| Index | PMID | Date | Reference |
|---|---|---|---|
| 1 | 7599218 | 1995 | Savontaus, M.L. (1995) mtDNA mutations in Leber's hereditary optic neuropathy Biochimica et Biophysica Acta . 1271 (1): 261-263 . |
| 2 | 11349229 | 2001 | Finnila, S., Lehtonen, M. S., Majamaa, K. (2001) Phylogenetic network for European mtDNA American Journal of Human Genetics . 68 (6): 1475-1484 . |
| 3 | 11406419 | 2001 | Finnila, S., Hassinen, I. E., Majamaa, K. (2001) Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region Mutation Research . 458 (40545): 31-39 . |
| 4 | 11938495 | 2002 | Herrnstadt, C., Elson, J. L., Fahy, E., Preston, G., Turnbull, D. M., Anderson, C., Ghosh, S. S., Olefsky, J. M., Beal, M. F., Davis, R. E., Howell, N. (2002) Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups American Journal of Human Genetics . 70 (5): 1152-1171 . |
| 5 | 15286228 | 2004 | Uusimaa, J., Finnila, S., Remes, A. M., Rantala, H., Vainionpaa, L., Hassinen, I. E., Majamaa, K. (2004) Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) genes Pediatrics . 114 (2): 443-450 . |
| 6 | 16901986 | 2006 | Fraumene, C., Belle, E. M., Castri, L., Sanna, S., Mancosu, G., Cosso, M., Marras, F., Barbujani, G., Pirastu, M., Angius, A. (2006) High resolution analysis and phylogenetic network construction using complete mtDNA sequences in Sardinian genetic isolates Molecular Biology and Evolution . 23 (11): 2101-2111 . |
| 7 | 17406640 | 2007 | Puomila, A., Hamalainen, P., Kivioja, S., Savontaus, M. L., Koivumaki, S., Huoponen, K., Nikoskelainen, E. (2007) Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland European Journal of Human Genetics . 15 (10): 1079-1089 . |
| 8 | 17620140 | 2007 | Gonzalez, A. M., Larruga, J. M., Abu-Amero, K. K., Shi, Y., Pestano, J., Cabrera, V. M. (2007) Mitochondrial lineage M1 traces an early human backflow to Africa BMC Genomics . 8 (-): 223 . |
| 9 | 18269758 | 2008 | Abu-Amero, K. K., Larruga, J. M., Cabrera, V. M., Gonzalez, A. M. (2008) Mitochondrial DNA structure in the Arabian Peninsula BMC Evolutionary Biology . 8 (-): 45 . |
| 10 | 19005266 | 2008 | Hendrickson, S. L., Hutcheson, H. B., Ruiz-Pesini, E., Poole, J. C., Lautenberger, J., Sezgin, E., Kingsley, L., Goedert, J. J., Vlahov, D., Donfield, S., Wallace, D. C., O'Brien, S. J. (2008) Mitochondrial DNA haplogroups influence AIDS progression AIDS . 22 (18): 2429-2439 . |
| 11 | 19370763 | 2009 | Dobrowolski, S. F., Gray, J., Miller, T., Sears, M. (2009) Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profiling Human Mutation (Online) . 30 (6): 891-898 . |
| 12 | 20053576 | 2010 | Tong, Y., Sun, Y. H., Zhou, X., Zhao, F., Mao, Y., Wei, Q. P., Yang, L., Qu, J., Guan, M. X. (2010) Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation Molecular Genetics and Metabolism . 99 (4): 417-424 . |
| 13 | 20939899 | 2010 | Palanichamy, M. G., Zhang, C. L., Mitra, B., Malyarchuk, B., Derenko, M., Chaudhuri, T. K., Zhang, Y. P. (2010) Mitochondrial haplogroup N1a phylogeography, with implication to the origin of European farmers BMC Evolutionary Biology . 10 (): 304 . |
| 14 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
| 15 | 29208909 | 2017 | Jiang, W., Li, R., Zhang, Y., Wang, P., Wu, T., Lin, J., Yu, J., Gu, M. (2017) Mitochondrial DNA mutations associated with type 2 diabetes mellitus in Chinese Uyghur population Scientific Reports . 7 (1): 16989 . |
| 16 | 31152278 | 2020 | Kytovuori, L., Junttila, J., Huikuri, H., Keinanen-Kiukaanniemi, S., Majamaa, K., Martikainen, M. H. (2020) Mitochondrial DNA variation in sudden cardiac death: a population-based study International Journal of Legal Medicine . 134 (1): 39-44 . |
| 17 | 32094358 | 2020 | Marcus, J. H., Posth, C., Ringbauer, H., Lai, L., Skeates, R., Sidore, C., Beckett, J., Furtwangler, A., Olivieri, A., Chiang, C. W. K., Al-Asadi, H., Dey, K., Joseph, T. A., Liu, C. C., Der Sarkissian, C., Radzeviciute, R., Michel, M., Gradoli, M. G., Marongiu, P., Rubino, S., Mazzarello, V., Rovina, D., La Fragola, A., Serra, R. M., Bandiera, P., Bianucci, R., Pompianu, E., Murgia, C., Guirguis, M., Orquin, R. P., Tuross, N., van Dommelen, P., Haak, W., Reich, D., Schlessinger, D., Cucca, F., Krause, J., Novembre, J. (2020) Genetic history from the Middle Neolithic to present on the Mediterranean island of Sardinia Nature Communications . 11 (1): 939 . |