Vascular and Alzheimer Disease in Dementia

Por Strandberg, Timo E., Tienari, Pentti J., Kivimäki, Mika
Publicado no Ann Neurol (2020)

Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study

Por Kero, Mia, Raunio, Anna, Polvikoski, Tuomo, Tienari, Pentti J., Paetau, Anders, Myllykangas, Liisa
Publicado no J Alzheimers Dis (2018)

Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families

Por Mustonen, Tuuli, Schmidt, Eeva-Kaisa, Valori, Miko, Tienari, Pentti J, Atula, Sari, Kiuru-Enari, Sari
Publicado no Eur J Hum Genet (2017)

Age-related penetrance of the C9orf72 repeat expansion

Por Murphy, Natalie A., Arthur, Karissa C., Tienari, Pentti J., Houlden, Henry, Chiò, Adriano, Traynor, Bryan J.
Publicado no Sci Rep (2017)

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

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

A novel class of somatic mutations in blood detected preferentially in CD8 + cells

Por Valori, Miko, Jansson, Lilja, Kiviharju, Anna, Ellonen, Pekka, Rajala, Hanna, Awad, Shady Adnan, Mustjoki, Satu, Tienari, Pentti J.
Publicado no Clin Immunol (2017)

POLG1 polyglutamine tract variants associated with Parkinson’s disease

Por Eerola, Johanna, Luoma, Petri T., Peuralinna, Terhi, Scholz, Sonja, Paisan-Ruiz, Coro, Suomalainen, Anu, Singleton, Andrew B., Tienari, Pentti J.
Publicado em 2010

Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85+

Por Raunio, Anna, Kaivola, Karri, Tuimala, Jarno, Kero, Mia, Oinas, Minna, Polvikoski, Tuomo, Paetau, Anders, Tienari, Pentti J., Myllykangas, Liisa
Publicado no Acta Neuropathol (2019)

Intracellular and secreted Alzheimer β-amyloid species are generated by distinct mechanisms in cultured hippocampal neurons

Por Tienari, Pentti J., Ida, Nobuo, Ikonen, Elina, Simons, Mikael, Weidemann, Andreas, Multhaup, Gerd, Masters, Colin L., Dotti, Carlos G., Beyreuther, Konrad
Publicado em 1997

A follow-up study of chromosome 19q13 in multiple sclerosis susceptibility

Por Bonetti, Alessandro, Koivisto, Keijo, Pirttilä, Tuula, Elovaara, Irina, Reunanen, Mauri, Laaksonen, Mikko, Ruutiainen, Juhani, Peltonen, Leena, Rantamäki, Terhi, Tienari, Pentti J.
Publicado em 2009

A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma

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

Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis

Por Keller, Margaux F., Ferrucci, Luigi, Singleton, Andrew B., Tienari, Pentti J., Laaksovirta, Hannu, Restagno, Gabriella, Chiò, Adriano, Traynor, Bryan J., Nalls, Michael A.
Publicado no JAMA Neurol (2014)

Population‐based analysis of pathological correlates of dementia in the oldest old

Por Tanskanen, Maarit, Mäkelä, Mira, Notkola, Irma‐Leena, Myllykangas, Liisa, Rastas, Sari, Oinas, Minna, Lindsberg, Perttu J., Polvikoski, Tuomo, Tienari, Pentti J., Paetau, Anders
Publicado no Ann Clin Transl Neurol (2017)

Conflicting Results Regarding the Semaphorin Gene (SEMA5A) and the Risk for Parkinson Disease

Por Clarimon, Jordi, Scholz, Sonja, Fung, Hon-Chung, Hardy, John, Eerola, Johanna, Hellström, Olli, Chen, Chiung-Mei, Wu, Yih-Ru, Tienari, Pentti J., Singleton, Andrew
Publicado em 2006

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

Por Solje, Eino, Aaltokallio, Heidi, Koivumaa-Honkanen, Heli, Suhonen, Noora M., Moilanen, Virpi, Kiviharju, Anna, Traynor, Bryan, Tienari, Pentti J., Hartikainen, Päivi, Remes, Anne M.
Publicado no PLoS One (2015)

Generation of GFAP::GFP astrocyte reporter lines from human adult fibroblast-derived iPS cells using zinc-finger nuclease technology

Por Zhang, Ping-Wu, Haidet-Phillips, Amanda M., Pham, Jacqueline T., Lee, Youngjin, Huo, Yuqing, Tienari, Pentti J., Maragakis, Nicholas J., Sattler, Rita, Rothstein, Jeffrey D.
Publicado no Glia (2015)

Genetics of dementia in a Finnish cohort

Por Pasanen, Petra, Myllykangas, Liisa, Pöyhönen, Minna, Kiviharju, Anna, Siitonen, Maija, Hardy, John, Bras, Jose, Paetau, Anders, Tienari, Pentti J., Guerreiro, Rita, Verkkoniemi-Ahola, Auli
Publicado no Eur J Hum Genet (2018)

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 em 2005

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

Por 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
Publicado no Dement Geriatr Cogn Dis Extra (2016)

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

Por Sulonen, Anna-Maija, Kallio, Suvi P., Ellonen, Pekka, Suvela, Minna, Elovaara, Irina, Koivisto, Keijo, Pirttilä, Tuula, Reunanen, Mauri, Tienari, Pentti J., Palotie, Aarno, Peltonen, Leena, Saarela, Janna
Publicado em 2008