Attrition in a 30-year follow-up of a perinatal birth risk cohort: factors change with age

by Launes, Jyrki, Hokkanen, Laura, Laasonen, Marja, Tuulio-Henriksson, Annamari, Virta, Maarit, Lipsanen, Jari, Tienari, Pentti J., Michelsson, Katarina
Published 2014

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

by Clarimon, Jordi, Xiromerisiou, Georgia, Eerola, Johanna, Gourbali, Vanesa, Hellström, Olli, Dardiotis, Euthimios, Peuralinna, Terhi, Papadimitriou, Alexandros, Hadjigeorgiou, George M, Tienari, Pentti J, Singleton, Andrew B
Published 2005

A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma

by Kero, Mia, Ferrari, Raffaele, Mok, Kin, Paetau, Anders, Tienari, Pentti J, Tynninen, Olli, Hardy, John, Momeni, Parastoo, Verkkoniemi-Ahola, Auli, Myllykangas, Liisa
Published 2013

Cerebrospinal Fluid TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis Patients with and without the C9ORF72 Hexanucleotide Expansion

by Junttila, Anna, Kuvaja, Mari, Hartikainen, Päivi, Siloaho, Maritta, Helisalmi, Seppo, Moilanen, Virpi, Kiviharju, Anna, Jansson, Lilja, Tienari, Pentti J., Remes, Anne Marja, Herukka, Sanna-Kaisa
Published 2016

The Phenotype of the C9ORF72 Expansion Carriers According to Revised Criteria for bvFTD

by Solje, Eino, Aaltokallio, Heidi, Koivumaa-Honkanen, Heli, Suhonen, Noora M., Moilanen, Virpi, Kiviharju, Anna, Traynor, Bryan, Tienari, Pentti J., Hartikainen, Päivi, Remes, Anne M.
Published 2015

PRKCA and Multiple Sclerosis: Association in Two Independent Populations

by Saarela, Janna, Kallio, Suvi P, Chen, Daniel, Montpetit, Alexandre, Jokiaho, Anne, Choi, Eva, Asselta, Rosanna, Bronnikov, Denis, Lincoln, Matthew R, Sadovnick, A. Dessa, Tienari, Pentti J, Koivisto, Keijo, Palotie, Aarno, Ebers, George C, Hudson, Thomas J, Peltonen, Leena
Published 2006

Genome-wide association study of neocortical Lewy-related pathology

by Peuralinna, Terhi, Myllykangas, Liisa, Oinas, Minna, Nalls, Mike A, Keage, Hannah A D, Isoviita, Veli-Matti, Valori, Miko, Polvikoski, Tuomo, Paetau, Anders, Sulkava, Raimo, Ince, Paul G, Zaccai, Julia, Brayne, Carol, Traynor, Bryan J, Hardy, John, Singleton, Andrew B, Tienari, Pentti J
Published 2015

The chromosome 9 ALS and FTD locus is probably derived from a single founder

by Mok, Kin, Traynor, Bryan J., Schymick, Jennifer, Tienari, Pentti J., Laaksovirta, Hannu, Peuralinna, Terhi, Myllykangas, Liisa, Chiò, Adriano, Shatunov, Aleksey, Boeve, Bradley F., Boxer, Adam L., DeJesus-Hernandez, Mariely, Mackenzie, Ian R., Waite, Adrian, Williams, Nigel, Morris, Huw R., Simón-Sánchez, Javier, van Swieten, John C., Heutink, Peter, Restagno, Gabriella, Mora, Gabriele, Morrison, Karen E., Shaw, Pamela J., Rollinson, Pamela Sara, Al-Chalabi, Ammar, Rademakers, Rosa, Pickering-Brown, Stuart, Orrell, Richard W., Nalls, Michael A., Hardy, John
Published 2012

Analysis of C9orf72 repeat expansions in a large international cohort of Dementia with Lewy Bodies

by Kun-Rodrigues, Celia, Ross, Owen A., Orme, Tatiana, Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Hernandez, Dena, Ansorge, Olaf, Clark, Lorraine N., Honig, Lawrence, Marder, Karen, Lemstra, Afina, Scheltens, Philip, Flier, Wiesje van der, Louwersheimer, Eva, Holstege, Henne, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda S., Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, C., Al-Sarraj, S., Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Trojanowski, John Q., Serrano, Geidy E., Beach, Thomas G., Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Diez, Monica, Pastor, Pau, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Bradley F., Petersen, Ronald C., Ferman, Tanis J., Escott-Price, Valentina, Graff-Radford, Neill R., Cairns, Nigel, Morris, John C., Stone, David, Pickering-Brown, Stuart, Mann, David, Dickson, Dennis W., Halliday, Glenda M., Singleton, Andrew, Guerreiro, Rita, Bras, Jose
Published 2016

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

by Majounie, Elisa, Renton, Alan E, Mok, Kin, Dopper, Elise GP, Waite, Adrian, Rollinson, Sara, Chiò, Adriano, Restagno, Gabriella, Nicolaou, Nayia, Simon-Sanchez, Javier, van Swieten, John C, Abramzon, Yevgeniya, Johnson, Janel O, Sendtner, Michael, Pamphlett, Roger, Orrell, Richard W, Mead, Simon, Sidle, Katie C, Houlden, Henry, Rohrer, Jonathan D, Morrison, Karen E, Pall, Hardev, Talbot, Kevin, Ansorge, Olaf, Hernandez, Dena G, Arepalli, Sampath, Sabatelli, Mario, Mora, Gabriele, Corbo, Massimo, Giannini, Fabio, Calvo, Andrea, Englund, Elisabet, Borghero, Giuseppe, Floris, Gian Luca, Remes, Anne M, Laaksovirta, Hannu, McCluskey, Leo, Trojanowski, John Q, Van Deerlin, Vivianna M, Schellenberg, Gerard D, Nalls, Michael A, Drory, Vivian E, Lu, Chin-Song, Yeh, Tu-Hsueh, Ishiura, Hiroyuki, Takahashi, Yuji, Tsuji, Shoji, Le Ber, Isabelle, Brice, Alexis, Drepper, Carsten, Williams, Nigel, Kirby, Janine, Shaw, Pamela, Hardy, John, Tienari, Pentti J, Heutink, Peter, Morris, Huw R, Pickering-Brown, Stuart, Traynor, Bryan J
Published 2012