The co‐occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific von Raule, Nicola, Sevini, Federica, Li, Shengting, Barbieri, Annalaura, Tallaro, Federica, Lomartire, Laura, Vianello, Dario, Montesanto, Alberto, Moilanen, Jukka S., Bezrukov, Vladyslav, Blanché, Hélène, Hervonen, Antti, Christensen, Kaare, Deiana, Luca, Gonos, Efstathios S., Kirkwood, Tom B. L., Kristensen, Peter, Leon, Alberta, Pelicci, Pier Giuseppe, Poulain, Michel, Rea, Irene M., Remacle, Josè, Robine, Jean Marie, Schreiber, Stefan, Sikora, Ewa, Eline Slagboom, Peternella, Spazzafumo, Liana, Antonietta Stazi, Maria, Toussaint, Olivier, Vaupel, James W., Rose, Giuseppina, Majamaa, Kari, Perola, Markus, Johnson, Thomas E., Bolund, Lars, Yang, Huanming, Passarino, Giuseppe, Franceschi, Claudio

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A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron loss von Paakkola, T., Vuopala, K., Kokkonen, H., Ignatius, J., Valkama, M., Moilanen, J.S., Fahiminiya, S., Majewski, J., Hinttala, R., Uusimaa, J.

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Identification of C12orf4 as a gene for autosomal recessive intellectual disability von Philips, A.K., Pinelli, M., de Bie, C.I., Mustonen, A., Määttä, T., Arts, H.H., Wu, K., Roepman, R., Moilanen, J.S., Raza, S., Varilo, T., Scala, G., Cocozza, S., Gilissen, C., van Gassen, K.L.I., Järvelä, I.

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Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation von von Salomé, Jenny, Liu, Tao, Keihäs, Markku, Morak, Moni, Holinski-Feder, Elke, Berry, Ian R., Moilanen, Jukka S., Baert-Desurmont, Stéphanie, Lindblom, Annika, Lagerstedt-Robinson, Kristina

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A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects von Niemi, Anna-Kaisa, Moilanen, Jukka S, Tanaka, Masashi, Hervonen, Antti, Hurme, Mikko, Lehtimäki, Terho, Arai, Yasumichi, Hirose, Nobuyoshi, Majamaa, Kari

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Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia von AUTERE, Jaana, MOILANEN, Jukka S, FINNILÄ, Saara, SOININEN, Hilkka, MANNERMAA, Arto, HARTIKAINEN, Päivi, HALLIKAINEN, Merja, MAJAMAA, Kari

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Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNA von Moilanen, Jukka S, Majamaa, Kari

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Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population von Majamaa, Kari, Moilanen, Jukka S., Uimonen, Seija, Remes, Anne M., Salmela, Pasi I., Kärppä, Mikko, Majamaa-Voltti, Kirsi A.M., Rusanen, Harri, Sorri, Martti, Peuhkurinen, Keijo J., Hassinen, Ilmo E.

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Haplotype analysis suggest that the MLH1 c.2059C>T mutation is a Swedish founder mutation von von, Salome J, Liu, T, Keihas, M, Morak, M, Holinski-Feder, E, Berry, IR, Moilanen, JS, Baert-Desurmont, S, Lindblom, A, Lagerstedt-Robinson, K

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Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J von Moilanen, Jukka S, Finnila, Saara, Majamaa, Kari

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Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population von REMES, A. M, MAJAMAA-VOLTTI, K, MAJAMAA, K, KÄRPPÄ, M, MOILANEN, J. S, UIMONEN, S, HELANDER, H, RUSANEN, H, SALMELA, P. I, SORRI, M, HASSINEN, I. E

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Increased variation in mtDNA in patients with familial sensorineural hearing impairment von LEHTONEN, Mervi S, MOILANEN, Jukka S, MAJAMAA, Kari

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Sequence variation in the tRNA genes of human mitochondrial DNA von Vilmi, Tiina, Moilanen, Jukka S, Finnilä, Saara, Majamaa, Kari

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Familial aggregation of Parkinson's disease in a Finnish population von Autere, Jaana M, Moilanen, Jukka S, Myllylä, Vilho V, Majamaa, Kari

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Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome von Remes, A M, Kärppä, M, Rusanen, H, Majamaa, K, Hassinen, I E, Moilanen, J S, Uimonen, S, Sorri, M, Salmela, P I, Karvonen, S-L, Karvonen, S-L

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Hearing impairment in patients with 3243A→G mtDNA mutation : phenotype and rate of progression von UIMONEN, Seija, MOILANEN, Jukka S, SORRI, Martti, HASSINEN, Ilmo E, MAJAMAA, Kari

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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL von ANNUNEN-RASILA, Johanna, FINNILÄ, Saara, MYKKÄNEN, Kati, MOILANEN, Jukka S, VEIJOLA, Johanna, PÖYHÖNEN, Minna, VIITANEN, Matti, KALIMO, Hannu, MAJAMAA, Kari

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Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G von Moilanen, J S, Majamaa, K

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Complex segregation analysis of Parkinson's disease in the Finnish population von MOILANEN, J. S, AUTERE, J. M, MYLLYLÄ, V. V, MAJAMAA, K

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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL von Annunen-Rasila, Johanna, Finnilä, Saara, Mykkänen, Kati, Moilanen, Jukka S., Veijola, Johanna, Pöyhönen, Minna, Viitanen, Matti, Kalimo, Hannu, Majamaa, Kari

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