Familial aggregation of Parkinson's disease in a Finnish population

od Autere, J., Moilanen, J., Myllyla, V., Majamaa, K.
Izdano 2000

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

od Hinttala, R, Smeets, R, Moilanen, J S, Ugalde, C, Uusimaa, J, Smeitink, J A M, Majamaa, K
Izdano 2006

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

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

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

od 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
Izdano 1998

Breast-Cancer Risk in Families with Mutations in PALB2

od 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.
Izdano 2014