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

por 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
Publicado 2005

Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)

por Mäkelä, Mira, Kaivola, Karri, Valori, Miko, Paetau, Anders, Polvikoski, Tuomo, Singleton, Andrew B., Traynor, Bryan J., Stone, David J., Peuralinna, Terhi, Tienari, Pentti J., Tanskanen, Maarit, Myllykangas, Liisa
Publicado 2018

Genome-wide association study of neocortical Lewy-related pathology

por 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
Publicado 2015

Melatonin receptor type 1A gene linked to Alzheimer’s disease in old age

por Sulkava, Sonja, Muggalla, Pranuthi, Sulkava, Raimo, Ollila, Hanna M, Peuralinna, Terhi, Myllykangas, Liisa, Kaivola, Karri, Stone, David J, Traynor, Bryan J, Renton, Alan E, Rivera, Alberto M, Helisalmi, Seppo, Soininen, Hilkka, Polvikoski, Tuomo, Hiltunen, Mikko, Tienari, Pentti J, Huttunen, Henri J, Paunio, Tiina
Publicado 2018

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

por 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
Publicado 2012

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

por Kasperavičiūtė, Dalia, Catarino, Claudia B., Heinzen, Erin L., Depondt, Chantal, Cavalleri, Gianpiero L., Caboclo, Luis O., Tate, Sarah K., Jamnadas-Khoda, Jenny, Chinthapalli, Krishna, Clayton, Lisa M.S., Shianna, Kevin V., Radtke, Rodney A., Mikati, Mohamad A., Gallentine, William B., Husain, Aatif M., Alhusaini, Saud, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Heuser, Kjell, Amos, Leslie, Ortega, Marcos, Zumsteg, Dominik, Wieser, Heinz-Gregor, Steinhoff, Bernhard J., Krämer, Günter, Hansen, Jörg, Dorn, Thomas, Kantanen, Anne-Mari, Gjerstad, Leif, Peuralinna, Terhi, Hernandez, Dena G., Eriksson, Kai J., Kälviäinen, Reetta K., Doherty, Colin P., Wood, Nicholas W., Pandolfo, Massimo, Duncan, John S., Sander, Josemir W., Delanty, Norman, Goldstein, David B., Sisodiya, Sanjay M.
Publicado 2010