MITOMAP References for Variant G>A at 12618

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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 .