Classification of European mtDNAs From an Analysis of Three European Populations von Torroni, A, Huoponen, K, Francalacci, P, Petrozzi, M, Morelli, L, Scozzari, R, Obinu, D, Savontaus, M. L, Wallace, D. C

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Migration Waves to the Baltic Sea Region von Lappalainen, T., Laitinen, V., Salmela, E., Andersen, P., Huoponen, K., Savontaus, M.‐L., Lahermo, P.

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Population Structure in Contemporary Sweden—A Y‐Chromosomal and Mitochondrial DNA Analysis von Lappalainen, T., Hannelius, U., Salmela, E., Von Döbeln, U., Lindgren, C. M., Huoponen, K., Savontaus, M.‐L., Kere, J., Lahermo, P.

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mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe von Torroni, Antonio, Bandelt, Hans-Jürgen, D'Urbano, Leila, Lahermo, Päivi, Moral, Pedro, Sellitto, Daniele, Rengo, Chiara, Forster, Peter, Savontaus, Marja-Liisa, Bonné-Tamir, Batsheva, Scozzari, Rosaria

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Identification of SLC7A7 , encoding y + LAT-1, as the lysinuric protein intolerance gene von Estévez, Raúl, Aula, Pertti, Pineda, Marta, Savontaus, Marja-Liisa, Zorzano, Antonio, Mykkänen, Juha, Reinikainen, Arja, Simell, Olli, Torrents, David, Feliubadaló, Lidia, Sanjurjo, Pablo, Huoponen, Kirsi, Palacín, Manuel, Cid, Rafael de, Nunes, Virginia

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A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy von HUOPONEN, K, VILKKI, J, AULA, P, NIKOSKELAINEN, E. K, SAVONTAUS, M.-L

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Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy von Nikoskelainen, E K, Marttila, R J, Huoponen, K, Juvonen, V, Lamminen, T, Sonninen, P, Savontaus, M L

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Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe von Salmela, Elina, Lappalainen, Tuuli, Fransson, Ingegerd, Andersen, Peter M, Dahlman-Wright, Karin, Fiebig, Andreas, Sistonen, Pertti, Savontaus, Marja-Liisa, Schreiber, Stefan, Kere, Juha, Lahermo, Päivi

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The genetic relationship between the Finns and the Finnish Saami (lapps) : Analysis of nuclear DNA and mtDNA von LAHERMO, P, SAJANTILA, A, SISTONEN, P, LUKKA, M, AULA, P, PELTONEN, L, SAVONTAUS, M.-L

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Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion von Juvonen, Vesa, Hietala, Marja, Päivärinta, Markku, Rantamäki, Maria, Hakamies, Lauri, Kaakkola, Seppo, Vierimaa, Outi, Penttinen, Maila, Savontaus, Marja-Liisa

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Tandem repeats and length variation in the mitochondrial DNA control region of Epirrita autumnata (Lepidoptera: Geometridae) von Snäll, N, Huoponen, K, Savontaus, M -L, Ruohomäki, K

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Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes von Salmela, E, Taskinen, O, Seppänen, J K, Sistonen, P, Daly, M J, Lahermo, P, Savontaus, M-L, Kere, J

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Ophthalmologic Findings in Leber Hereditary Optic Neuropathy, with Special Reference to mtDNA Mutations von Nikoskelainen, Eeva K., Huoponen, Kirsi, Juvonen, Vesa, Lamminen, Tarja, Nummelin, Kari, Savontaus, Marja-Liisa

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An expanded CAG repeat sequence in spinocerebellar ataxia type 7 von Lindblad, K, Savontaus, M L, Stevanin, G, Holmberg, M, Digre, K, Zander, C, Ehrsson, H, David, G, Benomar, A, Nikoskelainen, E, Trottier, Y, Holmgren, G, Ptacek, L J, Anttinen, A, Brice, A, Schalling, M

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Calculating predictive values for the large repeat alleles at the SCA8 locus in patients with ataxia von Juvonen, V, Kairisto, V, Hietala, M, Savontaus, M-L

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Swedish population substructure revealed by genome-wide single nucleotide polymorphism data von Salmela, Elina, Lappalainen, Tuuli, Liu, Jianjun, Sistonen, Pertti, Andersen, Peter M, Schreiber, Stefan, Savontaus, Marja-Liisa, Czene, Kamila, Lahermo, Päivi, Hall, Per, Kere, Juha

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Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON) von Majander, Anna, Huoponen, Kirsi, Savontaus, Marja-Liisa, Nikoskelainen, Eeva, Wikstro¨m, Ma˚rten

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MULTIPLE DELETIONS OF MITOCHONDRIAL-DNA IN SEVERAL TISSUES OF A PATIENT WITH SEVERE RETARDED DEPRESSION AND FAMILIAL PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA von SUOMALAINEN, A, MAJANDER, A, HALTIA, M, SOMER, H, LONNQVIST, J, SAVONTAUS, ML, PELTONEN, L

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The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion von KOENIG, M, BEGGS, A. H, DE LA CHAPELLE, A, KIURU, A, SAVONTAUS, M.-L, GILGENKRANTZ, H, RECAN, D, CHELLY, J, KAPLAN, J.-C, COVONE, A. E, ARCHIDIACONO, N, ROMEO, G, MOYER, M, SCHERPF, S, HEINDRICH, K, BETTECKEN, T, MENG, G, MÜLLER, C. R, LINDÖF, M, KAARIAINEN, H

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Genomic landscape of positive natural selection in Northern European populations von LAPPALAINEN, Tuuli, SALMELA, Elina, ANDERSEN, Peter M, DAHLMAN-WRIGHT, Karin, SISTONEN, Pertti, SAVONTAUS, Marja-Liisa, SCHREIBER, Stefan, LAHERMO, Päivi, KERE, Juha

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