Familial aggregation of Parkinson's disease in a Finnish population

Por Autere, J., Moilanen, J., Myllyla, V., Majamaa, K.
Publicado em 2000

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency

Por Hinttala, R, Smeets, R, Moilanen, J S, Ugalde, C, Uusimaa, J, Smeitink, J A M, Majamaa, K
Publicado em 2006

Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome

Por Remes, A, Karppa, M, Rusanen, H, Majamaa, K, Hassinen, I, Moilanen, J, Uimonen, S, Sorri, M, Salmela, P, Karvonen, S, Karvonen, S
Publicado em 2003

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

Por Majamaa, K, Moilanen, J S, Uimonen, S, Remes, A M, Salmela, P I, Kärppä, M, Majamaa-Voltti, K A, Rusanen, H, Sorri, M, Peuhkurinen, K J, Hassinen, I E
Publicado em 1998

Breast-Cancer Risk in Families with Mutations in PALB2

Por Antoniou, A.C., Casadei, S., Heikkinen, T., Barrowdale, D., Pylkäs, K., Roberts, J., Lee, A., Subramanian, D., De Leeneer, K., Fostira, F., Tomiak, E., Neuhausen, S.L., Teo, Z.L., Khan, S., Aittomäki, K., Moilanen, J.S., Turnbull, C., Seal, S., Mannermaa, A., Kallioniemi, A., Lindeman, G.J., Buys, S.S., Andrulis, I.L., Radice, P., Tondini, C., Manoukian, S., Toland, A.E., Miron, P., Weitzel, J.N., Domchek, S.M., Poppe, B., Claes, K.B.M., Yannoukakos, D., Concannon, P., Bernstein, J.L., James, P.A., Easton, D.F., Goldgar, D.E., Hopper, J.L., Rahman, N., Peterlongo, P., Nevanlinna, H., King, M.-C., Couch, F.J., Southey, M.C., Winqvist, R., Foulkes, W.D., Tischkowitz, M.
Publicado em 2014