Response to the letter by de Boer et al. (2022)

por Kaivola, Karri, Tienari, Pentti J.
Publicado 2022

CD8+ cell somatic mutations in multiple sclerosis patients and controls—Enrichment of mutations in STAT3 and other genes implicated in hematological malignancies

por Valori, Miko, Jansson, Lilja, Tienari, Pentti J.
Publicado 2021

Vascular and Alzheimer Disease in Dementia

por Strandberg, Timo E., Tienari, Pentti J., Kivimäki, Mika
Publicado 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 2018

ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the C9orf72 Hexanucleotide Repeat Expansion

por Laaksovirta, Hannu, Launes, Jyrki, Jansson, Lilja, Traynor, Bryan J., Kaivola, Karri, Tienari, Pentti J.
Publicado 2022

High prevalence of low-allele-fraction somatic mutations in STAT3 in peripheral blood CD8+ cells in multiple sclerosis patients and controls

por Valori, Miko, Lehikoinen, Joonas, Jansson, Lilja, Clancy, Jonna, Lundgren, Sofie A., Mustjoki, Satu, Tienari, Pentti
Publicado 2022

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 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 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 2017

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 2019

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 2013

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 2017

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 2015

Identification of two highly antigenic epitope markers predicting multiple sclerosis in optic neuritis patients

por Sadam, Helle, Pihlak, Arno, Jaago, Mariliis, Pupina, Nadežda, Rähni, Annika, Toots, Maarja, Vaheri, Antti, Nieminen, Janne K., Siuko, Mika, Tienari, Pentti J., Palm, Kaia
Publicado 2021

Alpha-synuclein pathology of olfactory bulbs/peduncles in the Vantaa85+ cohort exhibit two divergent patterns: a population-based study

por Kok, Eloise H., Savola, Sara, Raunio, Anna, Oinas, Minna, Tuimala, Jarno, Polvikoski, Tuomo, Kero, Mia, Kaivola, Karri, Tienari, Pentti J., Paetau, Anders, Myllykangas, Liisa
Publicado 2021

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

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 2016

C9orf72 hexanucleotide repeat allele tagging SNPs: Associations with ALS risk and longevity

por Kaivola, Karri, Pirinen, Matti, Laaksovirta, Hannu, Jansson, Lilja, Rautila, Osma, Launes, Jyrki, Hokkanen, Laura, Lahti, Jari, Eriksson, Johan G., Strandberg, Timo E., FinnGen, Tienari, Pentti J.
Publicado 2023

Primary age‐related tauopathy in a Finnish population‐based study of the oldest old (Vantaa 85+)

por Savola, Sara, Kaivola, Karri, Raunio, Anna, Kero, Mia, Mäkelä, Mira, Pärn, Kalle, Palta, Priit, Tanskanen, Maarit, Tuimala, Jarno, Polvikoski, Tuomo, Tienari, Pentti J., Paetau, Anders, Myllykangas, Liisa
Publicado 2022

Distribution of Lewy-related pathology in the brain, spinal cord, and periphery: the population-based Vantaa 85 + study

por Raunio, Anna, Kivistö, Ville, Kero, Mia, Tuimala, Jarno, Savola, Sara, Oinas, Minna, Kok, Eloise, Colangelo, Kia, Paetau, Anders, Polvikoski, Tuomo, Tienari, Pentti J., Puttonen, Henri, Myllykangas, Liisa
Publicado 2022