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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Leber hereditary optic neuropathy : clinical and molecular genetic findings von HUOPONEN, Kirsi

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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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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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Nutrient intake in lysinuric protein intolerance von Tanner, L. M, Näntö-Salonen, K, Venetoklis, J, Kotilainen, S, Niinikoski, H, Huoponen, K, Simell, O

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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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Mitochondrial DNA variation in an aboriginal Australian population: evidence for genetic isolation and regional differentiation von Huoponen, K, Schurr, T G, Chen, Y, Wallace, D C

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Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA–Haplogroup Background von Hudson, Gavin, Carelli, Valerio, Spruijt, Liesbeth, Gerards, Mike, Mowbray, Catherine, Achilli, Alessandro, Pyle, Angela, Elson, Joanna, Howell, Neil, La Morgia, Chiara, Valentino, Maria Lucia, Huoponen, Kirsi, Savontaus, Marja-Liisa, Nikoskelainen, Eeva, Sadun, Alfredo A., Salomao, Solange R., Belfort, Rubens, Griffiths, Philip, Man, Patrick Yu Wai, de Coo, Rene F.M., Horvath, Rita, Zeviani, Massimo, Smeets, Hubert J.T., Torroni, Antonio, Chinnery, Patrick F.

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New methods for molecular diagnosis and demonstration of the (CCTG) n mutation in myotonic dystrophy type 2 (DM2) von Sallinen, R, Vihola, A, Bachinski, L.L, Huoponen, K, Haapasalo, H, Hackman, P, Zhang, S, Sirito, M, Kalimo, H, Meola, G, Horelli-Kuitunen, N, Wessman, M, Krahe, R, Udd, B

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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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Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder von Hudson, Gavin, Keers, Sharon, Man, Patrick Yu Wai, Griffiths, Philip, Huoponen, Kirsi, Savontaus, Marja-Liisa, Nikoskelainen, Eeva, Zeviani, Massimo, Carrara, Franco, Horvath, Rita, Karcagi, Veronika, Spruijt, Liesbeth, de Coo, I.F.M., Smeets, Hubert J.M., Chinnery, Patrick F.

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Regional differences among the Finns: A Y-chromosomal perspective von Lappalainen, Tuuli, Koivumäki, Satu, Salmela, Elina, Huoponen, Kirsi, Sistonen, Pertti, Savontaus, Marja-Liisa, Lahermo, Päivi

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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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Pre-excitation syndrome in Leber's hereditary optic neuropathy von Nikoskelainen, E.K., Savontaus, M-L., Huoponen, K., Antila, K., Hartiala, J.

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Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups von Starikovskaya, Elena B., Sukernik, Rem I., Derbeneva, Olga A., Volodko, Natalia V., Ruiz‐Pesini, Eduardo, Torroni, Antonio, Brown, Michael D., Lott, Marie T., Hosseini, Seyed H., Huoponen, Kirsi, Wallace, Douglas C.

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A Signal, from Human mtDNA, of Postglacial Recolonization in Europe von Torroni, Antonio, Bandelt, Hans-Jürgen, Macaulay, Vincent, Richards, Martin, Cruciani, Fulvio, Rengo, Chiara, Martinez-Cabrera, Vicente, Villems, Richard, Kivisild, Toomas, Metspalu, Ene, Parik, Jüri, Tolk, Helle-Viivi, Tambets, Kristiina, Forster, Peter, Karger, Bernd, Francalacci, Paolo, Rudan, Pavao, Janicijevic, Branka, Rickards, Olga, Savontaus, Marja-Liisa, Huoponen, Kirsi, Laitinen, Virpi, Koivumäki, Satu, Sykes, Bryan, Hickey, Eileen, Novelletto, Andrea, Moral, Pedro, Sellitto, Daniele, Coppa, Alfredo, Al-Zaheri, Nadia, Santachiara-Benerecetti, A. Silvana, Semino, Ornella, 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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Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions von Vuorela, Pia, Ala-Mello, Sirpa, Saloranta, Carola, Penttinen, Maila, Pöyhönen, Minna, Huoponen, Kirsi, Borozdin, Wiktor, Bausch, Birke, Botzenhart, Elke M, Wilhelm, Christian, Kääriäinen, Helena, Kohlhase, Jürgen

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mtDNA Variation in the South African Kung and Khwe—and Their Genetic Relationships to Other African Populations von Chen, Yu-Sheng, Olckers, Antonel, Schurr, Theodore G., Kogelnik, Andreas M., Huoponen, Kirsi, Wallace, Douglas C.

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