Index | PMID | Date | Reference |
---|---|---|---|
1 | 11349229 | 2001 | Finnila, S., Lehtonen, M. S., Majamaa, K. (2001) Phylogenetic network for European mtDNA American Journal of Human Genetics . 68 (6): 1475-1484 . |
2 | 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 . |
3 | 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 . |
4 | 12192017 | 2002 | Schwartz, M., Vissing, J. (2002) Paternal inheritance of mitochondrial DNA New England Journal of Medicine . 347 (8): 576-580 . |
5 | 12402350 | 2002 | Crimi, M., Sciacco, M., Galbiati, S., Bordoni, A., Malferrari, G., Del Bo, R., Biunno, I., Bresolin, N., Comi, G.P. (2002) A collection of 33 novel human mtDNA homoplasmic variants Human Mutation . 20 (5): 409 . |
6 | NA | 2003 | Silva, W. A., Jr., Bonatto, S. L., Holanda, A. J., Ribeiro-Dos-Santos, A. K., Paixao, B. M., Goldman, G. H., Abe-Sandes, K., Rodriguez-Delfin, L., Barbosa, M., Paco-Larson, M. L., Petzl-Erler, M. L., Valente, V., Santos, S. E., Zago, M. A. (2003) Correction: mitochondrial DNA variation in Amerindians American Journal of Human Genetics . 72 (5): 1346-1348; in response to 1341-1346; further reply 1348-1349 . |
7 | 12802679 | 2003 | Lehtonen, M. S., Moilanen, J. S., Majamaa, K. (2003) Increased variation in mtDNA in patients with familial sensorineural hearing impairment Human Genetics . 113 (3): 220-227 . |
8 | 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 . |
9 | 16773565 | 2006 | Saxena, R., de Bakker, P. I., Singer, K., Mootha, V., Burtt, N., Hirschhorn, J. N., Gaudet, D., Isomaa, B., Daly, M. J., Groop, L., Ardlie, K. G., Altshuler, D. (2006) Comprehensive association testing of common mitochondrial DNA variation in metabolic disease American Journal of Human Genetics . 79 (1): 54-61 . |
10 | 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 . |
11 | 18477584 | 2008 | Malyarchuk, B., Grzybowski, T., Derenko, M., Perkova, M., Vanecek, T., Lazur, J., Gomolcak, P., Tsybovsky, I. (2008) Mitochondrial DNA phylogeny in Eastern and Western Slavs Molecular Biology and Evolution . 25 (8): 1651-1658 . |
12 | 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 . |
13 | 20003445 | 2009 | Ricaut, F. X., Razafindrazaka, H., Cox, M. P., Dugoujon, J. M., Guitard, E., Sambo, C., Mormina, M., Mirazon-Lahr, M., Ludes, B., Crubezy, E. (2009) A new deep branch of eurasian mtDNA macrohaplogroup M reveals additional complexity regarding the settlement of Madagascar BMC Genomics . 10 (): 605 . |
14 | 22333566 | 2012 | Bodner, M., Perego, U. A., Huber, G., Fendt, L., Rock, A. W., Zimmermann, B., Olivieri, A., Gomez-Carballa, A., Lancioni, H., Angerhofer, N., Bobillo, M. C., Corach, D., Woodward, S. R., Salas, A., Achilli, A., Torroni, A., Bandelt, H. J., Parson, W. (2012) Rapid coastal spread of First Americans: novel insights from South America's Southern Cone mitochondrial genomes Genome Research . 22 (5): 811-820 . |
15 | NA | 2014 | van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb . |
16 | 24467713 | 2014 | Summerer, M., Horst, J., Erhart, G., Weissensteiner, H., Schonherr, S., Pacher, D., Forer, L., Horst, D., Manhart, A., Horst, B., Sanguansermsri, T., Kloss-Brandstatter, A. (2014) Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar BMC Evolutionary Biology . 14 (): 184-192 . |
17 | 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 . |