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Plos One|December 7, 2021
CD8+ cell somatic mutations in multiple sclerosis patients and controls-Enrichment of mutations in STAT3 and other genes implicated in hematological malignanciesMiko Valori, Lilja Jansson, Pentti J Tienari
Neurology. Genetics|March 17, 2022
ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the <i>C9orf72</i> Hexanucleotide Repeat ExpansionHannu Laaksovirta, Jyrki Launes, Lilja Jansson, et al.
Neurocase|December 11, 2012
Brain ¹⁸F-FDG and ¹¹C-PiB PET findings in two siblings with FTD/ALS associated with the C9ORF72 repeat expansionMika H Martikainen, Maria Gardberg, Lilja Jansson, et al.
Plos One|November 28, 2022
High prevalence of low-allele-fraction somatic mutations in STAT3 in peripheral blood CD8+ cells in multiple sclerosis patients and controlsMiko Valori, Joonas Lehikoinen, Lilja Jansson, et al.
Neurobiology of Aging|October 30, 2012
Amyloid precursor protein (APP) A673T mutation in the elderly Finnish populationMia Kero, Anders Paetau, Tuomo Polvikoski, et al.
Clinical Immunology (Orlando, Fla.)|December 10, 2016
A novel class of somatic mutations in blood detected preferentially in CD8+ cellsMiko Valori, Lilja Jansson, Anna Kiviharju, et al.
Dementia and Geriatric Cognitive Disorders|March 21, 2015
Cerebrospinal fluid biomarkers for Alzheimer's disease in patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis with the C9ORF72 repeat expansionAnna Kämäläinen, Sanna-Kaisa Herukka, Päivi Hartikainen, et al.
Clinical and Experimental Immunology|October 20, 2023
Cultured lymphocytes' mitochondrial genome integrity is not altered by cladribineElina Järvinen, Fumi Suomi, James B Stewart, et al.
Neurobiology of Aging|January 17, 2018
Heterozygous TYROBP deletion (PLOSL<sub>FIN</sub>) is not a strong risk factor for cognitive impairmentKarri Kaivola, Lilja Jansson, Elmo Saarentaus, et al.
Dementia and Geriatric Cognitive Disorders Extra|May 20, 2016
Cerebrospinal Fluid TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis Patients with and without the C9ORF72 Hexanucleotide ExpansionAnna Junttila, Mari Kuvaja, Päivi Hartikainen, et al.
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