Apolipoprotein E ( APOE), PARKIN and catechol- O-methyltransferase ( COMT) genes and susceptibility to sporadic Parkinson's disease in Finland von Eerola, J, Launes, J, Hellström, O, Tienari, P.J

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Multiple sclerosis in Finland: incidence trends and differences in relapsing remitting and primary progressive disease courses von Sumelahti, M-L, Tienari, P J, Hakama, M, Wikström, J

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Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis von Öckinger, J, Stridh, P, Beyeen, A D, Lundmark, F, Seddighzadeh, M, Oturai, A, Sørensen, P S, Lorentzen, Å R, Celius, E G, Leppä, V, Koivisto, K, Tienari, P J, Alfredsson, L, Padyukov, L, Hillert, J, Kockum, I, Jagodic, M, Olsson, T

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BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groups von Xiromerisiou, G., Hadjigeorgiou, G.M., Eerola, J., Fernandez, H.H., Tsimourtou, V., Mandel, R., Hellström, O., Gwinn-Hardy, K., Okun, M.S., Tienari, P.J., Singleton, A.B.

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Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene von Tienari, P.J, Sajantila, A, Peltonen, L, Tienari, P.J, Wikström, J, Palo, J

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Association of Tau Haplotype-Tagging Polymorphisms with Parkinson’s Disease in Diverse Ethnic Parkinson’s Disease Cohorts von Fung, H.C., Xiromerisiou, G., Gibbs, J.R., Wu, Y.R., Eerola, J., Gourbali, V., Hellström, O., Chen, C.M., Duckworth, J., Papadimitriou, A., Tienari, P.J., Hadjigeorgiou, G.M., Hardy, J., Singleton, A.B.

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Regional and Temporal Variation in the Incidence of Multiple Sclerosis in Finland 1979–1993 von Sumelahti, M.-L., Tienari, P.J., Wikström, J., Palo, J., Hakama, M.

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Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland von Pihlaja, H, Rantamäki, T, Wikström, J, Sumelahti, M-L, Laaksonen, M, Ilonen, J, Ruutiainen, J, Pirttilä, T, Elovaara, I, Reunanen, M, Kuokkanen, S, Peltonen, L, Koivisto, K, Tienari, P J

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Orexin-A measurement in narcolepsy: a stability study and a comparison of LC-MS/MS and immunoassays von Lindstrom, M., Schinkelshoek, M., Tienari, P.J., Kukkonen, J.P., Renkonen, R., Fronczek, R., Lammers, G.J., Itkonen, O.

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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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Chromosome 19 locus apolipoprotein C-II association with multiple sclerosis von Tienari, P J, Reunanen, K

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Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis von Johnson, J.O., Chia, R., Miller, D.E., Li, R., Kumaran, R., Abramzon, Y., Alahmady, N., Renton, A.E., Topp, S.D., Gibbs, J.R., Cookson, M.R., Sabir, M.S., Dalgard, C.L., Troakes, C., Jones, A.R., Shatunov, A., Iacoangeli, A., Khleifat, A. al, Ticozzi, N., Silani, V., Gellera, C., Blair, I.P., Dobson-Stone, C., Kwok, J.B., Bonkowski, E.S., Palvadeau, R., Tienari, P.J., Morrison, K.E., Shaw, P.J., Al-Chalabi, A., Jr, R.H.B., Calvo, A., Mora, G., Al-Saif, H., Gotkine, M., Leigh, F., Chang, I.J., Perlman, S.J., Glass, I., Scott, A.I., Shaw, C.E., Basak, A.N., Landers, J.E., Chio, A., Crawford, T.O., Smith, B.N., Traynor, B.J.

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Investigation of autosomal genetic sex differences in Parkinson's disease von Blauwendraat, C., Iwaki, H., Makarious, M.B., Bandres-Ciga, S., Leonard, H.L., Grenn, F.P., Lake, J., Krohn, L., Tan, M., Kim, J.J., Gibbs, J.R., Hernandez, D.G., Ruskey, J.A., Pihlstrom, L., Toft, M., Hilten, J.J. van, Marinus, J., Schulte, C., Brockmann, K., Sharma, M., Siitonen, A., Majamaa, K., Eerola-Rautio, J., Tienari, P.J., Grosset, D.G., Lesage, S., Corvol, J.C., Brice, A., Wood, N., Hardy, J., Gan-Or, Z., Heutink, P., Gasser, T., Morris, H.R., Noyce, A.J., Nalls, M.A., Singleton, A.B.

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Two-Locus Linkage Analysis in Multiple Sclerosis (MS) von Tienari, Pentti J., Terwilliger, Joseph D., Ott, Jürg, Palo, Jorma, Peltonen, Leena

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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia von Blauwendraat, C., Reed, X., Krohn, L., Heilbron, K., Bandres-Ciga, S., Tan, M., Gibbs, J.R., Hernandez, D.G., Kumaran, R., Langston, R., Bonet-Ponce, L., Alcalay, R.N., Hassin-Baer, S., Greenbaum, L., Iwaki, H., Leonard, H.L., Grenn, F.P., Ruskey, J.A., Sabir, M., Ahmed, S., Makarious, M.B., Pihlstrom, L., Toft, M., Hilten, J.J. van, Marinus, J., Schulte, C., Brockmann, K., Sharma, M., Siitonen, A., Majamaa, K., Eerola-Rautio, J., Tienari, P.J., Pantelyat, A., Hillis, A.E., Dawson, T.M., Rosenthal, L.S., Albert, M.S., Resnick, S.M., Ferrucci, L., Morris, C.M., Pletnikova, O., Troncoso, J., Grosset, D., Lesage, S., Corvol, J.C., Brice, A., Noyce, A.J., Masliah, E., Wood, N., Hardy, J., Shulman, L.M., Jankovic, J., Shulman, J.M., Heutink, P., Gasser, T., Cannon, P., Scholz, S.W., Morris, H., Cookson, M.R., Nalls, M.A., Gan-Or, Z., Singleton, A.B.

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1-31-24 Immune system genes in multiple sclerosis: Genetic association and linkage analyses on TCRβ, IGH, IL-1ra/IL-1β and IFN-γ loci von Tienari, P.J., Wansen, K., Pastinen, T., Kuokkanen, S., Wikström, J., Peltonen, L., Palo, J.

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Genome-wide association study of neocortical Lewy-related pathology von Peuralinna, T, Myllykangas, L, Oinas, M, Nalls, M.A, Keage, H.A, Isoviita, V.M, Valori, M, Polvikoski, T, Paetau, A, Sulkava, R, Ince, P.G, Zaccai, J, Brayne, C, Traynor, B.J, Hardy, J, Singleton, A.B, Tienari, P.J

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The amyloid hypothesis in Alzheimer's disease and its implication for therapy: A review of evidence von Beyreuther, K., Tienari, P.J., Ikonenen, E., Multhaup, G., Hartmann, T., Simons, M., Dotti, C.G., Masters, C.L.

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APOE GENOTYPE-BY-SMOKING INTERACTIONS AND EARLY ATHEROSCLEROTIC LESIONS von Viiri, L.E., Viiri, K.M., Ilveskoski, E., Huhtala, H., Tienari, P.J., Perola, M., Lehtimaki, T., Karhunen, P.J.

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