Mika Martikainen
M.D., Ph.D., Professor of Neurology
mikmar@utu.fi Follow my tweets @mhmartikainen ORCID-tunniste: https://orcid.org/0000-0002-7604-8081 |
Mitokondriotaudit; liikehäiriösairaudet; perinnölliset neurologiset sairaudet; kliininen neurologia
My research team is part of the Turku Centre for Lifespan Research at the University of Turku.
Professor of neurology at the University of Oulu (since February 2023). Adjunct professor (docent) of neurology at the University of Turku since 2014. Associate Professor of neurology at University of Turku from September 2021 to January 2023. Post doc (Sigrid Jusélius Fellowship) at Wellcome Centre for Mitochondrial Research, Newcastle University, Newcastle-upon-Tyne, UK, in 2014-2015. Ph.D. (neurology) 2012. Medical specialist (neurology) 2009. M.D. 2002. Medical education and specialist training at the University of Turku, Finland. Erasmus Fellowship studies at the Trinity College, Dublin, Ireland, in 2001.
Our research interests are focussed on the clinical, genetic, and epidemiological aspects of human mitochondrial disease. We are also involved in movement disorder neurology research, particularly in the context of inherited neurological disease (e.g. monogenic Parkinson's disease). Part of the MJFF Global Genetic Parkinson's Disease Study Group; part of DystoniaNet Europe. Collaboration with researchers at University of Helsinki (FIN), Newcastle University (UK), University of Groningen (NED), University of Lübeck (GER).
Interest in Medical Education. Experience as a clinical teacher (neurology) since 2015. Special competence in Medical Education (Finnish Medical Association). Medical education studies at the University of Turku, Karolinska Institute (Sweden), ACGME (USA). National coordinator of postgraduate medical education development in Finland, 2018 - 2021.
- Associations between the brain glymphatic system and mitochondrial (dys)function: a systematic review (2026)
- Frontiers in Neuroscience
(A2 Vertaisarvioitu katsausartikkeli tieteellisessä lehdessä) - Next-Generation Genetic Testing in the Diagnostics of Neurological Disease in Southwest Finland in 2010-2021: A Register-Based Study (2026)
- Acta Neurologica Scandinavica
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Prevalence and treatment of mitochondrial diabetes in Southwest Finland (2026)
- Journal of diabetes and metabolic disorders
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Progressive White Matter Changes in Mitochondrial Disease: A Quantitative MRI Study (2026)
- JIMD Reports
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Aivo-selkäydinnesteen ja veren merkkiaineet yhä tärkeämpiä Alzheimer-diagnostiikassa (2025)
- Lääkärilehti
(A2 Vertaisarvioitu katsausartikkeli tieteellisessä lehdessä) - Clinical features and treatment of stroke-like episodes in mitochondrial disease: a cohort-based study (2025)
- Journal of Neurology
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Huntingtonin tauti : diagnostinen polku geenitutkimuksesta perinnöllisyysneuvontaan (2025)
- Duodecim
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Liver Involvement in POLG Disease-a Multicentre Cohort Study of 202 Patients (2025)
- Journal of Inherited Metabolic Disease
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Obstetric history of women with m.3243A>G: an observational cohort study (2025)
- Journal of Medical Genetics
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Widespread and progressive brain atrophy is a common feature in patients with mitochondrial disease (2025)
- Journal of Neurology
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )



