Mika Martikainen
M.D., Ph.D., Professor of Neurology
mikmar@utu.fi Follow my tweets @mhmartikainen ORCID identifier: https://orcid.org/0000-0002-7604-8081 |
Mitochondrial disease; movement disorders; neurogenetics; clinical neurology
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 Refereed review article in a scientific journal ) - 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 Refereed original research article in a scientific journal) - Aivo-selkäydinnesteen ja veren merkkiaineet yhä tärkeämpiä Alzheimer-diagnostiikassa (2025)
- Lääkärilehti
(A2 Refereed review article in a scientific journal ) - Clinical features and treatment of stroke-like episodes in mitochondrial disease: a cohort-based study (2025)
- Journal of Neurology
(A1 Refereed original research article in a scientific journal) - Huntingtonin tauti : diagnostinen polku geenitutkimuksesta perinnöllisyysneuvontaan (2025)
- Duodecim
(A1 Refereed original research article in a scientific journal) - Liver Involvement in POLG Disease-a Multicentre Cohort Study of 202 Patients (2025)
- Journal of Inherited Metabolic Disease
(A1 Refereed original research article in a scientific journal) - Obstetric history of women with m.3243A>G: an observational cohort study (2025)
- Journal of Medical Genetics
(A1 Refereed original research article in a scientific journal) - Widespread and progressive brain atrophy is a common feature in patients with mitochondrial disease (2025)
- Journal of Neurology
(A1 Refereed original research article in a scientific journal) - Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009-2022: an observational, population-based study (2024)
- BMJ neurology open
(A1 Refereed original research article in a scientific journal) - Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2 (2024)
- Case Reports in Neurological Medicine
(A1 Refereed original research article in a scientific journal) - Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort (2023)
- Movement Disorders
(A1 Refereed original research article in a scientific journal) - Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project (2023)
- PLoS ONE
(A1 Refereed original research article in a scientific journal) - Perheessä Parkinson: omaisen kuormitus sairauden eri vaiheissa (2023)
- Gerontologia
(B1 Non-refereed article in a scientific journal) - CANVAS - tasapainovaikeuksien ja kroonisen yskän mahdollinen aiheuttaja (2022)
- Duodecim
(D1 Article in a professional journal) - Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report (2022)
- BMC Neurology
(A1 Refereed original research article in a scientific journal) - Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease (2022)
- Annals of Neurology
(B1 Non-refereed article in a scientific journal) - Validation of the Finnish Version of the Unified Dyskinesia Rating Scale (2021)
- European Neurology
(A1 Refereed original research article in a scientific journal) - Deep brain stimulation for monogenic Parkinson’s disease: a systematic review (2020)
- Journal of Neurology
(A2 Refereed review article in a scientific journal ) - Mitochondrial DNA variation in sudden cardiac death: a population-based study (2020)
- International Journal of Legal Medicine
(A1 Refereed original research article in a scientific journal) - Consensus-based statements for the management of mitochondrial stroke-like episodes (2019)
- Wellcome Open Research
(A1 Refereed original research article in a scientific journal)



