CD8+cell somatic mutations in multiple sclerosis patients and controls-Enrichment of mutations in STAT3 and other genes implicated in hematological malignancies von Valori, Miko, Jansson, Lilja, Tienari, Pentti J.

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RNA Toxicity from the ALS/FTD C9ORF72 Expansion Is Mitigated by Antisense Intervention von Donnelly, Christopher J., Zhang, Ping-Wu, Pham, Jacqueline T., Haeusler, Aaron R., Mistry, Nipun A., Vidensky, Svetlana, Daley, Elizabeth L., Poth, Erin M., Hoover, Benjamin, Fines, Daniel M., Maragakis, Nicholas, Tienari, Pentti J., Petrucelli, Leonard, Traynor, Bryan J., Wang, Jiou, Rigo, Frank, Bennett, C. Frank, Blackshaw, Seth, Sattler, Rita, Rothstein, Jeffrey D.

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A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology von Pasanen, Petra, Myllykangas, Liisa, Siitonen, Maija, Raunio, Anna, Kaakkola, Seppo, Lyytinen, Jukka, Tienari, Pentti J, Pöyhönen, Minna, Paetau, Anders

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Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85 von Raunio, Anna, Kaivola, Karri, Tuimala, Jarno, Kero, Mia, Oinas, Minna, Polvikoski, Tuomo, Paetau, Anders, Tienari, Pentti J., Myllykangas, Liisa

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Age-related penetrance of the C9orf72 repeat expansion von Murphy, Natalie A., Arthur, Karissa C., Tienari, Pentti J., Houlden, Henry, Chiò, Adriano, Traynor, Bryan J.

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The Phenotype of the C9ORF72 Expansion Carriers According to Revised Criteria for bvFTD von Solje, Eino, Aaltokallio, Heidi, Koivumaa-Honkanen, Heli, Suhonen, Noora M, Moilanen, Virpi, Kiviharju, Anna, Traynor, Bryan, Tienari, Pentti J, Hartikainen, Päivi, Remes, Anne M

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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study von Laaksovirta, Hannu, MD, Peuralinna, Terhi, MSc, Schymick, Jennifer C, PhD, Scholz, Sonja W, MD, Lai, Shaoi-Lin, MD, Myllykangas, Liisa, MD, Sulkava, Raimo, MD, Jansson, Lilja, Hernandez, Dena G, MSc, Gibbs, J Raphael, BS, Nalls, Michael A, PhD, Heckerman, David, MD, Tienari, Pentti J, MD, Traynor, Bryan J, Dr

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Vascular and Alzheimer Disease in Dementia von Strandberg, Timo E., Tienari, Pentti J., Kivimäki, Mika

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A novel class of somatic mutations in blood detected preferentially in CD8 + cells von Valori, Miko, Jansson, Lilja, Kiviharju, Anna, Ellonen, Pekka, Rajala, Hanna, Awad, Shady Adnan, Mustjoki, Satu, Tienari, Pentti J

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Response to the letter by de Boer et al. (2022) von Kaivola, Karri, Tienari, Pentti J

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Fibrinolysis associated proteins and lipopolysaccharide bioactivity in plasma and cerebrospinal fluid in multiple sclerosis von Lehikoinen, Joonas, Strandin, Tomas, Parantainen, Jukka, Nurmi, Katariina, Eklund, Kari K., Rivera, Francisco J., Vaheri, Antti, Tienari, Pentti J.

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Incidental demyelination in magnetic resonance imaging and 10‐year risk of multiple sclerosis: A data lake cohort study von Maunula, Anna, Martola, Juha, Atula, Sari, Laakso, Sini M., Tienari, Pentti J.

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Job-related exhaustion risk variant in UST is associated with dementia and DNA methylation von Sulkava, Sonja, Haukka, Jari, Kaivola, Karri, Doagu, Fatma, Lahtinen, Alexandra, Kantojärvi, Katri, Pärn, Kalle, Palta, Priit, Myllykangas, Liisa, Sulkava, Raimo, Laatikainen, Tiina, Tienari, Pentti J., Paunio, Tiina

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APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study von Kurki, Samu N., Kantonen, Jonas, Kaivola, Karri, Hokkanen, Laura, Mayranpaa, Mikko I., Puttonen, Henri, Martola, Juha, Poyhonen, Minna, Kero, Mia, Tuimala, Jarno, Carpen, Olli, Kantele, Anu, Vapalahti, Olli, Tiainen, Marjaana, Tienari, Pentti J., Kaila, Kai, Hastbacka, Johanna, Myllykangas, Liisa

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Hemophagocytic lymphohistiocytosis in 2 patients with multiple sclerosis treated with alemtuzumab von Saarela, Mika, Senthil, Keerthi, Jones, Joanne, Tienari, Pentti J, Soilu-Hänninen, Merja, Airas, Laura, Coles, Alasdair, Saarinen, Jukka T

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The shared ancestry between the C9orf72 hexanucleotide repeat expansion and intermediate-length alleles using haplotype sharing trees and HAPTK von Rautila, Osma S., Kaivola, Karri, Rautila, Harri, Hokkanen, Laura, Launes, Jyrki, Strandberg, Timo E., Laaksovirta, Hannu, Palmio, Johanna, Tienari, Pentti J.

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Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis von Keller, Margaux F, Ferrucci, Luigi, Singleton, Andrew B, Tienari, Pentti J, Laaksovirta, Hannu, Restagno, Gabriella, Chiò, Adriano, Traynor, Bryan J, Nalls, Michael A

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Finnish neuroscience from past to present von Korpi, Esa R., Lindholm, Dan, Panula, Pertti, Tienari, Pentti J., Haltia, Matti

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Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study von Chia, Ruth, Saez-Atienzar, Sara, Murphy, Natalie, Chiò, Adriano, Blauwendraat, Cornelis, Roda, Ricardo H, Tienari, Pentti J, Kaminski, Henry J, Ricciardi, Roberta, Guida, Melania, De Rosa, Anna, Petrucci, Loredana, Evoli, Amelia, Provenzano, Carlo, Drachman, Daniel B, Traynor, Bryan J

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Differential patterns of cross-reactive antibody response against SARS-CoV-2 spike protein detected for chronically ill and healthy COVID-19 naïve individuals von Jaago, Mariliis, Rähni, Annika, Pupina, Nadežda, Pihlak, Arno, Sadam, Helle, Tuvikene, Jürgen, Avarlaid, Annela, Planken, Anu, Planken, Margus, Haring, Liina, Vasar, Eero, Baćević, Miljana, Lambert, France, Kalso, Eija, Pussinen, Pirkko, Tienari, Pentti J., Vaheri, Antti, Lindholm, Dan, Timmusk, Tõnis, Ghaemmaghami, Amir M., Palm, Kaia

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