Phylogenetic Network for European mtDNA von Finnilä, Saara, Lehtonen, Mervi S., Majamaa, Kari

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Biochemical Signals Mediate the Crosstalk between Cartilage and Bone in Osteoarthritis von Wu, Wei, Yuan, Yu, Cao, Hong, Zhou, Xuchang

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Variations of mitochondrial DNA polymerase γ in patients with Parkinson’s disease von Ylönen, S., Ylikotila, P., Siitonen, A., Finnilä, S., Autere, J., Majamaa, K.

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Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy von REMES, A. M, FINNILÄ, S, MONONEN, H, TUOMINEN, H, TAKALO, R, HERVA, R, MAJAMAA, K

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Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population von Finnilä, S., Majamaa, K.

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Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis von Finnilä, Saara, Hassinen, Ilmo E., Ala-Kokko, Leena, Majamaa, Kari

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Variations of mitochondrial DNA polymerase [gamma] in patients with Parkinson's disease von Ylönen, S, Ylikotila, P, Siitonen, A, Finnilä, S, Autere, J, Majamaa, K

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A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL von FINNILÄ, Saara, TUISKU, Seppo, HERVA, Riitta, MAJAMAA, Kari

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Evidence for mtDNA Admixture between the Finns and the Saami von Meinilä, Maria, Finnilä, Saara, Majamaa, Kari

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Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine von Majamaa, Kari, Finnila, Saara, Turkka, Jukka, Hassinen, Ilmo E

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Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study von Reunanen, K, Finnilä, S, Laaksonen, M, Sumelahti, M.-L, Wikström, J, Pastinen, T, Kuokkanen, S, Saarela, J, Uimari, P, Ruutiainen, J, Ilonen, J, Peltonen, L, Tienari, P.J

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A two-stage study on multiple sclerosis susceptibility and chromosome 2q33 von Bonetti, A, Reunanen, K, Finnilä, S, Koivisto, K, Wikström, J, Sumelahti, M-L, Pirttilä, T, Elovaara, I, Reunanen, M, Saarela, J, Peltonen, L, Rantamäki, T, Tienari, P J

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Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat von Sajanti, Juha, Björkstrand, Ann-Sofi, Finnilä, Saara, Heikkinen, Esa, Peltonen, Juha, 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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Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln von Finnilä, Saara, Autere, Jaana, Lehtovirta, Maarit, Hartikainen, Päivi, Mannermaa, Arto, Soininen, Hilkka, Majamaa, Kari

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Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1 von Mee, Lisa, Honkala, Heli, Kopra, Outi, Vesa, Jouni, Finnilä, Saara, Visapää, Ilona, Sang, Tzu-Kang, Jackson, George R., Salonen, Riitta, Kestilä, Marjo, Peltonen, Leena

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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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Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations von FINNILÄ, S, HASSINEN, I. E, MAJAMAA, K

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A Mutation in Mitochondrial DNA-Encoded Cytochrome c Oxidase II Gene in a Child With Alpers-Huttenlocher-Like Disease von Uusimaa, Johanna, Finnila, Saara, Vainionpaa, Leena, Karppa, Mikko, Herva, Riitta, Rantala, Heikki, Hassinen, Ilmo E, Majamaa, Kari

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Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24 von Saarela, Janna, Schoenberg Fejzo, Marlena, Chen, Daniel, Finnilä, Saara, Parkkonen, Maikki, Kuokkanen, Satu, Sobel, Eric, Tienari, Pentti J., Sumelahti, Marja-Liisa, Wikström, Juhani, Elovaara, Irina, Koivisto, Keijo, Pirttilä, Tuula, Reunanen, Mauri, Palotie, Aarno, Peltonen, Leena

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