Barboni P, Carbonelli M, Rizzo G, Tonon C, Lodi R, Martinuzzi A, De Nardo V, Rugolo M, Ferretti L, Gandini F, Pala M, Achilli A, Olivieri A, Torroni A, Carelli V. Carossa V, et al. Among authors: torroni a. Hum Mutat. 2014 Aug;35(8):954-8. doi: 10.1002/humu.22596. Epub 2014 Jun 28. Hum Mutat. 2014. PMID: 24863938
The worldwide spread of Aedes albopictus: New insights from mitogenomes.
Battaglia V, Agostini V, Moroni E, Colombo G, Lombardo G, Rambaldi Migliore N, Gabrieli P, Garofalo M, Gagliardi S, Gomulski LM, Ferretti L, Semino O, Malacrida AR, Gasperi G, Achilli A, Torroni A, Olivieri A. Battaglia V, et al. Among authors: torroni a. Front Genet. 2022 Aug 26;13:931163. doi: 10.3389/fgene.2022.931163. eCollection 2022. Front Genet. 2022. PMID: 36092930 Free PMC article.
The Worldwide Spread of the Tiger Mosquito as Revealed by Mitogenome Haplogroup Diversity.
Battaglia V, Gabrieli P, Brandini S, Capodiferro MR, Javier PA, Chen XG, Achilli A, Semino O, Gomulski LM, Malacrida AR, Gasperi G, Torroni A, Olivieri A. Battaglia V, et al. Among authors: torroni a. Front Genet. 2016 Nov 23;7:208. doi: 10.3389/fgene.2016.00208. eCollection 2016. Front Genet. 2016. PMID: 27933090 Free PMC article.
The multifaceted origin of taurine cattle reflected by the mitochondrial genome.
Achilli A, Bonfiglio S, Olivieri A, Malusà A, Pala M, Hooshiar Kashani B, Perego UA, Ajmone-Marsan P, Liotta L, Semino O, Bandelt HJ, Ferretti L, Torroni A. Achilli A, et al. Among authors: torroni a. PLoS One. 2009 Jun 1;4(6):e5753. doi: 10.1371/journal.pone.0005753. PLoS One. 2009. PMID: 19484124 Free PMC article.
271 results